Hmdb loader
You are using an unsupported browser. Please upgrade your browser to a newer version to get the best experience on Human Metabolome Database.
Record Information
Version5.0
StatusDetected but not Quantified
Creation Date2006-05-22 15:12:42 UTC
Update Date2022-09-22 18:34:17 UTC
HMDB IDHMDB0003219
Secondary Accession Numbers
  • HMDB03219
Metabolite Identification
Common NameSedoheptulose
DescriptionSedoheptulose (CAS: 3019-74-7) is a ketoheptose, a monosaccharide with seven carbon atoms and a ketone functional group. It is one of the few heptoses found in nature. Sedoheptulose is a seven-carbon ketose sugar originally found in Sedum spectabile, a common perennial garden plant. Later it was shown to be widely distributed in the plants of the Crassulaceae family. The Crassulaceae, or orpine family, is a family of dicotyledons. They store water in their succulent leaves. They are found worldwide, but mostly occur in the northern hemisphere and southern Africa, typically in dry and/or cold areas where water may be scarce. The family includes about 1,400 species in 33 genera. As a result, this sugar is often found to be part of the human diet. This sugar, D-sedoheptulose, is a significant intermediary compound in the cyclic regeneration of D-ribulose. It also plays an important role as a transitory compound in the cyclic regeneration of D-ribulose for carbon dioxide fixation in plant photosynthesis.
Structure
Data?1582752266
Synonyms
ValueSource
beta-D-SedoheptuloseChEBI
D-Altro-heptuloseChEBI
D-SedoheptuloseChEBI
VolemuloseChEBI
b-D-SedoheptuloseGenerator
Β-D-sedoheptuloseGenerator
b-D-SedoheptulopyranoseHMDB
Β-D-sedoheptulopyranoseHMDB
D-AltroheptuloseHMDB
beta-D-SedoheptulopyranoseHMDB
beta-D-Altro-2-heptulopyranoseHMDB
Β-D-altro-2-heptulopyranoseHMDB
SedoheptuloseHMDB
Chemical FormulaC7H14O7
Average Molecular Weight210.1819
Monoisotopic Molecular Weight210.073952802
IUPAC Name(2R,3S,4R,5S,6R)-2,6-bis(hydroxymethyl)oxane-2,3,4,5-tetrol
Traditional Nameβ-D-sedoheptulopyranose
CAS Registry Number470-46-2
SMILES
OC[C@H]1O[C@](O)(CO)[C@@H](O)[C@H](O)[C@@H]1O
InChI Identifier
InChI=1S/C7H14O7/c8-1-3-4(10)5(11)6(12)7(13,2-9)14-3/h3-6,8-13H,1-2H2/t3-,4-,5-,6+,7-/m1/s1
InChI KeyHAIWUXASLYEWLM-BNWJMWRWSA-N
Chemical Taxonomy
Description Belongs to the class of organic compounds known as c-glycosyl compounds. These are glycoside in which a sugar group is bonded through one carbon to another group via a C-glycosidic bond.
KingdomOrganic compounds
Super ClassOrganic oxygen compounds
ClassOrganooxygen compounds
Sub ClassCarbohydrates and carbohydrate conjugates
Direct ParentC-glycosyl compounds
Alternative Parents
Substituents
  • Hexose monosaccharide
  • C-glycosyl compound
  • Oxane
  • Monosaccharide
  • Secondary alcohol
  • Hemiacetal
  • Oxacycle
  • Organoheterocyclic compound
  • Polyol
  • Hydrocarbon derivative
  • Primary alcohol
  • Alcohol
  • Aliphatic heteromonocyclic compound
Molecular FrameworkAliphatic heteromonocyclic compounds
External Descriptors
Ontology
Disposition

Biological location

Source

Physical Properties
StateSolid
Experimental Molecular Properties
PropertyValueReference
Melting PointNot AvailableNot Available
Boiling PointNot AvailableNot Available
Water SolubilityNot AvailableNot Available
LogPNot AvailableNot Available
Experimental Chromatographic PropertiesNot Available
Predicted Molecular Properties
PropertyValueSource
Water Solubility227 g/LALOGPS
logP-2.6ALOGPS
logP-3.4ChemAxon
logS0.64ALOGPS
pKa (Strongest Acidic)10.28ChemAxon
pKa (Strongest Basic)-3ChemAxon
Physiological Charge0ChemAxon
Hydrogen Acceptor Count7ChemAxon
Hydrogen Donor Count6ChemAxon
Polar Surface Area130.61 ŲChemAxon
Rotatable Bond Count2ChemAxon
Refractivity42.32 m³·mol⁻¹ChemAxon
Polarizability18.79 ųChemAxon
Number of Rings1ChemAxon
BioavailabilityYesChemAxon
Rule of FiveNoChemAxon
Ghose FilterNoChemAxon
Veber's RuleNoChemAxon
MDDR-like RuleNoChemAxon
Predicted Chromatographic Properties

Predicted Collision Cross Sections

PredictorAdduct TypeCCS Value (Å2)Reference
DeepCCS[M+H]+144.16330932474
DeepCCS[M-H]-141.76830932474
DeepCCS[M-2H]-176.48830932474
DeepCCS[M+Na]+150.81730932474
AllCCS[M+H]+147.132859911
AllCCS[M+H-H2O]+143.132859911
AllCCS[M+NH4]+150.932859911
AllCCS[M+Na]+151.932859911
AllCCS[M-H]-138.132859911
AllCCS[M+Na-2H]-138.732859911
AllCCS[M+HCOO]-139.332859911

Predicted Kovats Retention Indices

Underivatized

MetaboliteSMILESKovats RI ValueColumn TypeReference
SedoheptuloseOC[C@H]1O[C@](O)(CO)[C@@H](O)[C@H](O)[C@@H]1O3672.1Standard polar33892256
SedoheptuloseOC[C@H]1O[C@](O)(CO)[C@@H](O)[C@H](O)[C@@H]1O2177.4Standard non polar33892256
SedoheptuloseOC[C@H]1O[C@](O)(CO)[C@@H](O)[C@H](O)[C@@H]1O1870.8Semi standard non polar33892256

Derivatized

Derivative Name / StructureSMILESKovats RI ValueColumn TypeReference
Sedoheptulose,1TMS,isomer #1C[Si](C)(C)OC[C@H]1O[C@](O)(CO)[C@@H](O)[C@H](O)[C@@H]1O1981.7Semi standard non polar33892256
Sedoheptulose,1TMS,isomer #2C[Si](C)(C)O[C@]1(CO)O[C@H](CO)[C@@H](O)[C@@H](O)[C@@H]1O1953.9Semi standard non polar33892256
Sedoheptulose,1TMS,isomer #3C[Si](C)(C)OC[C@@]1(O)O[C@H](CO)[C@@H](O)[C@@H](O)[C@@H]1O1984.5Semi standard non polar33892256
Sedoheptulose,1TMS,isomer #4C[Si](C)(C)O[C@H]1[C@H](O)[C@H](O)[C@@H](CO)O[C@]1(O)CO1965.1Semi standard non polar33892256
Sedoheptulose,1TMS,isomer #5C[Si](C)(C)O[C@H]1[C@H](O)[C@@](O)(CO)O[C@H](CO)[C@H]1O1950.8Semi standard non polar33892256
Sedoheptulose,1TMS,isomer #6C[Si](C)(C)O[C@H]1[C@@H](O)[C@H](O)[C@@](O)(CO)O[C@@H]1CO1933.9Semi standard non polar33892256
Sedoheptulose,2TMS,isomer #1C[Si](C)(C)OC[C@H]1O[C@@](CO)(O[Si](C)(C)C)[C@@H](O)[C@H](O)[C@@H]1O1952.0Semi standard non polar33892256
Sedoheptulose,2TMS,isomer #10C[Si](C)(C)OC[C@@]1(O)O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1O1929.9Semi standard non polar33892256
Sedoheptulose,2TMS,isomer #11C[Si](C)(C)OC[C@@]1(O)O[C@H](CO)[C@@H](O)[C@@H](O[Si](C)(C)C)[C@@H]1O1946.9Semi standard non polar33892256
Sedoheptulose,2TMS,isomer #12C[Si](C)(C)OC[C@@]1(O)O[C@H](CO)[C@@H](O)[C@@H](O)[C@@H]1O[Si](C)(C)C1954.9Semi standard non polar33892256
Sedoheptulose,2TMS,isomer #13C[Si](C)(C)O[C@H]1[C@H](O[Si](C)(C)C)[C@H](O)[C@@H](CO)O[C@]1(O)CO1919.2Semi standard non polar33892256
Sedoheptulose,2TMS,isomer #14C[Si](C)(C)O[C@@H]1[C@@H](CO)O[C@](O)(CO)[C@@H](O[Si](C)(C)C)[C@@H]1O1917.7Semi standard non polar33892256
Sedoheptulose,2TMS,isomer #15C[Si](C)(C)O[C@H]1[C@H](O)[C@@](O)(CO)O[C@H](CO)[C@H]1O[Si](C)(C)C1889.9Semi standard non polar33892256
Sedoheptulose,2TMS,isomer #2C[Si](C)(C)OC[C@H]1O[C@](O)(CO[Si](C)(C)C)[C@@H](O)[C@H](O)[C@@H]1O1951.1Semi standard non polar33892256
Sedoheptulose,2TMS,isomer #3C[Si](C)(C)OC[C@H]1O[C@](O)(CO)[C@@H](O[Si](C)(C)C)[C@H](O)[C@@H]1O1953.4Semi standard non polar33892256
Sedoheptulose,2TMS,isomer #4C[Si](C)(C)OC[C@H]1O[C@](O)(CO)[C@@H](O)[C@H](O[Si](C)(C)C)[C@@H]1O1933.0Semi standard non polar33892256
Sedoheptulose,2TMS,isomer #5C[Si](C)(C)OC[C@H]1O[C@](O)(CO)[C@@H](O)[C@H](O)[C@@H]1O[Si](C)(C)C1924.2Semi standard non polar33892256
Sedoheptulose,2TMS,isomer #6C[Si](C)(C)OC[C@@]1(O[Si](C)(C)C)O[C@H](CO)[C@@H](O)[C@@H](O)[C@@H]1O1950.2Semi standard non polar33892256
Sedoheptulose,2TMS,isomer #7C[Si](C)(C)O[C@H]1[C@@H](O)[C@H](O)[C@](CO)(O[Si](C)(C)C)O[C@@H]1CO1934.0Semi standard non polar33892256
Sedoheptulose,2TMS,isomer #8C[Si](C)(C)O[C@H]1[C@H](O)[C@](CO)(O[Si](C)(C)C)O[C@H](CO)[C@H]1O1939.2Semi standard non polar33892256
Sedoheptulose,2TMS,isomer #9C[Si](C)(C)O[C@H]1[C@H](O)[C@H](O)[C@@H](CO)O[C@@]1(CO)O[Si](C)(C)C1942.2Semi standard non polar33892256
Sedoheptulose,3TMS,isomer #1C[Si](C)(C)OC[C@H]1O[C@@](CO[Si](C)(C)C)(O[Si](C)(C)C)[C@@H](O)[C@H](O)[C@@H]1O1920.9Semi standard non polar33892256
Sedoheptulose,3TMS,isomer #10C[Si](C)(C)OC[C@H]1O[C@](O)(CO)[C@@H](O)[C@H](O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C1878.2Semi standard non polar33892256
Sedoheptulose,3TMS,isomer #11C[Si](C)(C)OC[C@@]1(O[Si](C)(C)C)O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1O1950.7Semi standard non polar33892256
Sedoheptulose,3TMS,isomer #12C[Si](C)(C)OC[C@@]1(O[Si](C)(C)C)O[C@H](CO)[C@@H](O)[C@@H](O[Si](C)(C)C)[C@@H]1O1964.6Semi standard non polar33892256
Sedoheptulose,3TMS,isomer #13C[Si](C)(C)OC[C@@]1(O[Si](C)(C)C)O[C@H](CO)[C@@H](O)[C@@H](O)[C@@H]1O[Si](C)(C)C1954.1Semi standard non polar33892256
Sedoheptulose,3TMS,isomer #14C[Si](C)(C)O[C@H]1[C@H](O)[C@](CO)(O[Si](C)(C)C)O[C@H](CO)[C@H]1O[Si](C)(C)C1942.5Semi standard non polar33892256
Sedoheptulose,3TMS,isomer #15C[Si](C)(C)O[C@@H]1[C@@H](CO)O[C@@](CO)(O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]1O1944.9Semi standard non polar33892256
Sedoheptulose,3TMS,isomer #16C[Si](C)(C)O[C@H]1[C@H](O[Si](C)(C)C)[C@H](O)[C@@H](CO)O[C@@]1(CO)O[Si](C)(C)C1950.1Semi standard non polar33892256
Sedoheptulose,3TMS,isomer #17C[Si](C)(C)OC[C@@]1(O)O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]1O1911.8Semi standard non polar33892256
Sedoheptulose,3TMS,isomer #18C[Si](C)(C)OC[C@@]1(O)O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1O[Si](C)(C)C1942.9Semi standard non polar33892256
Sedoheptulose,3TMS,isomer #19C[Si](C)(C)OC[C@@]1(O)O[C@H](CO)[C@@H](O)[C@@H](O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C1941.6Semi standard non polar33892256
Sedoheptulose,3TMS,isomer #2C[Si](C)(C)OC[C@H]1O[C@@](CO)(O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H](O)[C@@H]1O1942.6Semi standard non polar33892256
Sedoheptulose,3TMS,isomer #20C[Si](C)(C)O[C@H]1[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@@H](CO)O[C@]1(O)CO1910.1Semi standard non polar33892256
Sedoheptulose,3TMS,isomer #3C[Si](C)(C)OC[C@H]1O[C@@](CO)(O[Si](C)(C)C)[C@@H](O)[C@H](O[Si](C)(C)C)[C@@H]1O1958.3Semi standard non polar33892256
Sedoheptulose,3TMS,isomer #4C[Si](C)(C)OC[C@H]1O[C@@](CO)(O[Si](C)(C)C)[C@@H](O)[C@H](O)[C@@H]1O[Si](C)(C)C1946.2Semi standard non polar33892256
Sedoheptulose,3TMS,isomer #5C[Si](C)(C)OC[C@H]1O[C@](O)(CO[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H](O)[C@@H]1O1927.6Semi standard non polar33892256
Sedoheptulose,3TMS,isomer #6C[Si](C)(C)OC[C@H]1O[C@](O)(CO[Si](C)(C)C)[C@@H](O)[C@H](O[Si](C)(C)C)[C@@H]1O1932.7Semi standard non polar33892256
Sedoheptulose,3TMS,isomer #7C[Si](C)(C)OC[C@H]1O[C@](O)(CO[Si](C)(C)C)[C@@H](O)[C@H](O)[C@@H]1O[Si](C)(C)C1903.3Semi standard non polar33892256
Sedoheptulose,3TMS,isomer #8C[Si](C)(C)OC[C@H]1O[C@](O)(CO)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@@H]1O1921.0Semi standard non polar33892256
Sedoheptulose,3TMS,isomer #9C[Si](C)(C)OC[C@H]1O[C@](O)(CO)[C@@H](O[Si](C)(C)C)[C@H](O)[C@@H]1O[Si](C)(C)C1915.9Semi standard non polar33892256
Sedoheptulose,4TMS,isomer #1C[Si](C)(C)OC[C@H]1O[C@@](CO[Si](C)(C)C)(O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H](O)[C@@H]1O1949.7Semi standard non polar33892256
Sedoheptulose,4TMS,isomer #10C[Si](C)(C)OC[C@H]1O[C@](O)(CO)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C1943.0Semi standard non polar33892256
Sedoheptulose,4TMS,isomer #11C[Si](C)(C)OC[C@@]1(O[Si](C)(C)C)O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]1O1985.5Semi standard non polar33892256
Sedoheptulose,4TMS,isomer #12C[Si](C)(C)OC[C@@]1(O[Si](C)(C)C)O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1O[Si](C)(C)C1992.1Semi standard non polar33892256
Sedoheptulose,4TMS,isomer #13C[Si](C)(C)OC[C@@]1(O[Si](C)(C)C)O[C@H](CO)[C@@H](O)[C@@H](O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C2014.9Semi standard non polar33892256
Sedoheptulose,4TMS,isomer #14C[Si](C)(C)O[C@H]1[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@@H](CO)O[C@@]1(CO)O[Si](C)(C)C1997.3Semi standard non polar33892256
Sedoheptulose,4TMS,isomer #15C[Si](C)(C)OC[C@@]1(O)O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C1975.6Semi standard non polar33892256
Sedoheptulose,4TMS,isomer #2C[Si](C)(C)OC[C@H]1O[C@@](CO[Si](C)(C)C)(O[Si](C)(C)C)[C@@H](O)[C@H](O[Si](C)(C)C)[C@@H]1O1984.1Semi standard non polar33892256
Sedoheptulose,4TMS,isomer #3C[Si](C)(C)OC[C@H]1O[C@@](CO[Si](C)(C)C)(O[Si](C)(C)C)[C@@H](O)[C@H](O)[C@@H]1O[Si](C)(C)C1963.6Semi standard non polar33892256
Sedoheptulose,4TMS,isomer #4C[Si](C)(C)OC[C@H]1O[C@@](CO)(O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@@H]1O1993.3Semi standard non polar33892256
Sedoheptulose,4TMS,isomer #5C[Si](C)(C)OC[C@H]1O[C@@](CO)(O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H](O)[C@@H]1O[Si](C)(C)C1986.4Semi standard non polar33892256
Sedoheptulose,4TMS,isomer #6C[Si](C)(C)OC[C@H]1O[C@@](CO)(O[Si](C)(C)C)[C@@H](O)[C@H](O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C1974.6Semi standard non polar33892256
Sedoheptulose,4TMS,isomer #7C[Si](C)(C)OC[C@H]1O[C@](O)(CO[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@@H]1O1975.4Semi standard non polar33892256
Sedoheptulose,4TMS,isomer #8C[Si](C)(C)OC[C@H]1O[C@](O)(CO[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H](O)[C@@H]1O[Si](C)(C)C1979.7Semi standard non polar33892256
Sedoheptulose,4TMS,isomer #9C[Si](C)(C)OC[C@H]1O[C@](O)(CO[Si](C)(C)C)[C@@H](O)[C@H](O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C1937.7Semi standard non polar33892256
Sedoheptulose,5TMS,isomer #1C[Si](C)(C)OC[C@H]1O[C@@](CO[Si](C)(C)C)(O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@@H]1O2048.5Semi standard non polar33892256
Sedoheptulose,5TMS,isomer #2C[Si](C)(C)OC[C@H]1O[C@@](CO[Si](C)(C)C)(O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H](O)[C@@H]1O[Si](C)(C)C2027.5Semi standard non polar33892256
Sedoheptulose,5TMS,isomer #3C[Si](C)(C)OC[C@H]1O[C@@](CO[Si](C)(C)C)(O[Si](C)(C)C)[C@@H](O)[C@H](O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C2006.2Semi standard non polar33892256
Sedoheptulose,5TMS,isomer #4C[Si](C)(C)OC[C@H]1O[C@@](CO)(O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C2040.2Semi standard non polar33892256
Sedoheptulose,5TMS,isomer #5C[Si](C)(C)OC[C@H]1O[C@](O)(CO[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C1998.6Semi standard non polar33892256
Sedoheptulose,5TMS,isomer #6C[Si](C)(C)OC[C@@]1(O[Si](C)(C)C)O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C2065.6Semi standard non polar33892256
Sedoheptulose,6TMS,isomer #1C[Si](C)(C)OC[C@H]1O[C@@](CO[Si](C)(C)C)(O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C2108.6Semi standard non polar33892256
Sedoheptulose,1TBDMS,isomer #1CC(C)(C)[Si](C)(C)OC[C@H]1O[C@](O)(CO)[C@@H](O)[C@H](O)[C@@H]1O2232.2Semi standard non polar33892256
Sedoheptulose,1TBDMS,isomer #2CC(C)(C)[Si](C)(C)O[C@]1(CO)O[C@H](CO)[C@@H](O)[C@@H](O)[C@@H]1O2224.8Semi standard non polar33892256
Sedoheptulose,1TBDMS,isomer #3CC(C)(C)[Si](C)(C)OC[C@@]1(O)O[C@H](CO)[C@@H](O)[C@@H](O)[C@@H]1O2249.9Semi standard non polar33892256
Sedoheptulose,1TBDMS,isomer #4CC(C)(C)[Si](C)(C)O[C@H]1[C@H](O)[C@H](O)[C@@H](CO)O[C@]1(O)CO2196.7Semi standard non polar33892256
Sedoheptulose,1TBDMS,isomer #5CC(C)(C)[Si](C)(C)O[C@H]1[C@H](O)[C@@](O)(CO)O[C@H](CO)[C@H]1O2178.0Semi standard non polar33892256
Sedoheptulose,1TBDMS,isomer #6CC(C)(C)[Si](C)(C)O[C@H]1[C@@H](O)[C@H](O)[C@@](O)(CO)O[C@@H]1CO2186.5Semi standard non polar33892256
Sedoheptulose,2TBDMS,isomer #1CC(C)(C)[Si](C)(C)OC[C@H]1O[C@@](CO)(O[Si](C)(C)C(C)(C)C)[C@@H](O)[C@H](O)[C@@H]1O2433.0Semi standard non polar33892256
Sedoheptulose,2TBDMS,isomer #10CC(C)(C)[Si](C)(C)OC[C@@]1(O)O[C@H](CO)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H](O)[C@@H]1O2408.6Semi standard non polar33892256
Sedoheptulose,2TBDMS,isomer #11CC(C)(C)[Si](C)(C)OC[C@@]1(O)O[C@H](CO)[C@@H](O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H]1O2417.9Semi standard non polar33892256
Sedoheptulose,2TBDMS,isomer #12CC(C)(C)[Si](C)(C)OC[C@@]1(O)O[C@H](CO)[C@@H](O)[C@@H](O)[C@@H]1O[Si](C)(C)C(C)(C)C2428.6Semi standard non polar33892256
Sedoheptulose,2TBDMS,isomer #13CC(C)(C)[Si](C)(C)O[C@H]1[C@H](O[Si](C)(C)C(C)(C)C)[C@H](O)[C@@H](CO)O[C@]1(O)CO2388.4Semi standard non polar33892256
Sedoheptulose,2TBDMS,isomer #14CC(C)(C)[Si](C)(C)O[C@@H]1[C@@H](CO)O[C@](O)(CO)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H]1O2384.5Semi standard non polar33892256
Sedoheptulose,2TBDMS,isomer #15CC(C)(C)[Si](C)(C)O[C@H]1[C@H](O)[C@@](O)(CO)O[C@H](CO)[C@H]1O[Si](C)(C)C(C)(C)C2367.2Semi standard non polar33892256
Sedoheptulose,2TBDMS,isomer #2CC(C)(C)[Si](C)(C)OC[C@H]1O[C@](O)(CO[Si](C)(C)C(C)(C)C)[C@@H](O)[C@H](O)[C@@H]1O2456.5Semi standard non polar33892256
Sedoheptulose,2TBDMS,isomer #3CC(C)(C)[Si](C)(C)OC[C@H]1O[C@](O)(CO)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](O)[C@@H]1O2435.0Semi standard non polar33892256
Sedoheptulose,2TBDMS,isomer #4CC(C)(C)[Si](C)(C)OC[C@H]1O[C@](O)(CO)[C@@H](O)[C@H](O[Si](C)(C)C(C)(C)C)[C@@H]1O2408.4Semi standard non polar33892256
Sedoheptulose,2TBDMS,isomer #5CC(C)(C)[Si](C)(C)OC[C@H]1O[C@](O)(CO)[C@@H](O)[C@H](O)[C@@H]1O[Si](C)(C)C(C)(C)C2397.7Semi standard non polar33892256
Sedoheptulose,2TBDMS,isomer #6CC(C)(C)[Si](C)(C)OC[C@@]1(O[Si](C)(C)C(C)(C)C)O[C@H](CO)[C@@H](O)[C@@H](O)[C@@H]1O2433.2Semi standard non polar33892256
Sedoheptulose,2TBDMS,isomer #7CC(C)(C)[Si](C)(C)O[C@H]1[C@@H](O)[C@H](O)[C@](CO)(O[Si](C)(C)C(C)(C)C)O[C@@H]1CO2409.4Semi standard non polar33892256
Sedoheptulose,2TBDMS,isomer #8CC(C)(C)[Si](C)(C)O[C@H]1[C@H](O)[C@](CO)(O[Si](C)(C)C(C)(C)C)O[C@H](CO)[C@H]1O2410.1Semi standard non polar33892256
Sedoheptulose,2TBDMS,isomer #9CC(C)(C)[Si](C)(C)O[C@H]1[C@H](O)[C@H](O)[C@@H](CO)O[C@@]1(CO)O[Si](C)(C)C(C)(C)C2413.8Semi standard non polar33892256
Sedoheptulose,3TBDMS,isomer #1CC(C)(C)[Si](C)(C)OC[C@H]1O[C@@](CO[Si](C)(C)C(C)(C)C)(O[Si](C)(C)C(C)(C)C)[C@@H](O)[C@H](O)[C@@H]1O2641.6Semi standard non polar33892256
Sedoheptulose,3TBDMS,isomer #10CC(C)(C)[Si](C)(C)OC[C@H]1O[C@](O)(CO)[C@@H](O)[C@H](O[Si](C)(C)C(C)(C)C)[C@@H]1O[Si](C)(C)C(C)(C)C2599.6Semi standard non polar33892256
Sedoheptulose,3TBDMS,isomer #11CC(C)(C)[Si](C)(C)OC[C@@]1(O[Si](C)(C)C(C)(C)C)O[C@H](CO)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H](O)[C@@H]1O2645.8Semi standard non polar33892256
Sedoheptulose,3TBDMS,isomer #12CC(C)(C)[Si](C)(C)OC[C@@]1(O[Si](C)(C)C(C)(C)C)O[C@H](CO)[C@@H](O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H]1O2659.2Semi standard non polar33892256
Sedoheptulose,3TBDMS,isomer #13CC(C)(C)[Si](C)(C)OC[C@@]1(O[Si](C)(C)C(C)(C)C)O[C@H](CO)[C@@H](O)[C@@H](O)[C@@H]1O[Si](C)(C)C(C)(C)C2657.5Semi standard non polar33892256
Sedoheptulose,3TBDMS,isomer #14CC(C)(C)[Si](C)(C)O[C@H]1[C@H](O)[C@](CO)(O[Si](C)(C)C(C)(C)C)O[C@H](CO)[C@H]1O[Si](C)(C)C(C)(C)C2640.7Semi standard non polar33892256
Sedoheptulose,3TBDMS,isomer #15CC(C)(C)[Si](C)(C)O[C@@H]1[C@@H](CO)O[C@@](CO)(O[Si](C)(C)C(C)(C)C)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H]1O2636.1Semi standard non polar33892256
Sedoheptulose,3TBDMS,isomer #16CC(C)(C)[Si](C)(C)O[C@H]1[C@H](O[Si](C)(C)C(C)(C)C)[C@H](O)[C@@H](CO)O[C@@]1(CO)O[Si](C)(C)C(C)(C)C2647.3Semi standard non polar33892256
Sedoheptulose,3TBDMS,isomer #17CC(C)(C)[Si](C)(C)OC[C@@]1(O)O[C@H](CO)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H]1O2632.8Semi standard non polar33892256
Sedoheptulose,3TBDMS,isomer #18CC(C)(C)[Si](C)(C)OC[C@@]1(O)O[C@H](CO)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H](O)[C@@H]1O[Si](C)(C)C(C)(C)C2659.9Semi standard non polar33892256
Sedoheptulose,3TBDMS,isomer #19CC(C)(C)[Si](C)(C)OC[C@@]1(O)O[C@H](CO)[C@@H](O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H]1O[Si](C)(C)C(C)(C)C2660.5Semi standard non polar33892256
Sedoheptulose,3TBDMS,isomer #2CC(C)(C)[Si](C)(C)OC[C@H]1O[C@@](CO)(O[Si](C)(C)C(C)(C)C)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](O)[C@@H]1O2647.2Semi standard non polar33892256
Sedoheptulose,3TBDMS,isomer #20CC(C)(C)[Si](C)(C)O[C@H]1[C@H](O[Si](C)(C)C(C)(C)C)[C@H](O[Si](C)(C)C(C)(C)C)[C@@H](CO)O[C@]1(O)CO2630.4Semi standard non polar33892256
Sedoheptulose,3TBDMS,isomer #3CC(C)(C)[Si](C)(C)OC[C@H]1O[C@@](CO)(O[Si](C)(C)C(C)(C)C)[C@@H](O)[C@H](O[Si](C)(C)C(C)(C)C)[C@@H]1O2653.3Semi standard non polar33892256
Sedoheptulose,3TBDMS,isomer #4CC(C)(C)[Si](C)(C)OC[C@H]1O[C@@](CO)(O[Si](C)(C)C(C)(C)C)[C@@H](O)[C@H](O)[C@@H]1O[Si](C)(C)C(C)(C)C2641.9Semi standard non polar33892256
Sedoheptulose,3TBDMS,isomer #5CC(C)(C)[Si](C)(C)OC[C@H]1O[C@](O)(CO[Si](C)(C)C(C)(C)C)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](O)[C@@H]1O2673.2Semi standard non polar33892256
Sedoheptulose,3TBDMS,isomer #6CC(C)(C)[Si](C)(C)OC[C@H]1O[C@](O)(CO[Si](C)(C)C(C)(C)C)[C@@H](O)[C@H](O[Si](C)(C)C(C)(C)C)[C@@H]1O2650.2Semi standard non polar33892256
Sedoheptulose,3TBDMS,isomer #7CC(C)(C)[Si](C)(C)OC[C@H]1O[C@](O)(CO[Si](C)(C)C(C)(C)C)[C@@H](O)[C@H](O)[C@@H]1O[Si](C)(C)C(C)(C)C2630.5Semi standard non polar33892256
Sedoheptulose,3TBDMS,isomer #8CC(C)(C)[Si](C)(C)OC[C@H]1O[C@](O)(CO)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](O[Si](C)(C)C(C)(C)C)[C@@H]1O2641.9Semi standard non polar33892256
Sedoheptulose,3TBDMS,isomer #9CC(C)(C)[Si](C)(C)OC[C@H]1O[C@](O)(CO)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](O)[C@@H]1O[Si](C)(C)C(C)(C)C2646.4Semi standard non polar33892256
Sedoheptulose,4TBDMS,isomer #1CC(C)(C)[Si](C)(C)OC[C@H]1O[C@@](CO[Si](C)(C)C(C)(C)C)(O[Si](C)(C)C(C)(C)C)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](O)[C@@H]1O2861.1Semi standard non polar33892256
Sedoheptulose,4TBDMS,isomer #10CC(C)(C)[Si](C)(C)OC[C@H]1O[C@](O)(CO)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](O[Si](C)(C)C(C)(C)C)[C@@H]1O[Si](C)(C)C(C)(C)C2837.4Semi standard non polar33892256
Sedoheptulose,4TBDMS,isomer #11CC(C)(C)[Si](C)(C)OC[C@@]1(O[Si](C)(C)C(C)(C)C)O[C@H](CO)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H]1O2860.3Semi standard non polar33892256
Sedoheptulose,4TBDMS,isomer #12CC(C)(C)[Si](C)(C)OC[C@@]1(O[Si](C)(C)C(C)(C)C)O[C@H](CO)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H](O)[C@@H]1O[Si](C)(C)C(C)(C)C2866.3Semi standard non polar33892256
Sedoheptulose,4TBDMS,isomer #13CC(C)(C)[Si](C)(C)OC[C@@]1(O[Si](C)(C)C(C)(C)C)O[C@H](CO)[C@@H](O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H]1O[Si](C)(C)C(C)(C)C2868.7Semi standard non polar33892256
Sedoheptulose,4TBDMS,isomer #14CC(C)(C)[Si](C)(C)O[C@H]1[C@H](O[Si](C)(C)C(C)(C)C)[C@H](O[Si](C)(C)C(C)(C)C)[C@@H](CO)O[C@@]1(CO)O[Si](C)(C)C(C)(C)C2857.4Semi standard non polar33892256
Sedoheptulose,4TBDMS,isomer #15CC(C)(C)[Si](C)(C)OC[C@@]1(O)O[C@H](CO)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H]1O[Si](C)(C)C(C)(C)C2852.4Semi standard non polar33892256
Sedoheptulose,4TBDMS,isomer #2CC(C)(C)[Si](C)(C)OC[C@H]1O[C@@](CO[Si](C)(C)C(C)(C)C)(O[Si](C)(C)C(C)(C)C)[C@@H](O)[C@H](O[Si](C)(C)C(C)(C)C)[C@@H]1O2864.4Semi standard non polar33892256
Sedoheptulose,4TBDMS,isomer #3CC(C)(C)[Si](C)(C)OC[C@H]1O[C@@](CO[Si](C)(C)C(C)(C)C)(O[Si](C)(C)C(C)(C)C)[C@@H](O)[C@H](O)[C@@H]1O[Si](C)(C)C(C)(C)C2851.2Semi standard non polar33892256
Sedoheptulose,4TBDMS,isomer #4CC(C)(C)[Si](C)(C)OC[C@H]1O[C@@](CO)(O[Si](C)(C)C(C)(C)C)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](O[Si](C)(C)C(C)(C)C)[C@@H]1O2864.7Semi standard non polar33892256
Sedoheptulose,4TBDMS,isomer #5CC(C)(C)[Si](C)(C)OC[C@H]1O[C@@](CO)(O[Si](C)(C)C(C)(C)C)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](O)[C@@H]1O[Si](C)(C)C(C)(C)C2861.1Semi standard non polar33892256
Sedoheptulose,4TBDMS,isomer #6CC(C)(C)[Si](C)(C)OC[C@H]1O[C@@](CO)(O[Si](C)(C)C(C)(C)C)[C@@H](O)[C@H](O[Si](C)(C)C(C)(C)C)[C@@H]1O[Si](C)(C)C(C)(C)C2860.5Semi standard non polar33892256
Sedoheptulose,4TBDMS,isomer #7CC(C)(C)[Si](C)(C)OC[C@H]1O[C@](O)(CO[Si](C)(C)C(C)(C)C)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](O[Si](C)(C)C(C)(C)C)[C@@H]1O2867.1Semi standard non polar33892256
Sedoheptulose,4TBDMS,isomer #8CC(C)(C)[Si](C)(C)OC[C@H]1O[C@](O)(CO[Si](C)(C)C(C)(C)C)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](O)[C@@H]1O[Si](C)(C)C(C)(C)C2879.7Semi standard non polar33892256
Sedoheptulose,4TBDMS,isomer #9CC(C)(C)[Si](C)(C)OC[C@H]1O[C@](O)(CO[Si](C)(C)C(C)(C)C)[C@@H](O)[C@H](O[Si](C)(C)C(C)(C)C)[C@@H]1O[Si](C)(C)C(C)(C)C2841.6Semi standard non polar33892256
Sedoheptulose,5TBDMS,isomer #1CC(C)(C)[Si](C)(C)OC[C@H]1O[C@@](CO[Si](C)(C)C(C)(C)C)(O[Si](C)(C)C(C)(C)C)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](O[Si](C)(C)C(C)(C)C)[C@@H]1O3044.9Semi standard non polar33892256
Sedoheptulose,5TBDMS,isomer #2CC(C)(C)[Si](C)(C)OC[C@H]1O[C@@](CO[Si](C)(C)C(C)(C)C)(O[Si](C)(C)C(C)(C)C)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](O)[C@@H]1O[Si](C)(C)C(C)(C)C3039.5Semi standard non polar33892256
Sedoheptulose,5TBDMS,isomer #3CC(C)(C)[Si](C)(C)OC[C@H]1O[C@@](CO[Si](C)(C)C(C)(C)C)(O[Si](C)(C)C(C)(C)C)[C@@H](O)[C@H](O[Si](C)(C)C(C)(C)C)[C@@H]1O[Si](C)(C)C(C)(C)C3026.7Semi standard non polar33892256
Sedoheptulose,5TBDMS,isomer #4CC(C)(C)[Si](C)(C)OC[C@H]1O[C@@](CO)(O[Si](C)(C)C(C)(C)C)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](O[Si](C)(C)C(C)(C)C)[C@@H]1O[Si](C)(C)C(C)(C)C3046.8Semi standard non polar33892256
Sedoheptulose,5TBDMS,isomer #5CC(C)(C)[Si](C)(C)OC[C@H]1O[C@](O)(CO[Si](C)(C)C(C)(C)C)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](O[Si](C)(C)C(C)(C)C)[C@@H]1O[Si](C)(C)C(C)(C)C3058.4Semi standard non polar33892256
Sedoheptulose,5TBDMS,isomer #6CC(C)(C)[Si](C)(C)OC[C@@]1(O[Si](C)(C)C(C)(C)C)O[C@H](CO)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H]1O[Si](C)(C)C(C)(C)C3048.1Semi standard non polar33892256
Sedoheptulose,6TBDMS,isomer #1CC(C)(C)[Si](C)(C)OC[C@H]1O[C@@](CO[Si](C)(C)C(C)(C)C)(O[Si](C)(C)C(C)(C)C)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](O[Si](C)(C)C(C)(C)C)[C@@H]1O[Si](C)(C)C(C)(C)C3249.8Semi standard non polar33892256
Spectra

GC-MS Spectra

Spectrum TypeDescriptionSplash KeyDeposition DateSourceView
Predicted GC-MSPredicted GC-MS Spectrum - Sedoheptulose GC-MS (Non-derivatized) - 70eV, PositiveNot Available2021-10-12Wishart LabView Spectrum

MS/MS Spectra

Spectrum TypeDescriptionSplash KeyDeposition DateSourceView
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Sedoheptulose 10V, Negative-QTOFsplash10-0a4i-2290000000-b75209a2ded2569fd90d2021-09-22Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Sedoheptulose 20V, Negative-QTOFsplash10-0a4i-9110000000-469f32ec283b1ab3663a2021-09-22Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Sedoheptulose 40V, Negative-QTOFsplash10-0a4i-9000000000-e748c71d0610471789b62021-09-22Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Sedoheptulose 10V, Positive-QTOFsplash10-03di-0490000000-2c85b0b40e4eb7c699e12021-09-22Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Sedoheptulose 20V, Positive-QTOFsplash10-03di-9330000000-154c47472db8afc2b7be2021-09-22Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Sedoheptulose 40V, Positive-QTOFsplash10-0c29-9000000000-947d80d103b7151973d42021-09-22Wishart LabView Spectrum

NMR Spectra

Spectrum TypeDescriptionDeposition DateSourceView
Predicted 1D NMR1H NMR Spectrum (1D, 100 MHz, D2O, predicted)2021-09-25Wishart LabView Spectrum
Predicted 1D NMR13C NMR Spectrum (1D, 100 MHz, D2O, predicted)2021-09-25Wishart LabView Spectrum
Predicted 1D NMR1H NMR Spectrum (1D, 1000 MHz, D2O, predicted)2021-09-25Wishart LabView Spectrum
Predicted 1D NMR13C NMR Spectrum (1D, 1000 MHz, D2O, predicted)2021-09-25Wishart LabView Spectrum
Predicted 1D NMR1H NMR Spectrum (1D, 200 MHz, D2O, predicted)2021-09-25Wishart LabView Spectrum
Predicted 1D NMR13C NMR Spectrum (1D, 200 MHz, D2O, predicted)2021-09-25Wishart LabView Spectrum
Predicted 1D NMR1H NMR Spectrum (1D, 300 MHz, D2O, predicted)2021-09-25Wishart LabView Spectrum
Predicted 1D NMR13C NMR Spectrum (1D, 300 MHz, D2O, predicted)2021-09-25Wishart LabView Spectrum
Predicted 1D NMR1H NMR Spectrum (1D, 400 MHz, D2O, predicted)2021-09-25Wishart LabView Spectrum
Predicted 1D NMR13C NMR Spectrum (1D, 400 MHz, D2O, predicted)2021-09-25Wishart LabView Spectrum
Predicted 1D NMR1H NMR Spectrum (1D, 500 MHz, D2O, predicted)2021-09-25Wishart LabView Spectrum
Predicted 1D NMR13C NMR Spectrum (1D, 500 MHz, D2O, predicted)2021-09-25Wishart LabView Spectrum
Predicted 1D NMR1H NMR Spectrum (1D, 600 MHz, D2O, predicted)2021-09-25Wishart LabView Spectrum
Predicted 1D NMR13C NMR Spectrum (1D, 600 MHz, D2O, predicted)2021-09-25Wishart LabView Spectrum
Predicted 1D NMR1H NMR Spectrum (1D, 700 MHz, D2O, predicted)2021-09-25Wishart LabView Spectrum
Predicted 1D NMR13C NMR Spectrum (1D, 700 MHz, D2O, predicted)2021-09-25Wishart LabView Spectrum
Predicted 1D NMR1H NMR Spectrum (1D, 800 MHz, D2O, predicted)2021-09-25Wishart LabView Spectrum
Predicted 1D NMR13C NMR Spectrum (1D, 800 MHz, D2O, predicted)2021-09-25Wishart LabView Spectrum
Predicted 1D NMR1H NMR Spectrum (1D, 900 MHz, D2O, predicted)2021-09-25Wishart LabView Spectrum
Predicted 1D NMR13C NMR Spectrum (1D, 900 MHz, D2O, predicted)2021-09-25Wishart LabView Spectrum
Biological Properties
Cellular Locations
  • Cytoplasm (predicted from logP)
Biospecimen Locations
  • Blood
  • Feces
  • Urine
Tissue Locations
  • Placenta
Pathways
Normal Concentrations
BiospecimenStatusValueAgeSexConditionReferenceDetails
FecesDetected but not QuantifiedNot QuantifiedAdult (>18 years old)Both
Normal
details
Abnormal Concentrations
BiospecimenStatusValueAgeSexConditionReferenceDetails
BloodExpected but not QuantifiedNot QuantifiedNot SpecifiedNot SpecifiedCancer patients undergoing total body irradiation details
UrineDetected but not QuantifiedNot QuantifiedNot SpecifiedNot SpecifiedCancer patients undergoing total body irradiation details
Associated Disorders and Diseases
Disease ReferencesNone
Associated OMIM IDsNone
DrugBank IDNot Available
Phenol Explorer Compound IDNot Available
FooDB IDNot Available
KNApSAcK IDC00001132
Chemspider ID390207
KEGG Compound IDC08355
BioCyc IDNot Available
BiGG IDNot Available
Wikipedia LinkSedoheptulose
METLIN IDNot Available
PubChem Compound441483
PDB IDNot Available
ChEBI ID27520
Food Biomarker OntologyNot Available
VMH IDM03165
MarkerDB IDNot Available
Good Scents IDNot Available
References
Synthesis ReferenceNot Available
Material Safety Data Sheet (MSDS)Download (PDF)
General References
  1. Pitkanen E, Sahlstrom K: The occurrence of sedoheptulose in human urine. Ann Med Exp Biol Fenn. 1968;46(3):295-300. [PubMed:5731228 ]
  2. Elshenawy S, Pinney SE, Stuart T, Doulias PT, Zura G, Parry S, Elovitz MA, Bennett MJ, Bansal A, Strauss JF 3rd, Ischiropoulos H, Simmons RA: The Metabolomic Signature of the Placenta in Spontaneous Preterm Birth. Int J Mol Sci. 2020 Feb 4;21(3). pii: ijms21031043. doi: 10.3390/ijms21031043. [PubMed:32033212 ]

Enzymes

General function:
Involved in catalytic activity
Specific function:
Catalyzes the transfer of a two-carbon ketol group from a ketose donor to an aldose acceptor, via a covalent intermediate with the cofactor thiamine pyrophosphate (By similarity).
Gene Name:
TKTL1
Uniprot ID:
P51854
Molecular weight:
59302.195
General function:
Involved in catalytic activity
Specific function:
Transaldolase is important for the balance of metabolites in the pentose-phosphate pathway.
Gene Name:
TALDO1
Uniprot ID:
P37837
Molecular weight:
37539.74
General function:
Involved in catalytic activity
Specific function:
Catalyzes the transfer of a two-carbon ketol group from a ketose donor to an aldose acceptor, via a covalent intermediate with the cofactor thiamine pyrophosphate.
Gene Name:
TKT
Uniprot ID:
P29401
Molecular weight:
67876.95
General function:
Carbohydrate transport and metabolism
Specific function:
Not Available
Gene Name:
KHK
Uniprot ID:
P50053
Molecular weight:
32730.055
Reactions
Adenosine triphosphate + Sedoheptulose → ADP + Sedoheptulose 1-phosphatedetails
General function:
Involved in catalytic activity
Specific function:
Plays an essential role in total transketolase activity and cell proliferation in cancer cells; after transfection with anti-TKTL1 siRNA, total transketolase activity dramatically decreases and proliferation was significantly inhibited in cancer cells. Plays a pivotal role in carcinogenesis.
Gene Name:
TKTL2
Uniprot ID:
Q9H0I9
Molecular weight:
67876.625
General function:
Involved in phosphotransferase activity, alcohol group as acceptor
Specific function:
Acts as a modulator of macrophage activation through control of glucose metabolism (By similarity).
Gene Name:
SHPK
Uniprot ID:
Q9UHJ6
Molecular weight:
51504.425
Reactions
Adenosine triphosphate + Sedoheptulose → ADP + D-Sedoheptulose 7-phosphatedetails