NP-MRD: Showing NP-Card for (1r,2r,6r,7r,8r,9r,10s,12s)-9,12-dihydroxy-6-isopropyl-3,9-dimethyl-13-methylidene-15-oxatricyclo[6.6.1.0²,⁷]pentadec-3-en-10-yl acetate (NP0251380)

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Record Information

Version

2.0

Created at

2022-09-07 14:33:45 UTC

Updated at

2022-09-07 14:33:45 UTC

NP-MRD ID

NP0251380

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(1r,2r,6r,7r,8r,9r,10s,12s)-9,12-dihydroxy-6-isopropyl-3,9-dimethyl-13-methylidene-15-oxatricyclo[6.6.1.0²,⁷]pentadec-3-en-10-yl acetate

Description

(4R,4aR,5R,6R,7S,9S,12R,12aR)-3,4,4aalpha,5,6,7,8,9,10,11,12,12aalpha-Dodecahydro-1,6-dimethyl-10-methylene-4alpha-isopropyl-5,12-epoxybenzocyclodecene-6,7,9-triol 7-acetate belongs to the class of organic compounds known as eunicellane and asbestinane diterpenoids. These are diterpenoids with a structure based on either the eunicellane (5,14-cyclocembrane) or the asbestinane skeleton. (1r,2r,6r,7r,8r,9r,10s,12s)-9,12-dihydroxy-6-isopropyl-3,9-dimethyl-13-methylidene-15-oxatricyclo[6.6.1.0²,⁷]pentadec-3-en-10-yl acetate is found in Sinularia flexibilis. Based on a literature review very few articles have been published on (4R,4aR,5R,6R,7S,9S,12R,12aR)-3,4,4aalpha,5,6,7,8,9,10,11,12,12aalpha-Dodecahydro-1,6-dimethyl-10-methylene-4alpha-isopropyl-5,12-epoxybenzocyclodecene-6,7,9-triol 7-acetate.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309072216332D          

 27 29  0  0  1  0            999 V2000
    6.1282    0.9937    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6433    0.3263    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8587    0.5812    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0740    0.3263    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.3440   -0.7537    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.0740   -1.8336    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.5891   -1.1662    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.8746   -1.5787    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.8746   -2.4037    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1602   -2.8162    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5891   -2.8162    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1602   -1.1662    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1602   -0.3412    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8746    0.0713    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8746    0.8963    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5891   -0.3412    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.8587   -2.0886    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.3737   -2.7560    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3436   -2.7560    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.6433   -1.8336    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    6.1282   -2.5011    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.7926   -3.2547    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.2776   -3.9222    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9722   -3.3410    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.1282   -1.1662    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1282   -0.3412    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    6.9128   -0.0862    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  6  0  0  0
  6  5  1  6  0  0  0
  7  6  1  6  0  0  0
  7  8  1  0  0  0  0
  8  9  1  1  0  0  0
  9 10  1  0  0  0  0
  9 11  1  0  0  0  0
  8 12  1  0  0  0  0
 12 13  1  0  0  0  0
 13 14  2  0  0  0  0
 14 15  1  0  0  0  0
 16 14  1  6  0  0  0
  4 16  1  0  0  0  0
  7 16  1  0  0  0  0
  6 17  1  0  0  0  0
 17 18  1  6  0  0  0
 17 19  1  1  0  0  0
 17 20  1  0  0  0  0
 20 21  1  6  0  0  0
 21 22  1  0  0  0  0
 22 23  1  0  0  0  0
 22 24  2  0  0  0  0
 20 25  1  0  0  0  0
 25 26  1  0  0  0  0
  2 26  1  0  0  0  0
 26 27  1  1  0  0  0
M  END

     RDKit          3D

 61 63  0  0  0  0  0  0  0  0999 V2000
   -2.1993   -3.5193   -1.4516 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9807   -2.7915   -0.3864 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6599   -2.8766    0.2921 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2886   -1.9499   -0.4268 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.4221   -0.9982   -1.0918 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2265    0.2300   -0.5275 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.1519    0.1822    0.1250 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.2400    0.6831   -0.7608 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.3460    1.3178    0.0736 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4139    1.9198   -0.8180 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7346    2.4298    0.8996 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8372   -0.4065   -1.6317 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3800   -1.4333   -0.6899 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6121   -1.8226    0.3129 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1252   -2.8369    1.2593 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2699   -1.2720    0.4978 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.2028    0.6843    0.4635 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.8978    2.1399    0.7749 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9510   -0.0029    1.6771 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6379    0.5830    0.1617 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.0951    1.7512   -0.5026 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0570    2.6020    0.0201 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5241    3.8104   -0.6762 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5345    2.2919    1.1546 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0980   -0.5862   -0.6466 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0714   -1.8942    0.1154 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.9661   -1.6888    1.4857 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4396   -4.1728   -1.8378 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1483   -3.4711   -1.9556 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2741   -3.9256    0.1299 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7075   -2.7210    1.3743 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8697   -2.5257   -1.2075 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1546    0.9862   -1.3599 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1624    0.7459    1.0797 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8584    1.4676   -1.4398 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7759    0.5148    0.6962 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.9123    2.7175   -0.2466 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.1593    1.1448   -1.0616 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.9398    2.3616   -1.7133 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.4418    2.0812    1.8940 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8679    2.8593    0.3763 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5104    3.2503    0.9817 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0981   -0.7972   -2.3287 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.6711    0.0611   -2.1846 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.3633   -1.8091   -0.8662 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.5220   -2.8482    2.2133 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0013   -3.8569    0.8336 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.1859   -2.6096    1.4888 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9362   -1.4555    1.5377 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4798    2.5928   -0.1462 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8186    2.7031    1.0291 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1185    2.2461    1.5686 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3149    0.5681    2.4001 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2066    0.5439    1.1281 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7077    4.1840   -1.3160 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7475    4.6110    0.0678 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4481    3.6139   -1.2704 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1982   -0.3888   -0.8448 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6578   -0.6556   -1.6526 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0144   -2.4811   -0.0357 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7151   -2.0816    2.0013 H   0  0  0  0  0  0  0  0  0  0  0  0
 10  9  1  0
  9 11  1  0
  9  8  1  0
  8 12  1  0
 12 13  1  0
 13 14  2  0
 14 15  1  0
 14 16  1  0
 16  4  1  0
  4  3  1  0
  3  2  1  0
  2  1  2  3
  2 26  1  0
 26 27  1  0
 26 25  1  0
 25 20  1  0
 20 21  1  0
 21 22  1  0
 22 23  1  0
 22 24  2  0
 20 17  1  0
 17 18  1  0
 17 19  1  1
 17  6  1  0
  6  5  1  0
  6  7  1  0
  7  8  1  0
  7 16  1  0
  5  4  1  0
 10 37  1  0
 10 38  1  0
 10 39  1  0
  9 36  1  0
 11 40  1  0
 11 41  1  0
 11 42  1  0
  8 35  1  6
 12 43  1  0
 12 44  1  0
 13 45  1  0
 15 46  1  0
 15 47  1  0
 15 48  1  0
 16 49  1  1
  4 32  1  6
  3 30  1  0
  3 31  1  0
  1 28  1  0
  1 29  1  0
 26 60  1  1
 27 61  1  0
 25 58  1  0
 25 59  1  0
 20 54  1  1
 23 55  1  0
 23 56  1  0
 23 57  1  0
 18 50  1  0
 18 51  1  0
 18 52  1  0
 19 53  1  0
  6 33  1  6
  7 34  1  1
M  END


  Mrv1652309072216332D          

 27 29  0  0  1  0            999 V2000
    6.1282    0.9937    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6433    0.3263    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8587    0.5812    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0740    0.3263    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.3440   -0.7537    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.0740   -1.8336    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.5891   -1.1662    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.8746   -1.5787    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.8746   -2.4037    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1602   -2.8162    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5891   -2.8162    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1602   -1.1662    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1602   -0.3412    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8746    0.0713    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8746    0.8963    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5891   -0.3412    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.8587   -2.0886    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.3737   -2.7560    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3436   -2.7560    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.6433   -1.8336    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    6.1282   -2.5011    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.7926   -3.2547    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.2776   -3.9222    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9722   -3.3410    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.1282   -1.1662    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1282   -0.3412    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    6.9128   -0.0862    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  6  0  0  0
  6  5  1  6  0  0  0
  7  6  1  6  0  0  0
  7  8  1  0  0  0  0
  8  9  1  1  0  0  0
  9 10  1  0  0  0  0
  9 11  1  0  0  0  0
  8 12  1  0  0  0  0
 12 13  1  0  0  0  0
 13 14  2  0  0  0  0
 14 15  1  0  0  0  0
 16 14  1  6  0  0  0
  4 16  1  0  0  0  0
  7 16  1  0  0  0  0
  6 17  1  0  0  0  0
 17 18  1  6  0  0  0
 17 19  1  1  0  0  0
 17 20  1  0  0  0  0
 20 21  1  6  0  0  0
 21 22  1  0  0  0  0
 22 23  1  0  0  0  0
 22 24  2  0  0  0  0
 20 25  1  0  0  0  0
 25 26  1  0  0  0  0
  2 26  1  0  0  0  0
 26 27  1  1  0  0  0
M  END
> <DATABASE_ID>
NP0251380

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC(C)[C@H]1CC=C(C)[C@@H]2[C@H]3CC(=C)[C@@H](O)C[C@H](OC(C)=O)[C@@](C)(O)[C@H](O3)[C@H]12

> <INCHI_IDENTIFIER>
InChI=1S/C22H34O5/c1-11(2)15-8-7-12(3)19-17-9-13(4)16(24)10-18(26-14(5)23)22(6,25)21(27-17)20(15)19/h7,11,15-21,24-25H,4,8-10H2,1-3,5-6H3/t15-,16+,17-,18+,19-,20-,21-,22-/m1/s1

> <INCHI_KEY>
ZDDYROFVYQUUSR-DIHPLBBDSA-N

> <FORMULA>
C22H34O5

> <MOLECULAR_WEIGHT>
378.509

> <EXACT_MASS>
378.240624195

> <JCHEM_ACCEPTOR_COUNT>
4

> <JCHEM_ATOM_COUNT>
61

> <JCHEM_AVERAGE_POLARIZABILITY>
41.58496977195899

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(1R,2R,6R,7R,8R,9R,10S,12S)-9,12-dihydroxy-3,9-dimethyl-13-methylidene-6-(propan-2-yl)-15-oxatricyclo[6.6.1.0^{2,7}]pentadec-3-en-10-yl acetate

> <JCHEM_LOGP>
2.097019798

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
14.559852493651853

> <JCHEM_PKA_STRONGEST_ACIDIC>
13.057638880436947

> <JCHEM_PKA_STRONGEST_BASIC>
-3.000547643778538

> <JCHEM_POLAR_SURFACE_AREA>
75.99

> <JCHEM_REFRACTIVITY>
103.5894

> <JCHEM_ROTATABLE_BOND_COUNT>
3

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
(1R,2R,6R,7R,8R,9R,10S,12S)-9,12-dihydroxy-6-isopropyl-3,9-dimethyl-13-methylidene-15-oxatricyclo[6.6.1.0^{2,7}]pentadec-3-en-10-yl acetate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 07-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   07-SEP-22         0                                  
HETATM    1  C   UNK     0      11.439   1.855   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      10.534   0.609   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       9.070   1.085   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       7.605   0.609   0.000  0.00  0.00           C+0
HETATM    5  O   UNK     0       8.109  -1.407   0.000  0.00  0.00           O+0
HETATM    6  C   UNK     0       7.605  -3.423   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       6.700  -2.177   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       5.366  -2.947   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       5.366  -4.487   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       4.032  -5.257   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       6.700  -5.257   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       4.032  -2.177   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       4.032  -0.637   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       5.366   0.133   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       5.366   1.673   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       6.700  -0.637   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       9.070  -3.899   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       8.164  -5.145   0.000  0.00  0.00           C+0
HETATM   19  O   UNK     0       9.975  -5.145   0.000  0.00  0.00           O+0
HETATM   20  C   UNK     0      10.534  -3.423   0.000  0.00  0.00           C+0
HETATM   21  O   UNK     0      11.439  -4.669   0.000  0.00  0.00           O+0
HETATM   22  C   UNK     0      10.813  -6.075   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0      11.718  -7.321   0.000  0.00  0.00           C+0
HETATM   24  O   UNK     0       9.281  -6.236   0.000  0.00  0.00           O+0
HETATM   25  C   UNK     0      11.439  -2.177   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0      11.439  -0.637   0.000  0.00  0.00           C+0
HETATM   27  O   UNK     0      12.904  -0.161   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3   26                                                  
CONECT    3    2    4                                                       
CONECT    4    3    5   16                                                  
CONECT    5    4    6                                                       
CONECT    6    5    7   17                                                  
CONECT    7    6    8   16                                                  
CONECT    8    7    9   12                                                  
CONECT    9    8   10   11                                                  
CONECT   10    9                                                            
CONECT   11    9                                                            
CONECT   12    8   13                                                       
CONECT   13   12   14                                                       
CONECT   14   13   15   16                                                  
CONECT   15   14                                                            
CONECT   16   14    4    7                                                  
CONECT   17    6   18   19   20                                             
CONECT   18   17                                                            
CONECT   19   17                                                            
CONECT   20   17   21   25                                                  
CONECT   21   20   22                                                       
CONECT   22   21   23   24                                                  
CONECT   23   22                                                            
CONECT   24   22                                                            
CONECT   25   20   26                                                       
CONECT   26   25    2   27                                                  
CONECT   27   26                                                            
MASTER        0    0    0    0    0    0    0    0   27    0   58    0
END

View in JSmol

Synonyms

Value	Source
(4R,4AR,5R,6R,7S,9S,12R,12ar)-3,4,4aalpha,5,6,7,8,9,10,11,12,12aalpha-dodecahydro-1,6-dimethyl-10-methylene-4a-isopropyl-5,12-epoxybenzocyclodecene-6,7,9-triol 7-acetate	Generator
(4R,4AR,5R,6R,7S,9S,12R,12ar)-3,4,4aalpha,5,6,7,8,9,10,11,12,12aalpha-dodecahydro-1,6-dimethyl-10-methylene-4a-isopropyl-5,12-epoxybenzocyclodecene-6,7,9-triol 7-acetic acid	Generator
(4R,4AR,5R,6R,7S,9S,12R,12ar)-3,4,4aalpha,5,6,7,8,9,10,11,12,12aalpha-dodecahydro-1,6-dimethyl-10-methylene-4alpha-isopropyl-5,12-epoxybenzocyclodecene-6,7,9-triol 7-acetic acid	Generator
(4R,4AR,5R,6R,7S,9S,12R,12ar)-3,4,4aalpha,5,6,7,8,9,10,11,12,12aalpha-dodecahydro-1,6-dimethyl-10-methylene-4α-isopropyl-5,12-epoxybenzocyclodecene-6,7,9-triol 7-acetate	Generator
(4R,4AR,5R,6R,7S,9S,12R,12ar)-3,4,4aalpha,5,6,7,8,9,10,11,12,12aalpha-dodecahydro-1,6-dimethyl-10-methylene-4α-isopropyl-5,12-epoxybenzocyclodecene-6,7,9-triol 7-acetic acid	Generator

Chemical Formula

C₂₂H₃₄O₅

Average Mass

378.5090 Da

Monoisotopic Mass

378.24062 Da

IUPAC Name

(1R,2R,6R,7R,8R,9R,10S,12S)-9,12-dihydroxy-3,9-dimethyl-13-methylidene-6-(propan-2-yl)-15-oxatricyclo[6.6.1.0^{2,7}]pentadec-3-en-10-yl acetate

Traditional Name

(1R,2R,6R,7R,8R,9R,10S,12S)-9,12-dihydroxy-6-isopropyl-3,9-dimethyl-13-methylidene-15-oxatricyclo[6.6.1.0^{2,7}]pentadec-3-en-10-yl acetate

CAS Registry Number

Not Available

SMILES

CC(C)[C@H]1CC=C(C)[C@@H]2[C@H]3CC(=C)[C@@H](O)C[C@H](OC(C)=O)[C@@](C)(O)[C@H](O3)[C@H]12

InChI Identifier

InChI=1S/C22H34O5/c1-11(2)15-8-7-12(3)19-17-9-13(4)16(24)10-18(26-14(5)23)22(6,25)21(27-17)20(15)19/h7,11,15-21,24-25H,4,8-10H2,1-3,5-6H3/t15-,16+,17-,18+,19-,20-,21-,22-/m1/s1

InChI Key

ZDDYROFVYQUUSR-DIHPLBBDSA-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
Sinularia flexibilis	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as eunicellane and asbestinane diterpenoids. These are diterpenoids with a structure based on either the eunicellane (5,14-cyclocembrane) or the asbestinane skeleton.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Prenol lipids

Sub Class

Diterpenoids

Direct Parent

Eunicellane and asbestinane diterpenoids

Alternative Parents

Substituents

Cladiellane diterpenoid
Eunicellane-type diterpenoid
Cyclitol or derivatives
Tertiary alcohol
Tetrahydrofuran
Carboxylic acid ester
Secondary alcohol
Carboxylic acid derivative
Dialkyl ether
Ether
Monocarboxylic acid or derivatives
Oxacycle
Organoheterocyclic compound
Organic oxygen compound
Hydrocarbon derivative
Carbonyl group
Organooxygen compound
Alcohol
Organic oxide
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	2.1	ChemAxon
pKa (Strongest Acidic)	13.06	ChemAxon
pKa (Strongest Basic)	-3	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	4	ChemAxon
Hydrogen Donor Count	2	ChemAxon
Polar Surface Area	75.99 Å²	ChemAxon
Rotatable Bond Count	3	ChemAxon
Refractivity	103.59 m³·mol⁻¹	ChemAxon
Polarizability	41.58 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

10472357

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

14061137

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for (1r,2r,6r,7r,8r,9r,10s,12s)-9,12-dihydroxy-6-isopropyl-3,9-dimethyl-13-methylidene-15-oxatricyclo[6.6.1.0²,⁷]pentadec-3-en-10-yl acetate (NP0251380)

MOL for NP0251380 ((1r,2r,6r,7r,8r,9r,10s,12s)-9,12-dihydroxy-6-isopropyl-3,9-dimethyl-13-methylidene-15-oxatricyclo[6.6.1.0²,⁷]pentadec-3-en-10-yl acetate)

3D MOL for NP0251380 ((1r,2r,6r,7r,8r,9r,10s,12s)-9,12-dihydroxy-6-isopropyl-3,9-dimethyl-13-methylidene-15-oxatricyclo[6.6.1.0²,⁷]pentadec-3-en-10-yl acetate)

3D SDF for NP0251380 ((1r,2r,6r,7r,8r,9r,10s,12s)-9,12-dihydroxy-6-isopropyl-3,9-dimethyl-13-methylidene-15-oxatricyclo[6.6.1.0²,⁷]pentadec-3-en-10-yl acetate)

3D-SDF for NP0251380 ((1r,2r,6r,7r,8r,9r,10s,12s)-9,12-dihydroxy-6-isopropyl-3,9-dimethyl-13-methylidene-15-oxatricyclo[6.6.1.0²,⁷]pentadec-3-en-10-yl acetate)

PDB for NP0251380 ((1r,2r,6r,7r,8r,9r,10s,12s)-9,12-dihydroxy-6-isopropyl-3,9-dimethyl-13-methylidene-15-oxatricyclo[6.6.1.0²,⁷]pentadec-3-en-10-yl acetate)

3D PDB for NP0251380 ((1r,2r,6r,7r,8r,9r,10s,12s)-9,12-dihydroxy-6-isopropyl-3,9-dimethyl-13-methylidene-15-oxatricyclo[6.6.1.0²,⁷]pentadec-3-en-10-yl acetate)

SMILES for NP0251380 ((1r,2r,6r,7r,8r,9r,10s,12s)-9,12-dihydroxy-6-isopropyl-3,9-dimethyl-13-methylidene-15-oxatricyclo[6.6.1.0²,⁷]pentadec-3-en-10-yl acetate)

INCHI for NP0251380 ((1r,2r,6r,7r,8r,9r,10s,12s)-9,12-dihydroxy-6-isopropyl-3,9-dimethyl-13-methylidene-15-oxatricyclo[6.6.1.0²,⁷]pentadec-3-en-10-yl acetate)

Structure for NP0251380 ((1r,2r,6r,7r,8r,9r,10s,12s)-9,12-dihydroxy-6-isopropyl-3,9-dimethyl-13-methylidene-15-oxatricyclo[6.6.1.0²,⁷]pentadec-3-en-10-yl acetate)

3D Structure for NP0251380 ((1r,2r,6r,7r,8r,9r,10s,12s)-9,12-dihydroxy-6-isopropyl-3,9-dimethyl-13-methylidene-15-oxatricyclo[6.6.1.0²,⁷]pentadec-3-en-10-yl acetate)