NP-MRD: Showing NP-Card for (4e,8s,9r,10e,14r)-8-[(1s)-1-hydroxyethyl]-15-isopropyl-1,4,11-trimethyl-6-oxatricyclo[12.3.0.0⁵,⁹]heptadeca-4,10,15-triene-7,17-dione (NP0236933)

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Record Information

Version

2.0

Created at

2022-09-06 19:57:09 UTC

Updated at

2022-09-06 19:57:09 UTC

NP-MRD ID

NP0236933

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(4e,8s,9r,10e,14r)-8-[(1s)-1-hydroxyethyl]-15-isopropyl-1,4,11-trimethyl-6-oxatricyclo[12.3.0.0⁵,⁹]heptadeca-4,10,15-triene-7,17-dione

Description

(8S,9R,10E,14R)-8-[(1S)-1-hydroxyethyl]-1,4,11-trimethyl-15-(propan-2-yl)-6-oxatricyclo[12.3.0.0⁵,⁹]Heptadeca-4,10,15-triene-7,17-dione belongs to the class of organic compounds known as tetrahydrofurans. These are heterocyclic compounds containing a saturated, aliphatic, five-membered ring where a carbon is replaced by an oxygen. Based on a literature review very few articles have been published on (8S,9R,10E,14R)-8-[(1S)-1-hydroxyethyl]-1,4,11-trimethyl-15-(propan-2-yl)-6-oxatricyclo[12.3.0.0⁵,⁹]Heptadeca-4,10,15-triene-7,17-dione.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309062221572D          

 28 30  0  0  1  0            999 V2000
    3.6820    0.4140    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1970   -0.2534    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4520   -1.0380    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2135   -1.5229    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.2135   -2.3479    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4990   -2.7604    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4990   -3.5854    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7845   -2.3479    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0701   -2.7604    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3556   -2.3479    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2693   -3.1684    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5710   -2.6029    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3160   -3.3875    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0860   -1.9354    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5710   -1.2680    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3160   -0.4834    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4909   -0.3119    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8681    0.1297    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3556   -1.5229    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.1171   -1.0380    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3720   -0.2534    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9981   -2.6029    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.4830   -1.9354    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.3080   -1.9354    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.9981   -1.2680    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    5.2530   -0.4834    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.7010    0.1297    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0600   -0.3119    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  2  0  0  0  0
  3  4  1  0  0  0  0
  4  5  1  6  0  0  0
  5  6  2  0  0  0  0
  6  7  1  0  0  0  0
  6  8  1  0  0  0  0
  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
 10 11  1  0  0  0  0
 10 12  1  0  0  0  0
 12 13  2  0  0  0  0
 12 14  1  0  0  0  0
 14 15  2  0  0  0  0
 15 16  1  0  0  0  0
 16 17  1  0  0  0  0
 16 18  1  0  0  0  0
 19 15  1  1  0  0  0
 10 19  1  0  0  0  0
 19 20  1  0  0  0  0
 20 21  1  0  0  0  0
  2 21  1  0  0  0  0
  5 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
  4 25  1  0  0  0  0
 25 26  1  1  0  0  0
 26 27  1  0  0  0  0
 26 28  1  6  0  0  0
M  END

     RDKit          3D

 62 64  0  0  0  0  0  0  0  0999 V2000
   -0.6848    1.8705   -2.1850 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1624    1.4318   -1.0235 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3079    0.8372   -1.2667 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2723    0.3384   -0.2602 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.5540   -1.0896   -0.3387 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9537   -2.0525    0.3514 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3433   -3.4938    0.1751 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8718   -1.7188    1.3232 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4147   -1.8468    0.5889 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6000   -1.1403    1.1402 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.4451   -0.6458    2.5463 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6994   -2.1270    1.1657 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6123   -3.2985    1.5842 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8787   -1.4944    0.6240 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5829   -0.3073    0.0642 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6237    0.5291   -0.5581 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3092    0.7761   -2.0391 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8376    1.8780    0.0766 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1199   -0.1130    0.1840 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.8126    1.2866    0.5043 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3710    1.7157    0.3256 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5826   -1.2541   -1.2839 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.0390   -0.0142   -1.7063 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6651    0.2560   -2.7549 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.6314    0.9404   -0.6529 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.5104    0.7755    0.5944 C   0  0  2  0  0  0  0  0  0  0  0  0
    5.9561    1.0392    0.2092 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3642   -0.4886    1.1125 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0176    0.9504   -2.7025 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5036    2.5323   -1.9053 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0521    2.4097   -2.9396 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6057    0.6813   -2.3078 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1051    0.7238    0.7625 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.1367   -3.7634    0.8811 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4699   -4.1539    0.1909 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7915   -3.5669   -0.8477 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8565   -2.5132    2.1271 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1081   -0.7386    1.7303 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2345   -1.4772   -0.4645 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5765   -2.9560    0.4315 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5216   -1.5104    3.2719 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5220   -0.1337    2.7849 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2914    0.0167    2.8198 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9111   -1.9002    0.6463 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6236    0.0262   -0.5859 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7255   -0.0305   -2.4806 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2400    0.8917   -2.6323 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7636    1.7510   -2.1356 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5385    2.7347   -0.6011 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3995    1.9874    1.0751 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9632    2.0672    0.1627 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6437   -0.3450   -0.8040 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1355    1.5948    1.5421 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3792    1.9405   -0.1844 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4055    2.8497    0.3821 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2691    1.4314    1.1560 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5518    1.9738   -0.9775 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.2416    1.5569    1.3340 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.1554    0.6160   -0.8097 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.6149    0.5303    0.9690 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.0979    2.1263    0.1888 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.2215   -0.8931    1.4221 H   0  0  0  0  0  0  0  0  0  0  0  0
 17 16  1  0
 16 18  1  0
 16 15  1  0
 15 14  2  0
 14 12  1  0
 12 13  2  0
 12 10  1  0
 10 11  1  1
 10  9  1  0
  9  8  1  0
  8  6  1  0
  6  7  1  0
  6  5  2  0
  5 22  1  0
 22 23  1  0
 23 24  2  0
 23 25  1  0
 25 26  1  0
 26 27  1  0
 26 28  1  0
 25  4  1  0
  4  3  1  0
  3  2  2  0
  2  1  1  0
  2 21  1  0
 21 20  1  0
 20 19  1  0
 19 15  1  0
 19 10  1  0
  4  5  1  0
 17 46  1  0
 17 47  1  0
 17 48  1  0
 16 45  1  0
 18 49  1  0
 18 50  1  0
 18 51  1  0
 14 44  1  0
 11 41  1  0
 11 42  1  0
 11 43  1  0
  9 39  1  0
  9 40  1  0
  8 37  1  0
  8 38  1  0
  7 34  1  0
  7 35  1  0
  7 36  1  0
 25 57  1  6
 26 58  1  1
 27 59  1  0
 27 60  1  0
 27 61  1  0
 28 62  1  0
  4 33  1  1
  3 32  1  0
  1 29  1  0
  1 30  1  0
  1 31  1  0
 21 55  1  0
 21 56  1  0
 20 53  1  0
 20 54  1  0
 19 52  1  6
M  END


  Mrv1652309062221572D          

 28 30  0  0  1  0            999 V2000
    3.6820    0.4140    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1970   -0.2534    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4520   -1.0380    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2135   -1.5229    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.2135   -2.3479    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4990   -2.7604    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4990   -3.5854    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7845   -2.3479    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0701   -2.7604    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3556   -2.3479    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2693   -3.1684    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5710   -2.6029    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3160   -3.3875    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0860   -1.9354    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5710   -1.2680    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3160   -0.4834    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4909   -0.3119    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8681    0.1297    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3556   -1.5229    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.1171   -1.0380    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3720   -0.2534    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9981   -2.6029    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.4830   -1.9354    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.3080   -1.9354    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.9981   -1.2680    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    5.2530   -0.4834    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.7010    0.1297    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0600   -0.3119    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  2  0  0  0  0
  3  4  1  0  0  0  0
  4  5  1  6  0  0  0
  5  6  2  0  0  0  0
  6  7  1  0  0  0  0
  6  8  1  0  0  0  0
  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
 10 11  1  0  0  0  0
 10 12  1  0  0  0  0
 12 13  2  0  0  0  0
 12 14  1  0  0  0  0
 14 15  2  0  0  0  0
 15 16  1  0  0  0  0
 16 17  1  0  0  0  0
 16 18  1  0  0  0  0
 19 15  1  1  0  0  0
 10 19  1  0  0  0  0
 19 20  1  0  0  0  0
 20 21  1  0  0  0  0
  2 21  1  0  0  0  0
  5 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
  4 25  1  0  0  0  0
 25 26  1  1  0  0  0
 26 27  1  0  0  0  0
 26 28  1  6  0  0  0
M  END
> <DATABASE_ID>
NP0236933

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC(C)C1=CC(=O)C2(C)CC\C(C)=C3\OC(=O)[C@H]([C@H](C)O)[C@H]3\C=C(C)\CC[C@H]12

> <INCHI_IDENTIFIER>
InChI=1S/C24H34O4/c1-13(2)17-12-20(26)24(6)10-9-15(4)22-18(11-14(3)7-8-19(17)24)21(16(5)25)23(27)28-22/h11-13,16,18-19,21,25H,7-10H2,1-6H3/b14-11+,22-15+/t16-,18+,19+,21+,24?/m0/s1

> <INCHI_KEY>
CCMBGMOYVQDEBC-UIXNXTPYSA-N

> <FORMULA>
C24H34O4

> <MOLECULAR_WEIGHT>
386.532

> <EXACT_MASS>
386.245709575

> <JCHEM_ACCEPTOR_COUNT>
3

> <JCHEM_ATOM_COUNT>
62

> <JCHEM_AVERAGE_POLARIZABILITY>
44.011240426722765

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(8S,9R,10E,14R)-8-[(1S)-1-hydroxyethyl]-1,4,11-trimethyl-15-(propan-2-yl)-6-oxatricyclo[12.3.0.0^{5,9}]heptadeca-4,10,15-triene-7,17-dione

> <JCHEM_LOGP>
4.2890593053333355

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
18.375756206680787

> <JCHEM_PKA_STRONGEST_ACIDIC>
14.983470458555328

> <JCHEM_PKA_STRONGEST_BASIC>
-2.805952994653752

> <JCHEM_POLAR_SURFACE_AREA>
63.60000000000001

> <JCHEM_REFRACTIVITY>
113.05749999999999

> <JCHEM_ROTATABLE_BOND_COUNT>
2

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
(8S,9R,10E,14R)-8-[(1S)-1-hydroxyethyl]-15-isopropyl-1,4,11-trimethyl-6-oxatricyclo[12.3.0.0^{5,9}]heptadeca-4,10,15-triene-7,17-dione

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 06-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   06-SEP-22         0                                  
HETATM    1  C   UNK     0       6.873   0.773   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       5.968  -0.473   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       6.444  -1.938   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       7.865  -2.843   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       7.865  -4.383   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       6.531  -5.153   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       6.531  -6.693   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       5.198  -4.383   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       3.864  -5.153   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       2.530  -4.383   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       2.369  -5.914   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       1.066  -4.859   0.000  0.00  0.00           C+0
HETATM   13  O   UNK     0       0.590  -6.323   0.000  0.00  0.00           O+0
HETATM   14  C   UNK     0       0.161  -3.613   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       1.066  -2.367   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       0.590  -0.902   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      -0.916  -0.582   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       1.620   0.242   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       2.530  -2.843   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       3.952  -1.938   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       4.428  -0.473   0.000  0.00  0.00           C+0
HETATM   22  O   UNK     0       9.330  -4.859   0.000  0.00  0.00           O+0
HETATM   23  C   UNK     0      10.235  -3.613   0.000  0.00  0.00           C+0
HETATM   24  O   UNK     0      11.775  -3.613   0.000  0.00  0.00           O+0
HETATM   25  C   UNK     0       9.330  -2.367   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       9.806  -0.902   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0       8.775   0.242   0.000  0.00  0.00           C+0
HETATM   28  O   UNK     0      11.312  -0.582   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3   21                                                  
CONECT    3    2    4                                                       
CONECT    4    3    5   25                                                  
CONECT    5    4    6   22                                                  
CONECT    6    5    7    8                                                  
CONECT    7    6                                                            
CONECT    8    6    9                                                       
CONECT    9    8   10                                                       
CONECT   10    9   11   12   19                                             
CONECT   11   10                                                            
CONECT   12   10   13   14                                                  
CONECT   13   12                                                            
CONECT   14   12   15                                                       
CONECT   15   14   16   19                                                  
CONECT   16   15   17   18                                                  
CONECT   17   16                                                            
CONECT   18   16                                                            
CONECT   19   15   10   20                                                  
CONECT   20   19   21                                                       
CONECT   21   20    2                                                       
CONECT   22    5   23                                                       
CONECT   23   22   24   25                                                  
CONECT   24   23                                                            
CONECT   25   23    4   26                                                  
CONECT   26   25   27   28                                                  
CONECT   27   26                                                            
CONECT   28   26                                                            
MASTER        0    0    0    0    0    0    0    0   28    0   60    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₄H₃₄O₄

Average Mass

386.5320 Da

Monoisotopic Mass

386.24571 Da

IUPAC Name

Not Available

Traditional Name

Not Available

CAS Registry Number

Not Available

SMILES

CC(C)C1=CC(=O)C2(C)CC\C(C)=C3\OC(=O)[C@H]([C@H](C)O)[C@H]3\C=C(C)\CC[C@H]12

InChI Identifier

InChI=1S/C24H34O4/c1-13(2)17-12-20(26)24(6)10-9-15(4)22-18(11-14(3)7-8-19(17)24)21(16(5)25)23(27)28-22/h11-13,16,18-19,21,25H,7-10H2,1-6H3/b14-11+,22-15+/t16-,18+,19+,21+,24?/m0/s1

InChI Key

CCMBGMOYVQDEBC-UIXNXTPYSA-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

Not Available

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as tetrahydrofurans. These are heterocyclic compounds containing a saturated, aliphatic, five-membered ring where a carbon is replaced by an oxygen.

Kingdom

Organic compounds

Super Class

Organoheterocyclic compounds

Class

Tetrahydrofurans

Sub Class

Not Available

Direct Parent

Tetrahydrofurans

Alternative Parents

Substituents

Tetrahydrofuran
Enol ester
Secondary alcohol
Lactone
Ketone
Carboxylic acid ester
Oxacycle
Monocarboxylic acid or derivatives
Carboxylic acid derivative
Organic oxygen compound
Organic oxide
Hydrocarbon derivative
Organooxygen compound
Carbonyl group
Alcohol
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

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

Not Available

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

163187608

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for (4e,8s,9r,10e,14r)-8-[(1s)-1-hydroxyethyl]-15-isopropyl-1,4,11-trimethyl-6-oxatricyclo[12.3.0.0⁵,⁹]heptadeca-4,10,15-triene-7,17-dione (NP0236933)

MOL for NP0236933 ((4e,8s,9r,10e,14r)-8-[(1s)-1-hydroxyethyl]-15-isopropyl-1,4,11-trimethyl-6-oxatricyclo[12.3.0.0⁵,⁹]heptadeca-4,10,15-triene-7,17-dione)

3D MOL for NP0236933 ((4e,8s,9r,10e,14r)-8-[(1s)-1-hydroxyethyl]-15-isopropyl-1,4,11-trimethyl-6-oxatricyclo[12.3.0.0⁵,⁹]heptadeca-4,10,15-triene-7,17-dione)

3D SDF for NP0236933 ((4e,8s,9r,10e,14r)-8-[(1s)-1-hydroxyethyl]-15-isopropyl-1,4,11-trimethyl-6-oxatricyclo[12.3.0.0⁵,⁹]heptadeca-4,10,15-triene-7,17-dione)

3D-SDF for NP0236933 ((4e,8s,9r,10e,14r)-8-[(1s)-1-hydroxyethyl]-15-isopropyl-1,4,11-trimethyl-6-oxatricyclo[12.3.0.0⁵,⁹]heptadeca-4,10,15-triene-7,17-dione)

PDB for NP0236933 ((4e,8s,9r,10e,14r)-8-[(1s)-1-hydroxyethyl]-15-isopropyl-1,4,11-trimethyl-6-oxatricyclo[12.3.0.0⁵,⁹]heptadeca-4,10,15-triene-7,17-dione)

3D PDB for NP0236933 ((4e,8s,9r,10e,14r)-8-[(1s)-1-hydroxyethyl]-15-isopropyl-1,4,11-trimethyl-6-oxatricyclo[12.3.0.0⁵,⁹]heptadeca-4,10,15-triene-7,17-dione)

SMILES for NP0236933 ((4e,8s,9r,10e,14r)-8-[(1s)-1-hydroxyethyl]-15-isopropyl-1,4,11-trimethyl-6-oxatricyclo[12.3.0.0⁵,⁹]heptadeca-4,10,15-triene-7,17-dione)

INCHI for NP0236933 ((4e,8s,9r,10e,14r)-8-[(1s)-1-hydroxyethyl]-15-isopropyl-1,4,11-trimethyl-6-oxatricyclo[12.3.0.0⁵,⁹]heptadeca-4,10,15-triene-7,17-dione)

Structure for NP0236933 ((4e,8s,9r,10e,14r)-8-[(1s)-1-hydroxyethyl]-15-isopropyl-1,4,11-trimethyl-6-oxatricyclo[12.3.0.0⁵,⁹]heptadeca-4,10,15-triene-7,17-dione)

3D Structure for NP0236933 ((4e,8s,9r,10e,14r)-8-[(1s)-1-hydroxyethyl]-15-isopropyl-1,4,11-trimethyl-6-oxatricyclo[12.3.0.0⁵,⁹]heptadeca-4,10,15-triene-7,17-dione)