NP-MRD: Showing NP-Card for elisabethin H (NP0038722)

Jump To Section:

Identification Spectra BioTaxonomy ChemoTaxonomy Physical properties Links References XML

Record Information

Version

2.0

Created at

2021-06-20 21:20:05 UTC

Updated at

2021-06-30 00:11:39 UTC

NP-MRD ID

NP0038722

Secondary Accession Numbers

None

Natural Product Identification

Common Name

elisabethin H

Provided By

JEOL Database JEOL Logo

Description

(1S,3R,3aS,5R,7aR)-3a-hydroxy-3-[(2Z)-3-hydroxy-2-methylprop-2-enoyl]-1,5-dimethyl-octahydro-1H-inden-4-one belongs to the class of organic compounds known as b'-hydroxy-alpha,beta-unsaturated ketones. These are alpha,beta-unsaturated ketones that carry a hydroxyl group at the beta'-position. elisabethin H is found in Pseudopterogorgia elisabethae (Bayer). elisabethin H was first documented in 2009 (Shi, Y.-P., et al.). Based on a literature review very few articles have been published on (1S,3R,3aS,5R,7aR)-3a-hydroxy-3-[(2Z)-3-hydroxy-2-methylprop-2-enoyl]-1,5-dimethyl-octahydro-1H-inden-4-one.

Structure

MOL 3D MOL SDF 3D SDF PDB SMILES InChI


  Mrv1652306202123203D          

 41 42  0  0  0  0            999 V2000
   -0.4938    4.6185    0.0949 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2667    4.1190    1.2754 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3191    4.7979    1.7627 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0743    4.4556    2.8533 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8458    2.8410    1.9445 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2537    2.5892    3.0844 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0217    1.8472    1.1762 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.8438    1.0799    0.1562 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.8479   -0.3978    0.5900 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.2039   -1.0594    0.3849 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3985   -0.3699    2.0599 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.1298   -1.6991    2.6130 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.4657   -2.1311    2.0077 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.5263   -1.0336    2.1211 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.8349   -1.4763    1.4740 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9787    0.2389    1.4815 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5632    0.8164    0.5634 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.6467    0.7533    2.0696 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.9410    1.1746    3.3961 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.5627    4.7452    0.3524 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5734    3.9236   -0.7467 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8616    5.5911   -0.2507 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6909    5.7218    1.3335 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6487    3.6840    3.2894 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8040    2.4239    0.6741 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8620    1.4818    0.0978 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4106    1.1646   -0.8476 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1151   -0.9332   -0.0260 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1718   -2.1161    0.6675 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5042   -1.0030   -0.6667 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9808   -0.5723    0.9838 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2492   -0.0811    2.6933 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6107   -2.4927    2.4633 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2587   -1.5988    3.6986 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8128   -3.0355    2.5222 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3182   -2.4082    0.9568 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7253   -0.8125    3.1768 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.2212   -2.3806    1.9556 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.5972   -0.6949    1.5638 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7026   -1.6881    0.4072 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1287    1.5822    3.7655 H   0  0  0  0  0  0  0  0  0  0  0  0
  9  8  1  0  0  0  0
  8  7  1  0  0  0  0
  7 18  1  0  0  0  0
 14 15  1  0  0  0  0
 18 19  1  1  0  0  0
 12 13  1  0  0  0  0
 11 32  1  1  0  0  0
 16 17  2  0  0  0  0
  9 10  1  0  0  0  0
 18 11  1  0  0  0  0
  7  5  1  0  0  0  0
 16 14  1  0  0  0  0
  5  2  1  0  0  0  0
 14 13  1  0  0  0  0
  2  1  1  0  0  0  0
 16 18  1  0  0  0  0
  2  3  2  0  0  0  0
 12 11  1  0  0  0  0
  3 23  1  0  0  0  0
  3  4  1  0  0  0  0
 11  9  1  0  0  0  0
  5  6  2  0  0  0  0
 12 33  1  0  0  0  0
 12 34  1  0  0  0  0
 14 37  1  1  0  0  0
 13 35  1  0  0  0  0
 13 36  1  0  0  0  0
 15 38  1  0  0  0  0
 15 39  1  0  0  0  0
 15 40  1  0  0  0  0
  9 28  1  6  0  0  0
  8 26  1  0  0  0  0
  8 27  1  0  0  0  0
  7 25  1  6  0  0  0
 19 41  1  0  0  0  0
 10 29  1  0  0  0  0
 10 30  1  0  0  0  0
 10 31  1  0  0  0  0
  1 20  1  0  0  0  0
  1 21  1  0  0  0  0
  1 22  1  0  0  0  0
  4 24  1  0  0  0  0
M  END

     RDKit          3D

 41 42  0  0  0  0  0  0  0  0999 V2000
   -0.4938    4.6185    0.0949 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2667    4.1190    1.2754 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3191    4.7979    1.7627 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0743    4.4556    2.8533 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8458    2.8410    1.9445 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2537    2.5892    3.0844 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0217    1.8472    1.1762 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.8438    1.0799    0.1562 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8479   -0.3978    0.5900 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.2039   -1.0594    0.3849 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3985   -0.3699    2.0599 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.1298   -1.6991    2.6130 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4657   -2.1311    2.0077 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5263   -1.0336    2.1211 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.8349   -1.4763    1.4740 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9787    0.2389    1.4815 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5632    0.8164    0.5634 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.6467    0.7533    2.0696 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.9410    1.1746    3.3961 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.5627    4.7452    0.3524 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5734    3.9236   -0.7467 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8616    5.5911   -0.2507 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6909    5.7218    1.3335 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6487    3.6840    3.2894 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8040    2.4239    0.6741 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8620    1.4818    0.0978 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4106    1.1646   -0.8476 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1151   -0.9332   -0.0260 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1718   -2.1161    0.6675 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5042   -1.0030   -0.6667 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9808   -0.5723    0.9838 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2492   -0.0811    2.6933 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6107   -2.4927    2.4633 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2587   -1.5988    3.6986 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8128   -3.0355    2.5222 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3182   -2.4082    0.9568 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7253   -0.8125    3.1768 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.2212   -2.3806    1.9556 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.5972   -0.6949    1.5638 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7026   -1.6881    0.4072 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1287    1.5822    3.7655 H   0  0  0  0  0  0  0  0  0  0  0  0
  9  8  1  0
  8  7  1  0
  7 18  1  0
 14 15  1  0
 18 19  1  1
 12 13  1  0
 11 32  1  1
 16 17  2  0
  9 10  1  0
 18 11  1  0
  7  5  1  0
 16 14  1  0
  5  2  1  0
 14 13  1  0
  2  1  1  0
 16 18  1  0
  2  3  2  0
 12 11  1  0
  3 23  1  0
  3  4  1  0
 11  9  1  0
  5  6  2  0
 12 33  1  0
 12 34  1  0
 14 37  1  1
 13 35  1  0
 13 36  1  0
 15 38  1  0
 15 39  1  0
 15 40  1  0
  9 28  1  6
  8 26  1  0
  8 27  1  0
  7 25  1  6
 19 41  1  0
 10 29  1  0
 10 30  1  0
 10 31  1  0
  1 20  1  0
  1 21  1  0
  1 22  1  0
  4 24  1  0
M  END


  Mrv1652306202123203D          

 41 42  0  0  0  0            999 V2000
   -0.4938    4.6185    0.0949 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2667    4.1190    1.2754 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3191    4.7979    1.7627 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0743    4.4556    2.8533 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8458    2.8410    1.9445 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2537    2.5892    3.0844 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0217    1.8472    1.1762 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.8438    1.0799    0.1562 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.8479   -0.3978    0.5900 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.2039   -1.0594    0.3849 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3985   -0.3699    2.0599 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.1298   -1.6991    2.6130 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.4657   -2.1311    2.0077 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.5263   -1.0336    2.1211 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.8349   -1.4763    1.4740 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9787    0.2389    1.4815 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5632    0.8164    0.5634 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.6467    0.7533    2.0696 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.9410    1.1746    3.3961 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.5627    4.7452    0.3524 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5734    3.9236   -0.7467 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8616    5.5911   -0.2507 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6909    5.7218    1.3335 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6487    3.6840    3.2894 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8040    2.4239    0.6741 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8620    1.4818    0.0978 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4106    1.1646   -0.8476 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1151   -0.9332   -0.0260 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1718   -2.1161    0.6675 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5042   -1.0030   -0.6667 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9808   -0.5723    0.9838 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2492   -0.0811    2.6933 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6107   -2.4927    2.4633 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2587   -1.5988    3.6986 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8128   -3.0355    2.5222 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3182   -2.4082    0.9568 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7253   -0.8125    3.1768 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.2212   -2.3806    1.9556 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.5972   -0.6949    1.5638 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7026   -1.6881    0.4072 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1287    1.5822    3.7655 H   0  0  0  0  0  0  0  0  0  0  0  0
  9  8  1  0  0  0  0
  8  7  1  0  0  0  0
  7 18  1  0  0  0  0
 14 15  1  0  0  0  0
 18 19  1  1  0  0  0
 12 13  1  0  0  0  0
 11 32  1  1  0  0  0
 16 17  2  0  0  0  0
  9 10  1  0  0  0  0
 18 11  1  0  0  0  0
  7  5  1  0  0  0  0
 16 14  1  0  0  0  0
  5  2  1  0  0  0  0
 14 13  1  0  0  0  0
  2  1  1  0  0  0  0
 16 18  1  0  0  0  0
  2  3  2  0  0  0  0
 12 11  1  0  0  0  0
  3 23  1  0  0  0  0
  3  4  1  0  0  0  0
 11  9  1  0  0  0  0
  5  6  2  0  0  0  0
 12 33  1  0  0  0  0
 12 34  1  0  0  0  0
 14 37  1  1  0  0  0
 13 35  1  0  0  0  0
 13 36  1  0  0  0  0
 15 38  1  0  0  0  0
 15 39  1  0  0  0  0
 15 40  1  0  0  0  0
  9 28  1  6  0  0  0
  8 26  1  0  0  0  0
  8 27  1  0  0  0  0
  7 25  1  6  0  0  0
 19 41  1  0  0  0  0
 10 29  1  0  0  0  0
 10 30  1  0  0  0  0
 10 31  1  0  0  0  0
  1 20  1  0  0  0  0
  1 21  1  0  0  0  0
  1 22  1  0  0  0  0
  4 24  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0038722

> <DATABASE_NAME>
NP-MRD

> <SMILES>
[H]O\C([H])=C(/C(=O)[C@]1([H])C([H])([H])[C@]([H])(C([H])([H])[H])[C@@]2([H])C([H])([H])C([H])([H])[C@]([H])(C(=O)[C@@]12O[H])C([H])([H])[H])C([H])([H])[H]

> <INCHI_IDENTIFIER>
InChI=1S/C15H22O4/c1-8-4-5-11-9(2)6-12(13(17)10(3)7-16)15(11,19)14(8)18/h7-9,11-12,16,19H,4-6H2,1-3H3/b10-7-/t8-,9+,11-,12+,15+/m1/s1

> <INCHI_KEY>
JSEIKXDLHBMXHO-ODPKOALNSA-N

> <FORMULA>
C15H22O4

> <MOLECULAR_WEIGHT>
266.337

> <EXACT_MASS>
266.151809188

> <JCHEM_ACCEPTOR_COUNT>
4

> <JCHEM_ATOM_COUNT>
41

> <JCHEM_AVERAGE_POLARIZABILITY>
28.73847656073775

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(1S,3R,3aS,5R,7aR)-3a-hydroxy-3-[(2Z)-3-hydroxy-2-methylprop-2-enoyl]-1,5-dimethyl-octahydro-1H-inden-4-one

> <ALOGPS_LOGP>
1.28

> <JCHEM_LOGP>
2.573377444666666

> <ALOGPS_LOGS>
-1.94

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
2

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
12.599092725920865

> <JCHEM_PKA_STRONGEST_ACIDIC>
8.820331995391534

> <JCHEM_PKA_STRONGEST_BASIC>
-3.9053536001909768

> <JCHEM_POLAR_SURFACE_AREA>
74.6

> <JCHEM_REFRACTIVITY>
71.38889999999998

> <JCHEM_ROTATABLE_BOND_COUNT>
2

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
3.08e+00 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(1S,3R,3aS,5R,7aR)-3a-hydroxy-3-[(2Z)-3-hydroxy-2-methylprop-2-enoyl]-1,5-dimethyl-hexahydro-1H-inden-4-one

> <JCHEM_VEBER_RULE>
0

$$$$

     RDKit          3D

 41 42  0  0  0  0  0  0  0  0999 V2000
   -0.4938    4.6185    0.0949 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2667    4.1190    1.2754 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3191    4.7979    1.7627 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0743    4.4556    2.8533 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8458    2.8410    1.9445 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2537    2.5892    3.0844 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0217    1.8472    1.1762 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.8438    1.0799    0.1562 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8479   -0.3978    0.5900 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.2039   -1.0594    0.3849 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3985   -0.3699    2.0599 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.1298   -1.6991    2.6130 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4657   -2.1311    2.0077 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5263   -1.0336    2.1211 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.8349   -1.4763    1.4740 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9787    0.2389    1.4815 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5632    0.8164    0.5634 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.6467    0.7533    2.0696 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.9410    1.1746    3.3961 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.5627    4.7452    0.3524 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5734    3.9236   -0.7467 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8616    5.5911   -0.2507 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6909    5.7218    1.3335 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6487    3.6840    3.2894 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8040    2.4239    0.6741 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8620    1.4818    0.0978 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4106    1.1646   -0.8476 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1151   -0.9332   -0.0260 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1718   -2.1161    0.6675 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5042   -1.0030   -0.6667 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9808   -0.5723    0.9838 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2492   -0.0811    2.6933 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6107   -2.4927    2.4633 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2587   -1.5988    3.6986 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8128   -3.0355    2.5222 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3182   -2.4082    0.9568 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7253   -0.8125    3.1768 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.2212   -2.3806    1.9556 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.5972   -0.6949    1.5638 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7026   -1.6881    0.4072 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1287    1.5822    3.7655 H   0  0  0  0  0  0  0  0  0  0  0  0
  9  8  1  0
  8  7  1  0
  7 18  1  0
 14 15  1  0
 18 19  1  1
 12 13  1  0
 11 32  1  1
 16 17  2  0
  9 10  1  0
 18 11  1  0
  7  5  1  0
 16 14  1  0
  5  2  1  0
 14 13  1  0
  2  1  1  0
 16 18  1  0
  2  3  2  0
 12 11  1  0
  3 23  1  0
  3  4  1  0
 11  9  1  0
  5  6  2  0
 12 33  1  0
 12 34  1  0
 14 37  1  1
 13 35  1  0
 13 36  1  0
 15 38  1  0
 15 39  1  0
 15 40  1  0
  9 28  1  6
  8 26  1  0
  8 27  1  0
  7 25  1  6
 19 41  1  0
 10 29  1  0
 10 30  1  0
 10 31  1  0
  1 20  1  0
  1 21  1  0
  1 22  1  0
  4 24  1  0
M  END

HEADER    PROTEIN                                 20-JUN-21   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   20-JUN-21         0                                  
HETATM    1  C   UNK     0      -0.494   4.619   0.095  0.00  0.00           C+0
HETATM    2  C   UNK     0      -1.267   4.119   1.275  0.00  0.00           C+0
HETATM    3  C   UNK     0      -2.319   4.798   1.763  0.00  0.00           C+0
HETATM    4  O   UNK     0      -3.074   4.456   2.853  0.00  0.00           O+0
HETATM    5  C   UNK     0      -0.846   2.841   1.944  0.00  0.00           C+0
HETATM    6  O   UNK     0      -1.254   2.589   3.084  0.00  0.00           O+0
HETATM    7  C   UNK     0       0.022   1.847   1.176  0.00  0.00           C+0
HETATM    8  C   UNK     0      -0.844   1.080   0.156  0.00  0.00           C+0
HETATM    9  C   UNK     0      -0.848  -0.398   0.590  0.00  0.00           C+0
HETATM   10  C   UNK     0      -2.204  -1.059   0.385  0.00  0.00           C+0
HETATM   11  C   UNK     0      -0.399  -0.370   2.060  0.00  0.00           C+0
HETATM   12  C   UNK     0       0.130  -1.699   2.613  0.00  0.00           C+0
HETATM   13  C   UNK     0       1.466  -2.131   2.008  0.00  0.00           C+0
HETATM   14  C   UNK     0       2.526  -1.034   2.121  0.00  0.00           C+0
HETATM   15  C   UNK     0       3.835  -1.476   1.474  0.00  0.00           C+0
HETATM   16  C   UNK     0       1.979   0.239   1.482  0.00  0.00           C+0
HETATM   17  O   UNK     0       2.563   0.816   0.563  0.00  0.00           O+0
HETATM   18  C   UNK     0       0.647   0.753   2.070  0.00  0.00           C+0
HETATM   19  O   UNK     0       0.941   1.175   3.396  0.00  0.00           O+0
HETATM   20  H   UNK     0       0.563   4.745   0.352  0.00  0.00           H+0
HETATM   21  H   UNK     0      -0.573   3.924  -0.747  0.00  0.00           H+0
HETATM   22  H   UNK     0      -0.862   5.591  -0.251  0.00  0.00           H+0
HETATM   23  H   UNK     0      -2.691   5.722   1.333  0.00  0.00           H+0
HETATM   24  H   UNK     0      -2.649   3.684   3.289  0.00  0.00           H+0
HETATM   25  H   UNK     0       0.804   2.424   0.674  0.00  0.00           H+0
HETATM   26  H   UNK     0      -1.862   1.482   0.098  0.00  0.00           H+0
HETATM   27  H   UNK     0      -0.411   1.165  -0.848  0.00  0.00           H+0
HETATM   28  H   UNK     0      -0.115  -0.933  -0.026  0.00  0.00           H+0
HETATM   29  H   UNK     0      -2.172  -2.116   0.668  0.00  0.00           H+0
HETATM   30  H   UNK     0      -2.504  -1.003  -0.667  0.00  0.00           H+0
HETATM   31  H   UNK     0      -2.981  -0.572   0.984  0.00  0.00           H+0
HETATM   32  H   UNK     0      -1.249  -0.081   2.693  0.00  0.00           H+0
HETATM   33  H   UNK     0      -0.611  -2.493   2.463  0.00  0.00           H+0
HETATM   34  H   UNK     0       0.259  -1.599   3.699  0.00  0.00           H+0
HETATM   35  H   UNK     0       1.813  -3.035   2.522  0.00  0.00           H+0
HETATM   36  H   UNK     0       1.318  -2.408   0.957  0.00  0.00           H+0
HETATM   37  H   UNK     0       2.725  -0.813   3.177  0.00  0.00           H+0
HETATM   38  H   UNK     0       4.221  -2.381   1.956  0.00  0.00           H+0
HETATM   39  H   UNK     0       4.597  -0.695   1.564  0.00  0.00           H+0
HETATM   40  H   UNK     0       3.703  -1.688   0.407  0.00  0.00           H+0
HETATM   41  H   UNK     0       0.129   1.582   3.765  0.00  0.00           H+0
CONECT    1    2   20   21   22                                             
CONECT    2    5    1    3                                                  
CONECT    3    2   23    4                                                  
CONECT    4    3   24                                                       
CONECT    5    7    2    6                                                  
CONECT    6    5                                                            
CONECT    7    8   18    5   25                                             
CONECT    8    9    7   26   27                                             
CONECT    9    8   10   11   28                                             
CONECT   10    9   29   30   31                                             
CONECT   11   32   18   12    9                                             
CONECT   12   13   11   33   34                                             
CONECT   13   12   14   35   36                                             
CONECT   14   15   16   13   37                                             
CONECT   15   14   38   39   40                                             
CONECT   16   17   14   18                                                  
CONECT   17   16                                                            
CONECT   18    7   19   11   16                                             
CONECT   19   18   41                                                       
CONECT   20    1                                                            
CONECT   21    1                                                            
CONECT   22    1                                                            
CONECT   23    3                                                            
CONECT   24    4                                                            
CONECT   25    7                                                            
CONECT   26    8                                                            
CONECT   27    8                                                            
CONECT   28    9                                                            
CONECT   29   10                                                            
CONECT   30   10                                                            
CONECT   31   10                                                            
CONECT   32   11                                                            
CONECT   33   12                                                            
CONECT   34   12                                                            
CONECT   35   13                                                            
CONECT   36   13                                                            
CONECT   37   14                                                            
CONECT   38   15                                                            
CONECT   39   15                                                            
CONECT   40   15                                                            
CONECT   41   19                                                            
MASTER        0    0    0    0    0    0    0    0   41    0   84    0
END

RDKit          3D

41 42  0  0  0  0  0  0  0  0999 V2000
   -0.4938    4.6185    0.0949 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2667    4.1190    1.2754 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3191    4.7979    1.7627 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0743    4.4556    2.8533 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8458    2.8410    1.9445 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2537    2.5892    3.0844 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0217    1.8472    1.1762 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.8438    1.0799    0.1562 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8479   -0.3978    0.5900 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.2039   -1.0594    0.3849 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3985   -0.3699    2.0599 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.1298   -1.6991    2.6130 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4657   -2.1311    2.0077 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5263   -1.0336    2.1211 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.8349   -1.4763    1.4740 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9787    0.2389    1.4815 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5632    0.8164    0.5634 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.6467    0.7533    2.0696 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.9410    1.1746    3.3961 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.5627    4.7452    0.3524 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5734    3.9236   -0.7467 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8616    5.5911   -0.2507 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6909    5.7218    1.3335 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6487    3.6840    3.2894 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8040    2.4239    0.6741 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8620    1.4818    0.0978 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4106    1.1646   -0.8476 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1151   -0.9332   -0.0260 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1718   -2.1161    0.6675 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5042   -1.0030   -0.6667 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9808   -0.5723    0.9838 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2492   -0.0811    2.6933 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6107   -2.4927    2.4633 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2587   -1.5988    3.6986 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8128   -3.0355    2.5222 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3182   -2.4082    0.9568 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7253   -0.8125    3.1768 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.2212   -2.3806    1.9556 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.5972   -0.6949    1.5638 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7026   -1.6881    0.4072 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1287    1.5822    3.7655 H   0  0  0  0  0  0  0  0  0  0  0  0
  9  8  1  0
  8  7  1  0
  7 18  1  0
 14 15  1  0
 18 19  1  1
 12 13  1  0
 11 32  1  1
 16 17  2  0
  9 10  1  0
 18 11  1  0
  7  5  1  0
 16 14  1  0
  5  2  1  0
 14 13  1  0
  2  1  1  0
 16 18  1  0
  2  3  2  0
 12 11  1  0
  3 23  1  0
  3  4  1  0
 11  9  1  0
  5  6  2  0
 12 33  1  0
 12 34  1  0
 14 37  1  1
 13 35  1  0
 13 36  1  0
 15 38  1  0
 15 39  1  0
 15 40  1  0
  9 28  1  6
  8 26  1  0
  8 27  1  0
  7 25  1  6
 19 41  1  0
 10 29  1  0
 10 30  1  0
 10 31  1  0
  1 20  1  0
  1 21  1  0
  1 22  1  0
  4 24  1  0
M  END

View in JSmol View DFT Assignments 3D Conformers

Synonyms

Not Available

Chemical Formula

C₁₅H₂₂O₄

Average Mass

266.3370 Da

Monoisotopic Mass

266.15181 Da

IUPAC Name

(1S,3R,3aS,5R,7aR)-3a-hydroxy-3-[(2Z)-3-hydroxy-2-methylprop-2-enoyl]-1,5-dimethyl-octahydro-1H-inden-4-one

Traditional Name

(1S,3R,3aS,5R,7aR)-3a-hydroxy-3-[(2Z)-3-hydroxy-2-methylprop-2-enoyl]-1,5-dimethyl-hexahydro-1H-inden-4-one

CAS Registry Number

Not Available

SMILES

[H]O\C([H])=C(/C(=O)[C@]1([H])C([H])([H])[C@]([H])(C([H])([H])[H])[C@@]2([H])C([H])([H])C([H])([H])[C@]([H])(C(=O)[C@@]12O[H])C([H])([H])[H])C([H])([H])[H]

InChI Identifier

InChI=1S/C15H22O4/c1-8-4-5-11-9(2)6-12(13(17)10(3)7-16)15(11,19)14(8)18/h7-9,11-12,16,19H,4-6H2,1-3H3/b10-7-/t8-,9+,11-,12+,15+/m1/s1

InChI Key

JSEIKXDLHBMXHO-ODPKOALNSA-N

Experimental Spectra

Spectrum Type	Description	Depositor Email	Depositor Organization	Depositor	Deposition Date	View
1D NMR	¹³C NMR Spectrum (1D, 500 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 500 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 100 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 100 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 200 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 200 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 300 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 300 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 400 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 600 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 600 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 700 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 700 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 800 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 800 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 900 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 900 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 1000 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 1000 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, 100 MHz, chcl3, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 125 MHz, chcl3, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 150 MHz, chcl3, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 175 MHz, chcl3, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 200 MHz, chcl3, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 225 MHz, chcl3, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 25 MHz, chcl3, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 250 MHz, chcl3, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 50 MHz, chcl3, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 75 MHz, chcl3, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 100 MHz, chcl3, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 1000 MHz, chcl3, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 200 MHz, chcl3, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 300 MHz, chcl3, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, chcl3, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 500 MHz, chcl3, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 600 MHz, chcl3, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 700 MHz, chcl3, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 800 MHz, chcl3, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 900 MHz, chcl3, 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
Antillogorgia elisabethae	JEOL database	Shi, Y.-P., et al, EurJ. Org. Chem. 2009, 493.

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as b'-hydroxy-alpha,beta-unsaturated ketones. These are alpha,beta-unsaturated ketones that carry a hydroxyl group at the beta'-position.

Kingdom

Organic compounds

Super Class

Organic oxygen compounds

Class

Organooxygen compounds

Sub Class

Carbonyl compounds

Direct Parent

b'-hydroxy-alpha,beta-unsaturated ketones

Alternative Parents

Substituents

B'-hydroxy-alpha,beta-unsaturated-ketone
Alpha-branched alpha,beta-unsaturated-ketone
Vinylogous acid
Tertiary alcohol
Enone
Cyclic alcohol
Acryloyl-group
Ketone
Enol
Organic oxide
Hydrocarbon derivative
Alcohol
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	1.28	ALOGPS
logP	2.57	ChemAxon
logS	-1.9	ALOGPS
pKa (Strongest Acidic)	8.82	ChemAxon
pKa (Strongest Basic)	-3.9	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	4	ChemAxon
Hydrogen Donor Count	2	ChemAxon
Polar Surface Area	74.6 Å²	ChemAxon
Rotatable Bond Count	2	ChemAxon
Refractivity	71.39 m³·mol⁻¹	ChemAxon
Polarizability	28.74 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

Not Available

Chemspider ID

27024026

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

25215788

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Shi, Y.-P., et al. (2009). Shi, Y.-P., et al, EurJ. Org. Chem. 2009, 493.. Eur. J. Org. Chem..

Showing NP-Card for elisabethin H (NP0038722)

MOL for NP0038722 (elisabethin H)

3D MOL for NP0038722 (elisabethin H)

3D SDF for NP0038722 (elisabethin H)

3D-SDF for NP0038722 (elisabethin H)

PDB for NP0038722 (elisabethin H)

3D PDB for NP0038722 (elisabethin H)

SMILES for NP0038722 (elisabethin H)

INCHI for NP0038722 (elisabethin H)

Structure for NP0038722 (elisabethin H)

3D Structure for NP0038722 (elisabethin H)