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Record Information

Version

5.0

Status

Expected but not Quantified

Creation Date

2005-11-16 15:48:42 UTC

Update Date

2022-03-07 02:49:09 UTC

HMDB ID

HMDB0001376

Secondary Accession Numbers

HMDB01376

Metabolite Identification

Common Name

2-Keto-3-deoxy-6-phosphogluconic acid

Description

2-Keto-3-deoxy-6-phosphogluconic acid, also known as 2-dehydro-3-deoxy-D-gluconate 6-phosphate or 6-phospho-2-dehydro-3-deoxy-D-gluconate, belongs to the class of organic compounds known as medium-chain keto acids and derivatives. These are keto acids with a 6 to 12 carbon atoms long side chain. 2-Keto-3-deoxy-6-phosphogluconic acid exists in all living organisms, ranging from bacteria to humans. 2-Keto-3-deoxy-6-phosphogluconic acid has been detected, but not quantified in, a few different foods, such as anatidaes (Anatidae), chickens (Gallus gallus), and domestic pigs (Sus scrofa domestica). This could make 2-keto-3-deoxy-6-phosphogluconic acid a potential biomarker for the consumption of these foods. 2-Keto-3-deoxy-6-phosphogluconic acid is a primary metabolite. Primary metabolites are metabolically or physiologically essential metabolites. They are directly involved in an organism’s growth, development or reproduction. Based on a literature review a small amount of articles have been published on 2-Keto-3-deoxy-6-phosphogluconic acid.

Structure

MOL 3D MOL SDF 3D SDF PDB 3D PDB SMILES InChI


  Mrv0541 02231219062D          

 16 15  0  0  1  0            999 V2000
   12.2997  -17.4671    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.0167  -17.0532    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.0167  -16.2282    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   13.7312  -17.4657    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   14.4456  -17.0532    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   14.4456  -16.2282    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   15.1601  -17.4657    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   15.1601  -18.2907    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   15.8746  -17.0532    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   16.5891  -17.4657    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   17.3036  -17.0532    0.0000 P   0  0  0  0  0  0  0  0  0  0  0  0
   17.3036  -16.2282    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   18.0180  -17.4657    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   18.0180  -16.6407    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   12.2997  -18.2921    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   11.5853  -17.0546    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  2  0  0  0  0
  2  4  1  0  0  0  0
  4  5  1  0  0  0  0
  5  6  1  6  0  0  0
  5  7  1  0  0  0  0
  7  8  1  1  0  0  0
  7  9  1  0  0  0  0
  9 10  1  0  0  0  0
 10 11  1  0  0  0  0
 11 12  1  0  0  0  0
 11 13  1  0  0  0  0
 11 14  2  0  0  0  0
  1 15  2  0  0  0  0
  1 16  1  0  0  0  0
M  END
> <DATABASE_ID>
HMDB0001376

> <DATABASE_NAME>
hmdb

> <SMILES>
O[C@H](COP(O)(O)=O)[C@@H](O)CC(=O)C(O)=O

> <INCHI_IDENTIFIER>
InChI=1S/C6H11O9P/c7-3(1-4(8)6(10)11)5(9)2-15-16(12,13)14/h3,5,7,9H,1-2H2,(H,10,11)(H2,12,13,14)/t3-,5+/m0/s1

> <INCHI_KEY>
OVPRPPOVAXRCED-WVZVXSGGSA-N

> <FORMULA>
C6H11O9P

> <MOLECULAR_WEIGHT>
258.1199

> <EXACT_MASS>
258.014068462

> <JCHEM_ACCEPTOR_COUNT>
8

> <JCHEM_AVERAGE_POLARIZABILITY>
20.166331383317747

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
5

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(4S,5R)-4,5-dihydroxy-2-oxo-6-(phosphonooxy)hexanoic acid

> <ALOGPS_LOGP>
-2.36

> <JCHEM_LOGP>
-1.8985972716666666

> <ALOGPS_LOGS>
-1.26

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
0

> <JCHEM_PHYSIOLOGICAL_CHARGE>
-3

> <JCHEM_PKA>
2.98091974057207

> <JCHEM_PKA_STRONGEST_ACIDIC>
1.479791419702818

> <JCHEM_PKA_STRONGEST_BASIC>
-3.266803065880614

> <JCHEM_POLAR_SURFACE_AREA>
161.59

> <JCHEM_REFRACTIVITY>
47.1892

> <JCHEM_ROTATABLE_BOND_COUNT>
7

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
1.43e+01 g/l

> <JCHEM_TRADITIONAL_IUPAC>
kdpg intermediate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 23-FEB-12   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   23-FEB-12         0                                  
HETATM    1  C   UNK     0      22.959 -32.605   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      24.298 -31.833   0.000  0.00  0.00           C+0
HETATM    3  O   UNK     0      24.298 -30.293   0.000  0.00  0.00           O+0
HETATM    4  C   UNK     0      25.632 -32.603   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      26.965 -31.833   0.000  0.00  0.00           C+0
HETATM    6  O   UNK     0      26.965 -30.293   0.000  0.00  0.00           O+0
HETATM    7  C   UNK     0      28.299 -32.603   0.000  0.00  0.00           C+0
HETATM    8  O   UNK     0      28.299 -34.143   0.000  0.00  0.00           O+0
HETATM    9  C   UNK     0      29.633 -31.833   0.000  0.00  0.00           C+0
HETATM   10  O   UNK     0      30.966 -32.603   0.000  0.00  0.00           O+0
HETATM   11  P   UNK     0      32.300 -31.833   0.000  0.00  0.00           P+0
HETATM   12  O   UNK     0      32.300 -30.293   0.000  0.00  0.00           O+0
HETATM   13  O   UNK     0      33.634 -32.603   0.000  0.00  0.00           O+0
HETATM   14  O   UNK     0      33.634 -31.063   0.000  0.00  0.00           O+0
HETATM   15  O   UNK     0      22.959 -34.145   0.000  0.00  0.00           O+0
HETATM   16  O   UNK     0      21.626 -31.835   0.000  0.00  0.00           O+0
CONECT    1    2   15   16                                                  
CONECT    2    1    3    4                                                  
CONECT    3    2                                                            
CONECT    4    2    5                                                       
CONECT    5    4    6    7                                                  
CONECT    6    5                                                            
CONECT    7    5    8    9                                                  
CONECT    8    7                                                            
CONECT    9    7   10                                                       
CONECT   10    9   11                                                       
CONECT   11   10   12   13   14                                             
CONECT   12   11                                                            
CONECT   13   11                                                            
CONECT   14   11                                                            
CONECT   15    1                                                            
CONECT   16    1                                                            
MASTER        0    0    0    0    0    0    0    0   16    0   30    0
END

COMPND    HMDB0001376
HETATM    1  O1  UNL     1       3.173   1.903   0.490  1.00  0.00           O  
HETATM    2  C1  UNL     1       3.572   0.743   0.279  1.00  0.00           C  
HETATM    3  O2  UNL     1       4.699   0.290   1.028  1.00  0.00           O  
HETATM    4  C2  UNL     1       3.015  -0.213  -0.649  1.00  0.00           C  
HETATM    5  O3  UNL     1       3.532  -1.333  -0.735  1.00  0.00           O  
HETATM    6  C3  UNL     1       1.860   0.164  -1.455  1.00  0.00           C  
HETATM    7  C4  UNL     1       0.560   0.213  -0.751  1.00  0.00           C  
HETATM    8  O4  UNL     1       0.649   1.170   0.299  1.00  0.00           O  
HETATM    9  C5  UNL     1       0.135  -1.057  -0.073  1.00  0.00           C  
HETATM   10  O5  UNL     1      -0.016  -2.049  -1.030  1.00  0.00           O  
HETATM   11  C6  UNL     1      -1.132  -0.845   0.728  1.00  0.00           C  
HETATM   12  O6  UNL     1      -2.206  -0.466  -0.061  1.00  0.00           O  
HETATM   13  P1  UNL     1      -3.592  -0.222   0.870  1.00  0.00           P  
HETATM   14  O7  UNL     1      -3.424  -0.671   2.286  1.00  0.00           O  
HETATM   15  O8  UNL     1      -4.890  -0.957   0.082  1.00  0.00           O  
HETATM   16  O9  UNL     1      -3.832   1.472   0.933  1.00  0.00           O  
HETATM   17  H1  UNL     1       5.619   0.282   0.633  1.00  0.00           H  
HETATM   18  H2  UNL     1       1.991   1.165  -1.961  1.00  0.00           H  
HETATM   19  H3  UNL     1       1.808  -0.545  -2.335  1.00  0.00           H  
HETATM   20  H4  UNL     1      -0.207   0.610  -1.434  1.00  0.00           H  
HETATM   21  H5  UNL     1       0.494   2.080  -0.071  1.00  0.00           H  
HETATM   22  H6  UNL     1       0.884  -1.439   0.646  1.00  0.00           H  
HETATM   23  H7  UNL     1      -0.826  -1.978  -1.556  1.00  0.00           H  
HETATM   24  H8  UNL     1      -1.428  -1.725   1.298  1.00  0.00           H  
HETATM   25  H9  UNL     1      -0.925  -0.019   1.463  1.00  0.00           H  
HETATM   26  H10 UNL     1      -5.157  -0.343  -0.666  1.00  0.00           H  
HETATM   27  H11 UNL     1      -4.354   1.659   1.741  1.00  0.00           H  
CONECT    1    2    2
CONECT    2    3    4
CONECT    3   17
CONECT    4    5    5    6
CONECT    6    7   18   19
CONECT    7    8    9   20
CONECT    8   21
CONECT    9   10   11   22
CONECT   10   23
CONECT   11   12   24   25
CONECT   12   13
CONECT   13   14   14   15   16
CONECT   15   26
CONECT   16   27
END

View in JSmol View NMR Assignments View Stereo Labels

Synonyms

Value	Source
2-Dehydro-3-deoxy-6-phospho-D-gluconate	ChEBI
2-Dehydro-3-deoxy-D-gluconate 6-phosphate	ChEBI
2-Keto-3-deoxy-6-phosphogluconate	ChEBI
3-Deoxy-D-erythro-hex-2-ulosonic acid 6-phosphate	ChEBI
6-Phospho-2-dehydro-3-deoxy-D-gluconate	ChEBI
KDPG Intermediate	ChEBI
2-Dehydro-3-deoxy-6-phospho-D-gluconic acid	Generator
2-Dehydro-3-deoxy-D-gluconic acid 6-phosphoric acid	Generator
3-Deoxy-D-erythro-hex-2-ulosonate 6-phosphate	Generator
3-Deoxy-D-erythro-hex-2-ulosonic acid 6-phosphoric acid	Generator
6-Phospho-2-dehydro-3-deoxy-D-gluconic acid	Generator
KDPG Intermediic acid	Generator
2-dehydro-3-Deoxy-D-gluconate-6-phosphate	HMDB
2-keto-3-Deoxy-6-P-gluconate	HMDB
2-keto-3-Deoxy-6-phospho-gluconate	HMDB
2-keto-3-Deoxygluconate-6-P	HMDB
6-P-2-K-3-deo-Gluconate	HMDB
6-phospho-2-dehydro-3-Deoxygluconate	HMDB
6-phospho-2-keto-3-Deoxygluconate	HMDB

Chemical Formula

C₆H₁₁O₉P

Average Molecular Weight

258.1199

Monoisotopic Molecular Weight

258.014068462

IUPAC Name

(4S,5R)-4,5-dihydroxy-2-oxo-6-(phosphonooxy)hexanoic acid

Traditional Name

kdpg intermediate

CAS Registry Number

27244-54-8

SMILES

O[C@H](COP(O)(O)=O)[C@@H](O)CC(=O)C(O)=O

InChI Identifier

InChI=1S/C6H11O9P/c7-3(1-4(8)6(10)11)5(9)2-15-16(12,13)14/h3,5,7,9H,1-2H2,(H,10,11)(H2,12,13,14)/t3-,5+/m0/s1

InChI Key

OVPRPPOVAXRCED-WVZVXSGGSA-N

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as medium-chain keto acids and derivatives. These are keto acids with a 6 to 12 carbon atoms long side chain.

Kingdom

Organic compounds

Super Class

Organic acids and derivatives

Class

Keto acids and derivatives

Sub Class

Medium-chain keto acids and derivatives

Direct Parent

Medium-chain keto acids and derivatives

Alternative Parents

Substituents

Medium-chain keto acid
Monoalkyl phosphate
Alpha-keto acid
Beta-hydroxy ketone
Organic phosphoric acid derivative
Phosphoric acid ester
Alkyl phosphate
Alpha-hydroxy ketone
Ketone
1,2-diol
Secondary alcohol
Monocarboxylic acid or derivatives
Carboxylic acid
Carboxylic acid derivative
Organooxygen compound
Organic oxygen compound
Carbonyl group
Alcohol
Organic oxide
Hydrocarbon derivative
Aliphatic acyclic compound

Molecular Framework

Aliphatic acyclic compounds

External Descriptors

ketoaldonic acid phosphate (CHEBI:15925 )

Ontology

Not Available

Endogenous (HMDB: HMDB0001376)

Microbe

Microbe (HMDB: HMDB0001376)
Clostridium (HMDB: HMDB0001376)
Achromobacter (HMDB: HMDB0001376)
Alcaligenes (HMDB: HMDB0001376)
Rlzodopseudomonas spheroides (HMDB: HMDB0001376)

Exogenous

Exogenous (HMDB: HMDB0001376)

Food

Animal origin

Poultry

Pheasant (FooDB: FOOD00430)
Squab (FooDB: FOOD00481)
Turkey (FooDB: FOOD00494)
Quail (FooDB: FOOD00541)
Anatidae (FooDB: FOOD00576)
Rock ptarmigan (FooDB: FOOD00597)
Columbidae (Dove, Pigeon) (FooDB: FOOD00610)
Chicken (FooDB: FOOD00329)
Mallard duck (FooDB: FOOD00353)
Emu (FooDB: FOOD00360)
Greylag goose (FooDB: FOOD00368)
Guinea hen (FooDB: FOOD00373)
Ostrich (FooDB: FOOD00422)
Velvet duck (FooDB: FOOD00427)

Lagomorph

Ovis

Sheep (Mutton, Lamb) (FooDB: FOOD00473)

Bovine

Venison

Deer (FooDB: FOOD00524)
Mule deer (FooDB: FOOD00348)
Elk (FooDB: FOOD00359)

Caprae

Domestic goat (FooDB: FOOD00529)

Swine

Domestic pig (FooDB: FOOD00536)
Wild boar (FooDB: FOOD00307)

Equine

Horse (FooDB: FOOD00378)

Process

Naturally occurring process

Biological process

Biochemical pathway

Metabolic pathway

Ketogluconate Metabolism (PathBank: SMP0122204)
Hexuronide and Hexuronate Degradation (PathBank: SMP0000854)

Role

Not Available

Physical Properties

State

Solid

Experimental Molecular Properties

Property	Value	Reference
Melting Point	Not Available	Not Available
Boiling Point	Not Available	Not Available
Water Solubility	Not Available	Not Available
LogP	Not Available	Not Available

Experimental Chromatographic Properties

Experimental Collision Cross Sections

Adduct Type	Data Source	CCS Value (Å²)	Reference
[M-H]-	Not Available	144.133	http://allccs.zhulab.cn/database/detail?ID=AllCCS00001773

Predicted Molecular Properties

Property	Value	Source
Water Solubility	14.3 g/L	ALOGPS
logP	-2.4	ALOGPS
logP	-1.9	ChemAxon
logS	-1.3	ALOGPS
pKa (Strongest Acidic)	1.48	ChemAxon
pKa (Strongest Basic)	-3.3	ChemAxon
Physiological Charge	-3	ChemAxon
Hydrogen Acceptor Count	8	ChemAxon
Hydrogen Donor Count	5	ChemAxon
Polar Surface Area	161.59 Å²	ChemAxon
Rotatable Bond Count	7	ChemAxon
Refractivity	47.19 m³·mol⁻¹	ChemAxon
Polarizability	20.17 Å³	ChemAxon
Number of Rings	0	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	Yes	ChemAxon
Ghose Filter	No	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	No	ChemAxon

Predicted Chromatographic Properties

Predicted Collision Cross Sections

Predictor	Adduct Type	CCS Value (Å²)	Reference
DarkChem	[M+H]+	160.516	31661259
DarkChem	[M-H]-	151.681	31661259
AllCCS	[M+H]+	154.271	32859911
AllCCS	[M-H]-	146.714	32859911
DeepCCS	[M+H]+	145.921	30932474
DeepCCS	[M-H]-	143.526	30932474
DeepCCS	[M-2H]-	176.422	30932474
DeepCCS	[M+Na]+	151.893	30932474
AllCCS	[M+H]+	154.3	32859911
AllCCS	[M+H-H2O]+	150.9	32859911
AllCCS	[M+NH4]+	157.4	32859911
AllCCS	[M+Na]+	158.2	32859911
AllCCS	[M-H]-	146.7	32859911
AllCCS	[M+Na-2H]-	147.3	32859911
AllCCS	[M+HCOO]-	148.1	32859911

Predicted Retention Times

Underivatized

Chromatographic Method	Retention Time	Reference
Measured using a Waters Acquity ultraperformance liquid chromatography (UPLC) ethylene-bridged hybrid (BEH) C18 column (100 mm × 2.1 mm; 1.7 μmparticle diameter). Predicted by Afia on May 17, 2022. Predicted by Afia on May 17, 2022.	2.14 minutes	32390414
Predicted by Siyang on May 30, 2022	9.7924 minutes	33406817
Predicted by Siyang using ReTip algorithm on June 8, 2022	9.11 minutes	32390414
AjsUoB = Accucore 150 Amide HILIC with 10mM Ammonium Formate, 0.1% Formic Acid	432.2 seconds	40023050
Fem_Long = Waters ACQUITY UPLC HSS T3 C18 with Water:MeOH and 0.1% Formic Acid	448.7 seconds	40023050
Fem_Lipids = Ascentis Express C18 with (60:40 water:ACN):(90:10 IPA:ACN) and 10mM NH4COOH + 0.1% Formic Acid	294.1 seconds	40023050
Life_Old = Waters ACQUITY UPLC BEH C18 with Water:(20:80 acetone:ACN) and 0.1% Formic Acid	28.9 seconds	40023050
Life_New = RP Waters ACQUITY UPLC HSS T3 C18 with Water:(30:70 MeOH:ACN) and 0.1% Formic Acid	176.5 seconds	40023050
RIKEN = Waters ACQUITY UPLC BEH C18 with Water:ACN and 0.1% Formic Acid	70.4 seconds	40023050
Eawag_XBridgeC18 = XBridge C18 3.5u 2.1x50 mm with Water:MeOH and 0.1% Formic Acid	293.6 seconds	40023050
BfG_NTS_RP1 =Agilent Zorbax Eclipse Plus C18 (2.1 mm x 150 mm, 3.5 um) with Water:ACN and 0.1% Formic Acid	236.8 seconds	40023050
HILIC_BDD_2 = Merck SeQuant ZIC-HILIC with ACN(0.1% formic acid):water(16 mM ammonium formate)	856.2 seconds	40023050
UniToyama_Atlantis = RP Waters Atlantis T3 (2.1 x 150 mm, 5 um) with ACN:Water and 0.1% Formic Acid	579.3 seconds	40023050
BDD_C18 = Hypersil Gold 1.9µm C18 with Water:ACN and 0.1% Formic Acid	44.5 seconds	40023050
UFZ_Phenomenex = Kinetex Core-Shell C18 2.6 um, 3.0 x 100 mm, Phenomenex with Water:MeOH and 0.1% Formic Acid	667.0 seconds	40023050
SNU_RIKEN_POS = Waters ACQUITY UPLC BEH C18 with Water:ACN and 0.1% Formic Acid	189.6 seconds	40023050
RPMMFDA = Waters ACQUITY UPLC BEH C18 with Water:ACN and 0.1% Formic Acid	295.3 seconds	40023050
MTBLS87 = Merck SeQuant ZIC-pHILIC column with ACN:Water and :ammonium carbonate	783.4 seconds	40023050
KI_GIAR_zic_HILIC_pH2_7 = Merck SeQuant ZIC-HILIC with ACN:Water and 0.1% FA	413.5 seconds	40023050
Meister zic-pHILIC pH9.3 = Merck SeQuant ZIC-pHILIC column with ACN:Water 5mM NH4Ac pH9.3 and 5mM ammonium acetate in water	519.1 seconds	40023050

Predicted Kovats Retention Indices

Underivatized

Metabolite	SMILES	Kovats RI Value	Column Type	Reference
2-Keto-3-deoxy-6-phosphogluconic acid	O[C@H](COP(O)(O)=O)[C@@H](O)CC(=O)C(O)=O	3609.5	Standard polar	33892256
2-Keto-3-deoxy-6-phosphogluconic acid	O[C@H](COP(O)(O)=O)[C@@H](O)CC(=O)C(O)=O	1707.8	Standard non polar	33892256
2-Keto-3-deoxy-6-phosphogluconic acid	O[C@H](COP(O)(O)=O)[C@@H](O)CC(=O)C(O)=O	2285.8	Semi standard non polar	33892256

Derivatized

Derivative Name / Structure	SMILES	Kovats RI Value	Column Type	Reference
2-Keto-3-deoxy-6-phosphogluconic acid,1TMS,isomer #1	C[Si](C)(C)O[C@H](COP(=O)(O)O)[C@@H](O)CC(=O)C(=O)O	2162.4	Semi standard non polar	33892256
2-Keto-3-deoxy-6-phosphogluconic acid,1TMS,isomer #2	C[Si](C)(C)O[C@@H](CC(=O)C(=O)O)[C@H](O)COP(=O)(O)O	2155.0	Semi standard non polar	33892256
2-Keto-3-deoxy-6-phosphogluconic acid,1TMS,isomer #3	C[Si](C)(C)OC(=O)C(=O)C[C@H](O)[C@H](O)COP(=O)(O)O	2117.2	Semi standard non polar	33892256
2-Keto-3-deoxy-6-phosphogluconic acid,1TMS,isomer #4	C[Si](C)(C)OP(=O)(O)OC[C@@H](O)[C@@H](O)CC(=O)C(=O)O	2227.0	Semi standard non polar	33892256
2-Keto-3-deoxy-6-phosphogluconic acid,1TMS,isomer #5	C[Si](C)(C)OC(=C[C@H](O)[C@H](O)COP(=O)(O)O)C(=O)O	2266.4	Semi standard non polar	33892256
2-Keto-3-deoxy-6-phosphogluconic acid,2TMS,isomer #1	C[Si](C)(C)O[C@@H](CC(=O)C(=O)O)[C@@H](COP(=O)(O)O)O[Si](C)(C)C	2143.5	Semi standard non polar	33892256
2-Keto-3-deoxy-6-phosphogluconic acid,2TMS,isomer #10	C[Si](C)(C)OP(=O)(OC[C@@H](O)[C@@H](O)CC(=O)C(=O)O)O[Si](C)(C)C	2280.9	Semi standard non polar	33892256
2-Keto-3-deoxy-6-phosphogluconic acid,2TMS,isomer #11	C[Si](C)(C)OC(=C[C@H](O)[C@H](O)COP(=O)(O)O[Si](C)(C)C)C(=O)O	2321.3	Semi standard non polar	33892256
2-Keto-3-deoxy-6-phosphogluconic acid,2TMS,isomer #2	C[Si](C)(C)OC(=O)C(=O)C[C@H](O)[C@@H](COP(=O)(O)O)O[Si](C)(C)C	2128.7	Semi standard non polar	33892256
2-Keto-3-deoxy-6-phosphogluconic acid,2TMS,isomer #3	C[Si](C)(C)O[C@H](COP(=O)(O)O[Si](C)(C)C)[C@@H](O)CC(=O)C(=O)O	2232.3	Semi standard non polar	33892256
2-Keto-3-deoxy-6-phosphogluconic acid,2TMS,isomer #4	C[Si](C)(C)OC(=C[C@H](O)[C@@H](COP(=O)(O)O)O[Si](C)(C)C)C(=O)O	2273.7	Semi standard non polar	33892256
2-Keto-3-deoxy-6-phosphogluconic acid,2TMS,isomer #5	C[Si](C)(C)OC(=O)C(=O)C[C@H](O[Si](C)(C)C)[C@H](O)COP(=O)(O)O	2122.6	Semi standard non polar	33892256
2-Keto-3-deoxy-6-phosphogluconic acid,2TMS,isomer #6	C[Si](C)(C)O[C@@H](CC(=O)C(=O)O)[C@H](O)COP(=O)(O)O[Si](C)(C)C	2222.4	Semi standard non polar	33892256
2-Keto-3-deoxy-6-phosphogluconic acid,2TMS,isomer #7	C[Si](C)(C)OC(=C[C@H](O[Si](C)(C)C)[C@H](O)COP(=O)(O)O)C(=O)O	2280.1	Semi standard non polar	33892256
2-Keto-3-deoxy-6-phosphogluconic acid,2TMS,isomer #8	C[Si](C)(C)OC(=O)C(=O)C[C@H](O)[C@H](O)COP(=O)(O)O[Si](C)(C)C	2193.2	Semi standard non polar	33892256
2-Keto-3-deoxy-6-phosphogluconic acid,2TMS,isomer #9	C[Si](C)(C)OC(=O)C(=C[C@H](O)[C@H](O)COP(=O)(O)O)O[Si](C)(C)C	2210.1	Semi standard non polar	33892256
2-Keto-3-deoxy-6-phosphogluconic acid,3TMS,isomer #1	C[Si](C)(C)OC(=O)C(=O)C[C@H](O[Si](C)(C)C)[C@@H](COP(=O)(O)O)O[Si](C)(C)C	2153.1	Semi standard non polar	33892256
2-Keto-3-deoxy-6-phosphogluconic acid,3TMS,isomer #10	C[Si](C)(C)O[C@@H](CC(=O)C(=O)O)[C@H](O)COP(=O)(O[Si](C)(C)C)O[Si](C)(C)C	2270.2	Semi standard non polar	33892256
2-Keto-3-deoxy-6-phosphogluconic acid,3TMS,isomer #11	C[Si](C)(C)OC(=C[C@H](O[Si](C)(C)C)[C@H](O)COP(=O)(O)O[Si](C)(C)C)C(=O)O	2331.6	Semi standard non polar	33892256
2-Keto-3-deoxy-6-phosphogluconic acid,3TMS,isomer #12	C[Si](C)(C)OC(=O)C(=O)C[C@H](O)[C@H](O)COP(=O)(O[Si](C)(C)C)O[Si](C)(C)C	2227.7	Semi standard non polar	33892256
2-Keto-3-deoxy-6-phosphogluconic acid,3TMS,isomer #13	C[Si](C)(C)OC(=O)C(=C[C@H](O)[C@H](O)COP(=O)(O)O[Si](C)(C)C)O[Si](C)(C)C	2247.5	Semi standard non polar	33892256
2-Keto-3-deoxy-6-phosphogluconic acid,3TMS,isomer #14	C[Si](C)(C)OC(=C[C@H](O)[C@H](O)COP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)C(=O)O	2330.1	Semi standard non polar	33892256
2-Keto-3-deoxy-6-phosphogluconic acid,3TMS,isomer #2	C[Si](C)(C)O[C@@H](CC(=O)C(=O)O)[C@@H](COP(=O)(O)O[Si](C)(C)C)O[Si](C)(C)C	2220.9	Semi standard non polar	33892256
2-Keto-3-deoxy-6-phosphogluconic acid,3TMS,isomer #3	C[Si](C)(C)OC(=C[C@H](O[Si](C)(C)C)[C@@H](COP(=O)(O)O)O[Si](C)(C)C)C(=O)O	2282.2	Semi standard non polar	33892256
2-Keto-3-deoxy-6-phosphogluconic acid,3TMS,isomer #4	C[Si](C)(C)OC(=O)C(=O)C[C@H](O)[C@@H](COP(=O)(O)O[Si](C)(C)C)O[Si](C)(C)C	2215.3	Semi standard non polar	33892256
2-Keto-3-deoxy-6-phosphogluconic acid,3TMS,isomer #5	C[Si](C)(C)OC(=O)C(=C[C@H](O)[C@@H](COP(=O)(O)O)O[Si](C)(C)C)O[Si](C)(C)C	2226.9	Semi standard non polar	33892256
2-Keto-3-deoxy-6-phosphogluconic acid,3TMS,isomer #6	C[Si](C)(C)O[C@H](COP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)[C@@H](O)CC(=O)C(=O)O	2280.1	Semi standard non polar	33892256
2-Keto-3-deoxy-6-phosphogluconic acid,3TMS,isomer #7	C[Si](C)(C)OC(=C[C@H](O)[C@@H](COP(=O)(O)O[Si](C)(C)C)O[Si](C)(C)C)C(=O)O	2319.5	Semi standard non polar	33892256
2-Keto-3-deoxy-6-phosphogluconic acid,3TMS,isomer #8	C[Si](C)(C)OC(=O)C(=O)C[C@H](O[Si](C)(C)C)[C@H](O)COP(=O)(O)O[Si](C)(C)C	2193.8	Semi standard non polar	33892256
2-Keto-3-deoxy-6-phosphogluconic acid,3TMS,isomer #9	C[Si](C)(C)OC(=O)C(=C[C@H](O[Si](C)(C)C)[C@H](O)COP(=O)(O)O)O[Si](C)(C)C	2238.7	Semi standard non polar	33892256
2-Keto-3-deoxy-6-phosphogluconic acid,4TMS,isomer #1	C[Si](C)(C)OC(=O)C(=O)C[C@H](O[Si](C)(C)C)[C@@H](COP(=O)(O)O[Si](C)(C)C)O[Si](C)(C)C	2234.8	Semi standard non polar	33892256
2-Keto-3-deoxy-6-phosphogluconic acid,4TMS,isomer #1	C[Si](C)(C)OC(=O)C(=O)C[C@H](O[Si](C)(C)C)[C@@H](COP(=O)(O)O[Si](C)(C)C)O[Si](C)(C)C	2226.8	Standard non polar	33892256
2-Keto-3-deoxy-6-phosphogluconic acid,4TMS,isomer #1	C[Si](C)(C)OC(=O)C(=O)C[C@H](O[Si](C)(C)C)[C@@H](COP(=O)(O)O[Si](C)(C)C)O[Si](C)(C)C	2707.5	Standard polar	33892256
2-Keto-3-deoxy-6-phosphogluconic acid,4TMS,isomer #10	C[Si](C)(C)OC(=C[C@H](O[Si](C)(C)C)[C@H](O)COP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)C(=O)O	2379.3	Semi standard non polar	33892256
2-Keto-3-deoxy-6-phosphogluconic acid,4TMS,isomer #10	C[Si](C)(C)OC(=C[C@H](O[Si](C)(C)C)[C@H](O)COP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)C(=O)O	2310.3	Standard non polar	33892256
2-Keto-3-deoxy-6-phosphogluconic acid,4TMS,isomer #10	C[Si](C)(C)OC(=C[C@H](O[Si](C)(C)C)[C@H](O)COP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)C(=O)O	2740.2	Standard polar	33892256
2-Keto-3-deoxy-6-phosphogluconic acid,4TMS,isomer #11	C[Si](C)(C)OC(=O)C(=C[C@H](O)[C@H](O)COP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)O[Si](C)(C)C	2266.5	Semi standard non polar	33892256
2-Keto-3-deoxy-6-phosphogluconic acid,4TMS,isomer #11	C[Si](C)(C)OC(=O)C(=C[C@H](O)[C@H](O)COP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)O[Si](C)(C)C	2284.0	Standard non polar	33892256
2-Keto-3-deoxy-6-phosphogluconic acid,4TMS,isomer #11	C[Si](C)(C)OC(=O)C(=C[C@H](O)[C@H](O)COP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)O[Si](C)(C)C	2733.8	Standard polar	33892256
2-Keto-3-deoxy-6-phosphogluconic acid,4TMS,isomer #2	C[Si](C)(C)OC(=O)C(=C[C@H](O[Si](C)(C)C)[C@@H](COP(=O)(O)O)O[Si](C)(C)C)O[Si](C)(C)C	2242.8	Semi standard non polar	33892256
2-Keto-3-deoxy-6-phosphogluconic acid,4TMS,isomer #2	C[Si](C)(C)OC(=O)C(=C[C@H](O[Si](C)(C)C)[C@@H](COP(=O)(O)O)O[Si](C)(C)C)O[Si](C)(C)C	2276.7	Standard non polar	33892256
2-Keto-3-deoxy-6-phosphogluconic acid,4TMS,isomer #2	C[Si](C)(C)OC(=O)C(=C[C@H](O[Si](C)(C)C)[C@@H](COP(=O)(O)O)O[Si](C)(C)C)O[Si](C)(C)C	3003.6	Standard polar	33892256
2-Keto-3-deoxy-6-phosphogluconic acid,4TMS,isomer #3	C[Si](C)(C)O[C@@H](CC(=O)C(=O)O)[C@@H](COP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)O[Si](C)(C)C	2294.2	Semi standard non polar	33892256
2-Keto-3-deoxy-6-phosphogluconic acid,4TMS,isomer #3	C[Si](C)(C)O[C@@H](CC(=O)C(=O)O)[C@@H](COP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)O[Si](C)(C)C	2284.3	Standard non polar	33892256
2-Keto-3-deoxy-6-phosphogluconic acid,4TMS,isomer #3	C[Si](C)(C)O[C@@H](CC(=O)C(=O)O)[C@@H](COP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)O[Si](C)(C)C	2585.2	Standard polar	33892256
2-Keto-3-deoxy-6-phosphogluconic acid,4TMS,isomer #4	C[Si](C)(C)OC(=C[C@H](O[Si](C)(C)C)[C@@H](COP(=O)(O)O[Si](C)(C)C)O[Si](C)(C)C)C(=O)O	2350.2	Semi standard non polar	33892256
2-Keto-3-deoxy-6-phosphogluconic acid,4TMS,isomer #4	C[Si](C)(C)OC(=C[C@H](O[Si](C)(C)C)[C@@H](COP(=O)(O)O[Si](C)(C)C)O[Si](C)(C)C)C(=O)O	2293.1	Standard non polar	33892256
2-Keto-3-deoxy-6-phosphogluconic acid,4TMS,isomer #4	C[Si](C)(C)OC(=C[C@H](O[Si](C)(C)C)[C@@H](COP(=O)(O)O[Si](C)(C)C)O[Si](C)(C)C)C(=O)O	2870.2	Standard polar	33892256
2-Keto-3-deoxy-6-phosphogluconic acid,4TMS,isomer #5	C[Si](C)(C)OC(=O)C(=O)C[C@H](O)[C@@H](COP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)O[Si](C)(C)C	2282.2	Semi standard non polar	33892256
2-Keto-3-deoxy-6-phosphogluconic acid,4TMS,isomer #5	C[Si](C)(C)OC(=O)C(=O)C[C@H](O)[C@@H](COP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)O[Si](C)(C)C	2253.0	Standard non polar	33892256
2-Keto-3-deoxy-6-phosphogluconic acid,4TMS,isomer #5	C[Si](C)(C)OC(=O)C(=O)C[C@H](O)[C@@H](COP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)O[Si](C)(C)C	2556.2	Standard polar	33892256
2-Keto-3-deoxy-6-phosphogluconic acid,4TMS,isomer #6	C[Si](C)(C)OC(=O)C(=C[C@H](O)[C@@H](COP(=O)(O)O[Si](C)(C)C)O[Si](C)(C)C)O[Si](C)(C)C	2281.5	Semi standard non polar	33892256
2-Keto-3-deoxy-6-phosphogluconic acid,4TMS,isomer #6	C[Si](C)(C)OC(=O)C(=C[C@H](O)[C@@H](COP(=O)(O)O[Si](C)(C)C)O[Si](C)(C)C)O[Si](C)(C)C	2257.6	Standard non polar	33892256
2-Keto-3-deoxy-6-phosphogluconic acid,4TMS,isomer #6	C[Si](C)(C)OC(=O)C(=C[C@H](O)[C@@H](COP(=O)(O)O[Si](C)(C)C)O[Si](C)(C)C)O[Si](C)(C)C	2853.9	Standard polar	33892256
2-Keto-3-deoxy-6-phosphogluconic acid,4TMS,isomer #7	C[Si](C)(C)OC(=C[C@H](O)[C@@H](COP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)O[Si](C)(C)C)C(=O)O	2372.2	Semi standard non polar	33892256
2-Keto-3-deoxy-6-phosphogluconic acid,4TMS,isomer #7	C[Si](C)(C)OC(=C[C@H](O)[C@@H](COP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)O[Si](C)(C)C)C(=O)O	2331.3	Standard non polar	33892256
2-Keto-3-deoxy-6-phosphogluconic acid,4TMS,isomer #7	C[Si](C)(C)OC(=C[C@H](O)[C@@H](COP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)O[Si](C)(C)C)C(=O)O	2738.1	Standard polar	33892256
2-Keto-3-deoxy-6-phosphogluconic acid,4TMS,isomer #8	C[Si](C)(C)OC(=O)C(=O)C[C@H](O[Si](C)(C)C)[C@H](O)COP(=O)(O[Si](C)(C)C)O[Si](C)(C)C	2258.0	Semi standard non polar	33892256
2-Keto-3-deoxy-6-phosphogluconic acid,4TMS,isomer #8	C[Si](C)(C)OC(=O)C(=O)C[C@H](O[Si](C)(C)C)[C@H](O)COP(=O)(O[Si](C)(C)C)O[Si](C)(C)C	2252.4	Standard non polar	33892256
2-Keto-3-deoxy-6-phosphogluconic acid,4TMS,isomer #8	C[Si](C)(C)OC(=O)C(=O)C[C@H](O[Si](C)(C)C)[C@H](O)COP(=O)(O[Si](C)(C)C)O[Si](C)(C)C	2552.0	Standard polar	33892256
2-Keto-3-deoxy-6-phosphogluconic acid,4TMS,isomer #9	C[Si](C)(C)OC(=O)C(=C[C@H](O[Si](C)(C)C)[C@H](O)COP(=O)(O)O[Si](C)(C)C)O[Si](C)(C)C	2266.7	Semi standard non polar	33892256
2-Keto-3-deoxy-6-phosphogluconic acid,4TMS,isomer #9	C[Si](C)(C)OC(=O)C(=C[C@H](O[Si](C)(C)C)[C@H](O)COP(=O)(O)O[Si](C)(C)C)O[Si](C)(C)C	2237.6	Standard non polar	33892256
2-Keto-3-deoxy-6-phosphogluconic acid,4TMS,isomer #9	C[Si](C)(C)OC(=O)C(=C[C@H](O[Si](C)(C)C)[C@H](O)COP(=O)(O)O[Si](C)(C)C)O[Si](C)(C)C	2867.2	Standard polar	33892256
2-Keto-3-deoxy-6-phosphogluconic acid,5TMS,isomer #1	C[Si](C)(C)OC(=O)C(=O)C[C@H](O[Si](C)(C)C)[C@@H](COP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)O[Si](C)(C)C	2272.4	Semi standard non polar	33892256
2-Keto-3-deoxy-6-phosphogluconic acid,5TMS,isomer #1	C[Si](C)(C)OC(=O)C(=O)C[C@H](O[Si](C)(C)C)[C@@H](COP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)O[Si](C)(C)C	2275.1	Standard non polar	33892256
2-Keto-3-deoxy-6-phosphogluconic acid,5TMS,isomer #1	C[Si](C)(C)OC(=O)C(=O)C[C@H](O[Si](C)(C)C)[C@@H](COP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)O[Si](C)(C)C	2441.6	Standard polar	33892256
2-Keto-3-deoxy-6-phosphogluconic acid,5TMS,isomer #2	C[Si](C)(C)OC(=O)C(=C[C@H](O[Si](C)(C)C)[C@@H](COP(=O)(O)O[Si](C)(C)C)O[Si](C)(C)C)O[Si](C)(C)C	2291.6	Semi standard non polar	33892256
2-Keto-3-deoxy-6-phosphogluconic acid,5TMS,isomer #2	C[Si](C)(C)OC(=O)C(=C[C@H](O[Si](C)(C)C)[C@@H](COP(=O)(O)O[Si](C)(C)C)O[Si](C)(C)C)O[Si](C)(C)C	2255.9	Standard non polar	33892256
2-Keto-3-deoxy-6-phosphogluconic acid,5TMS,isomer #2	C[Si](C)(C)OC(=O)C(=C[C@H](O[Si](C)(C)C)[C@@H](COP(=O)(O)O[Si](C)(C)C)O[Si](C)(C)C)O[Si](C)(C)C	2638.3	Standard polar	33892256
2-Keto-3-deoxy-6-phosphogluconic acid,5TMS,isomer #3	C[Si](C)(C)OC(=C[C@H](O[Si](C)(C)C)[C@@H](COP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)O[Si](C)(C)C)C(=O)O	2407.8	Semi standard non polar	33892256
2-Keto-3-deoxy-6-phosphogluconic acid,5TMS,isomer #3	C[Si](C)(C)OC(=C[C@H](O[Si](C)(C)C)[C@@H](COP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)O[Si](C)(C)C)C(=O)O	2313.6	Standard non polar	33892256
2-Keto-3-deoxy-6-phosphogluconic acid,5TMS,isomer #3	C[Si](C)(C)OC(=C[C@H](O[Si](C)(C)C)[C@@H](COP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)O[Si](C)(C)C)C(=O)O	2562.3	Standard polar	33892256
2-Keto-3-deoxy-6-phosphogluconic acid,5TMS,isomer #4	C[Si](C)(C)OC(=O)C(=C[C@H](O)[C@@H](COP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)O[Si](C)(C)C)O[Si](C)(C)C	2318.8	Semi standard non polar	33892256
2-Keto-3-deoxy-6-phosphogluconic acid,5TMS,isomer #4	C[Si](C)(C)OC(=O)C(=C[C@H](O)[C@@H](COP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)O[Si](C)(C)C)O[Si](C)(C)C	2292.6	Standard non polar	33892256
2-Keto-3-deoxy-6-phosphogluconic acid,5TMS,isomer #4	C[Si](C)(C)OC(=O)C(=C[C@H](O)[C@@H](COP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)O[Si](C)(C)C)O[Si](C)(C)C	2561.3	Standard polar	33892256
2-Keto-3-deoxy-6-phosphogluconic acid,5TMS,isomer #5	C[Si](C)(C)OC(=O)C(=C[C@H](O[Si](C)(C)C)[C@H](O)COP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)O[Si](C)(C)C	2317.0	Semi standard non polar	33892256
2-Keto-3-deoxy-6-phosphogluconic acid,5TMS,isomer #5	C[Si](C)(C)OC(=O)C(=C[C@H](O[Si](C)(C)C)[C@H](O)COP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)O[Si](C)(C)C	2273.5	Standard non polar	33892256
2-Keto-3-deoxy-6-phosphogluconic acid,5TMS,isomer #5	C[Si](C)(C)OC(=O)C(=C[C@H](O[Si](C)(C)C)[C@H](O)COP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)O[Si](C)(C)C	2582.2	Standard polar	33892256
2-Keto-3-deoxy-6-phosphogluconic acid,6TMS,isomer #1	C[Si](C)(C)OC(=O)C(=C[C@H](O[Si](C)(C)C)[C@@H](COP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)O[Si](C)(C)C)O[Si](C)(C)C	2327.4	Semi standard non polar	33892256
2-Keto-3-deoxy-6-phosphogluconic acid,6TMS,isomer #1	C[Si](C)(C)OC(=O)C(=C[C@H](O[Si](C)(C)C)[C@@H](COP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)O[Si](C)(C)C)O[Si](C)(C)C	2297.9	Standard non polar	33892256
2-Keto-3-deoxy-6-phosphogluconic acid,6TMS,isomer #1	C[Si](C)(C)OC(=O)C(=C[C@H](O[Si](C)(C)C)[C@@H](COP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)O[Si](C)(C)C)O[Si](C)(C)C	2429.4	Standard polar	33892256
2-Keto-3-deoxy-6-phosphogluconic acid,1TBDMS,isomer #1	CC(C)(C)[Si](C)(C)O[C@H](COP(=O)(O)O)[C@@H](O)CC(=O)C(=O)O	2398.0	Semi standard non polar	33892256
2-Keto-3-deoxy-6-phosphogluconic acid,1TBDMS,isomer #2	CC(C)(C)[Si](C)(C)O[C@@H](CC(=O)C(=O)O)[C@H](O)COP(=O)(O)O	2386.7	Semi standard non polar	33892256
2-Keto-3-deoxy-6-phosphogluconic acid,1TBDMS,isomer #3	CC(C)(C)[Si](C)(C)OC(=O)C(=O)C[C@H](O)[C@H](O)COP(=O)(O)O	2377.3	Semi standard non polar	33892256
2-Keto-3-deoxy-6-phosphogluconic acid,1TBDMS,isomer #4	CC(C)(C)[Si](C)(C)OP(=O)(O)OC[C@@H](O)[C@@H](O)CC(=O)C(=O)O	2457.2	Semi standard non polar	33892256
2-Keto-3-deoxy-6-phosphogluconic acid,1TBDMS,isomer #5	CC(C)(C)[Si](C)(C)OC(=C[C@H](O)[C@H](O)COP(=O)(O)O)C(=O)O	2484.0	Semi standard non polar	33892256
2-Keto-3-deoxy-6-phosphogluconic acid,2TBDMS,isomer #1	CC(C)(C)[Si](C)(C)O[C@@H](CC(=O)C(=O)O)[C@@H](COP(=O)(O)O)O[Si](C)(C)C(C)(C)C	2558.9	Semi standard non polar	33892256
2-Keto-3-deoxy-6-phosphogluconic acid,2TBDMS,isomer #10	CC(C)(C)[Si](C)(C)OP(=O)(OC[C@@H](O)[C@@H](O)CC(=O)C(=O)O)O[Si](C)(C)C(C)(C)C	2688.5	Semi standard non polar	33892256
2-Keto-3-deoxy-6-phosphogluconic acid,2TBDMS,isomer #11	CC(C)(C)[Si](C)(C)OC(=C[C@H](O)[C@H](O)COP(=O)(O)O[Si](C)(C)C(C)(C)C)C(=O)O	2713.3	Semi standard non polar	33892256
2-Keto-3-deoxy-6-phosphogluconic acid,2TBDMS,isomer #2	CC(C)(C)[Si](C)(C)OC(=O)C(=O)C[C@H](O)[C@@H](COP(=O)(O)O)O[Si](C)(C)C(C)(C)C	2577.0	Semi standard non polar	33892256
2-Keto-3-deoxy-6-phosphogluconic acid,2TBDMS,isomer #3	CC(C)(C)[Si](C)(C)O[C@H](COP(=O)(O)O[Si](C)(C)C(C)(C)C)[C@@H](O)CC(=O)C(=O)O	2650.5	Semi standard non polar	33892256
2-Keto-3-deoxy-6-phosphogluconic acid,2TBDMS,isomer #4	CC(C)(C)[Si](C)(C)OC(=C[C@H](O)[C@@H](COP(=O)(O)O)O[Si](C)(C)C(C)(C)C)C(=O)O	2680.5	Semi standard non polar	33892256
2-Keto-3-deoxy-6-phosphogluconic acid,2TBDMS,isomer #5	CC(C)(C)[Si](C)(C)OC(=O)C(=O)C[C@H](O[Si](C)(C)C(C)(C)C)[C@H](O)COP(=O)(O)O	2573.1	Semi standard non polar	33892256
2-Keto-3-deoxy-6-phosphogluconic acid,2TBDMS,isomer #6	CC(C)(C)[Si](C)(C)O[C@@H](CC(=O)C(=O)O)[C@H](O)COP(=O)(O)O[Si](C)(C)C(C)(C)C	2634.6	Semi standard non polar	33892256
2-Keto-3-deoxy-6-phosphogluconic acid,2TBDMS,isomer #7	CC(C)(C)[Si](C)(C)OC(=C[C@H](O[Si](C)(C)C(C)(C)C)[C@H](O)COP(=O)(O)O)C(=O)O	2681.7	Semi standard non polar	33892256
2-Keto-3-deoxy-6-phosphogluconic acid,2TBDMS,isomer #8	CC(C)(C)[Si](C)(C)OC(=O)C(=O)C[C@H](O)[C@H](O)COP(=O)(O)O[Si](C)(C)C(C)(C)C	2647.2	Semi standard non polar	33892256
2-Keto-3-deoxy-6-phosphogluconic acid,2TBDMS,isomer #9	CC(C)(C)[Si](C)(C)OC(=O)C(=C[C@H](O)[C@H](O)COP(=O)(O)O)O[Si](C)(C)C(C)(C)C	2610.4	Semi standard non polar	33892256
2-Keto-3-deoxy-6-phosphogluconic acid,3TBDMS,isomer #1	CC(C)(C)[Si](C)(C)OC(=O)C(=O)C[C@H](O[Si](C)(C)C(C)(C)C)[C@@H](COP(=O)(O)O)O[Si](C)(C)C(C)(C)C	2801.2	Semi standard non polar	33892256
2-Keto-3-deoxy-6-phosphogluconic acid,3TBDMS,isomer #10	CC(C)(C)[Si](C)(C)O[C@@H](CC(=O)C(=O)O)[C@H](O)COP(=O)(O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C	2887.9	Semi standard non polar	33892256
2-Keto-3-deoxy-6-phosphogluconic acid,3TBDMS,isomer #11	CC(C)(C)[Si](C)(C)OC(=C[C@H](O[Si](C)(C)C(C)(C)C)[C@H](O)COP(=O)(O)O[Si](C)(C)C(C)(C)C)C(=O)O	2966.3	Semi standard non polar	33892256
2-Keto-3-deoxy-6-phosphogluconic acid,3TBDMS,isomer #12	CC(C)(C)[Si](C)(C)OC(=O)C(=O)C[C@H](O)[C@H](O)COP(=O)(O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C	2890.3	Semi standard non polar	33892256
2-Keto-3-deoxy-6-phosphogluconic acid,3TBDMS,isomer #13	CC(C)(C)[Si](C)(C)OC(=O)C(=C[C@H](O)[C@H](O)COP(=O)(O)O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C	2853.7	Semi standard non polar	33892256
2-Keto-3-deoxy-6-phosphogluconic acid,3TBDMS,isomer #14	CC(C)(C)[Si](C)(C)OC(=C[C@H](O)[C@H](O)COP(=O)(O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C)C(=O)O	2948.8	Semi standard non polar	33892256
2-Keto-3-deoxy-6-phosphogluconic acid,3TBDMS,isomer #2	CC(C)(C)[Si](C)(C)O[C@@H](CC(=O)C(=O)O)[C@@H](COP(=O)(O)O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C	2868.0	Semi standard non polar	33892256
2-Keto-3-deoxy-6-phosphogluconic acid,3TBDMS,isomer #3	CC(C)(C)[Si](C)(C)OC(=C[C@H](O[Si](C)(C)C(C)(C)C)[C@@H](COP(=O)(O)O)O[Si](C)(C)C(C)(C)C)C(=O)O	2913.0	Semi standard non polar	33892256
2-Keto-3-deoxy-6-phosphogluconic acid,3TBDMS,isomer #4	CC(C)(C)[Si](C)(C)OC(=O)C(=O)C[C@H](O)[C@@H](COP(=O)(O)O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C	2869.0	Semi standard non polar	33892256
2-Keto-3-deoxy-6-phosphogluconic acid,3TBDMS,isomer #5	CC(C)(C)[Si](C)(C)OC(=O)C(=C[C@H](O)[C@@H](COP(=O)(O)O)O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C	2839.5	Semi standard non polar	33892256
2-Keto-3-deoxy-6-phosphogluconic acid,3TBDMS,isomer #6	CC(C)(C)[Si](C)(C)O[C@H](COP(=O)(O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C)[C@@H](O)CC(=O)C(=O)O	2908.4	Semi standard non polar	33892256
2-Keto-3-deoxy-6-phosphogluconic acid,3TBDMS,isomer #7	CC(C)(C)[Si](C)(C)OC(=C[C@H](O)[C@@H](COP(=O)(O)O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C)C(=O)O	2955.0	Semi standard non polar	33892256
2-Keto-3-deoxy-6-phosphogluconic acid,3TBDMS,isomer #8	CC(C)(C)[Si](C)(C)OC(=O)C(=O)C[C@H](O[Si](C)(C)C(C)(C)C)[C@H](O)COP(=O)(O)O[Si](C)(C)C(C)(C)C	2858.2	Semi standard non polar	33892256
2-Keto-3-deoxy-6-phosphogluconic acid,3TBDMS,isomer #9	CC(C)(C)[Si](C)(C)OC(=O)C(=C[C@H](O[Si](C)(C)C(C)(C)C)[C@H](O)COP(=O)(O)O)O[Si](C)(C)C(C)(C)C	2855.2	Semi standard non polar	33892256
2-Keto-3-deoxy-6-phosphogluconic acid,4TBDMS,isomer #1	CC(C)(C)[Si](C)(C)OC(=O)C(=O)C[C@H](O[Si](C)(C)C(C)(C)C)[C@@H](COP(=O)(O)O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C	3076.4	Semi standard non polar	33892256
2-Keto-3-deoxy-6-phosphogluconic acid,4TBDMS,isomer #1	CC(C)(C)[Si](C)(C)OC(=O)C(=O)C[C@H](O[Si](C)(C)C(C)(C)C)[C@@H](COP(=O)(O)O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C	2968.2	Standard non polar	33892256
2-Keto-3-deoxy-6-phosphogluconic acid,4TBDMS,isomer #1	CC(C)(C)[Si](C)(C)OC(=O)C(=O)C[C@H](O[Si](C)(C)C(C)(C)C)[C@@H](COP(=O)(O)O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C	3018.1	Standard polar	33892256
2-Keto-3-deoxy-6-phosphogluconic acid,4TBDMS,isomer #10	CC(C)(C)[Si](C)(C)OC(=C[C@H](O[Si](C)(C)C(C)(C)C)[C@H](O)COP(=O)(O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C)C(=O)O	3189.1	Semi standard non polar	33892256
2-Keto-3-deoxy-6-phosphogluconic acid,4TBDMS,isomer #10	CC(C)(C)[Si](C)(C)OC(=C[C@H](O[Si](C)(C)C(C)(C)C)[C@H](O)COP(=O)(O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C)C(=O)O	2896.8	Standard non polar	33892256
2-Keto-3-deoxy-6-phosphogluconic acid,4TBDMS,isomer #10	CC(C)(C)[Si](C)(C)OC(=C[C@H](O[Si](C)(C)C(C)(C)C)[C@H](O)COP(=O)(O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C)C(=O)O	3040.3	Standard polar	33892256
2-Keto-3-deoxy-6-phosphogluconic acid,4TBDMS,isomer #11	CC(C)(C)[Si](C)(C)OC(=O)C(=C[C@H](O)[C@H](O)COP(=O)(O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C	3071.7	Semi standard non polar	33892256
2-Keto-3-deoxy-6-phosphogluconic acid,4TBDMS,isomer #11	CC(C)(C)[Si](C)(C)OC(=O)C(=C[C@H](O)[C@H](O)COP(=O)(O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C	2879.3	Standard non polar	33892256
2-Keto-3-deoxy-6-phosphogluconic acid,4TBDMS,isomer #11	CC(C)(C)[Si](C)(C)OC(=O)C(=C[C@H](O)[C@H](O)COP(=O)(O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C	3029.0	Standard polar	33892256
2-Keto-3-deoxy-6-phosphogluconic acid,4TBDMS,isomer #2	CC(C)(C)[Si](C)(C)OC(=O)C(=C[C@H](O[Si](C)(C)C(C)(C)C)[C@@H](COP(=O)(O)O)O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C	3074.5	Semi standard non polar	33892256
2-Keto-3-deoxy-6-phosphogluconic acid,4TBDMS,isomer #2	CC(C)(C)[Si](C)(C)OC(=O)C(=C[C@H](O[Si](C)(C)C(C)(C)C)[C@@H](COP(=O)(O)O)O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C	2923.0	Standard non polar	33892256
2-Keto-3-deoxy-6-phosphogluconic acid,4TBDMS,isomer #2	CC(C)(C)[Si](C)(C)OC(=O)C(=C[C@H](O[Si](C)(C)C(C)(C)C)[C@@H](COP(=O)(O)O)O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C	3187.7	Standard polar	33892256
2-Keto-3-deoxy-6-phosphogluconic acid,4TBDMS,isomer #3	CC(C)(C)[Si](C)(C)O[C@@H](CC(=O)C(=O)O)[C@@H](COP(=O)(O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C	3124.9	Semi standard non polar	33892256
2-Keto-3-deoxy-6-phosphogluconic acid,4TBDMS,isomer #3	CC(C)(C)[Si](C)(C)O[C@@H](CC(=O)C(=O)O)[C@@H](COP(=O)(O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C	2937.7	Standard non polar	33892256
2-Keto-3-deoxy-6-phosphogluconic acid,4TBDMS,isomer #3	CC(C)(C)[Si](C)(C)O[C@@H](CC(=O)C(=O)O)[C@@H](COP(=O)(O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C	2931.8	Standard polar	33892256
2-Keto-3-deoxy-6-phosphogluconic acid,4TBDMS,isomer #4	CC(C)(C)[Si](C)(C)OC(=C[C@H](O[Si](C)(C)C(C)(C)C)[C@@H](COP(=O)(O)O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C)C(=O)O	3201.1	Semi standard non polar	33892256
2-Keto-3-deoxy-6-phosphogluconic acid,4TBDMS,isomer #4	CC(C)(C)[Si](C)(C)OC(=C[C@H](O[Si](C)(C)C(C)(C)C)[C@@H](COP(=O)(O)O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C)C(=O)O	2934.1	Standard non polar	33892256
2-Keto-3-deoxy-6-phosphogluconic acid,4TBDMS,isomer #4	CC(C)(C)[Si](C)(C)OC(=C[C@H](O[Si](C)(C)C(C)(C)C)[C@@H](COP(=O)(O)O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C)C(=O)O	3113.5	Standard polar	33892256
2-Keto-3-deoxy-6-phosphogluconic acid,4TBDMS,isomer #5	CC(C)(C)[Si](C)(C)OC(=O)C(=O)C[C@H](O)[C@@H](COP(=O)(O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C	3094.2	Semi standard non polar	33892256
2-Keto-3-deoxy-6-phosphogluconic acid,4TBDMS,isomer #5	CC(C)(C)[Si](C)(C)OC(=O)C(=O)C[C@H](O)[C@@H](COP(=O)(O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C	2938.7	Standard non polar	33892256
2-Keto-3-deoxy-6-phosphogluconic acid,4TBDMS,isomer #5	CC(C)(C)[Si](C)(C)OC(=O)C(=O)C[C@H](O)[C@@H](COP(=O)(O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C	2917.0	Standard polar	33892256
2-Keto-3-deoxy-6-phosphogluconic acid,4TBDMS,isomer #6	CC(C)(C)[Si](C)(C)OC(=O)C(=C[C@H](O)[C@@H](COP(=O)(O)O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C	3102.8	Semi standard non polar	33892256
2-Keto-3-deoxy-6-phosphogluconic acid,4TBDMS,isomer #6	CC(C)(C)[Si](C)(C)OC(=O)C(=C[C@H](O)[C@@H](COP(=O)(O)O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C	2910.1	Standard non polar	33892256
2-Keto-3-deoxy-6-phosphogluconic acid,4TBDMS,isomer #6	CC(C)(C)[Si](C)(C)OC(=O)C(=C[C@H](O)[C@@H](COP(=O)(O)O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C	3088.3	Standard polar	33892256
2-Keto-3-deoxy-6-phosphogluconic acid,4TBDMS,isomer #7	CC(C)(C)[Si](C)(C)OC(=C[C@H](O)[C@@H](COP(=O)(O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C)C(=O)O	3187.3	Semi standard non polar	33892256
2-Keto-3-deoxy-6-phosphogluconic acid,4TBDMS,isomer #7	CC(C)(C)[Si](C)(C)OC(=C[C@H](O)[C@@H](COP(=O)(O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C)C(=O)O	2926.1	Standard non polar	33892256
2-Keto-3-deoxy-6-phosphogluconic acid,4TBDMS,isomer #7	CC(C)(C)[Si](C)(C)OC(=C[C@H](O)[C@@H](COP(=O)(O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C)C(=O)O	3033.7	Standard polar	33892256
2-Keto-3-deoxy-6-phosphogluconic acid,4TBDMS,isomer #8	CC(C)(C)[Si](C)(C)OC(=O)C(=O)C[C@H](O[Si](C)(C)C(C)(C)C)[C@H](O)COP(=O)(O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C	3077.4	Semi standard non polar	33892256
2-Keto-3-deoxy-6-phosphogluconic acid,4TBDMS,isomer #8	CC(C)(C)[Si](C)(C)OC(=O)C(=O)C[C@H](O[Si](C)(C)C(C)(C)C)[C@H](O)COP(=O)(O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C	2934.0	Standard non polar	33892256
2-Keto-3-deoxy-6-phosphogluconic acid,4TBDMS,isomer #8	CC(C)(C)[Si](C)(C)OC(=O)C(=O)C[C@H](O[Si](C)(C)C(C)(C)C)[C@H](O)COP(=O)(O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C	2918.6	Standard polar	33892256
2-Keto-3-deoxy-6-phosphogluconic acid,4TBDMS,isomer #9	CC(C)(C)[Si](C)(C)OC(=O)C(=C[C@H](O[Si](C)(C)C(C)(C)C)[C@H](O)COP(=O)(O)O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C	3118.6	Semi standard non polar	33892256
2-Keto-3-deoxy-6-phosphogluconic acid,4TBDMS,isomer #9	CC(C)(C)[Si](C)(C)OC(=O)C(=C[C@H](O[Si](C)(C)C(C)(C)C)[C@H](O)COP(=O)(O)O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C	2888.3	Standard non polar	33892256
2-Keto-3-deoxy-6-phosphogluconic acid,4TBDMS,isomer #9	CC(C)(C)[Si](C)(C)OC(=O)C(=C[C@H](O[Si](C)(C)C(C)(C)C)[C@H](O)COP(=O)(O)O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C	3103.1	Standard polar	33892256
2-Keto-3-deoxy-6-phosphogluconic acid,5TBDMS,isomer #1	CC(C)(C)[Si](C)(C)OC(=O)C(=O)C[C@H](O[Si](C)(C)C(C)(C)C)[C@@H](COP(=O)(O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C	3312.5	Semi standard non polar	33892256
2-Keto-3-deoxy-6-phosphogluconic acid,5TBDMS,isomer #1	CC(C)(C)[Si](C)(C)OC(=O)C(=O)C[C@H](O[Si](C)(C)C(C)(C)C)[C@@H](COP(=O)(O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C	3068.3	Standard non polar	33892256
2-Keto-3-deoxy-6-phosphogluconic acid,5TBDMS,isomer #1	CC(C)(C)[Si](C)(C)OC(=O)C(=O)C[C@H](O[Si](C)(C)C(C)(C)C)[C@@H](COP(=O)(O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C	2902.6	Standard polar	33892256
2-Keto-3-deoxy-6-phosphogluconic acid,5TBDMS,isomer #2	CC(C)(C)[Si](C)(C)OC(=O)C(=C[C@H](O[Si](C)(C)C(C)(C)C)[C@@H](COP(=O)(O)O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C	3306.3	Semi standard non polar	33892256
2-Keto-3-deoxy-6-phosphogluconic acid,5TBDMS,isomer #2	CC(C)(C)[Si](C)(C)OC(=O)C(=C[C@H](O[Si](C)(C)C(C)(C)C)[C@@H](COP(=O)(O)O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C	3014.7	Standard non polar	33892256
2-Keto-3-deoxy-6-phosphogluconic acid,5TBDMS,isomer #2	CC(C)(C)[Si](C)(C)OC(=O)C(=C[C@H](O[Si](C)(C)C(C)(C)C)[C@@H](COP(=O)(O)O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C	3012.6	Standard polar	33892256
2-Keto-3-deoxy-6-phosphogluconic acid,5TBDMS,isomer #3	CC(C)(C)[Si](C)(C)OC(=C[C@H](O[Si](C)(C)C(C)(C)C)[C@@H](COP(=O)(O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C)C(=O)O	3409.4	Semi standard non polar	33892256
2-Keto-3-deoxy-6-phosphogluconic acid,5TBDMS,isomer #3	CC(C)(C)[Si](C)(C)OC(=C[C@H](O[Si](C)(C)C(C)(C)C)[C@@H](COP(=O)(O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C)C(=O)O	3015.8	Standard non polar	33892256
2-Keto-3-deoxy-6-phosphogluconic acid,5TBDMS,isomer #3	CC(C)(C)[Si](C)(C)OC(=C[C@H](O[Si](C)(C)C(C)(C)C)[C@@H](COP(=O)(O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C)C(=O)O	2975.6	Standard polar	33892256
2-Keto-3-deoxy-6-phosphogluconic acid,5TBDMS,isomer #4	CC(C)(C)[Si](C)(C)OC(=O)C(=C[C@H](O)[C@@H](COP(=O)(O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C	3312.7	Semi standard non polar	33892256
2-Keto-3-deoxy-6-phosphogluconic acid,5TBDMS,isomer #4	CC(C)(C)[Si](C)(C)OC(=O)C(=C[C@H](O)[C@@H](COP(=O)(O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C	3007.9	Standard non polar	33892256
2-Keto-3-deoxy-6-phosphogluconic acid,5TBDMS,isomer #4	CC(C)(C)[Si](C)(C)OC(=O)C(=C[C@H](O)[C@@H](COP(=O)(O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C	2969.3	Standard polar	33892256
2-Keto-3-deoxy-6-phosphogluconic acid,5TBDMS,isomer #5	CC(C)(C)[Si](C)(C)OC(=O)C(=C[C@H](O[Si](C)(C)C(C)(C)C)[C@H](O)COP(=O)(O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C	3310.1	Semi standard non polar	33892256
2-Keto-3-deoxy-6-phosphogluconic acid,5TBDMS,isomer #5	CC(C)(C)[Si](C)(C)OC(=O)C(=C[C@H](O[Si](C)(C)C(C)(C)C)[C@H](O)COP(=O)(O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C	2984.8	Standard non polar	33892256
2-Keto-3-deoxy-6-phosphogluconic acid,5TBDMS,isomer #5	CC(C)(C)[Si](C)(C)OC(=O)C(=C[C@H](O[Si](C)(C)C(C)(C)C)[C@H](O)COP(=O)(O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C	2984.6	Standard polar	33892256

Spectra

Biological Properties

Cellular Locations

Not Available

Biospecimen Locations

Not Available

Tissue Locations

Not Available

Pathways

Not Available

Name	SMPDB/PathBank	KEGG

Normal Concentrations

Not Available

Abnormal Concentrations

Not Available

Associated Disorders and Diseases

Disease References

None

Associated OMIM IDs

None

External Links

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FooDB ID

KNApSAcK ID

Chemspider ID

KEGG Compound ID

BioCyc ID

2-KETO-3-DEOXY-6-P-GLUCONATE

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

6202

PubChem Compound

3080745

PDB ID

Not Available

ChEBI ID

15925

Food Biomarker Ontology

Not Available

VMH ID

Not Available

MarkerDB ID

Not Available

Good Scents ID

Not Available

References

Synthesis Reference

Not Available

Material Safety Data Sheet (MSDS)

Not Available

General References

Andreesen JR, Gottschalk G: The occurrence of a modified Entner-doudoroff pathway in Clostridium aceticum. Arch Mikrobiol. 1969;69(2):160-70. [PubMed:5383859 ]
Kersters K, De Ley J: The occurrence of the Entner-Doudoroff pathway in bacteria. Antonie Van Leeuwenhoek. 1968;34(4):393-408. [PubMed:5304016 ]

Showing metabocard for 2-Keto-3-deoxy-6-phosphogluconic acid (HMDB0001376)

MOL for HMDB0001376 (2-Keto-3-deoxy-6-phosphogluconic acid)

3D MOL for HMDB0001376 (2-Keto-3-deoxy-6-phosphogluconic acid)

3D SDF for HMDB0001376 (2-Keto-3-deoxy-6-phosphogluconic acid)

3D-SDF for HMDB0001376 (2-Keto-3-deoxy-6-phosphogluconic acid)

PDB for HMDB0001376 (2-Keto-3-deoxy-6-phosphogluconic acid)

3D PDB for HMDB0001376 (2-Keto-3-deoxy-6-phosphogluconic acid)

SMILES for HMDB0001376 (2-Keto-3-deoxy-6-phosphogluconic acid)

INCHI for HMDB0001376 (2-Keto-3-deoxy-6-phosphogluconic acid)

Structure for HMDB0001376 (2-Keto-3-deoxy-6-phosphogluconic acid)

3D Structure for HMDB0001376 (2-Keto-3-deoxy-6-phosphogluconic acid)

Experimental Collision Cross Sections

Predicted Collision Cross Sections

Predicted Retention Times

Underivatized

Predicted Kovats Retention Indices

Underivatized

Derivatized