NP-MRD: Showing NP-Card for (3r,4as,5s,6ar,12r,12as)-3-[(1s)-1-bromo-2-hydroxyethyl]-5,12-dihydroxy-3,12a-dimethyl-2h,4h,4ah,5h,6h,6ah,8h,9h,10h,12h-cycloocta[a]naphthalene-7,11-dione (NP0147256)

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Record Information

Version

2.0

Created at

2022-09-02 02:49:19 UTC

Updated at

2022-09-02 02:49:19 UTC

NP-MRD ID

NP0147256

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(3r,4as,5s,6ar,12r,12as)-3-[(1s)-1-bromo-2-hydroxyethyl]-5,12-dihydroxy-3,12a-dimethyl-2h,4h,4ah,5h,6h,6ah,8h,9h,10h,12h-cycloocta[a]naphthalene-7,11-dione

Description

Neopargueroldione belongs to the class of organic compounds known as cyclic alcohols and derivatives. These are organic compounds containing an aliphatic ring substituted with at least one hydroxyl group. (3r,4as,5s,6ar,12r,12as)-3-[(1s)-1-bromo-2-hydroxyethyl]-5,12-dihydroxy-3,12a-dimethyl-2h,4h,4ah,5h,6h,6ah,8h,9h,10h,12h-cycloocta[a]naphthalene-7,11-dione is found in Aplysia punctata. Based on a literature review very few articles have been published on Neopargueroldione.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309022204492D          

 26 28  0  0  1  0            999 V2000
    2.5381    1.0068    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0704    0.3272    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.8943    0.3699    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2693    1.1047    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0932    1.1473    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5421    0.4551    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    5.1458    1.0174    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2006   -0.0418    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    5.0996   -0.8606    0.0000 Br  0  0  0  0  0  0  0  0  0  0  0  0
    5.9603    0.2801    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.6188   -0.2169    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.1671   -0.2797    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3432   -0.3223    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.9681   -1.0572    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.4170   -1.7494    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1442   -1.0998    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6954   -0.4076    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.9106   -0.6620    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8453   -1.4845    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.1758   -0.2870    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0787    0.4978    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2964    1.2326    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0811    1.4870    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1464    2.3095    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.8160    1.1120    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.4437    1.6474    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  2  1  1  1  0  0  0
  2  3  1  0  0  0  0
  3  4  2  0  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  6  7  1  6  0  0  0
  6  8  1  1  0  0  0
  8  9  1  1  0  0  0
  8 10  1  0  0  0  0
 10 11  1  0  0  0  0
  6 12  1  0  0  0  0
 13 12  1  6  0  0  0
  3 13  1  0  0  0  0
 13 14  1  0  0  0  0
 14 15  1  1  0  0  0
 14 16  1  0  0  0  0
 17 16  1  1  0  0  0
  2 17  1  0  0  0  0
 17 18  1  0  0  0  0
 18 19  2  0  0  0  0
 18 20  1  0  0  0  0
 20 21  1  0  0  0  0
 21 22  1  0  0  0  0
 22 23  1  0  0  0  0
 23 24  2  0  0  0  0
 23 25  1  0  0  0  0
  2 25  1  0  0  0  0
 25 26  1  6  0  0  0
M  END

     RDKit          3D

 55 57  0  0  0  0  0  0  0  0999 V2000
   -1.0399   -1.4004    1.5013 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9553   -0.0229    0.8423 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.4259    0.1033    0.3502 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1440    1.1613    0.6486 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5440    1.3488    0.1846 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6934    0.6755   -1.1373 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.7936    1.3442   -2.1883 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0885    0.7595   -1.6959 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.2167   -0.1633   -3.3918 Br  0  0  0  0  0  0  0  0  0  0  0  0
    5.1534    0.2360   -0.7914 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4175    0.3597   -1.4003 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.3303   -0.7672   -0.9858 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9338   -1.0241   -0.4856 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.0133   -1.4633   -1.5442 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.0775   -2.8585   -1.7795 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4268   -1.1147   -1.3876 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7816   -0.0061   -0.4381 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.2302    0.0605   -0.2140 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7374    1.1068   -0.5848 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2368   -0.8528    0.3615 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6677   -0.5033    1.7563 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1569    0.8409    2.2209 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6888    0.7169    2.4247 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4987    0.1523    3.5143 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4318    1.0692    1.7122 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.6144    2.2105    0.9062 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2265   -1.5490    2.2287 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9927   -1.5629    2.0359 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0183   -2.1421    0.6729 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7089    1.9349    1.2531 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.1853    0.7759    0.9120 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8024    2.4247    0.1710 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8092    0.7756   -3.1345 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7616    1.2674   -1.7926 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0335    2.4020   -2.3028 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.3744    1.8314   -1.9200 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.1812    0.8253    0.1686 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.0747   -0.8140   -0.4994 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.0426   -0.1733   -0.8538 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.1048   -1.2368   -0.3257 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.4650   -1.2454   -1.9857 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0242   -1.8871    0.2420 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3526   -1.0243   -2.5163 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9633   -3.1993   -1.5104 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0532   -2.0024   -1.0748 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8881   -0.8174   -2.3780 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4610    0.9460   -0.9600 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8909   -1.9229    0.3336 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1788   -0.8784   -0.2623 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3591   -1.2886    2.4929 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7941   -0.4804    1.8590 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6767    1.0013    3.2210 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4452    1.6536    1.5358 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7321    1.3723    2.5176 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5058    3.0452    1.3863 H   0  0  0  0  0  0  0  0  0  0  0  0
  6  7  1  6
  6  5  1  0
  5  4  1  0
  4  3  2  0
  3 13  1  0
 13 12  1  0
 13 14  1  0
 14 15  1  0
 14 16  1  0
 16 17  1  0
 17 18  1  0
 18 19  2  0
 18 20  1  0
 20 21  1  0
 21 22  1  0
 22 23  1  0
 23 24  2  0
 23 25  1  0
 25 26  1  0
 25  2  1  0
  2  1  1  1
  6  8  1  0
  8  9  1  0
  8 10  1  0
 10 11  1  0
 12  6  1  0
  2 17  1  0
  2  3  1  0
  7 33  1  0
  7 34  1  0
  7 35  1  0
  5 31  1  0
  5 32  1  0
  4 30  1  0
 13 42  1  1
 12 40  1  0
 12 41  1  0
 14 43  1  6
 15 44  1  0
 16 45  1  0
 16 46  1  0
 17 47  1  6
 20 48  1  0
 20 49  1  0
 21 50  1  0
 21 51  1  0
 22 52  1  0
 22 53  1  0
 25 54  1  1
 26 55  1  0
  1 27  1  0
  1 28  1  0
  1 29  1  0
  8 36  1  6
 10 37  1  0
 10 38  1  0
 11 39  1  0
M  END


  Mrv1652309022204492D          

 26 28  0  0  1  0            999 V2000
    2.5381    1.0068    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0704    0.3272    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.8943    0.3699    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2693    1.1047    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0932    1.1473    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5421    0.4551    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    5.1458    1.0174    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2006   -0.0418    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    5.0996   -0.8606    0.0000 Br  0  0  0  0  0  0  0  0  0  0  0  0
    5.9603    0.2801    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.6188   -0.2169    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.1671   -0.2797    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3432   -0.3223    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.9681   -1.0572    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.4170   -1.7494    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1442   -1.0998    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6954   -0.4076    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.9106   -0.6620    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8453   -1.4845    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.1758   -0.2870    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0787    0.4978    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2964    1.2326    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0811    1.4870    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1464    2.3095    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.8160    1.1120    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.4437    1.6474    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  2  1  1  1  0  0  0
  2  3  1  0  0  0  0
  3  4  2  0  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  6  7  1  6  0  0  0
  6  8  1  1  0  0  0
  8  9  1  1  0  0  0
  8 10  1  0  0  0  0
 10 11  1  0  0  0  0
  6 12  1  0  0  0  0
 13 12  1  6  0  0  0
  3 13  1  0  0  0  0
 13 14  1  0  0  0  0
 14 15  1  1  0  0  0
 14 16  1  0  0  0  0
 17 16  1  1  0  0  0
  2 17  1  0  0  0  0
 17 18  1  0  0  0  0
 18 19  2  0  0  0  0
 18 20  1  0  0  0  0
 20 21  1  0  0  0  0
 21 22  1  0  0  0  0
 22 23  1  0  0  0  0
 23 24  2  0  0  0  0
 23 25  1  0  0  0  0
  2 25  1  0  0  0  0
 25 26  1  6  0  0  0
M  END
> <DATABASE_ID>
NP0147256

> <DATABASE_NAME>
NP-MRD

> <SMILES>
C[C@]1(CC=C2[C@H](C1)[C@@H](O)C[C@H]1C(=O)CCCC(=O)[C@H](O)[C@]21C)[C@H](Br)CO

> <INCHI_IDENTIFIER>
InChI=1S/C20H29BrO5/c1-19(17(21)10-22)7-6-12-11(9-19)16(25)8-13-14(23)4-3-5-15(24)18(26)20(12,13)2/h6,11,13,16-18,22,25-26H,3-5,7-10H2,1-2H3/t11-,13-,16-,17+,18-,19+,20+/m0/s1

> <INCHI_KEY>
BXBRFJCICVSQSF-YOWBZOQOSA-N

> <FORMULA>
C20H29BrO5

> <MOLECULAR_WEIGHT>
429.351

> <EXACT_MASS>
428.119837

> <JCHEM_ACCEPTOR_COUNT>
5

> <JCHEM_ATOM_COUNT>
55

> <JCHEM_AVERAGE_POLARIZABILITY>
41.36768764768385

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
3

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(3R,4aS,5S,6aR,12R,12aS)-3-[(1S)-1-bromo-2-hydroxyethyl]-5,12-dihydroxy-3,12a-dimethyl-2H,3H,4H,4aH,5H,6H,6aH,7H,8H,9H,10H,11H,12H,12aH-cycloocta[a]naphthalene-7,11-dione

> <ALOGPS_LOGP>
2.08

> <JCHEM_LOGP>
1.5395719086666664

> <ALOGPS_LOGS>
-3.14

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
14.357145919643752

> <JCHEM_PKA_STRONGEST_ACIDIC>
12.872302342343819

> <JCHEM_PKA_STRONGEST_BASIC>
-2.86101429276295

> <JCHEM_POLAR_SURFACE_AREA>
94.83

> <JCHEM_REFRACTIVITY>
102.16189999999997

> <JCHEM_ROTATABLE_BOND_COUNT>
2

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
3.11e-01 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(3R,4aS,5S,6aR,12R,12aS)-3-[(1S)-1-bromo-2-hydroxyethyl]-5,12-dihydroxy-3,12a-dimethyl-2H,4H,4aH,5H,6H,6aH,8H,9H,10H,12H-cycloocta[a]naphthalene-7,11-dione

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 02-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   02-SEP-22         0                                  
HETATM    1  C   UNK     0       4.738   1.879   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       3.865   0.611   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       5.403   0.690   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       6.103   2.062   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       7.641   2.142   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       8.479   0.850   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       9.606   1.899   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       9.708  -0.078   0.000  0.00  0.00           C+0
HETATM    9 Br   UNK     0       9.519  -1.606   0.000  0.00  0.00          Br+0
HETATM   10  C   UNK     0      11.126   0.523   0.000  0.00  0.00           C+0
HETATM   11  O   UNK     0      12.355  -0.405   0.000  0.00  0.00           O+0
HETATM   12  C   UNK     0       7.779  -0.522   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       6.241  -0.602   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       5.541  -1.973   0.000  0.00  0.00           C+0
HETATM   15  O   UNK     0       6.378  -3.265   0.000  0.00  0.00           O+0
HETATM   16  C   UNK     0       4.003  -2.053   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       3.165  -0.761   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       1.700  -1.236   0.000  0.00  0.00           C+0
HETATM   19  O   UNK     0       1.578  -2.771   0.000  0.00  0.00           O+0
HETATM   20  C   UNK     0       0.328  -0.536   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0      -0.147   0.929   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       0.553   2.301   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       2.018   2.776   0.000  0.00  0.00           C+0
HETATM   24  O   UNK     0       2.140   4.311   0.000  0.00  0.00           O+0
HETATM   25  C   UNK     0       3.390   2.076   0.000  0.00  0.00           C+0
HETATM   26  O   UNK     0       4.561   3.075   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3   17   25                                             
CONECT    3    2    4   13                                                  
CONECT    4    3    5                                                       
CONECT    5    4    6                                                       
CONECT    6    5    7    8   12                                             
CONECT    7    6                                                            
CONECT    8    6    9   10                                                  
CONECT    9    8                                                            
CONECT   10    8   11                                                       
CONECT   11   10                                                            
CONECT   12    6   13                                                       
CONECT   13   12    3   14                                                  
CONECT   14   13   15   16                                                  
CONECT   15   14                                                            
CONECT   16   14   17                                                       
CONECT   17   16    2   18                                                  
CONECT   18   17   19   20                                                  
CONECT   19   18                                                            
CONECT   20   18   21                                                       
CONECT   21   20   22                                                       
CONECT   22   21   23                                                       
CONECT   23   22   24   25                                                  
CONECT   24   23                                                            
CONECT   25   23    2   26                                                  
CONECT   26   25                                                            
MASTER        0    0    0    0    0    0    0    0   26    0   56    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₀H₂₉BrO₅

Average Mass

429.3510 Da

Monoisotopic Mass

428.11984 Da

IUPAC Name

(3R,4aS,5S,6aR,12R,12aS)-3-[(1S)-1-bromo-2-hydroxyethyl]-5,12-dihydroxy-3,12a-dimethyl-2H,3H,4H,4aH,5H,6H,6aH,7H,8H,9H,10H,11H,12H,12aH-cycloocta[a]naphthalene-7,11-dione

Traditional Name

(3R,4aS,5S,6aR,12R,12aS)-3-[(1S)-1-bromo-2-hydroxyethyl]-5,12-dihydroxy-3,12a-dimethyl-2H,4H,4aH,5H,6H,6aH,8H,9H,10H,12H-cycloocta[a]naphthalene-7,11-dione

CAS Registry Number

Not Available

SMILES

C[C@]1(CC=C2[C@H](C1)[C@@H](O)C[C@H]1C(=O)CCCC(=O)[C@H](O)[C@]21C)[C@H](Br)CO

InChI Identifier

InChI=1S/C20H29BrO5/c1-19(17(21)10-22)7-6-12-11(9-19)16(25)8-13-14(23)4-3-5-15(24)18(26)20(12,13)2/h6,11,13,16-18,22,25-26H,3-5,7-10H2,1-2H3/t11-,13-,16-,17+,18-,19+,20+/m0/s1

InChI Key

BXBRFJCICVSQSF-YOWBZOQOSA-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
Aplysia punctata	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as cyclic alcohols and derivatives. These are organic compounds containing an aliphatic ring substituted with at least one hydroxyl group.

Kingdom

Organic compounds

Super Class

Organic oxygen compounds

Class

Organooxygen compounds

Sub Class

Alcohols and polyols

Direct Parent

Cyclic alcohols and derivatives

Alternative Parents

Substituents

Cyclic alcohol
Cyclic ketone
Secondary alcohol
Ketone
Halohydrin
Bromohydrin
Organic oxide
Hydrocarbon derivative
Primary alcohol
Organobromide
Organohalogen compound
Carbonyl group
Alkyl halide
Alkyl bromide
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	2.08	ALOGPS
logP	1.54	ChemAxon
logS	-3.1	ALOGPS
pKa (Strongest Acidic)	12.87	ChemAxon
pKa (Strongest Basic)	-2.9	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	5	ChemAxon
Hydrogen Donor Count	3	ChemAxon
Polar Surface Area	94.83 Å²	ChemAxon
Rotatable Bond Count	2	ChemAxon
Refractivity	102.16 m³·mol⁻¹	ChemAxon
Polarizability	41.37 Å³	ChemAxon
Number of Rings	3	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

29213173

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

12967309

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for (3r,4as,5s,6ar,12r,12as)-3-[(1s)-1-bromo-2-hydroxyethyl]-5,12-dihydroxy-3,12a-dimethyl-2h,4h,4ah,5h,6h,6ah,8h,9h,10h,12h-cycloocta[a]naphthalene-7,11-dione (NP0147256)

MOL for NP0147256 ((3r,4as,5s,6ar,12r,12as)-3-[(1s)-1-bromo-2-hydroxyethyl]-5,12-dihydroxy-3,12a-dimethyl-2h,4h,4ah,5h,6h,6ah,8h,9h,10h,12h-cycloocta[a]naphthalene-7,11-dione)

3D MOL for NP0147256 ((3r,4as,5s,6ar,12r,12as)-3-[(1s)-1-bromo-2-hydroxyethyl]-5,12-dihydroxy-3,12a-dimethyl-2h,4h,4ah,5h,6h,6ah,8h,9h,10h,12h-cycloocta[a]naphthalene-7,11-dione)

3D SDF for NP0147256 ((3r,4as,5s,6ar,12r,12as)-3-[(1s)-1-bromo-2-hydroxyethyl]-5,12-dihydroxy-3,12a-dimethyl-2h,4h,4ah,5h,6h,6ah,8h,9h,10h,12h-cycloocta[a]naphthalene-7,11-dione)

3D-SDF for NP0147256 ((3r,4as,5s,6ar,12r,12as)-3-[(1s)-1-bromo-2-hydroxyethyl]-5,12-dihydroxy-3,12a-dimethyl-2h,4h,4ah,5h,6h,6ah,8h,9h,10h,12h-cycloocta[a]naphthalene-7,11-dione)

PDB for NP0147256 ((3r,4as,5s,6ar,12r,12as)-3-[(1s)-1-bromo-2-hydroxyethyl]-5,12-dihydroxy-3,12a-dimethyl-2h,4h,4ah,5h,6h,6ah,8h,9h,10h,12h-cycloocta[a]naphthalene-7,11-dione)

3D PDB for NP0147256 ((3r,4as,5s,6ar,12r,12as)-3-[(1s)-1-bromo-2-hydroxyethyl]-5,12-dihydroxy-3,12a-dimethyl-2h,4h,4ah,5h,6h,6ah,8h,9h,10h,12h-cycloocta[a]naphthalene-7,11-dione)

SMILES for NP0147256 ((3r,4as,5s,6ar,12r,12as)-3-[(1s)-1-bromo-2-hydroxyethyl]-5,12-dihydroxy-3,12a-dimethyl-2h,4h,4ah,5h,6h,6ah,8h,9h,10h,12h-cycloocta[a]naphthalene-7,11-dione)

INCHI for NP0147256 ((3r,4as,5s,6ar,12r,12as)-3-[(1s)-1-bromo-2-hydroxyethyl]-5,12-dihydroxy-3,12a-dimethyl-2h,4h,4ah,5h,6h,6ah,8h,9h,10h,12h-cycloocta[a]naphthalene-7,11-dione)

Structure for NP0147256 ((3r,4as,5s,6ar,12r,12as)-3-[(1s)-1-bromo-2-hydroxyethyl]-5,12-dihydroxy-3,12a-dimethyl-2h,4h,4ah,5h,6h,6ah,8h,9h,10h,12h-cycloocta[a]naphthalene-7,11-dione)

3D Structure for NP0147256 ((3r,4as,5s,6ar,12r,12as)-3-[(1s)-1-bromo-2-hydroxyethyl]-5,12-dihydroxy-3,12a-dimethyl-2h,4h,4ah,5h,6h,6ah,8h,9h,10h,12h-cycloocta[a]naphthalene-7,11-dione)