NP-MRD: Showing NP-Card for n-[(1s,2e,4e,6r,8e,10e,12s,14e,17r)-6,12-dihydroxy-3,9,15,17-tetramethyl-16-oxocycloheptadeca-2,4,8,10,14-pentaen-1-yl]ethanimidic acid (NP0327334)

Jump To Section:

Identification Spectra BioTaxonomy ChemoTaxonomy Physical properties Links References XML

Record Information

Version

2.0

Created at

2022-09-12 09:49:30 UTC

Updated at

2022-09-12 09:49:30 UTC

NP-MRD ID

NP0327334

Secondary Accession Numbers

None

Natural Product Identification

Common Name

n-[(1s,2e,4e,6r,8e,10e,12s,14e,17r)-6,12-dihydroxy-3,9,15,17-tetramethyl-16-oxocycloheptadeca-2,4,8,10,14-pentaen-1-yl]ethanimidic acid

Description

Chejuenolide A belongs to the class of organic compounds known as acetamides. These are organic compounds with the general formula RNHC(=O)CH3, where R= organyl group. n-[(1s,2e,4e,6r,8e,10e,12s,14e,17r)-6,12-dihydroxy-3,9,15,17-tetramethyl-16-oxocycloheptadeca-2,4,8,10,14-pentaen-1-yl]ethanimidic acid is found in Hahella chejuensis. Based on a literature review very few articles have been published on Chejuenolide A.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309122211492D          

 28 28  0  0  1  0            999 V2000
    2.6514    3.4994    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3762    2.7217    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5651    2.5711    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.9122    2.0945    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.6371    1.3167    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.1866    0.7014    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9943    0.8695    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2525    1.6531    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5438    0.2542    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2856   -0.5294    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8351   -1.1448    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    5.6427   -0.9766    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.5769   -1.9283    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7692   -2.0965    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2197   -1.4811    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4779   -0.6976    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4120   -1.6493    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8625   -1.0339    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0549   -1.2021    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.7967   -1.9857    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.5054   -0.5867    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7504    0.2822    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4180    1.0372    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3883    1.2121    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0334    1.5867    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9505    2.4075    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.7461    1.1712    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.5960    0.3600    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  2  1  1  4  0  0  0
  2  3  1  0  0  0  0
  2  4  2  0  0  0  0
  5  4  1  1  0  0  0
  5  6  1  0  0  0  0
  6  7  2  0  0  0  0
  7  8  1  0  0  0  0
  7  9  1  0  0  0  0
  9 10  2  0  0  0  0
 10 11  1  0  0  0  0
 11 12  1  6  0  0  0
 11 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
 15 17  1  0  0  0  0
 17 18  2  0  0  0  0
 18 19  1  0  0  0  0
 19 20  1  1  0  0  0
 19 21  1  0  0  0  0
 21 22  1  0  0  0  0
 22 23  2  0  0  0  0
 23 24  1  0  0  0  0
 23 25  1  0  0  0  0
 25 26  2  0  0  0  0
 25 27  1  0  0  0  0
  5 27  1  0  0  0  0
 27 28  1  1  0  0  0
M  END

     RDKit          3D

 61 61  0  0  0  0  0  0  0  0999 V2000
    3.8128   -0.3098   -3.2561 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5989   -0.2876   -1.7447 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2719    0.8890   -1.2395 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0099    1.2074    0.1811 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0127    2.3650    0.3426 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.1688    2.3514   -0.7288 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4032    2.2019    1.6712 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1690    2.4150    2.0681 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9928    2.8728    1.3343 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4521    4.3146    1.5419 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7445    2.1840    0.4904 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5852    0.7842    0.0766 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.5412    0.4574   -0.9644 N   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2278   -0.0323   -2.0910 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2615   -0.3481   -3.1220 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9159   -0.2896   -2.4006 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0104   -0.0981    1.2736 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.4024    0.4040    1.6812 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1361   -1.5109    0.8818 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0028   -1.7515   -0.0500 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4040   -2.6438    1.4209 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2751   -3.8143    1.8603 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0957   -2.7455    1.5488 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9339   -1.7645    1.1988 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4165   -1.8792   -0.2351 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.7005   -2.9167   -0.8281 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8631   -2.2241   -0.3428 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7676   -1.5233   -0.9961 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5873   -1.0482   -3.5383 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8855   -0.5940   -3.7881 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.1983    0.6806   -3.5822 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.1656    1.7665   -1.9021 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.9892    1.6289    0.5828 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7916    0.3716    0.8324 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.5770    3.3402    0.2700 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9192    3.2437   -1.0803 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1293    1.8363    2.4436 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0607    2.2596    3.1753 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5646    4.3665    1.3840 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2851    4.6542    2.5663 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9998    4.9468    0.7784 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6046    2.7230    0.0246 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5869    0.4766   -0.1893 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8030   -0.6508   -4.0793 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8929   -1.1735   -2.7721 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9100    0.5138   -3.3200 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6408   -1.2127   -2.6927 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3926    0.0485    2.1451 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7185   -0.0672    2.6381 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0809    0.1471    0.8443 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4011    1.5086    1.7672 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1896   -3.8946    1.2565 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7196   -4.7633    1.7210 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5729   -3.6741    2.9152 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2856   -3.6979    1.9757 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8499   -1.9970    1.8230 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7078   -0.7153    1.4708 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1773   -0.9645   -0.8167 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1593   -3.2780   -1.6234 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.1207   -3.1556    0.1962 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.7987   -1.9330   -0.9983 H   0  0  0  0  0  0  0  0  0  0  0  0
 18 17  1  0
 17 12  1  0
 12 11  1  0
 11  9  2  0
  9 10  1  0
  9  8  1  0
  8  7  2  0
  7  5  1  0
  5  6  1  0
  5  4  1  0
  4  3  1  0
  3  2  2  0
  2  1  1  0
  2 28  1  0
 28 27  2  0
 27 25  1  0
 25 26  1  0
 25 24  1  0
 24 23  1  0
 23 21  2  0
 21 22  1  0
 21 19  1  0
 19 20  2  0
 12 13  1  0
 13 14  2  0
 14 15  1  0
 14 16  1  0
 19 17  1  0
 18 49  1  0
 18 50  1  0
 18 51  1  0
 17 48  1  1
 12 43  1  6
 11 42  1  0
 10 39  1  0
 10 40  1  0
 10 41  1  0
  8 38  1  0
  7 37  1  0
  5 35  1  1
  6 36  1  0
  4 33  1  0
  4 34  1  0
  3 32  1  0
  1 29  1  0
  1 30  1  0
  1 31  1  0
 28 61  1  0
 27 60  1  0
 25 58  1  6
 26 59  1  0
 24 56  1  0
 24 57  1  0
 23 55  1  0
 22 52  1  0
 22 53  1  0
 22 54  1  0
 15 44  1  0
 15 45  1  0
 15 46  1  0
 16 47  1  0
M  END


  Mrv1652309122211492D          

 28 28  0  0  1  0            999 V2000
    2.6514    3.4994    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3762    2.7217    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5651    2.5711    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.9122    2.0945    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.6371    1.3167    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.1866    0.7014    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9943    0.8695    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2525    1.6531    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5438    0.2542    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2856   -0.5294    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8351   -1.1448    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    5.6427   -0.9766    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.5769   -1.9283    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7692   -2.0965    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2197   -1.4811    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4779   -0.6976    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4120   -1.6493    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8625   -1.0339    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0549   -1.2021    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.7967   -1.9857    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.5054   -0.5867    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7504    0.2822    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4180    1.0372    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3883    1.2121    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0334    1.5867    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9505    2.4075    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.7461    1.1712    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.5960    0.3600    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  2  1  1  4  0  0  0
  2  3  1  0  0  0  0
  2  4  2  0  0  0  0
  5  4  1  1  0  0  0
  5  6  1  0  0  0  0
  6  7  2  0  0  0  0
  7  8  1  0  0  0  0
  7  9  1  0  0  0  0
  9 10  2  0  0  0  0
 10 11  1  0  0  0  0
 11 12  1  6  0  0  0
 11 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
 15 17  1  0  0  0  0
 17 18  2  0  0  0  0
 18 19  1  0  0  0  0
 19 20  1  1  0  0  0
 19 21  1  0  0  0  0
 21 22  1  0  0  0  0
 22 23  2  0  0  0  0
 23 24  1  0  0  0  0
 23 25  1  0  0  0  0
 25 26  2  0  0  0  0
 25 27  1  0  0  0  0
  5 27  1  0  0  0  0
 27 28  1  1  0  0  0
M  END
> <DATABASE_ID>
NP0327334

> <DATABASE_NAME>
NP-MRD

> <SMILES>
C[C@@H]1[C@H](\C=C(/C)\C=C\[C@H](O)C\C=C(/C)\C=C\[C@@H](O)C\C=C(C)\C1=O)N=C(C)O

> <INCHI_IDENTIFIER>
InChI=1S/C23H33NO4/c1-15-6-10-20(26)12-8-16(2)14-22(24-19(5)25)18(4)23(28)17(3)9-13-21(27)11-7-15/h6-9,11-12,14,18,20-22,26-27H,10,13H2,1-5H3,(H,24,25)/b11-7+,12-8+,15-6+,16-14+,17-9+/t18-,20-,21-,22+/m1/s1

> <INCHI_KEY>
UTURGGMCWRWPTG-YOFHZKFDSA-N

> <FORMULA>
C23H33NO4

> <MOLECULAR_WEIGHT>
387.52

> <EXACT_MASS>
387.240958547

> <JCHEM_ACCEPTOR_COUNT>
5

> <JCHEM_ATOM_COUNT>
61

> <JCHEM_AVERAGE_POLARIZABILITY>
43.80432150401941

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
3

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
N-[(1S,2E,4E,6R,8E,10E,12S,14E,17R)-6,12-dihydroxy-3,9,15,17-tetramethyl-16-oxocycloheptadeca-2,4,8,10,14-pentaen-1-yl]ethanimidic acid

> <JCHEM_LOGP>
3.3488889459999998

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
1

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
17.73355516356844

> <JCHEM_PKA_STRONGEST_ACIDIC>
6.228294821940849

> <JCHEM_PKA_STRONGEST_BASIC>
3.706837306064133

> <JCHEM_POLAR_SURFACE_AREA>
90.12

> <JCHEM_REFRACTIVITY>
117.9292

> <JCHEM_ROTATABLE_BOND_COUNT>
1

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
N-[(1S,2E,4E,6R,8E,10E,12S,14E,17R)-6,12-dihydroxy-3,9,15,17-tetramethyl-16-oxocycloheptadeca-2,4,8,10,14-pentaen-1-yl]ethanimidic acid

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 12-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   12-SEP-22         0                                  
HETATM    1  C   UNK     0       4.949   6.532   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       4.436   5.080   0.000  0.00  0.00           C+0
HETATM    3  O   UNK     0       2.922   4.799   0.000  0.00  0.00           O+0
HETATM    4  N   UNK     0       5.436   3.910   0.000  0.00  0.00           N+0
HETATM    5  C   UNK     0       4.923   2.458   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       5.948   1.309   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       7.456   1.623   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       7.938   3.086   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       8.482   0.474   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       8.000  -0.988   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       9.025  -2.137   0.000  0.00  0.00           C+0
HETATM   12  O   UNK     0      10.533  -1.823   0.000  0.00  0.00           O+0
HETATM   13  C   UNK     0       8.543  -3.600   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       7.036  -3.913   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       6.010  -2.765   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       6.492  -1.302   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       4.502  -3.079   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       3.477  -1.930   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       1.969  -2.244   0.000  0.00  0.00           C+0
HETATM   20  O   UNK     0       1.487  -3.707   0.000  0.00  0.00           O+0
HETATM   21  C   UNK     0       0.943  -1.095   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       1.401   0.527   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       0.780   1.936   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0      -0.725   2.263   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       1.929   2.962   0.000  0.00  0.00           C+0
HETATM   26  O   UNK     0       1.774   4.494   0.000  0.00  0.00           O+0
HETATM   27  C   UNK     0       3.259   2.186   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0       2.979   0.672   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3    4                                                  
CONECT    3    2                                                            
CONECT    4    2    5                                                       
CONECT    5    4    6   27                                                  
CONECT    6    5    7                                                       
CONECT    7    6    8    9                                                  
CONECT    8    7                                                            
CONECT    9    7   10                                                       
CONECT   10    9   11                                                       
CONECT   11   10   12   13                                                  
CONECT   12   11                                                            
CONECT   13   11   14                                                       
CONECT   14   13   15                                                       
CONECT   15   14   16   17                                                  
CONECT   16   15                                                            
CONECT   17   15   18                                                       
CONECT   18   17   19                                                       
CONECT   19   18   20   21                                                  
CONECT   20   19                                                            
CONECT   21   19   22                                                       
CONECT   22   21   23                                                       
CONECT   23   22   24   25                                                  
CONECT   24   23                                                            
CONECT   25   23   26   27                                                  
CONECT   26   25                                                            
CONECT   27   25    5   28                                                  
CONECT   28   27                                                            
MASTER        0    0    0    0    0    0    0    0   28    0   56    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₃H₃₃NO₄

Average Mass

387.5200 Da

Monoisotopic Mass

387.24096 Da

IUPAC Name

N-[(1S,2E,4E,6R,8E,10E,12S,14E,17R)-6,12-dihydroxy-3,9,15,17-tetramethyl-16-oxocycloheptadeca-2,4,8,10,14-pentaen-1-yl]ethanimidic acid

Traditional Name

N-[(1S,2E,4E,6R,8E,10E,12S,14E,17R)-6,12-dihydroxy-3,9,15,17-tetramethyl-16-oxocycloheptadeca-2,4,8,10,14-pentaen-1-yl]ethanimidic acid

CAS Registry Number

Not Available

SMILES

C[C@@H]1[C@H](\C=C(/C)\C=C\[C@H](O)C\C=C(/C)\C=C\[C@@H](O)C\C=C(C)\C1=O)N=C(C)O

InChI Identifier

InChI=1S/C23H33NO4/c1-15-6-10-20(26)12-8-16(2)14-22(24-19(5)25)18(4)23(28)17(3)9-13-21(27)11-7-15/h6-9,11-12,14,18,20-22,26-27H,10,13H2,1-5H3,(H,24,25)/b11-7+,12-8+,15-6+,16-14+,17-9+/t18-,20-,21-,22+/m1/s1

InChI Key

UTURGGMCWRWPTG-YOFHZKFDSA-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, 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

Species Name	Source	Reference
Hahella chejuensis	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as acetamides. These are organic compounds with the general formula RNHC(=O)CH3, where R= organyl group.

Kingdom

Organic compounds

Super Class

Organic acids and derivatives

Class

Carboxylic acids and derivatives

Sub Class

Carboxylic acid derivatives

Direct Parent

Acetamides

Alternative Parents

Substituents

Acetamide
Cyclic ketone
Secondary carboxylic acid amide
Secondary alcohol
Ketone
Organic nitrogen compound
Organic oxygen compound
Organic oxide
Hydrocarbon derivative
Organooxygen compound
Organonitrogen compound
Carbonyl group
Alcohol
Aliphatic homomonocyclic compound

Molecular Framework

Aliphatic homomonocyclic 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	3.35	ChemAxon
pKa (Strongest Acidic)	6.23	ChemAxon
pKa (Strongest Basic)	3.71	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	5	ChemAxon
Hydrogen Donor Count	3	ChemAxon
Polar Surface Area	90.12 Å²	ChemAxon
Rotatable Bond Count	1	ChemAxon
Refractivity	117.93 m³·mol⁻¹	ChemAxon
Polarizability	43.8 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

HMDB ID

Not Available

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FoodDB ID

Not Available

KNApSAcK ID

Not Available

Chemspider ID

27023447

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

25150198

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for n-[(1s,2e,4e,6r,8e,10e,12s,14e,17r)-6,12-dihydroxy-3,9,15,17-tetramethyl-16-oxocycloheptadeca-2,4,8,10,14-pentaen-1-yl]ethanimidic acid (NP0327334)

MOL for NP0327334 (n-[(1s,2e,4e,6r,8e,10e,12s,14e,17r)-6,12-dihydroxy-3,9,15,17-tetramethyl-16-oxocycloheptadeca-2,4,8,10,14-pentaen-1-yl]ethanimidic acid)

3D MOL for NP0327334 (n-[(1s,2e,4e,6r,8e,10e,12s,14e,17r)-6,12-dihydroxy-3,9,15,17-tetramethyl-16-oxocycloheptadeca-2,4,8,10,14-pentaen-1-yl]ethanimidic acid)

3D SDF for NP0327334 (n-[(1s,2e,4e,6r,8e,10e,12s,14e,17r)-6,12-dihydroxy-3,9,15,17-tetramethyl-16-oxocycloheptadeca-2,4,8,10,14-pentaen-1-yl]ethanimidic acid)

3D-SDF for NP0327334 (n-[(1s,2e,4e,6r,8e,10e,12s,14e,17r)-6,12-dihydroxy-3,9,15,17-tetramethyl-16-oxocycloheptadeca-2,4,8,10,14-pentaen-1-yl]ethanimidic acid)

PDB for NP0327334 (n-[(1s,2e,4e,6r,8e,10e,12s,14e,17r)-6,12-dihydroxy-3,9,15,17-tetramethyl-16-oxocycloheptadeca-2,4,8,10,14-pentaen-1-yl]ethanimidic acid)

3D PDB for NP0327334 (n-[(1s,2e,4e,6r,8e,10e,12s,14e,17r)-6,12-dihydroxy-3,9,15,17-tetramethyl-16-oxocycloheptadeca-2,4,8,10,14-pentaen-1-yl]ethanimidic acid)

SMILES for NP0327334 (n-[(1s,2e,4e,6r,8e,10e,12s,14e,17r)-6,12-dihydroxy-3,9,15,17-tetramethyl-16-oxocycloheptadeca-2,4,8,10,14-pentaen-1-yl]ethanimidic acid)

INCHI for NP0327334 (n-[(1s,2e,4e,6r,8e,10e,12s,14e,17r)-6,12-dihydroxy-3,9,15,17-tetramethyl-16-oxocycloheptadeca-2,4,8,10,14-pentaen-1-yl]ethanimidic acid)

Structure for NP0327334 (n-[(1s,2e,4e,6r,8e,10e,12s,14e,17r)-6,12-dihydroxy-3,9,15,17-tetramethyl-16-oxocycloheptadeca-2,4,8,10,14-pentaen-1-yl]ethanimidic acid)

3D Structure for NP0327334 (n-[(1s,2e,4e,6r,8e,10e,12s,14e,17r)-6,12-dihydroxy-3,9,15,17-tetramethyl-16-oxocycloheptadeca-2,4,8,10,14-pentaen-1-yl]ethanimidic acid)