NP-MRD: Showing NP-Card for Cladosin C (major tautomer) (NP0012499)

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Record Information

Version

2.0

Created at

2021-01-05 21:52:25 UTC

Updated at

2021-07-15 17:11:56 UTC

NP-MRD ID

NP0012499

Secondary Accession Numbers

None

Natural Product Identification

Common Name

Cladosin C (major tautomer)

Provided By

NPAtlas

Description

Cladosin C (major tautomer) belongs to the class of organic compounds known as cyclic carboximidic acids. These are organic acids with the general formula RC(=N)-OH (R=H, organic group), where the carboximidic acid group is part of a cycle. Cladosin C (major tautomer) is found in Cladosporium. Based on a literature review very few articles have been published on Cladosin C (major tautomer).

Structure

MOL 3D MOL SDF 3D SDF PDB SMILES InChI


  Mrv1652306242117093D          

 36 36  0  0  0  0            999 V2000
   -5.2929    0.4068    1.4612 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4155   -0.1239    0.3632 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0532   -0.7638   -0.7831 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0879    0.0283    0.5163 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4299    0.6327    1.5960 N   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0091    0.5608    1.3317 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2118    1.0365    2.1568 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8231   -0.1073    0.0549 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3894   -0.4417   -0.6609 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2687   -1.0851   -1.8184 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.7672   -0.2115   -0.3664 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3873    0.3535    0.5945 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8864    0.4746    0.6818 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.6069   -0.1184   -0.4749 C   0  0  2  0  0  0  0  0  0  0  0  0
    6.1061    0.0940   -0.1936 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3814    0.5857   -1.6646 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0529   -0.4117   -0.4081 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4096   -1.0603   -1.6017 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4933    1.4626    1.2307 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7383    0.2791    2.4249 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.2327   -0.1809    1.5203 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0971   -1.0813   -0.4947 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5345   -1.7454   -0.9764 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0737   -0.1739   -1.7069 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8797    1.0571    2.4346 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5734   -1.3465   -2.2173 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.5006   -0.6199   -1.1472 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8680    0.7749    1.3905 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.1859   -0.0762    1.5956 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.1268    1.5394    0.8064 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.4471   -1.1942   -0.5535 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.2750    0.1307    0.9124 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.4352    1.0645   -0.5953 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.6983   -0.6964   -0.6818 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.8677    1.4262   -1.6002 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7892   -0.4689   -2.3398 H   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  2  3  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  6  7  2  0  0  0  0
  6  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  1  0  0  0  0
 14 16  1  0  0  0  0
  8 17  2  0  0  0  0
 17 18  1  0  0  0  0
 17  4  1  0  0  0  0
  1 19  1  0  0  0  0
  1 20  1  0  0  0  0
  1 21  1  0  0  0  0
  3 22  1  0  0  0  0
  3 23  1  0  0  0  0
  3 24  1  0  0  0  0
  5 25  1  0  0  0  0
 10 26  1  0  0  0  0
 11 27  1  0  0  0  0
 12 28  1  0  0  0  0
 13 29  1  0  0  0  0
 13 30  1  0  0  0  0
 14 31  1  6  0  0  0
 15 32  1  0  0  0  0
 15 33  1  0  0  0  0
 15 34  1  0  0  0  0
 16 35  1  0  0  0  0
 18 36  1  0  0  0  0
M  END

     RDKit          3D

 36 36  0  0  0  0  0  0  0  0999 V2000
   -5.2929    0.4068    1.4612 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4155   -0.1239    0.3632 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0532   -0.7638   -0.7831 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0879    0.0283    0.5163 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4299    0.6327    1.5960 N   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0091    0.5608    1.3317 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2118    1.0365    2.1568 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8231   -0.1073    0.0549 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3894   -0.4417   -0.6609 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2687   -1.0851   -1.8184 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.7672   -0.2115   -0.3664 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3873    0.3535    0.5945 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8864    0.4746    0.6818 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6069   -0.1184   -0.4749 C   0  0  2  0  0  0  0  0  0  0  0  0
    6.1061    0.0940   -0.1936 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3814    0.5857   -1.6646 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0529   -0.4117   -0.4081 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4096   -1.0603   -1.6017 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4933    1.4626    1.2307 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7383    0.2791    2.4249 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.2327   -0.1809    1.5203 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0971   -1.0813   -0.4947 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5345   -1.7454   -0.9764 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0737   -0.1739   -1.7069 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8797    1.0571    2.4346 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5734   -1.3465   -2.2173 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.5006   -0.6199   -1.1472 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8680    0.7749    1.3905 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.1859   -0.0762    1.5956 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.1268    1.5394    0.8064 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.4471   -1.1942   -0.5535 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.2750    0.1307    0.9124 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.4352    1.0645   -0.5953 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.6983   -0.6964   -0.6818 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.8677    1.4262   -1.6002 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7892   -0.4689   -2.3398 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  2  4  2  3
  4  5  1  0
  5  6  1  0
  6  7  2  0
  6  8  1  0
  8  9  1  0
  9 10  2  0
  9 11  1  0
 11 12  2  0
 12 13  1  0
 13 14  1  0
 14 15  1  0
 14 16  1  0
  8 17  2  0
 17 18  1  0
 17  4  1  0
  1 19  1  0
  1 20  1  0
  1 21  1  0
  3 22  1  0
  3 23  1  0
  3 24  1  0
  5 25  1  0
 10 26  1  0
 11 27  1  0
 12 28  1  0
 13 29  1  0
 13 30  1  0
 14 31  1  6
 15 32  1  0
 15 33  1  0
 15 34  1  0
 16 35  1  0
 18 36  1  0
M  END


  Mrv1652306242117093D          

 36 36  0  0  0  0            999 V2000
   -5.2929    0.4068    1.4612 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4155   -0.1239    0.3632 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0532   -0.7638   -0.7831 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0879    0.0283    0.5163 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4299    0.6327    1.5960 N   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0091    0.5608    1.3317 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2118    1.0365    2.1568 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8231   -0.1073    0.0549 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3894   -0.4417   -0.6609 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2687   -1.0851   -1.8184 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.7672   -0.2115   -0.3664 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3873    0.3535    0.5945 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8864    0.4746    0.6818 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.6069   -0.1184   -0.4749 C   0  0  2  0  0  0  0  0  0  0  0  0
    6.1061    0.0940   -0.1936 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3814    0.5857   -1.6646 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0529   -0.4117   -0.4081 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4096   -1.0603   -1.6017 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4933    1.4626    1.2307 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7383    0.2791    2.4249 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.2327   -0.1809    1.5203 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0971   -1.0813   -0.4947 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5345   -1.7454   -0.9764 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0737   -0.1739   -1.7069 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8797    1.0571    2.4346 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5734   -1.3465   -2.2173 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.5006   -0.6199   -1.1472 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8680    0.7749    1.3905 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.1859   -0.0762    1.5956 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.1268    1.5394    0.8064 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.4471   -1.1942   -0.5535 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.2750    0.1307    0.9124 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.4352    1.0645   -0.5953 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.6983   -0.6964   -0.6818 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.8677    1.4262   -1.6002 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7892   -0.4689   -2.3398 H   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  2  3  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  6  7  2  0  0  0  0
  6  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  1  0  0  0  0
 14 16  1  0  0  0  0
  8 17  2  0  0  0  0
 17 18  1  0  0  0  0
 17  4  1  0  0  0  0
  1 19  1  0  0  0  0
  1 20  1  0  0  0  0
  1 21  1  0  0  0  0
  3 22  1  0  0  0  0
  3 23  1  0  0  0  0
  3 24  1  0  0  0  0
  5 25  1  0  0  0  0
 10 26  1  0  0  0  0
 11 27  1  0  0  0  0
 12 28  1  0  0  0  0
 13 29  1  0  0  0  0
 13 30  1  0  0  0  0
 14 31  1  6  0  0  0
 15 32  1  0  0  0  0
 15 33  1  0  0  0  0
 15 34  1  0  0  0  0
 16 35  1  0  0  0  0
 18 36  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0012499

> <DATABASE_NAME>
NP-MRD

> <SMILES>
[H]OC1=C(C(=N[H])C(\[H])=C(/[H])C([H])([H])[C@@]([H])(O[H])C([H])([H])[H])C(=O)N([H])C1=C(C([H])([H])[H])C([H])([H])[H]

> <INCHI_IDENTIFIER>
InChI=1S/C13H18N2O3/c1-7(2)11-12(17)10(13(18)15-11)9(14)6-4-5-8(3)16/h4,6,8,14,16-17H,5H2,1-3H3,(H,15,18)/b6-4+,14-9-/t8-/m0/s1

> <INCHI_KEY>
NRYAZWLSPQPXOQ-KWXKUKOQSA-N

> <FORMULA>
C13H18N2O3

> <MOLECULAR_WEIGHT>
250.298

> <EXACT_MASS>
250.131742448

> <JCHEM_ACCEPTOR_COUNT>
4

> <JCHEM_ATOM_COUNT>
36

> <JCHEM_AVERAGE_POLARIZABILITY>
27.584780345898757

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
4

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
4-hydroxy-3-[(2E,5S)-5-hydroxyhex-2-enimidoyl]-5-(propan-2-ylidene)-2,5-dihydro-1H-pyrrol-2-one

> <ALOGPS_LOGP>
0.59

> <JCHEM_LOGP>
0.2504000396666672

> <ALOGPS_LOGS>
-3.01

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
1

> <JCHEM_PHYSIOLOGICAL_CHARGE>
1

> <JCHEM_PKA>
11.1661370930293

> <JCHEM_PKA_STRONGEST_ACIDIC>
10.059433179369613

> <JCHEM_PKA_STRONGEST_BASIC>
7.286909856509202

> <JCHEM_POLAR_SURFACE_AREA>
93.41000000000001

> <JCHEM_REFRACTIVITY>
83.1748

> <JCHEM_ROTATABLE_BOND_COUNT>
4

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
2.44e-01 g/l

> <JCHEM_TRADITIONAL_IUPAC>
4-hydroxy-3-[(2E,5S)-5-hydroxyhex-2-enimidoyl]-5-(propan-2-ylidene)-1H-pyrrol-2-one

> <JCHEM_VEBER_RULE>
0

$$$$

     RDKit          3D

 36 36  0  0  0  0  0  0  0  0999 V2000
   -5.2929    0.4068    1.4612 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4155   -0.1239    0.3632 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0532   -0.7638   -0.7831 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0879    0.0283    0.5163 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4299    0.6327    1.5960 N   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0091    0.5608    1.3317 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2118    1.0365    2.1568 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8231   -0.1073    0.0549 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3894   -0.4417   -0.6609 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2687   -1.0851   -1.8184 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.7672   -0.2115   -0.3664 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3873    0.3535    0.5945 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8864    0.4746    0.6818 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6069   -0.1184   -0.4749 C   0  0  2  0  0  0  0  0  0  0  0  0
    6.1061    0.0940   -0.1936 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3814    0.5857   -1.6646 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0529   -0.4117   -0.4081 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4096   -1.0603   -1.6017 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4933    1.4626    1.2307 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7383    0.2791    2.4249 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.2327   -0.1809    1.5203 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0971   -1.0813   -0.4947 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5345   -1.7454   -0.9764 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0737   -0.1739   -1.7069 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8797    1.0571    2.4346 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5734   -1.3465   -2.2173 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.5006   -0.6199   -1.1472 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8680    0.7749    1.3905 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.1859   -0.0762    1.5956 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.1268    1.5394    0.8064 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.4471   -1.1942   -0.5535 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.2750    0.1307    0.9124 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.4352    1.0645   -0.5953 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.6983   -0.6964   -0.6818 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.8677    1.4262   -1.6002 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7892   -0.4689   -2.3398 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  2  4  2  3
  4  5  1  0
  5  6  1  0
  6  7  2  0
  6  8  1  0
  8  9  1  0
  9 10  2  0
  9 11  1  0
 11 12  2  0
 12 13  1  0
 13 14  1  0
 14 15  1  0
 14 16  1  0
  8 17  2  0
 17 18  1  0
 17  4  1  0
  1 19  1  0
  1 20  1  0
  1 21  1  0
  3 22  1  0
  3 23  1  0
  3 24  1  0
  5 25  1  0
 10 26  1  0
 11 27  1  0
 12 28  1  0
 13 29  1  0
 13 30  1  0
 14 31  1  6
 15 32  1  0
 15 33  1  0
 15 34  1  0
 16 35  1  0
 18 36  1  0
M  END

HEADER    PROTEIN                                 24-JUN-21   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   24-JUN-21         0                                  
HETATM    1  C   UNK     0      -5.293   0.407   1.461  0.00  0.00           C+0
HETATM    2  C   UNK     0      -4.415  -0.124   0.363  0.00  0.00           C+0
HETATM    3  C   UNK     0      -5.053  -0.764  -0.783  0.00  0.00           C+0
HETATM    4  C   UNK     0      -3.088   0.028   0.516  0.00  0.00           C+0
HETATM    5  N   UNK     0      -2.430   0.633   1.596  0.00  0.00           N+0
HETATM    6  C   UNK     0      -1.009   0.561   1.332  0.00  0.00           C+0
HETATM    7  O   UNK     0      -0.212   1.036   2.157  0.00  0.00           O+0
HETATM    8  C   UNK     0      -0.823  -0.107   0.055  0.00  0.00           C+0
HETATM    9  C   UNK     0       0.389  -0.442  -0.661  0.00  0.00           C+0
HETATM   10  N   UNK     0       0.269  -1.085  -1.818  0.00  0.00           N+0
HETATM   11  C   UNK     0       1.767  -0.212  -0.366  0.00  0.00           C+0
HETATM   12  C   UNK     0       2.387   0.354   0.595  0.00  0.00           C+0
HETATM   13  C   UNK     0       3.886   0.475   0.682  0.00  0.00           C+0
HETATM   14  C   UNK     0       4.607  -0.118  -0.475  0.00  0.00           C+0
HETATM   15  C   UNK     0       6.106   0.094  -0.194  0.00  0.00           C+0
HETATM   16  O   UNK     0       4.381   0.586  -1.665  0.00  0.00           O+0
HETATM   17  C   UNK     0      -2.053  -0.412  -0.408  0.00  0.00           C+0
HETATM   18  O   UNK     0      -2.410  -1.060  -1.602  0.00  0.00           O+0
HETATM   19  H   UNK     0      -5.493   1.463   1.231  0.00  0.00           H+0
HETATM   20  H   UNK     0      -4.738   0.279   2.425  0.00  0.00           H+0
HETATM   21  H   UNK     0      -6.233  -0.181   1.520  0.00  0.00           H+0
HETATM   22  H   UNK     0      -6.097  -1.081  -0.495  0.00  0.00           H+0
HETATM   23  H   UNK     0      -4.535  -1.745  -0.976  0.00  0.00           H+0
HETATM   24  H   UNK     0      -5.074  -0.174  -1.707  0.00  0.00           H+0
HETATM   25  H   UNK     0      -2.880   1.057   2.435  0.00  0.00           H+0
HETATM   26  H   UNK     0      -0.573  -1.347  -2.217  0.00  0.00           H+0
HETATM   27  H   UNK     0       2.501  -0.620  -1.147  0.00  0.00           H+0
HETATM   28  H   UNK     0       1.868   0.775   1.391  0.00  0.00           H+0
HETATM   29  H   UNK     0       4.186  -0.076   1.596  0.00  0.00           H+0
HETATM   30  H   UNK     0       4.127   1.539   0.806  0.00  0.00           H+0
HETATM   31  H   UNK     0       4.447  -1.194  -0.554  0.00  0.00           H+0
HETATM   32  H   UNK     0       6.275   0.131   0.912  0.00  0.00           H+0
HETATM   33  H   UNK     0       6.435   1.065  -0.595  0.00  0.00           H+0
HETATM   34  H   UNK     0       6.698  -0.696  -0.682  0.00  0.00           H+0
HETATM   35  H   UNK     0       4.868   1.426  -1.600  0.00  0.00           H+0
HETATM   36  H   UNK     0      -2.789  -0.469  -2.340  0.00  0.00           H+0
CONECT    1    2   19   20   21                                             
CONECT    2    1    3    4                                                  
CONECT    3    2   22   23   24                                             
CONECT    4    2    5   17                                                  
CONECT    5    4    6   25                                                  
CONECT    6    5    7    8                                                  
CONECT    7    6                                                            
CONECT    8    6    9   17                                                  
CONECT    9    8   10   11                                                  
CONECT   10    9   26                                                       
CONECT   11    9   12   27                                                  
CONECT   12   11   13   28                                                  
CONECT   13   12   14   29   30                                             
CONECT   14   13   15   16   31                                             
CONECT   15   14   32   33   34                                             
CONECT   16   14   35                                                       
CONECT   17    8   18    4                                                  
CONECT   18   17   36                                                       
CONECT   19    1                                                            
CONECT   20    1                                                            
CONECT   21    1                                                            
CONECT   22    3                                                            
CONECT   23    3                                                            
CONECT   24    3                                                            
CONECT   25    5                                                            
CONECT   26   10                                                            
CONECT   27   11                                                            
CONECT   28   12                                                            
CONECT   29   13                                                            
CONECT   30   13                                                            
CONECT   31   14                                                            
CONECT   32   15                                                            
CONECT   33   15                                                            
CONECT   34   15                                                            
CONECT   35   16                                                            
CONECT   36   18                                                            
MASTER        0    0    0    0    0    0    0    0   36    0   72    0
END

RDKit          3D

36 36  0  0  0  0  0  0  0  0999 V2000
   -5.2929    0.4068    1.4612 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4155   -0.1239    0.3632 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0532   -0.7638   -0.7831 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0879    0.0283    0.5163 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4299    0.6327    1.5960 N   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0091    0.5608    1.3317 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2118    1.0365    2.1568 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8231   -0.1073    0.0549 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3894   -0.4417   -0.6609 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2687   -1.0851   -1.8184 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.7672   -0.2115   -0.3664 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3873    0.3535    0.5945 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8864    0.4746    0.6818 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6069   -0.1184   -0.4749 C   0  0  2  0  0  0  0  0  0  0  0  0
    6.1061    0.0940   -0.1936 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3814    0.5857   -1.6646 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0529   -0.4117   -0.4081 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4096   -1.0603   -1.6017 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4933    1.4626    1.2307 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7383    0.2791    2.4249 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.2327   -0.1809    1.5203 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0971   -1.0813   -0.4947 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5345   -1.7454   -0.9764 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0737   -0.1739   -1.7069 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8797    1.0571    2.4346 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5734   -1.3465   -2.2173 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.5006   -0.6199   -1.1472 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8680    0.7749    1.3905 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.1859   -0.0762    1.5956 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.1268    1.5394    0.8064 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.4471   -1.1942   -0.5535 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.2750    0.1307    0.9124 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.4352    1.0645   -0.5953 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.6983   -0.6964   -0.6818 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.8677    1.4262   -1.6002 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7892   -0.4689   -2.3398 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  2  4  2  3
  4  5  1  0
  5  6  1  0
  6  7  2  0
  6  8  1  0
  8  9  1  0
  9 10  2  0
  9 11  1  0
 11 12  2  0
 12 13  1  0
 13 14  1  0
 14 15  1  0
 14 16  1  0
  8 17  2  0
 17 18  1  0
 17  4  1  0
  1 19  1  0
  1 20  1  0
  1 21  1  0
  3 22  1  0
  3 23  1  0
  3 24  1  0
  5 25  1  0
 10 26  1  0
 11 27  1  0
 12 28  1  0
 13 29  1  0
 13 30  1  0
 14 31  1  6
 15 32  1  0
 15 33  1  0
 15 34  1  0
 16 35  1  0
 18 36  1  0
M  END

View in JSmol View NMR Assignments

Synonyms

Not Available

Chemical Formula

C₁₃H₁₈N₂O₃

Average Mass

250.2980 Da

Monoisotopic Mass

250.13174 Da

IUPAC Name

4-hydroxy-3-[(2E,5S)-5-hydroxyhex-2-enimidoyl]-5-(propan-2-ylidene)-2,5-dihydro-1H-pyrrol-2-one

Traditional Name

4-hydroxy-3-[(2E,5S)-5-hydroxyhex-2-enimidoyl]-5-(propan-2-ylidene)-1H-pyrrol-2-one

CAS Registry Number

Not Available

SMILES

C[C@H](O)C\C=C\C(=N)C1=C(O)C(NC1=O)=C(C)C

InChI Identifier

InChI=1S/C13H18N2O3/c1-7(2)11-12(17)10(13(18)15-11)9(14)6-4-5-8(3)16/h4,6,8,14,16-17H,5H2,1-3H3,(H,15,18)/b6-4+,14-9?/t8-/m0/s1

InChI Key

NRYAZWLSPQPXOQ-KWXKUKOQSA-N

Experimental Spectra

Not Available

Predicted Spectra

Spectrum Type	Description	Depositor ID	Depositor Organization	Depositor	Deposition Date	View
1D NMR	¹³C NMR Spectrum (1D, 25 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 100 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 252 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 1000 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 50 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 200 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 75 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 300 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 101 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 126 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 500 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 151 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 600 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 176 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 700 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 201 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 800 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 226 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 900 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum

Chemical Shift Submissions

Not Available

Species

Species of Origin

Species Name	Source	Reference
Cladosporium	NPAtlas	24499327

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as cyclic carboximidic acids. These are organic acids with the general formula RC(=N)-OH (R=H, organic group), where the carboximidic acid group is part of a cycle.

Kingdom

Organic compounds

Super Class

Organic acids and derivatives

Class

Carboximidic acids and derivatives

Sub Class

Carboximidic acids

Direct Parent

Cyclic carboximidic acids

Alternative Parents

Substituents

Cyclic carboximidic acid
Secondary alcohol
Ketimine
Azacycle
Organoheterocyclic compound
Organic 1,3-dipolar compound
Propargyl-type 1,3-dipolar organic compound
Enol
Organic nitrogen compound
Organic oxygen compound
Organopnictogen compound
Hydrocarbon derivative
Organooxygen compound
Organonitrogen compound
Imine
Carbonyl group
Alcohol
Aliphatic heteromonocyclic compound

Molecular Framework

Aliphatic heteromonocyclic 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	0.59	ALOGPS
logP	0.25	ChemAxon
logS	-3	ALOGPS
pKa (Strongest Acidic)	10.06	ChemAxon
pKa (Strongest Basic)	7.29	ChemAxon
Physiological Charge	1	ChemAxon
Hydrogen Acceptor Count	4	ChemAxon
Hydrogen Donor Count	4	ChemAxon
Polar Surface Area	93.41 Å²	ChemAxon
Rotatable Bond Count	4	ChemAxon
Refractivity	83.17 m³·mol⁻¹	ChemAxon
Polarizability	27.58 Å³	ChemAxon
Number of Rings	1	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

NPAtlas ID

NPA002903

HMDB ID

Not Available

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FoodDB ID

Not Available

KNApSAcK ID

Not Available

Chemspider ID

78436576

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

136249374

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Showing NP-Card for Cladosin C (major tautomer) (NP0012499)

MOL for NP0012499 (Cladosin C (major tautomer))

3D MOL for NP0012499 (Cladosin C (major tautomer))

3D SDF for NP0012499 (Cladosin C (major tautomer))

3D-SDF for NP0012499 (Cladosin C (major tautomer))

PDB for NP0012499 (Cladosin C (major tautomer))

3D PDB for NP0012499 (Cladosin C (major tautomer))

SMILES for NP0012499 (Cladosin C (major tautomer))

INCHI for NP0012499 (Cladosin C (major tautomer))

Structure for NP0012499 (Cladosin C (major tautomer))

3D Structure for NP0012499 (Cladosin C (major tautomer))