NP-MRD: Showing NP-Card for (1s,2s,3s,5s,8r,9s,10r,11s,12r,13s)-3,12,13-trihydroxy-11-methyl-6-methylidene-16-oxo-15-oxapentacyclo[9.3.2.1⁵,⁸.0¹,¹⁰.0²,⁸]heptadecane-9-carboxylic acid (NP0287342)

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Record Information

Version

2.0

Created at

2022-09-09 16:22:05 UTC

Updated at

2022-09-09 16:22:05 UTC

NP-MRD ID

NP0287342

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(1s,2s,3s,5s,8r,9s,10r,11s,12r,13s)-3,12,13-trihydroxy-11-methyl-6-methylidene-16-oxo-15-oxapentacyclo[9.3.2.1⁵,⁸.0¹,¹⁰.0²,⁸]heptadecane-9-carboxylic acid

Description

68062-25-9 Belongs to the class of organic compounds known as c19-gibberellin 6-carboxylic acids. These are c19-gibberellins with a carboxyl group at the 6-position. (1s,2s,3s,5s,8r,9s,10r,11s,12r,13s)-3,12,13-trihydroxy-11-methyl-6-methylidene-16-oxo-15-oxapentacyclo[9.3.2.1⁵,⁸.0¹,¹⁰.0²,⁸]heptadecane-9-carboxylic acid is found in Eriobotrya japonica and Lagenaria siceraria. Based on a literature review very few articles have been published on 68062-25-9.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309092218222D          

 26 30  0  0  1  0            999 V2000
    6.2619   -0.7938    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4341   -1.0711    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6331   -0.7208    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0102   -1.3568    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.6689   -1.6867    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3493   -1.9378    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    5.0080   -2.7384    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1559   -2.8690    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.8196   -3.6694    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.6513   -2.1599    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.8111   -2.0778    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.4387   -1.5422    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4841   -0.4960    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.2900   -0.1149    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.7495   -0.2250    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.0584    0.7260    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.9517   -0.4353    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.2491    0.0845    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6187   -1.1901    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7590   -1.2608    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.0012   -1.9210    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.5867   -1.1491    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.3307   -0.8465    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.3059    0.1412    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4273    0.5715    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.9697    0.8128    0.0000 O   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
  4  5  1  1  0  0  0
  6  5  1  1  0  0  0
  2  6  1  0  0  0  0
  6  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  1  6  0  0  0
  8 10  1  0  0  0  0
 10  4  1  1  0  0  0
 10 11  1  0  0  0  0
 11 12  1  0  0  0  0
 12 13  1  0  0  0  0
 13 14  1  1  0  0  0
 13 15  1  0  0  0  0
 15 16  1  1  0  0  0
 15 17  1  0  0  0  0
 17 18  1  1  0  0  0
 17 19  1  0  0  0  0
 19 20  2  0  0  0  0
 19 21  1  0  0  0  0
 11 21  1  6  0  0  0
 22 17  1  1  0  0  0
 11 22  1  0  0  0  0
 22 23  1  0  0  0  0
  4 23  1  0  0  0  0
 23 24  1  6  0  0  0
 24 25  2  0  0  0  0
 24 26  1  0  0  0  0
M  END

     RDKit          3D

 50 54  0  0  0  0  0  0  0  0999 V2000
   -4.7176   -0.8283   -0.8208 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5332   -0.5474   -0.3238 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2218   -0.6272   -1.0097 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1757   -0.4594    0.0713 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.9235   -0.7787    1.3307 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2631   -0.0830    1.0559 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.0144    1.3926    1.0287 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5321    1.7424    1.1678 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.4529    3.1165    0.8387 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7314    1.0073    0.1492 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.7152    0.8818    0.4265 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.5238    2.1107    0.1131 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8143    1.7692   -0.6014 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.6458    1.7887   -2.0002 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.4266    0.4955   -0.1255 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.4385    0.1425   -1.0311 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.4567   -0.6103    0.1076 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.9780   -1.9636   -0.2872 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0905   -0.5831    1.5636 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6212   -1.2627    2.4649 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.0474    0.3527    1.6733 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.1140   -0.2788   -0.5002 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.0508   -1.2844   -0.1194 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.0387   -2.3257   -1.1451 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6381   -2.3421   -2.2172 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9373   -3.3877   -0.9345 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8483   -1.1658   -1.8451 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6123   -0.7349   -0.2291 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1447    0.2634   -1.6842 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0886   -1.5033   -1.6416 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5077   -0.3568    2.2414 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0621   -1.8668    1.4883 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0302   -0.3934    1.7814 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3909    1.8809    0.1065 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5334    1.9120    1.8724 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1759    1.6534    2.1908 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5522    3.1935   -0.1540 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8531    1.4532   -0.8631 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8056    2.5821    1.0780 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9567    2.8655   -0.4607 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5662    2.5882   -0.3984 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9895    2.5946   -2.4153 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.9727    0.7339    0.8339 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.2068   -0.2624   -0.5541 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2196   -1.9804   -1.3494 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.8620   -2.1629    0.3668 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2300   -2.7307   -0.0120 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1341   -0.0026   -1.5434 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3969   -1.7530    0.8360 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5596   -4.2449   -0.5206 H   0  0  0  0  0  0  0  0  0  0  0  0
 17 18  1  6
 17 22  1  0
 22 23  1  0
 23 24  1  0
 24 26  1  0
 24 25  2  0
 23  4  1  0
  4  5  1  0
  5  6  1  0
  6  7  1  0
  7  8  1  0
  8  9  1  0
  8 10  1  0
 10 11  1  0
 11 12  1  0
 12 13  1  0
 13 14  1  0
 13 15  1  0
 15 16  1  0
 11 21  1  1
 21 19  1  0
 19 20  2  0
  6  2  1  0
  2  1  2  3
  2  3  1  0
 15 17  1  0
 19 17  1  0
 11 22  1  0
 10  4  1  0
  4  3  1  6
 18 45  1  0
 18 46  1  0
 18 47  1  0
 22 48  1  6
 23 49  1  1
 26 50  1  0
  5 31  1  0
  5 32  1  0
  6 33  1  1
  7 34  1  0
  7 35  1  0
  8 36  1  1
  9 37  1  0
 10 38  1  6
 12 39  1  0
 12 40  1  0
 13 41  1  6
 14 42  1  0
 15 43  1  1
 16 44  1  0
  1 27  1  0
  1 28  1  0
  3 29  1  0
  3 30  1  0
M  END


  Mrv1652309092218222D          

 26 30  0  0  1  0            999 V2000
    6.2619   -0.7938    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4341   -1.0711    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6331   -0.7208    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0102   -1.3568    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.6689   -1.6867    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3493   -1.9378    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    5.0080   -2.7384    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1559   -2.8690    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.8196   -3.6694    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.6513   -2.1599    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.8111   -2.0778    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.4387   -1.5422    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4841   -0.4960    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.2900   -0.1149    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.7495   -0.2250    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.0584    0.7260    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.9517   -0.4353    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.2491    0.0845    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6187   -1.1901    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7590   -1.2608    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.0012   -1.9210    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.5867   -1.1491    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.3307   -0.8465    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.3059    0.1412    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4273    0.5715    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.9697    0.8128    0.0000 O   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
  4  5  1  1  0  0  0
  6  5  1  1  0  0  0
  2  6  1  0  0  0  0
  6  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  1  6  0  0  0
  8 10  1  0  0  0  0
 10  4  1  1  0  0  0
 10 11  1  0  0  0  0
 11 12  1  0  0  0  0
 12 13  1  0  0  0  0
 13 14  1  1  0  0  0
 13 15  1  0  0  0  0
 15 16  1  1  0  0  0
 15 17  1  0  0  0  0
 17 18  1  1  0  0  0
 17 19  1  0  0  0  0
 19 20  2  0  0  0  0
 19 21  1  0  0  0  0
 11 21  1  6  0  0  0
 22 17  1  1  0  0  0
 11 22  1  0  0  0  0
 22 23  1  0  0  0  0
  4 23  1  0  0  0  0
 23 24  1  6  0  0  0
 24 25  2  0  0  0  0
 24 26  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0287342

> <DATABASE_NAME>
NP-MRD

> <SMILES>
C[C@]12[C@H]3[C@H](C(O)=O)[C@@]45C[C@@H](C[C@H](O)[C@H]4[C@@]3(C[C@H](O)[C@@H]1O)OC2=O)C(=C)C5

> <INCHI_IDENTIFIER>
InChI=1S/C19H24O7/c1-7-4-18-5-8(7)3-9(20)12(18)19-6-10(21)14(22)17(2,16(25)26-19)13(19)11(18)15(23)24/h8-14,20-22H,1,3-6H2,2H3,(H,23,24)/t8-,9+,10+,11-,12-,13-,14+,17+,18-,19-/m1/s1

> <INCHI_KEY>
FKMJLJSSQHSAEF-WQODXWHISA-N

> <FORMULA>
C19H24O7

> <MOLECULAR_WEIGHT>
364.394

> <EXACT_MASS>
364.152203113

> <JCHEM_ACCEPTOR_COUNT>
6

> <JCHEM_ATOM_COUNT>
50

> <JCHEM_AVERAGE_POLARIZABILITY>
36.379067868684274

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
4

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(1S,2S,3S,5S,8R,9S,10R,11S,12R,13S)-3,12,13-trihydroxy-11-methyl-6-methylidene-16-oxo-15-oxapentacyclo[9.3.2.1^{5,8}.0^{1,10}.0^{2,8}]heptadecane-9-carboxylic acid

> <JCHEM_LOGP>
-0.9325396276666666

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
5

> <JCHEM_PHYSIOLOGICAL_CHARGE>
-1

> <JCHEM_PKA>
13.385141993887036

> <JCHEM_PKA_STRONGEST_ACIDIC>
4.110556987157025

> <JCHEM_PKA_STRONGEST_BASIC>
-2.877965610374737

> <JCHEM_POLAR_SURFACE_AREA>
124.29

> <JCHEM_REFRACTIVITY>
86.96739999999998

> <JCHEM_ROTATABLE_BOND_COUNT>
1

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
(1S,2S,3S,5S,8R,9S,10R,11S,12R,13S)-3,12,13-trihydroxy-11-methyl-6-methylidene-16-oxo-15-oxapentacyclo[9.3.2.1^{5,8}.0^{1,10}.0^{2,8}]heptadecane-9-carboxylic acid

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 09-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   09-SEP-22         0                                  
HETATM    1  C   UNK     0      11.689  -1.482   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      10.144  -1.999   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       8.649  -1.346   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       7.486  -2.533   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       8.715  -3.149   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       9.985  -3.617   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       9.348  -5.112   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       7.758  -5.355   0.000  0.00  0.00           C+0
HETATM    9  O   UNK     0       7.130  -6.850   0.000  0.00  0.00           O+0
HETATM   10  C   UNK     0       6.816  -4.032   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       5.247  -3.879   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       6.419  -2.879   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       6.504  -0.926   0.000  0.00  0.00           C+0
HETATM   14  O   UNK     0       8.008  -0.214   0.000  0.00  0.00           O+0
HETATM   15  C   UNK     0       5.132  -0.420   0.000  0.00  0.00           C+0
HETATM   16  O   UNK     0       5.709   1.355   0.000  0.00  0.00           O+0
HETATM   17  C   UNK     0       3.643  -0.813   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       2.332   0.158   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       3.022  -2.221   0.000  0.00  0.00           C+0
HETATM   20  O   UNK     0       1.417  -2.353   0.000  0.00  0.00           O+0
HETATM   21  O   UNK     0       3.735  -3.586   0.000  0.00  0.00           O+0
HETATM   22  C   UNK     0       4.829  -2.145   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       6.217  -1.580   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       6.171   0.264   0.000  0.00  0.00           C+0
HETATM   25  O   UNK     0       4.531   1.067   0.000  0.00  0.00           O+0
HETATM   26  O   UNK     0       7.410   1.517   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3    6                                                  
CONECT    3    2    4                                                       
CONECT    4    3    5   10   23                                             
CONECT    5    4    6                                                       
CONECT    6    5    2    7                                                  
CONECT    7    6    8                                                       
CONECT    8    7    9   10                                                  
CONECT    9    8                                                            
CONECT   10    8    4   11                                                  
CONECT   11   10   12   21   22                                             
CONECT   12   11   13                                                       
CONECT   13   12   14   15                                                  
CONECT   14   13                                                            
CONECT   15   13   16   17                                                  
CONECT   16   15                                                            
CONECT   17   15   18   19   22                                             
CONECT   18   17                                                            
CONECT   19   17   20   21                                                  
CONECT   20   19                                                            
CONECT   21   19   11                                                       
CONECT   22   17   11   23                                                  
CONECT   23   22    4   24                                                  
CONECT   24   23   25   26                                                  
CONECT   25   24                                                            
CONECT   26   24                                                            
MASTER        0    0    0    0    0    0    0    0   26    0   60    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₁₉H₂₄O₇

Average Mass

364.3940 Da

Monoisotopic Mass

364.15220 Da

IUPAC Name

(1S,2S,3S,5S,8R,9S,10R,11S,12R,13S)-3,12,13-trihydroxy-11-methyl-6-methylidene-16-oxo-15-oxapentacyclo[9.3.2.1^{5,8}.0^{1,10}.0^{2,8}]heptadecane-9-carboxylic acid

Traditional Name

(1S,2S,3S,5S,8R,9S,10R,11S,12R,13S)-3,12,13-trihydroxy-11-methyl-6-methylidene-16-oxo-15-oxapentacyclo[9.3.2.1^{5,8}.0^{1,10}.0^{2,8}]heptadecane-9-carboxylic acid

CAS Registry Number

Not Available

SMILES

C[C@]12[C@H]3[C@H](C(O)=O)[C@@]45C[C@@H](C[C@H](O)[C@H]4[C@@]3(C[C@H](O)[C@@H]1O)OC2=O)C(=C)C5

InChI Identifier

InChI=1S/C19H24O7/c1-7-4-18-5-8(7)3-9(20)12(18)19-6-10(21)14(22)17(2,16(25)26-19)13(19)11(18)15(23)24/h8-14,20-22H,1,3-6H2,2H3,(H,23,24)/t8-,9+,10+,11-,12-,13-,14+,17+,18-,19-/m1/s1

InChI Key

FKMJLJSSQHSAEF-WQODXWHISA-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
Eriobotrya japonica	LOTUS Database	35616633
Lagenaria siceraria	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as c19-gibberellin 6-carboxylic acids. These are c19-gibberellins with a carboxyl group at the 6-position.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Prenol lipids

Sub Class

Diterpenoids

Direct Parent

C19-gibberellin 6-carboxylic acids

Alternative Parents

Substituents

20-norgibberellane-6-carboxylic acid
2-hydroxy,20-norgibberellane
Diterpene lactone
Caprolactone
Oxepane
Dicarboxylic acid or derivatives
Gamma butyrolactone
Cyclic alcohol
Tetrahydrofuran
Carboxylic acid ester
Secondary alcohol
Lactone
Carboxylic acid derivative
Carboxylic acid
Oxacycle
Organoheterocyclic compound
Polyol
Organic oxide
Hydrocarbon derivative
Organic oxygen compound
Carbonyl group
Alcohol
Organooxygen compound
Aliphatic heteropolycyclic compound

Molecular Framework

Aliphatic heteropolycyclic 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	-0.93	ChemAxon
pKa (Strongest Acidic)	4.11	ChemAxon
pKa (Strongest Basic)	-2.9	ChemAxon
Physiological Charge	-1	ChemAxon
Hydrogen Acceptor Count	6	ChemAxon
Hydrogen Donor Count	4	ChemAxon
Polar Surface Area	124.29 Å²	ChemAxon
Rotatable Bond Count	1	ChemAxon
Refractivity	86.97 m³·mol⁻¹	ChemAxon
Polarizability	36.38 Å³	ChemAxon
Number of Rings	5	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	Yes	ChemAxon
Ghose Filter	No	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

C00000050

Chemspider ID

103884609

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

101603121

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for (1s,2s,3s,5s,8r,9s,10r,11s,12r,13s)-3,12,13-trihydroxy-11-methyl-6-methylidene-16-oxo-15-oxapentacyclo[9.3.2.1⁵,⁸.0¹,¹⁰.0²,⁸]heptadecane-9-carboxylic acid (NP0287342)

MOL for NP0287342 ((1s,2s,3s,5s,8r,9s,10r,11s,12r,13s)-3,12,13-trihydroxy-11-methyl-6-methylidene-16-oxo-15-oxapentacyclo[9.3.2.1⁵,⁸.0¹,¹⁰.0²,⁸]heptadecane-9-carboxylic acid)

3D MOL for NP0287342 ((1s,2s,3s,5s,8r,9s,10r,11s,12r,13s)-3,12,13-trihydroxy-11-methyl-6-methylidene-16-oxo-15-oxapentacyclo[9.3.2.1⁵,⁸.0¹,¹⁰.0²,⁸]heptadecane-9-carboxylic acid)

3D SDF for NP0287342 ((1s,2s,3s,5s,8r,9s,10r,11s,12r,13s)-3,12,13-trihydroxy-11-methyl-6-methylidene-16-oxo-15-oxapentacyclo[9.3.2.1⁵,⁸.0¹,¹⁰.0²,⁸]heptadecane-9-carboxylic acid)

3D-SDF for NP0287342 ((1s,2s,3s,5s,8r,9s,10r,11s,12r,13s)-3,12,13-trihydroxy-11-methyl-6-methylidene-16-oxo-15-oxapentacyclo[9.3.2.1⁵,⁸.0¹,¹⁰.0²,⁸]heptadecane-9-carboxylic acid)

PDB for NP0287342 ((1s,2s,3s,5s,8r,9s,10r,11s,12r,13s)-3,12,13-trihydroxy-11-methyl-6-methylidene-16-oxo-15-oxapentacyclo[9.3.2.1⁵,⁸.0¹,¹⁰.0²,⁸]heptadecane-9-carboxylic acid)

3D PDB for NP0287342 ((1s,2s,3s,5s,8r,9s,10r,11s,12r,13s)-3,12,13-trihydroxy-11-methyl-6-methylidene-16-oxo-15-oxapentacyclo[9.3.2.1⁵,⁸.0¹,¹⁰.0²,⁸]heptadecane-9-carboxylic acid)

SMILES for NP0287342 ((1s,2s,3s,5s,8r,9s,10r,11s,12r,13s)-3,12,13-trihydroxy-11-methyl-6-methylidene-16-oxo-15-oxapentacyclo[9.3.2.1⁵,⁸.0¹,¹⁰.0²,⁸]heptadecane-9-carboxylic acid)

INCHI for NP0287342 ((1s,2s,3s,5s,8r,9s,10r,11s,12r,13s)-3,12,13-trihydroxy-11-methyl-6-methylidene-16-oxo-15-oxapentacyclo[9.3.2.1⁵,⁸.0¹,¹⁰.0²,⁸]heptadecane-9-carboxylic acid)

Structure for NP0287342 ((1s,2s,3s,5s,8r,9s,10r,11s,12r,13s)-3,12,13-trihydroxy-11-methyl-6-methylidene-16-oxo-15-oxapentacyclo[9.3.2.1⁵,⁸.0¹,¹⁰.0²,⁸]heptadecane-9-carboxylic acid)

3D Structure for NP0287342 ((1s,2s,3s,5s,8r,9s,10r,11s,12r,13s)-3,12,13-trihydroxy-11-methyl-6-methylidene-16-oxo-15-oxapentacyclo[9.3.2.1⁵,⁸.0¹,¹⁰.0²,⁸]heptadecane-9-carboxylic acid)