NP-MRD: Showing NP-Card for Cryptoporic Acid A (NP0331366)

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Record Information

Version

1.0

Created at

2022-12-23 04:05:58 UTC

Updated at

2024-04-19 09:38:47 UTC

NP-MRD ID

NP0331366

Secondary Accession Numbers

None

Natural Product Identification

Common Name

Cryptoporic Acid A

Description

Cryptoporic acid A, also known as cryptopate a, belongs to the class of organic compounds known as tricarboxylic acids and derivatives. These are carboxylic acids containing exactly three carboxyl groups. Based on a literature review very few articles have been published on Cryptoporic acid A.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309102222562D          

 30 31  0  0  1  0            999 V2000
    5.7158   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013   -2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013   -2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868   -3.3000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -2.8875    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.8579   -3.3000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3882   -3.9320    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3276   -3.9320    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -2.0625    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.5724   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868   -1.6500    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.2868   -0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013   -0.4125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013    0.4125    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.2868    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868    1.6500    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724    0.4125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7158    0.8250    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    5.7158    1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4302    2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4302    2.8875    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.1447    1.6500    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.4302    0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4302   -0.4125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.1447    0.8250    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.8592    0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  0  0  0  0
  2  3  1  0  0  0  0
  3  4  1  0  0  0  0
  5  4  1  1  0  0  0
  5  6  1  0  0  0  0
  6  7  1  0  0  0  0
  6  8  1  0  0  0  0
  6  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
  5 12  1  0  0  0  0
 12 13  1  1  0  0  0
 12 14  1  0  0  0  0
  2 14  1  0  0  0  0
 14 15  1  1  0  0  0
 15 16  1  0  0  0  0
 17 16  1  1  0  0  0
 17 18  1  0  0  0  0
 18 19  2  0  0  0  0
 18 20  1  0  0  0  0
 20 21  1  0  0  0  0
 17 22  1  0  0  0  0
 22 23  1  6  0  0  0
 23 24  1  0  0  0  0
 24 25  2  0  0  0  0
 24 26  1  0  0  0  0
 22 27  1  0  0  0  0
 27 28  2  0  0  0  0
 27 29  1  0  0  0  0
 29 30  1  0  0  0  0
M  END

     RDKit          3D

 66 67  0  0  0  0  0  0  0  0999 V2000
   -1.4022   -3.1296   -1.9661 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8476   -2.2377   -1.0716 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9850   -2.5652   -0.2057 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8879   -1.3981   -0.1053 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2520   -0.0611   -0.3639 C   0  0  1  0  0  0  0  0  0  0  0  0
   -4.1011    1.0390    0.2142 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4889    0.8558   -0.4068 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2630    1.0674    1.6817 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6270    2.4060   -0.2378 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1375    2.5404   -0.0061 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3672    1.4210   -0.6196 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7904    0.0393   -0.1361 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.3111   -0.2370    1.2506 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1079   -0.9508   -1.0523 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.3003   -1.2586   -0.6638 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1509   -0.1781   -0.5978 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.4362   -0.4858   -0.2416 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.4179   -0.2653   -1.3333 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1148    0.1426   -2.4845 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.7426   -0.5201   -1.0796 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.7973   -0.3686   -1.9864 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8045    0.1204    1.0628 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.5331    1.5781    1.2176 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3800    2.4621    0.3948 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0341    2.7074   -0.7873 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.5529    3.0483    0.8529 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.2062   -0.2355    1.4263 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0665    0.5687    1.8080 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.5580   -1.5757    1.3234 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.8747   -2.0177    1.6479 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5845   -2.9620   -2.6271 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9072   -4.0841   -2.0203 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6969   -3.0166    0.7857 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5459   -3.4262   -0.6871 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7593   -1.5739   -0.8071 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3630   -1.4220    0.9026 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3687    0.0935   -1.4863 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9467   -0.0952   -0.0221 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.1143    1.6756    0.0088 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4583    0.8413   -1.5026 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6100    1.8513    2.1760 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2174    0.1128    2.2154 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2998    1.4701    1.9025 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8605    2.5247   -1.3052 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1292    3.1851    0.3670 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8241    3.4728   -0.5191 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9260    2.6745    1.0700 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3098    1.6301   -0.5305 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6009    1.4321   -1.7237 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8316    0.2556    2.0581 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2478    0.1442    1.2937 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2166   -1.3097    1.5069 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1786   -0.5094   -2.0780 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7116   -1.9541   -1.4238 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3546   -1.7953    0.3036 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.4290   -1.6106   -0.0754 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.8847   -1.2623   -2.6636 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.7410   -0.3513   -1.4033 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.7337    0.5649   -2.5635 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1786   -0.3956    1.8524 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4529    1.7969    1.0813 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7372    1.8747    2.2904 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.7375    4.0313    0.7292 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.0923   -1.5718    2.6591 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.9217   -3.1002    1.7809 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.6212   -1.7027    0.9202 H   0  0  0  0  0  0  0  0  0  0  0  0
 30 29  1  0
 29 27  1  0
 27 28  2  0
 27 22  1  0
 22 23  1  0
 23 24  1  0
 24 26  1  0
 24 25  2  0
 22 17  1  0
 17 16  1  0
 16 15  1  0
 15 14  1  0
 14  2  1  0
  2  1  2  3
  2  3  1  0
  3  4  1  0
  4  5  1  0
  5  6  1  0
  6  7  1  0
  6  8  1  0
  6  9  1  0
  9 10  1  0
 10 11  1  0
 11 12  1  0
 12 13  1  1
 17 18  1  0
 18 19  2  0
 18 20  1  0
 20 21  1  0
 12 14  1  0
 12  5  1  0
 30 64  1  0
 30 65  1  0
 30 66  1  0
 22 60  1  1
 23 61  1  0
 23 62  1  0
 26 63  1  0
 17 56  1  1
 15 54  1  0
 15 55  1  0
 14 53  1  6
  1 31  1  0
  1 32  1  0
  3 33  1  0
  3 34  1  0
  4 35  1  0
  4 36  1  0
  5 37  1  6
  7 38  1  0
  7 39  1  0
  7 40  1  0
  8 41  1  0
  8 42  1  0
  8 43  1  0
  9 44  1  0
  9 45  1  0
 10 46  1  0
 10 47  1  0
 11 48  1  0
 11 49  1  0
 13 50  1  0
 13 51  1  0
 13 52  1  0
 21 57  1  0
 21 58  1  0
 21 59  1  0
M  END


  Mrv1652309102222562D          

 30 31  0  0  1  0            999 V2000
    5.7158   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013   -2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013   -2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868   -3.3000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -2.8875    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.8579   -3.3000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3882   -3.9320    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3276   -3.9320    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -2.0625    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.5724   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868   -1.6500    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.2868   -0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013   -0.4125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013    0.4125    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.2868    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868    1.6500    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724    0.4125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7158    0.8250    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    5.7158    1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4302    2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4302    2.8875    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.1447    1.6500    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.4302    0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4302   -0.4125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.1447    0.8250    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.8592    0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  0  0  0  0
  2  3  1  0  0  0  0
  3  4  1  0  0  0  0
  5  4  1  1  0  0  0
  5  6  1  0  0  0  0
  6  7  1  0  0  0  0
  6  8  1  0  0  0  0
  6  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
  5 12  1  0  0  0  0
 12 13  1  1  0  0  0
 12 14  1  0  0  0  0
  2 14  1  0  0  0  0
 14 15  1  1  0  0  0
 15 16  1  0  0  0  0
 17 16  1  1  0  0  0
 17 18  1  0  0  0  0
 18 19  2  0  0  0  0
 18 20  1  0  0  0  0
 20 21  1  0  0  0  0
 17 22  1  0  0  0  0
 22 23  1  6  0  0  0
 23 24  1  0  0  0  0
 24 25  2  0  0  0  0
 24 26  1  0  0  0  0
 22 27  1  0  0  0  0
 27 28  2  0  0  0  0
 27 29  1  0  0  0  0
 29 30  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0331366

> <DATABASE_NAME>
NP-MRD

> <SMILES>
COC(=O)[C@@H](CC(O)=O)[C@@H](OC[C@H]1C(=C)CC[C@H]2C(C)(C)CCC[C@]12C)C(=O)OC

> <INCHI_IDENTIFIER>
InChI=1S/C23H36O7/c1-14-8-9-17-22(2,3)10-7-11-23(17,4)16(14)13-30-19(21(27)29-6)15(12-18(24)25)20(26)28-5/h15-17,19H,1,7-13H2,2-6H3,(H,24,25)/t15-,16-,17-,19+,23+/m0/s1

> <INCHI_KEY>
OCKYURAITHEIMQ-UGECPWBJSA-N

> <FORMULA>
C23H36O7

> <MOLECULAR_WEIGHT>
424.534

> <EXACT_MASS>
424.246103499

> <JCHEM_ACCEPTOR_COUNT>
5

> <JCHEM_ATOM_COUNT>
66

> <JCHEM_AVERAGE_POLARIZABILITY>
46.048076137140626

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(3S,4R)-4-{[(1S,4aS,8aS)-5,5,8a-trimethyl-2-methylidene-decahydronaphthalen-1-yl]methoxy}-5-methoxy-3-(methyl carboxy)-5-oxopentanoic acid

> <JCHEM_LOGP>
3.428805876

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
2

> <JCHEM_PHYSIOLOGICAL_CHARGE>
-1

> <JCHEM_PKA_STRONGEST_ACIDIC>
4.1399784278952865

> <JCHEM_PKA_STRONGEST_BASIC>
-4.224237356333241

> <JCHEM_POLAR_SURFACE_AREA>
99.13000000000001

> <JCHEM_REFRACTIVITY>
110.07239999999996

> <JCHEM_ROTATABLE_BOND_COUNT>
10

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
(3S,4R)-4-{[(1S,4aS,8aS)-5,5,8a-trimethyl-2-methylidene-hexahydro-1H-naphthalen-1-yl]methoxy}-5-methoxy-3-(methyl carboxy)-5-oxopentanoic acid

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 10-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   10-SEP-22         0                                  
HETATM    1  C   UNK     0      10.669  -3.080   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       9.336  -3.850   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       9.336  -5.390   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       8.002  -6.160   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       6.668  -5.390   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       5.335  -6.160   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       6.325  -7.340   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       4.345  -7.340   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       4.001  -5.390   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       4.001  -3.850   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       5.335  -3.080   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       6.668  -3.850   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       6.668  -2.310   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       8.002  -3.080   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       8.002  -1.540   0.000  0.00  0.00           C+0
HETATM   16  O   UNK     0       9.336  -0.770   0.000  0.00  0.00           O+0
HETATM   17  C   UNK     0       9.336   0.770   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       8.002   1.540   0.000  0.00  0.00           C+0
HETATM   19  O   UNK     0       8.002   3.080   0.000  0.00  0.00           O+0
HETATM   20  O   UNK     0       6.668   0.770   0.000  0.00  0.00           O+0
HETATM   21  C   UNK     0       5.335   1.540   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0      10.669   1.540   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0      10.669   3.080   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0      12.003   3.850   0.000  0.00  0.00           C+0
HETATM   25  O   UNK     0      12.003   5.390   0.000  0.00  0.00           O+0
HETATM   26  O   UNK     0      13.337   3.080   0.000  0.00  0.00           O+0
HETATM   27  C   UNK     0      12.003   0.770   0.000  0.00  0.00           C+0
HETATM   28  O   UNK     0      12.003  -0.770   0.000  0.00  0.00           O+0
HETATM   29  O   UNK     0      13.337   1.540   0.000  0.00  0.00           O+0
HETATM   30  C   UNK     0      14.670   0.770   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3   14                                                  
CONECT    3    2    4                                                       
CONECT    4    3    5                                                       
CONECT    5    4    6   12                                                  
CONECT    6    5    7    8    9                                             
CONECT    7    6                                                            
CONECT    8    6                                                            
CONECT    9    6   10                                                       
CONECT   10    9   11                                                       
CONECT   11   10   12                                                       
CONECT   12   11    5   13   14                                             
CONECT   13   12                                                            
CONECT   14   12    2   15                                                  
CONECT   15   14   16                                                       
CONECT   16   15   17                                                       
CONECT   17   16   18   22                                                  
CONECT   18   17   19   20                                                  
CONECT   19   18                                                            
CONECT   20   18   21                                                       
CONECT   21   20                                                            
CONECT   22   17   23   27                                                  
CONECT   23   22   24                                                       
CONECT   24   23   25   26                                                  
CONECT   25   24                                                            
CONECT   26   24                                                            
CONECT   27   22   28   29                                                  
CONECT   28   27                                                            
CONECT   29   27   30                                                       
CONECT   30   29                                                            
MASTER        0    0    0    0    0    0    0    0   30    0   62    0
END

View in JSmol

Synonyms

Value	Source
Cryptopate a	Generator
Cryptopic acid a	Generator

Chemical Formula

C₂₃H₃₆O₇

Average Mass

424.5340 Da

Monoisotopic Mass

424.24610 Da

IUPAC Name

(3S,4R)-4-{[(1S,4aS,8aS)-5,5,8a-trimethyl-2-methylidene-decahydronaphthalen-1-yl]methoxy}-5-methoxy-3-(methyl carboxy)-5-oxopentanoic acid

Traditional Name

(3S,4R)-4-{[(1S,4aS,8aS)-5,5,8a-trimethyl-2-methylidene-hexahydro-1H-naphthalen-1-yl]methoxy}-5-methoxy-3-(methyl carboxy)-5-oxopentanoic acid

CAS Registry Number

Not Available

SMILES

COC(=O)[C@@H](CC(O)=O)[C@@H](OC[C@H]1C(=C)CC[C@H]2C(C)(C)CCC[C@]12C)C(=O)OC

InChI Identifier

InChI=1S/C23H36O7/c1-14-8-9-17-22(2,3)10-7-11-23(17,4)16(14)13-30-19(21(27)29-6)15(12-18(24)25)20(26)28-5/h15-17,19H,1,7-13H2,2-6H3,(H,24,25)/t15-,16-,17-,19+,23+/m0/s1

InChI Key

OCKYURAITHEIMQ-UGECPWBJSA-N

Experimental Spectra

Spectrum Type	Description	Depositor Email	Depositor Organization	Depositor	Deposition Date	View
1D NMR	[¹³C, ] NMR Spectrum (2D, 126 MHz, CDCl3, experimental)	phamthihuong@sookmyung.ac.kr	Not Available	Not Available	2022-12-23	View Spectrum
1D NMR	[¹H, ] NMR Spectrum (2D, 500 MHz, CDCl3, experimental)	phamthihuong@sookmyung.ac.kr	Not Available	Not Available	2022-12-23	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 500.18 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 125.78 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum

Predicted Spectra

Spectrum Type	Description	Depositor ID	Depositor Organization	Depositor	Deposition Date	View
1D NMR	¹³C NMR Spectrum (1D, 25 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 100 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 252 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 1000 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 50 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 200 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 75 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 300 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 101 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 126 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 500 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 151 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 600 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 176 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 700 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 201 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 800 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 226 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 900 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum

Chemical Shift Submissions

Not Available

Species

Species of Origin

Not Available

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as tricarboxylic acids and derivatives. These are carboxylic acids containing exactly three carboxyl groups.

Kingdom

Organic compounds

Super Class

Organic acids and derivatives

Class

Carboxylic acids and derivatives

Sub Class

Tricarboxylic acids and derivatives

Direct Parent

Tricarboxylic acids and derivatives

Alternative Parents

Substituents

Tricarboxylic acid or derivatives
Fatty acid ester
Fatty acyl
Monosaccharide
Methyl ester
Carboxylic acid ester
Ether
Dialkyl ether
Carboxylic acid
Organic oxygen compound
Organic oxide
Hydrocarbon derivative
Organooxygen compound
Carbonyl group
Aliphatic homopolycyclic compound

Molecular Framework

Aliphatic homopolycyclic compounds

External Descriptors

Not Available

Physical Properties

State

Not Available

Experimental 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

Predicted Properties

Property	Value	Source
logP	3.43	ChemAxon
pKa (Strongest Acidic)	4.14	ChemAxon
pKa (Strongest Basic)	-4.2	ChemAxon
Physiological Charge	-1	ChemAxon
Hydrogen Acceptor Count	5	ChemAxon
Hydrogen Donor Count	1	ChemAxon
Polar Surface Area	99.13 Å²	ChemAxon
Rotatable Bond Count	10	ChemAxon
Refractivity	110.07 m³·mol⁻¹	ChemAxon
Polarizability	46.05 Å³	ChemAxon
Number of Rings	2	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	Yes	ChemAxon
Ghose Filter	Yes	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	No	ChemAxon

External Links

HMDB ID

Not Available

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FoodDB ID

Not Available

KNApSAcK ID

C00031693

Chemspider ID

10203155

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

13993281

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Not Available

Showing NP-Card for Cryptoporic Acid A (NP0331366)

MOL for NP0331366 (Cryptoporic Acid A)

3D MOL for NP0331366 (Cryptoporic Acid A)

3D SDF for NP0331366 (Cryptoporic Acid A)

3D-SDF for NP0331366 (Cryptoporic Acid A)

PDB for NP0331366 (Cryptoporic Acid A)

3D PDB for NP0331366 (Cryptoporic Acid A)

SMILES for NP0331366 (Cryptoporic Acid A)

INCHI for NP0331366 (Cryptoporic Acid A)

Structure for NP0331366 (Cryptoporic Acid A)

3D Structure for NP0331366 (Cryptoporic Acid A)