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Record Information

Version

5.0

Status

Detected but not Quantified

Creation Date

2021-09-11 00:49:52 UTC

Update Date

2021-09-26 22:57:36 UTC

HMDB ID

HMDB0247738

Secondary Accession Numbers

None

Metabolite Identification

Common Name

AB-Chminaca

Description

AB-Chminaca belongs to the class of organic compounds known as n-acyl-alpha amino acids and derivatives. N-acyl-alpha amino acids and derivatives are compounds containing an alpha amino acid (or a derivative thereof) which bears an acyl group at its terminal nitrogen atom. Based on a literature review a significant number of articles have been published on AB-Chminaca. This compound has been identified in human blood as reported by (PMID: 31557052 ). Ab-chminaca is not a naturally occurring metabolite and is only found in those individuals exposed to this compound or its derivatives. Technically AB-Chminaca is part of the human exposome. The exposome can be defined as the collection of all the exposures of an individual in a lifetime and how those exposures relate to health. An individual's exposure begins before birth and includes insults from environmental and occupational sources.

Structure

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

  Mrv1652309112102502D          

 26 28  0  0  0  0            999 V2000
    2.4820    0.5756    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1964    0.1631    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1964   -0.6619    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9109    0.5756    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9109    1.4006    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6254    1.8131    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.1964    1.8131    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    4.6254    0.1631    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    5.3399    0.5756    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3399    1.4006    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.0543    0.1631    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.8080    0.4987    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    7.3600   -0.1144    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    6.9475   -0.8289    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.2025   -1.6135    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.6504   -2.2266    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8435   -2.0551    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5885   -1.2704    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1406   -0.6573    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.1805   -0.0282    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.6654   -0.6956    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.4859   -0.6094    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.9708   -1.2768    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.6353   -2.0305    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.8148   -2.1167    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.3299   -1.4493    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  1  0  0  0  0
  2  4  1  0  0  0  0
  4  5  1  0  0  0  0
  5  6  2  0  0  0  0
  5  7  1  0  0  0  0
  4  8  1  0  0  0  0
  8  9  1  0  0  0  0
  9 10  2  0  0  0  0
  9 11  1  0  0  0  0
 11 12  2  0  0  0  0
 12 13  1  0  0  0  0
 13 14  1  0  0  0  0
 14 15  2  0  0  0  0
 15 16  1  0  0  0  0
 16 17  2  0  0  0  0
 17 18  1  0  0  0  0
 18 19  2  0  0  0  0
 14 19  1  0  0  0  0
 11 19  1  0  0  0  0
 13 20  1  0  0  0  0
 20 21  1  0  0  0  0
 21 22  1  0  0  0  0
 22 23  1  0  0  0  0
 23 24  1  0  0  0  0
 24 25  1  0  0  0  0
 25 26  1  0  0  0  0
 21 26  1  0  0  0  0
M  END

HMDB0247738
     RDKit          3D
AB-Chminaca
 54 56  0  0  0  0  0  0  0  0999 V2000
   -6.3112    0.2721   -0.5328 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9134   -0.2485   -0.3970 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6874   -1.2399   -1.5648 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8493    0.8195   -0.4459 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5237    0.2735   -0.2922 N   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5992    0.1284   -1.3475 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8812    0.4594   -2.5149 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2557   -0.4348   -1.0779 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3990   -0.3764    0.0804 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.5549   -1.0384   -0.0149 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.5131   -1.1733    1.0565 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5702   -0.0841    0.9570 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0485    1.2978    1.0043 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2873    2.1118    2.2046 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7288    1.9188    2.6248 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7952    0.4681    3.0963 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6782   -0.4037    1.8939 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6313   -1.5339   -1.2660 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5468   -2.2980   -1.9579 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3903   -2.6882   -3.2573 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2427   -2.3003   -3.9430 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3129   -1.5419   -3.2782 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4803   -1.1516   -1.9624 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0836    2.0001    0.3721 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3146    2.7064    0.3513 N   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2040    2.4636    1.1365 O   0  0  0  0  0  0  0  0  0  0  0  0
   -6.7696    0.6393    0.3940 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.3161    1.0937   -1.2784 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.9868   -0.5150   -0.9641 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8187   -0.8260    0.5195 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8868   -1.9191   -1.2295 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3401   -0.5961   -2.4027 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6001   -1.7869   -1.8062 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8740    1.1739   -1.5365 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2490   -0.0302    0.6506 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9973   -1.0063    2.0355 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9640   -2.1780    1.1236 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.0119   -0.2400   -0.0839 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9405    1.2723    0.8408 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.4433    1.8870    0.1262 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2039    3.2056    1.9110 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6553    1.9198    3.0740 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.0192    2.5831    3.4451 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.4079    1.9696    1.7481 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.8095    0.3385    3.5313 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.0508    0.2824    3.9036 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.5480   -1.4588    2.2641 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.6775   -0.3877    1.3753 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.4503   -2.6057   -1.4319 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.1226   -3.2890   -3.7754 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1410   -2.6265   -4.9693 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5724   -1.2623   -3.8600 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6525    3.2118   -0.5018 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9333    2.7444    1.1893 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  2  4  1  0
  4  5  1  0
  5  6  1  0
  6  7  2  0
  6  8  1  0
  8  9  2  0
  9 10  1  0
 10 11  1  0
 11 12  1  0
 12 13  1  0
 13 14  1  0
 14 15  1  0
 15 16  1  0
 16 17  1  0
 10 18  1  0
 18 19  2  0
 19 20  1  0
 20 21  2  0
 21 22  1  0
 22 23  2  0
  4 24  1  0
 24 25  1  0
 24 26  2  0
 23  8  1  0
 17 12  1  0
 23 18  1  0
  1 27  1  0
  1 28  1  0
  1 29  1  0
  2 30  1  0
  3 31  1  0
  3 32  1  0
  3 33  1  0
  4 34  1  0
  5 35  1  0
 11 36  1  0
 11 37  1  0
 12 38  1  0
 13 39  1  0
 13 40  1  0
 14 41  1  0
 14 42  1  0
 15 43  1  0
 15 44  1  0
 16 45  1  0
 16 46  1  0
 17 47  1  0
 17 48  1  0
 19 49  1  0
 20 50  1  0
 21 51  1  0
 22 52  1  0
 25 53  1  0
 25 54  1  0
M  END

  Mrv1652309112102502D          

 26 28  0  0  0  0            999 V2000
    2.4820    0.5756    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1964    0.1631    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1964   -0.6619    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9109    0.5756    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9109    1.4006    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6254    1.8131    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.1964    1.8131    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    4.6254    0.1631    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    5.3399    0.5756    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3399    1.4006    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.0543    0.1631    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.8080    0.4987    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    7.3600   -0.1144    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    6.9475   -0.8289    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.2025   -1.6135    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.6504   -2.2266    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8435   -2.0551    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5885   -1.2704    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1406   -0.6573    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.1805   -0.0282    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.6654   -0.6956    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.4859   -0.6094    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.9708   -1.2768    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.6353   -2.0305    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.8148   -2.1167    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.3299   -1.4493    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  1  0  0  0  0
  2  4  1  0  0  0  0
  4  5  1  0  0  0  0
  5  6  2  0  0  0  0
  5  7  1  0  0  0  0
  4  8  1  0  0  0  0
  8  9  1  0  0  0  0
  9 10  2  0  0  0  0
  9 11  1  0  0  0  0
 11 12  2  0  0  0  0
 12 13  1  0  0  0  0
 13 14  1  0  0  0  0
 14 15  2  0  0  0  0
 15 16  1  0  0  0  0
 16 17  2  0  0  0  0
 17 18  1  0  0  0  0
 18 19  2  0  0  0  0
 14 19  1  0  0  0  0
 11 19  1  0  0  0  0
 13 20  1  0  0  0  0
 20 21  1  0  0  0  0
 21 22  1  0  0  0  0
 22 23  1  0  0  0  0
 23 24  1  0  0  0  0
 24 25  1  0  0  0  0
 25 26  1  0  0  0  0
 21 26  1  0  0  0  0
M  END
> <DATABASE_ID>
HMDB0247738

> <DATABASE_NAME>
hmdb

> <SMILES>
CC(C)C(NC(=O)C1=NN(CC2CCCCC2)C2=CC=CC=C12)C(N)=O

> <INCHI_IDENTIFIER>
InChI=1S/C20H28N4O2/c1-13(2)17(19(21)25)22-20(26)18-15-10-6-7-11-16(15)24(23-18)12-14-8-4-3-5-9-14/h6-7,10-11,13-14,17H,3-5,8-9,12H2,1-2H3,(H2,21,25)(H,22,26)

> <INCHI_KEY>
KJNZIEGLNLCWTQ-UHFFFAOYSA-N

> <FORMULA>
C20H28N4O2

> <MOLECULAR_WEIGHT>
356.47

> <EXACT_MASS>
356.221226158

> <JCHEM_ACCEPTOR_COUNT>
3

> <JCHEM_ATOM_COUNT>
54

> <JCHEM_AVERAGE_POLARIZABILITY>
40.187823105155644

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
2-{[1-(cyclohexylmethyl)-1H-indazol-3-yl]formamido}-3-methylbutanamide

> <ALOGPS_LOGP>
3.26

> <JCHEM_LOGP>
3.121733866333334

> <ALOGPS_LOGS>
-4.33

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
15.795059273583867

> <JCHEM_PKA_STRONGEST_ACIDIC>
14.651137036561384

> <JCHEM_PKA_STRONGEST_BASIC>
-0.43570838095913145

> <JCHEM_POLAR_SURFACE_AREA>
90.00999999999999

> <JCHEM_REFRACTIVITY>
112.0335

> <JCHEM_ROTATABLE_BOND_COUNT>
6

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
1.67e-02 g/l

> <JCHEM_TRADITIONAL_IUPAC>
2-{[1-(cyclohexylmethyl)indazol-3-yl]formamido}-3-methylbutanamide

> <JCHEM_VEBER_RULE>
0

$$$$

HMDB0247738
     RDKit          3D
AB-Chminaca
 54 56  0  0  0  0  0  0  0  0999 V2000
   -6.3112    0.2721   -0.5328 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9134   -0.2485   -0.3970 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6874   -1.2399   -1.5648 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8493    0.8195   -0.4459 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5237    0.2735   -0.2922 N   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5992    0.1284   -1.3475 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8812    0.4594   -2.5149 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2557   -0.4348   -1.0779 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3990   -0.3764    0.0804 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.5549   -1.0384   -0.0149 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.5131   -1.1733    1.0565 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5702   -0.0841    0.9570 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0485    1.2978    1.0043 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2873    2.1118    2.2046 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7288    1.9188    2.6248 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7952    0.4681    3.0963 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6782   -0.4037    1.8939 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6313   -1.5339   -1.2660 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5468   -2.2980   -1.9579 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3903   -2.6882   -3.2573 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2427   -2.3003   -3.9430 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3129   -1.5419   -3.2782 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4803   -1.1516   -1.9624 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0836    2.0001    0.3721 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3146    2.7064    0.3513 N   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2040    2.4636    1.1365 O   0  0  0  0  0  0  0  0  0  0  0  0
   -6.7696    0.6393    0.3940 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.3161    1.0937   -1.2784 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.9868   -0.5150   -0.9641 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8187   -0.8260    0.5195 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8868   -1.9191   -1.2295 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3401   -0.5961   -2.4027 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6001   -1.7869   -1.8062 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8740    1.1739   -1.5365 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2490   -0.0302    0.6506 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9973   -1.0063    2.0355 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9640   -2.1780    1.1236 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.0119   -0.2400   -0.0839 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9405    1.2723    0.8408 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.4433    1.8870    0.1262 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2039    3.2056    1.9110 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6553    1.9198    3.0740 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.0192    2.5831    3.4451 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.4079    1.9696    1.7481 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.8095    0.3385    3.5313 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.0508    0.2824    3.9036 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.5480   -1.4588    2.2641 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.6775   -0.3877    1.3753 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.4503   -2.6057   -1.4319 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.1226   -3.2890   -3.7754 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1410   -2.6265   -4.9693 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5724   -1.2623   -3.8600 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6525    3.2118   -0.5018 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9333    2.7444    1.1893 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  2  4  1  0
  4  5  1  0
  5  6  1  0
  6  7  2  0
  6  8  1  0
  8  9  2  0
  9 10  1  0
 10 11  1  0
 11 12  1  0
 12 13  1  0
 13 14  1  0
 14 15  1  0
 15 16  1  0
 16 17  1  0
 10 18  1  0
 18 19  2  0
 19 20  1  0
 20 21  2  0
 21 22  1  0
 22 23  2  0
  4 24  1  0
 24 25  1  0
 24 26  2  0
 23  8  1  0
 17 12  1  0
 23 18  1  0
  1 27  1  0
  1 28  1  0
  1 29  1  0
  2 30  1  0
  3 31  1  0
  3 32  1  0
  3 33  1  0
  4 34  1  0
  5 35  1  0
 11 36  1  0
 11 37  1  0
 12 38  1  0
 13 39  1  0
 13 40  1  0
 14 41  1  0
 14 42  1  0
 15 43  1  0
 15 44  1  0
 16 45  1  0
 16 46  1  0
 17 47  1  0
 17 48  1  0
 19 49  1  0
 20 50  1  0
 21 51  1  0
 22 52  1  0
 25 53  1  0
 25 54  1  0
M  END

HEADER    PROTEIN                                 11-SEP-21   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   11-SEP-21         0                                  
HETATM    1  C   UNK     0       4.633   1.075   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       5.967   0.305   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       5.967  -1.235   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       7.300   1.075   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       7.300   2.615   0.000  0.00  0.00           C+0
HETATM    6  O   UNK     0       8.634   3.385   0.000  0.00  0.00           O+0
HETATM    7  N   UNK     0       5.967   3.385   0.000  0.00  0.00           N+0
HETATM    8  N   UNK     0       8.634   0.305   0.000  0.00  0.00           N+0
HETATM    9  C   UNK     0       9.968   1.075   0.000  0.00  0.00           C+0
HETATM   10  O   UNK     0       9.968   2.615   0.000  0.00  0.00           O+0
HETATM   11  C   UNK     0      11.301   0.305   0.000  0.00  0.00           C+0
HETATM   12  N   UNK     0      12.708   0.931   0.000  0.00  0.00           N+0
HETATM   13  N   UNK     0      13.739  -0.214   0.000  0.00  0.00           N+0
HETATM   14  C   UNK     0      12.969  -1.547   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      13.445  -3.012   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      12.414  -4.156   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      10.908  -3.836   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      10.432  -2.371   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0      11.462  -1.227   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0      15.270  -0.053   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0      16.175  -1.298   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0      17.707  -1.137   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0      18.612  -2.383   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0      17.986  -3.790   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0      16.454  -3.951   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0      15.549  -2.705   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3    4                                                  
CONECT    3    2                                                            
CONECT    4    2    5    8                                                  
CONECT    5    4    6    7                                                  
CONECT    6    5                                                            
CONECT    7    5                                                            
CONECT    8    4    9                                                       
CONECT    9    8   10   11                                                  
CONECT   10    9                                                            
CONECT   11    9   12   19                                                  
CONECT   12   11   13                                                       
CONECT   13   12   14   20                                                  
CONECT   14   13   15   19                                                  
CONECT   15   14   16                                                       
CONECT   16   15   17                                                       
CONECT   17   16   18                                                       
CONECT   18   17   19                                                       
CONECT   19   18   14   11                                                  
CONECT   20   13   21                                                       
CONECT   21   20   22   26                                                  
CONECT   22   21   23                                                       
CONECT   23   22   24                                                       
CONECT   24   23   25                                                       
CONECT   25   24   26                                                       
CONECT   26   25   21                                                       
MASTER        0    0    0    0    0    0    0    0   26    0   56    0
END

COMPND    HMDB0247738
HETATM    1  C1  UNL     1      -6.311   0.272  -0.533  1.00  0.00           C  
HETATM    2  C2  UNL     1      -4.913  -0.249  -0.397  1.00  0.00           C  
HETATM    3  C3  UNL     1      -4.687  -1.240  -1.565  1.00  0.00           C  
HETATM    4  C4  UNL     1      -3.849   0.819  -0.446  1.00  0.00           C  
HETATM    5  N1  UNL     1      -2.524   0.273  -0.292  1.00  0.00           N  
HETATM    6  C5  UNL     1      -1.599   0.128  -1.348  1.00  0.00           C  
HETATM    7  O1  UNL     1      -1.881   0.459  -2.515  1.00  0.00           O  
HETATM    8  C6  UNL     1      -0.256  -0.435  -1.078  1.00  0.00           C  
HETATM    9  N2  UNL     1       0.399  -0.376   0.080  1.00  0.00           N  
HETATM   10  N3  UNL     1       1.555  -1.038  -0.015  1.00  0.00           N  
HETATM   11  C7  UNL     1       2.513  -1.173   1.057  1.00  0.00           C  
HETATM   12  C8  UNL     1       3.570  -0.084   0.957  1.00  0.00           C  
HETATM   13  C9  UNL     1       3.049   1.298   1.004  1.00  0.00           C  
HETATM   14  C10 UNL     1       3.287   2.112   2.205  1.00  0.00           C  
HETATM   15  C11 UNL     1       4.729   1.919   2.625  1.00  0.00           C  
HETATM   16  C12 UNL     1       4.795   0.468   3.096  1.00  0.00           C  
HETATM   17  C13 UNL     1       4.678  -0.404   1.894  1.00  0.00           C  
HETATM   18  C14 UNL     1       1.631  -1.534  -1.266  1.00  0.00           C  
HETATM   19  C15 UNL     1       2.547  -2.298  -1.958  1.00  0.00           C  
HETATM   20  C16 UNL     1       2.390  -2.688  -3.257  1.00  0.00           C  
HETATM   21  C17 UNL     1       1.243  -2.300  -3.943  1.00  0.00           C  
HETATM   22  C18 UNL     1       0.313  -1.542  -3.278  1.00  0.00           C  
HETATM   23  C19 UNL     1       0.480  -1.152  -1.962  1.00  0.00           C  
HETATM   24  C20 UNL     1      -4.084   2.000   0.372  1.00  0.00           C  
HETATM   25  N4  UNL     1      -5.315   2.706   0.351  1.00  0.00           N  
HETATM   26  O2  UNL     1      -3.204   2.464   1.136  1.00  0.00           O  
HETATM   27  H1  UNL     1      -6.770   0.639   0.394  1.00  0.00           H  
HETATM   28  H2  UNL     1      -6.316   1.094  -1.278  1.00  0.00           H  
HETATM   29  H3  UNL     1      -6.987  -0.515  -0.964  1.00  0.00           H  
HETATM   30  H4  UNL     1      -4.819  -0.826   0.520  1.00  0.00           H  
HETATM   31  H5  UNL     1      -3.887  -1.919  -1.229  1.00  0.00           H  
HETATM   32  H6  UNL     1      -4.340  -0.596  -2.403  1.00  0.00           H  
HETATM   33  H7  UNL     1      -5.600  -1.787  -1.806  1.00  0.00           H  
HETATM   34  H8  UNL     1      -3.874   1.174  -1.537  1.00  0.00           H  
HETATM   35  H9  UNL     1      -2.249  -0.030   0.651  1.00  0.00           H  
HETATM   36  H10 UNL     1       1.997  -1.006   2.035  1.00  0.00           H  
HETATM   37  H11 UNL     1       2.964  -2.178   1.124  1.00  0.00           H  
HETATM   38  H12 UNL     1       4.012  -0.240  -0.084  1.00  0.00           H  
HETATM   39  H13 UNL     1       1.940   1.272   0.841  1.00  0.00           H  
HETATM   40  H14 UNL     1       3.443   1.887   0.126  1.00  0.00           H  
HETATM   41  H15 UNL     1       3.204   3.206   1.911  1.00  0.00           H  
HETATM   42  H16 UNL     1       2.655   1.920   3.074  1.00  0.00           H  
HETATM   43  H17 UNL     1       5.019   2.583   3.445  1.00  0.00           H  
HETATM   44  H18 UNL     1       5.408   1.970   1.748  1.00  0.00           H  
HETATM   45  H19 UNL     1       5.809   0.339   3.531  1.00  0.00           H  
HETATM   46  H20 UNL     1       4.051   0.282   3.904  1.00  0.00           H  
HETATM   47  H21 UNL     1       4.548  -1.459   2.264  1.00  0.00           H  
HETATM   48  H22 UNL     1       5.677  -0.388   1.375  1.00  0.00           H  
HETATM   49  H23 UNL     1       3.450  -2.606  -1.432  1.00  0.00           H  
HETATM   50  H24 UNL     1       3.123  -3.289  -3.775  1.00  0.00           H  
HETATM   51  H25 UNL     1       1.141  -2.626  -4.969  1.00  0.00           H  
HETATM   52  H26 UNL     1      -0.572  -1.262  -3.860  1.00  0.00           H  
HETATM   53  H27 UNL     1      -5.653   3.212  -0.502  1.00  0.00           H  
HETATM   54  H28 UNL     1      -5.933   2.744   1.189  1.00  0.00           H  
CONECT    1    2   27   28   29
CONECT    2    3    4   30
CONECT    3   31   32   33
CONECT    4    5   24   34
CONECT    5    6   35
CONECT    6    7    7    8
CONECT    8    9    9   23
CONECT    9   10
CONECT   10   11   18
CONECT   11   12   36   37
CONECT   12   13   17   38
CONECT   13   14   39   40
CONECT   14   15   41   42
CONECT   15   16   43   44
CONECT   16   17   45   46
CONECT   17   47   48
CONECT   18   19   19   23
CONECT   19   20   49
CONECT   20   21   21   50
CONECT   21   22   51
CONECT   22   23   23   52
CONECT   24   25   26   26
CONECT   25   53   54
END

HMDB0247738
     RDKit          3D
AB-Chminaca
 54 56  0  0  0  0  0  0  0  0999 V2000
   -6.3112    0.2721   -0.5328 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9134   -0.2485   -0.3970 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6874   -1.2399   -1.5648 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8493    0.8195   -0.4459 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5237    0.2735   -0.2922 N   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5992    0.1284   -1.3475 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8812    0.4594   -2.5149 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2557   -0.4348   -1.0779 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3990   -0.3764    0.0804 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.5549   -1.0384   -0.0149 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.5131   -1.1733    1.0565 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5702   -0.0841    0.9570 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0485    1.2978    1.0043 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2873    2.1118    2.2046 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7288    1.9188    2.6248 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7952    0.4681    3.0963 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6782   -0.4037    1.8939 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6313   -1.5339   -1.2660 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5468   -2.2980   -1.9579 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3903   -2.6882   -3.2573 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2427   -2.3003   -3.9430 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3129   -1.5419   -3.2782 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4803   -1.1516   -1.9624 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0836    2.0001    0.3721 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3146    2.7064    0.3513 N   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2040    2.4636    1.1365 O   0  0  0  0  0  0  0  0  0  0  0  0
   -6.7696    0.6393    0.3940 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.3161    1.0937   -1.2784 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.9868   -0.5150   -0.9641 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8187   -0.8260    0.5195 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8868   -1.9191   -1.2295 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3401   -0.5961   -2.4027 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6001   -1.7869   -1.8062 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8740    1.1739   -1.5365 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2490   -0.0302    0.6506 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9973   -1.0063    2.0355 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9640   -2.1780    1.1236 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.0119   -0.2400   -0.0839 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9405    1.2723    0.8408 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.4433    1.8870    0.1262 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2039    3.2056    1.9110 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6553    1.9198    3.0740 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.0192    2.5831    3.4451 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.4079    1.9696    1.7481 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.8095    0.3385    3.5313 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.0508    0.2824    3.9036 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.5480   -1.4588    2.2641 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.6775   -0.3877    1.3753 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.4503   -2.6057   -1.4319 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.1226   -3.2890   -3.7754 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1410   -2.6265   -4.9693 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5724   -1.2623   -3.8600 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6525    3.2118   -0.5018 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9333    2.7444    1.1893 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  2  4  1  0
  4  5  1  0
  5  6  1  0
  6  7  2  0
  6  8  1  0
  8  9  2  0
  9 10  1  0
 10 11  1  0
 11 12  1  0
 12 13  1  0
 13 14  1  0
 14 15  1  0
 15 16  1  0
 16 17  1  0
 10 18  1  0
 18 19  2  0
 19 20  1  0
 20 21  2  0
 21 22  1  0
 22 23  2  0
  4 24  1  0
 24 25  1  0
 24 26  2  0
 23  8  1  0
 17 12  1  0
 23 18  1  0
  1 27  1  0
  1 28  1  0
  1 29  1  0
  2 30  1  0
  3 31  1  0
  3 32  1  0
  3 33  1  0
  4 34  1  0
  5 35  1  0
 11 36  1  0
 11 37  1  0
 12 38  1  0
 13 39  1  0
 13 40  1  0
 14 41  1  0
 14 42  1  0
 15 43  1  0
 15 44  1  0
 16 45  1  0
 16 46  1  0
 17 47  1  0
 17 48  1  0
 19 49  1  0
 20 50  1  0
 21 51  1  0
 22 52  1  0
 25 53  1  0
 25 54  1  0
M  END

View in JSmol View Stereo Labels

Synonyms

Value	Source
2-{[1-(cyclohexylmethyl)-1H-indazol-3-yl]formamido}-3-methylbutanimidate	HMDB
N-(1-Amino-3-methyl-1-oxobutan-2-yl)-1-(cyclohexylmethyl)-1H-indazole-3-carboxamide	HMDB
N-(1-(Aminocarbonyl)-2-methylpropyl)-1-(cyclohexylmethyl)-1H-indazole-3-carboxamide	HMDB

Chemical Formula

C₂₀H₂₈N₄O₂

Average Molecular Weight

356.47

Monoisotopic Molecular Weight

356.221226158

IUPAC Name

2-{[1-(cyclohexylmethyl)-1H-indazol-3-yl]formamido}-3-methylbutanamide

Traditional Name

2-{[1-(cyclohexylmethyl)indazol-3-yl]formamido}-3-methylbutanamide

CAS Registry Number

Not Available

SMILES

CC(C)C(NC(=O)C1=NN(CC2CCCCC2)C2=CC=CC=C12)C(N)=O

InChI Identifier

InChI=1S/C20H28N4O2/c1-13(2)17(19(21)25)22-20(26)18-15-10-6-7-11-16(15)24(23-18)12-14-8-4-3-5-9-14/h6-7,10-11,13-14,17H,3-5,8-9,12H2,1-2H3,(H2,21,25)(H,22,26)

InChI Key

KJNZIEGLNLCWTQ-UHFFFAOYSA-N

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as n-acyl-alpha amino acids and derivatives. N-acyl-alpha amino acids and derivatives are compounds containing an alpha amino acid (or a derivative thereof) which bears an acyl group at its terminal nitrogen atom.

Kingdom

Organic compounds

Super Class

Organic acids and derivatives

Class

Carboxylic acids and derivatives

Sub Class

Amino acids, peptides, and analogues

Direct Parent

N-acyl-alpha amino acids and derivatives

Alternative Parents

Substituents

N-acyl-alpha amino acid or derivatives
Valine or derivatives
Indazole-3-carboxamide
Benzopyrazole
Indazole
2-heteroaryl carboxamide
Pyrazole-5-carboxamide
Fatty amide
Fatty acyl
Benzenoid
Azole
Heteroaromatic compound
Pyrazole
Carboxamide group
Primary carboxylic acid amide
Secondary carboxylic acid amide
Azacycle
Organoheterocyclic compound
Organooxygen compound
Organonitrogen compound
Organic oxygen compound
Organic nitrogen compound
Organic oxide
Carbonyl group
Hydrocarbon derivative
Aromatic heteropolycyclic compound

Molecular Framework

Aromatic heteropolycyclic compounds

External Descriptors

Not Available

Ontology

Physiological effect

Not Available

Disposition

Biological location

Non-excretory biofluid

Biofluid or Excreta

Blood (PMID: 31557052)

Source

Exogenous

Exogenous (PMID: 31557052)

Process

Not Available

Role

Not Available

Physical Properties

State

Not Available

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

Not Available

Predicted Molecular Properties

Property	Value	Source
logP	3.26	ALOGPS
logP	3.12	ChemAxon
logS	-4.3	ALOGPS
pKa (Strongest Acidic)	14.65	ChemAxon
pKa (Strongest Basic)	-0.44	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	3	ChemAxon
Hydrogen Donor Count	2	ChemAxon
Polar Surface Area	90.01 Å²	ChemAxon
Rotatable Bond Count	6	ChemAxon
Refractivity	112.03 m³·mol⁻¹	ChemAxon
Polarizability	40.19 Å³	ChemAxon
Number of Rings	3	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	Yes	ChemAxon
Ghose Filter	Yes	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	Yes	ChemAxon

Predicted Chromatographic Properties

Predicted Collision Cross Sections

Predictor	Adduct Type	CCS Value (Å²)	Reference
DeepCCS	[M-2H]-	217.513	30932474
DeepCCS	[M+Na]+	192.958	30932474
AllCCS	[M+H]+	186.1	32859911
AllCCS	[M+H-H2O]+	183.5	32859911
AllCCS	[M+NH4]+	188.5	32859911
AllCCS	[M+Na]+	189.2	32859911
AllCCS	[M-H]-	185.4	32859911
AllCCS	[M+Na-2H]-	185.7	32859911
AllCCS	[M+HCOO]-	186.3	32859911

Predicted Kovats Retention Indices

Underivatized

Metabolite	SMILES	Kovats RI Value	Column Type	Reference
AB-Chminaca	CC(C)C(NC(=O)C1=NN(CC2CCCCC2)C2=CC=CC=C12)C(N)=O	3702.5	Standard polar	33892256
AB-Chminaca	CC(C)C(NC(=O)C1=NN(CC2CCCCC2)C2=CC=CC=C12)C(N)=O	2839.7	Standard non polar	33892256
AB-Chminaca	CC(C)C(NC(=O)C1=NN(CC2CCCCC2)C2=CC=CC=C12)C(N)=O	3199.7	Semi standard non polar	33892256

Derivatized

Derivative Name / Structure	SMILES	Kovats RI Value	Column Type	Reference
AB-Chminaca,1TMS,isomer #1	CC(C)C(NC(=O)C1=NN(CC2CCCCC2)C2=CC=CC=C12)C(=O)N[Si](C)(C)C	2993.3	Semi standard non polar	33892256
AB-Chminaca,1TMS,isomer #1	CC(C)C(NC(=O)C1=NN(CC2CCCCC2)C2=CC=CC=C12)C(=O)N[Si](C)(C)C	2782.7	Standard non polar	33892256
AB-Chminaca,1TMS,isomer #1	CC(C)C(NC(=O)C1=NN(CC2CCCCC2)C2=CC=CC=C12)C(=O)N[Si](C)(C)C	4038.6	Standard polar	33892256
AB-Chminaca,1TMS,isomer #2	CC(C)C(C(N)=O)N(C(=O)C1=NN(CC2CCCCC2)C2=CC=CC=C12)[Si](C)(C)C	3020.1	Semi standard non polar	33892256
AB-Chminaca,1TMS,isomer #2	CC(C)C(C(N)=O)N(C(=O)C1=NN(CC2CCCCC2)C2=CC=CC=C12)[Si](C)(C)C	2755.2	Standard non polar	33892256
AB-Chminaca,1TMS,isomer #2	CC(C)C(C(N)=O)N(C(=O)C1=NN(CC2CCCCC2)C2=CC=CC=C12)[Si](C)(C)C	4230.9	Standard polar	33892256
AB-Chminaca,2TMS,isomer #1	CC(C)C(C(=O)N[Si](C)(C)C)N(C(=O)C1=NN(CC2CCCCC2)C2=CC=CC=C12)[Si](C)(C)C	2954.0	Semi standard non polar	33892256
AB-Chminaca,2TMS,isomer #1	CC(C)C(C(=O)N[Si](C)(C)C)N(C(=O)C1=NN(CC2CCCCC2)C2=CC=CC=C12)[Si](C)(C)C	2880.9	Standard non polar	33892256
AB-Chminaca,2TMS,isomer #1	CC(C)C(C(=O)N[Si](C)(C)C)N(C(=O)C1=NN(CC2CCCCC2)C2=CC=CC=C12)[Si](C)(C)C	3741.7	Standard polar	33892256
AB-Chminaca,2TMS,isomer #2	CC(C)C(NC(=O)C1=NN(CC2CCCCC2)C2=CC=CC=C12)C(=O)N([Si](C)(C)C)[Si](C)(C)C	3029.3	Semi standard non polar	33892256
AB-Chminaca,2TMS,isomer #2	CC(C)C(NC(=O)C1=NN(CC2CCCCC2)C2=CC=CC=C12)C(=O)N([Si](C)(C)C)[Si](C)(C)C	2927.2	Standard non polar	33892256
AB-Chminaca,2TMS,isomer #2	CC(C)C(NC(=O)C1=NN(CC2CCCCC2)C2=CC=CC=C12)C(=O)N([Si](C)(C)C)[Si](C)(C)C	3909.5	Standard polar	33892256
AB-Chminaca,3TMS,isomer #1	CC(C)C(C(=O)N([Si](C)(C)C)[Si](C)(C)C)N(C(=O)C1=NN(CC2CCCCC2)C2=CC=CC=C12)[Si](C)(C)C	3045.3	Semi standard non polar	33892256
AB-Chminaca,3TMS,isomer #1	CC(C)C(C(=O)N([Si](C)(C)C)[Si](C)(C)C)N(C(=O)C1=NN(CC2CCCCC2)C2=CC=CC=C12)[Si](C)(C)C	3034.0	Standard non polar	33892256
AB-Chminaca,3TMS,isomer #1	CC(C)C(C(=O)N([Si](C)(C)C)[Si](C)(C)C)N(C(=O)C1=NN(CC2CCCCC2)C2=CC=CC=C12)[Si](C)(C)C	3597.0	Standard polar	33892256
AB-Chminaca,1TBDMS,isomer #1	CC(C)C(NC(=O)C1=NN(CC2CCCCC2)C2=CC=CC=C12)C(=O)N[Si](C)(C)C(C)(C)C	3202.5	Semi standard non polar	33892256
AB-Chminaca,1TBDMS,isomer #1	CC(C)C(NC(=O)C1=NN(CC2CCCCC2)C2=CC=CC=C12)C(=O)N[Si](C)(C)C(C)(C)C	2982.7	Standard non polar	33892256
AB-Chminaca,1TBDMS,isomer #1	CC(C)C(NC(=O)C1=NN(CC2CCCCC2)C2=CC=CC=C12)C(=O)N[Si](C)(C)C(C)(C)C	4103.9	Standard polar	33892256
AB-Chminaca,1TBDMS,isomer #2	CC(C)C(C(N)=O)N(C(=O)C1=NN(CC2CCCCC2)C2=CC=CC=C12)[Si](C)(C)C(C)(C)C	3237.3	Semi standard non polar	33892256
AB-Chminaca,1TBDMS,isomer #2	CC(C)C(C(N)=O)N(C(=O)C1=NN(CC2CCCCC2)C2=CC=CC=C12)[Si](C)(C)C(C)(C)C	2951.9	Standard non polar	33892256
AB-Chminaca,1TBDMS,isomer #2	CC(C)C(C(N)=O)N(C(=O)C1=NN(CC2CCCCC2)C2=CC=CC=C12)[Si](C)(C)C(C)(C)C	4282.5	Standard polar	33892256
AB-Chminaca,2TBDMS,isomer #1	CC(C)C(C(=O)N[Si](C)(C)C(C)(C)C)N(C(=O)C1=NN(CC2CCCCC2)C2=CC=CC=C12)[Si](C)(C)C(C)(C)C	3347.6	Semi standard non polar	33892256
AB-Chminaca,2TBDMS,isomer #1	CC(C)C(C(=O)N[Si](C)(C)C(C)(C)C)N(C(=O)C1=NN(CC2CCCCC2)C2=CC=CC=C12)[Si](C)(C)C(C)(C)C	3240.1	Standard non polar	33892256
AB-Chminaca,2TBDMS,isomer #1	CC(C)C(C(=O)N[Si](C)(C)C(C)(C)C)N(C(=O)C1=NN(CC2CCCCC2)C2=CC=CC=C12)[Si](C)(C)C(C)(C)C	3874.8	Standard polar	33892256
AB-Chminaca,2TBDMS,isomer #2	CC(C)C(NC(=O)C1=NN(CC2CCCCC2)C2=CC=CC=C12)C(=O)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	3461.3	Semi standard non polar	33892256
AB-Chminaca,2TBDMS,isomer #2	CC(C)C(NC(=O)C1=NN(CC2CCCCC2)C2=CC=CC=C12)C(=O)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	3264.5	Standard non polar	33892256
AB-Chminaca,2TBDMS,isomer #2	CC(C)C(NC(=O)C1=NN(CC2CCCCC2)C2=CC=CC=C12)C(=O)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	3985.9	Standard polar	33892256
AB-Chminaca,3TBDMS,isomer #1	CC(C)C(C(=O)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)N(C(=O)C1=NN(CC2CCCCC2)C2=CC=CC=C12)[Si](C)(C)C(C)(C)C	3628.7	Semi standard non polar	33892256
AB-Chminaca,3TBDMS,isomer #1	CC(C)C(C(=O)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)N(C(=O)C1=NN(CC2CCCCC2)C2=CC=CC=C12)[Si](C)(C)C(C)(C)C	3537.6	Standard non polar	33892256
AB-Chminaca,3TBDMS,isomer #1	CC(C)C(C(=O)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)N(C(=O)C1=NN(CC2CCCCC2)C2=CC=CC=C12)[Si](C)(C)C(C)(C)C	3760.5	Standard polar	33892256

Spectra

GC-MS Spectra

Spectrum Type	Description	Splash Key	Deposition Date	Source	View
Predicted GC-MS	Predicted GC-MS Spectrum - AB-Chminaca GC-MS (Non-derivatized) - 70eV, Positive	splash10-01ox-9436000000-8d8dfc66706b71aa4be5	2021-09-23	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - AB-Chminaca GC-MS (Non-derivatized) - 70eV, Positive	Not Available	2021-10-12	Wishart Lab	View Spectrum

MS/MS Spectra

Spectrum Type	Description	Splash Key	Deposition Date	Source	View
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - AB-Chminaca 10V, Positive-QTOF	splash10-052f-0039000000-2b7bb0059540e5470da7	2021-10-12	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - AB-Chminaca 20V, Positive-QTOF	splash10-0006-2293000000-1c079d1b4afdac2188e2	2021-10-12	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - AB-Chminaca 40V, Positive-QTOF	splash10-052b-9101000000-210f911f7c3e4fb0c7b8	2021-10-12	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - AB-Chminaca 10V, Negative-QTOF	splash10-0a4i-0019000000-24df2af20933608123bd	2021-10-12	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - AB-Chminaca 20V, Negative-QTOF	splash10-05mo-6469000000-8c43aee86497fbb1e679	2021-10-12	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - AB-Chminaca 40V, Negative-QTOF	splash10-0006-7921000000-3a9343b4874c95bc95ed	2021-10-12	Wishart Lab	View Spectrum

Biological Properties

Cellular Locations

Not Available

Biospecimen Locations

Blood

Tissue Locations

Not Available

Pathways

Not Available

Name	SMPDB/PathBank	KEGG

Normal Concentrations

Biospecimen	Status	Value	Age	Sex	Condition	Reference	Details
Blood	Detected but not Quantified	Not Quantified	Not Specified	Not Specified	Normal	31557052	details

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

Not Available

KNApSAcK ID

Not Available

Chemspider ID

52084458

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

70969900

PDB ID

Not Available

ChEBI ID

Not Available

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

Barupal DK, Fiehn O: Generating the Blood Exposome Database Using a Comprehensive Text Mining and Database Fusion Approach. Environ Health Perspect. 2019 Sep;127(9):97008. doi: 10.1289/EHP4713. Epub 2019 Sep 26. [PubMed:31557052 ]

Showing metabocard for AB-Chminaca (HMDB0247738)

MOL for HMDB0247738 (AB-Chminaca)

3D MOL for HMDB0247738 (AB-Chminaca)

3D SDF for HMDB0247738 (AB-Chminaca)

3D-SDF for HMDB0247738 (AB-Chminaca)

PDB for HMDB0247738 (AB-Chminaca)

3D PDB for HMDB0247738 (AB-Chminaca)

SMILES for HMDB0247738 (AB-Chminaca)

INCHI for HMDB0247738 (AB-Chminaca)

Structure for HMDB0247738 (AB-Chminaca)

3D Structure for HMDB0247738 (AB-Chminaca)

Predicted Collision Cross Sections

Predicted Kovats Retention Indices

Underivatized

Derivatized

GC-MS Spectra

MS/MS Spectra