NP-MRD: Showing NP-Card for (1s,8s,9s,12r)-8-(acetyloxy)-12-formyl-5-isopropyl-1,11,11-trimethyl-10-oxotricyclo[7.3.1.0²,⁷]trideca-2(7),3,5-trien-4-yl acetate (NP0294686)

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Record Information

Version

2.0

Created at

2022-09-10 03:20:52 UTC

Updated at

2022-09-10 03:20:52 UTC

NP-MRD ID

NP0294686

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(1s,8s,9s,12r)-8-(acetyloxy)-12-formyl-5-isopropyl-1,11,11-trimethyl-10-oxotricyclo[7.3.1.0²,⁷]trideca-2(7),3,5-trien-4-yl acetate

Description

(1S,8S,9S,12R)-8-(acetyloxy)-12-formyl-1,11,11-trimethyl-10-oxo-5-(propan-2-yl)tricyclo[7.3.1.0²,⁷]Trideca-2,4,6-trien-4-yl acetate belongs to the class of organic compounds known as tetralins. These are polycyclic aromatic compounds containing a tetralin moiety, which consists of a benzene fused to a cyclohexane. (1s,8s,9s,12r)-8-(acetyloxy)-12-formyl-5-isopropyl-1,11,11-trimethyl-10-oxotricyclo[7.3.1.0²,⁷]trideca-2(7),3,5-trien-4-yl acetate is found in Chamaecyparis obtusa. Based on a literature review very few articles have been published on (1S,8S,9S,12R)-8-(acetyloxy)-12-formyl-1,11,11-trimethyl-10-oxo-5-(propan-2-yl)tricyclo[7.3.1.0²,⁷]Trideca-2,4,6-trien-4-yl acetate.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309102205202D          

 30 32  0  0  1  0            999 V2000
    3.7843   -1.3367    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5265   -0.9765    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2095   -1.4392    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.5856   -0.1536    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.9026    0.3090    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1604   -0.0512    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4773    0.4115    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5365    1.2344    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2787    1.5946    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9618    1.1319    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7040    1.4921    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3870    1.0294    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7631    2.3150    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9965    1.8581    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.3660    2.5957    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.1896    2.6444    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6436    1.9556    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5591    3.3820    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.1736    1.9172    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.7693    0.9794    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8536   -0.1285    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.1139   -0.9114    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0308   -0.0694    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.6612   -0.8070    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1624   -0.8557    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.4907    0.5543    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0281   -0.1287    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2888    0.8245    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5499    1.3772    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1877    1.7468    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
  2  4  1  0  0  0  0
  4  5  1  0  0  0  0
  5  6  2  0  0  0  0
  6  7  1  0  0  0  0
  7  8  2  0  0  0  0
  8  9  1  0  0  0  0
  9 10  2  0  0  0  0
  5 10  1  0  0  0  0
 10 11  1  0  0  0  0
 11 12  1  0  0  0  0
 11 13  1  0  0  0  0
  8 14  1  0  0  0  0
 14 15  1  6  0  0  0
 15 16  1  0  0  0  0
 16 17  1  0  0  0  0
 16 18  2  0  0  0  0
 14 19  1  0  0  0  0
 19 20  1  1  0  0  0
 20 21  1  0  0  0  0
  7 21  1  0  0  0  0
 21 22  1  1  0  0  0
 21 23  1  0  0  0  0
 23 24  1  1  0  0  0
 24 25  2  0  0  0  0
 23 26  1  0  0  0  0
 26 27  1  0  0  0  0
 26 28  1  0  0  0  0
 26 29  1  0  0  0  0
 19 29  1  0  0  0  0
 29 30  2  0  0  0  0
M  END

     RDKit          3D

 60 62  0  0  0  0  0  0  0  0999 V2000
   -4.0771   -4.0265    1.0861 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1695   -2.9116    0.7976 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3887   -2.5376    1.7514 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0398   -2.2079   -0.3749 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0959   -1.1651   -0.4963 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7642   -1.5469   -0.7446 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2209   -0.5649   -0.8802 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1765    0.7250   -0.7500 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5139    1.0948   -0.5037 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4955    0.1369   -0.3770 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9065    0.4568   -0.0839 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2441    1.7390   -0.9014 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0910    0.9965    1.3644 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7505    1.9057   -0.7194 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.5994    2.5288    0.5565 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.1518    3.8111    0.6912 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0022    4.4569    2.0360 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1522    4.5172   -0.3024 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1614    1.3824   -0.8435 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.1761    0.3300   -1.9086 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6065   -0.9557   -1.2868 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.5313   -1.9478   -2.4514 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4906   -1.4980   -0.2337 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.5121   -2.4048   -0.8653 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1732   -2.0673   -1.8323 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.1835   -0.4506    0.6055 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6296   -0.2283    0.2319 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1884   -0.9923    2.0419 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4660    0.8172    0.5162 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1361    1.3752    1.5521 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1328   -4.7464    0.2341 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0785   -3.6622    1.4115 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6628   -4.5810    1.9955 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4933   -2.5790   -0.8221 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7721    2.1242   -0.3941 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5767   -0.3338   -0.3371 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4296    2.4458   -0.9693 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5922    1.4419   -1.9319 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1169    2.2647   -0.4597 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9403    0.2106    2.0778 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1441    1.4219    1.3426 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4218    1.8875    1.4340 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4947    2.5601   -1.5387 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9802    4.4240    2.5378 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3027    5.4985    1.9319 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7911    3.9367    2.6503 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8722    2.2298   -1.0878 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.1529    0.1609   -2.3949 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4268    0.6002   -2.7185 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4542   -2.2255   -2.5609 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0945   -2.8570   -2.2826 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8264   -1.4851   -3.4229 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8523   -2.1751    0.4098 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7019   -3.4141   -0.4766 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.1221    0.2085    1.1562 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.1856   -1.1560    0.0271 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.7436    0.5416   -0.5533 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.6323   -2.0212    1.9684 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1770   -1.0862    2.4579 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.8780   -0.4024    2.6402 H   0  0  0  0  0  0  0  0  0  0  0  0
 12 11  1  0
 11 13  1  0
 11 10  1  0
 10  9  2  0
  9  8  1  0
  8  7  2  0
  7  6  1  0
  6  5  2  0
  5  4  1  0
  4  2  1  0
  2  1  1  0
  2  3  2  0
  7 21  1  0
 21 22  1  6
 21 20  1  0
 20 19  1  0
 19 14  1  0
 14 15  1  0
 15 16  1  0
 16 17  1  0
 16 18  2  0
 19 29  1  0
 29 30  2  0
 29 26  1  0
 26 27  1  0
 26 28  1  0
 26 23  1  0
 23 24  1  0
 24 25  2  0
  5 10  1  0
 23 21  1  0
 14  8  1  0
 12 37  1  0
 12 38  1  0
 12 39  1  0
 11 36  1  0
 13 40  1  0
 13 41  1  0
 13 42  1  0
  9 35  1  0
  6 34  1  0
  1 31  1  0
  1 32  1  0
  1 33  1  0
 22 50  1  0
 22 51  1  0
 22 52  1  0
 20 48  1  0
 20 49  1  0
 19 47  1  6
 14 43  1  6
 17 44  1  0
 17 45  1  0
 17 46  1  0
 27 55  1  0
 27 56  1  0
 27 57  1  0
 28 58  1  0
 28 59  1  0
 28 60  1  0
 23 53  1  1
 24 54  1  0
M  END


  Mrv1652309102205202D          

 30 32  0  0  1  0            999 V2000
    3.7843   -1.3367    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5265   -0.9765    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2095   -1.4392    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.5856   -0.1536    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.9026    0.3090    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1604   -0.0512    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4773    0.4115    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5365    1.2344    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2787    1.5946    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9618    1.1319    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7040    1.4921    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3870    1.0294    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7631    2.3150    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9965    1.8581    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.3660    2.5957    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.1896    2.6444    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6436    1.9556    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5591    3.3820    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.1736    1.9172    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.7693    0.9794    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8536   -0.1285    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.1139   -0.9114    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0308   -0.0694    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.6612   -0.8070    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1624   -0.8557    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.4907    0.5543    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0281   -0.1287    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2888    0.8245    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5499    1.3772    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1877    1.7468    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
  2  4  1  0  0  0  0
  4  5  1  0  0  0  0
  5  6  2  0  0  0  0
  6  7  1  0  0  0  0
  7  8  2  0  0  0  0
  8  9  1  0  0  0  0
  9 10  2  0  0  0  0
  5 10  1  0  0  0  0
 10 11  1  0  0  0  0
 11 12  1  0  0  0  0
 11 13  1  0  0  0  0
  8 14  1  0  0  0  0
 14 15  1  6  0  0  0
 15 16  1  0  0  0  0
 16 17  1  0  0  0  0
 16 18  2  0  0  0  0
 14 19  1  0  0  0  0
 19 20  1  1  0  0  0
 20 21  1  0  0  0  0
  7 21  1  0  0  0  0
 21 22  1  1  0  0  0
 21 23  1  0  0  0  0
 23 24  1  1  0  0  0
 24 25  2  0  0  0  0
 23 26  1  0  0  0  0
 26 27  1  0  0  0  0
 26 28  1  0  0  0  0
 26 29  1  0  0  0  0
 19 29  1  0  0  0  0
 29 30  2  0  0  0  0
M  END
> <DATABASE_ID>
NP0294686

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC(C)C1=CC2=C(C=C1OC(C)=O)[C@@]1(C)C[C@@H]([C@@H]2OC(C)=O)C(=O)C(C)(C)[C@@H]1C=O

> <INCHI_IDENTIFIER>
InChI=1S/C24H30O6/c1-12(2)15-8-16-18(9-19(15)29-13(3)26)24(7)10-17(21(16)30-14(4)27)22(28)23(5,6)20(24)11-25/h8-9,11-12,17,20-21H,10H2,1-7H3/t17-,20-,21+,24+/m0/s1

> <INCHI_KEY>
WPFFFCFKBSDSFI-CTLLREPQSA-N

> <FORMULA>
C24H30O6

> <MOLECULAR_WEIGHT>
414.498

> <EXACT_MASS>
414.204238686

> <JCHEM_ACCEPTOR_COUNT>
4

> <JCHEM_ATOM_COUNT>
60

> <JCHEM_AVERAGE_POLARIZABILITY>
44.66573842369968

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
0

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(1S,8S,9S,12R)-8-(acetyloxy)-12-formyl-1,11,11-trimethyl-10-oxo-5-(propan-2-yl)tricyclo[7.3.1.0^{2,7}]trideca-2(7),3,5-trien-4-yl acetate

> <JCHEM_LOGP>
3.7387983233333335

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
18.25730243760785

> <JCHEM_PKA_STRONGEST_ACIDIC>
16.661956810605318

> <JCHEM_PKA_STRONGEST_BASIC>
-6.552439883367362

> <JCHEM_POLAR_SURFACE_AREA>
86.74000000000001

> <JCHEM_REFRACTIVITY>
110.80479999999999

> <JCHEM_ROTATABLE_BOND_COUNT>
6

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
(1S,8S,9S,12R)-8-(acetyloxy)-12-formyl-5-isopropyl-1,11,11-trimethyl-10-oxotricyclo[7.3.1.0^{2,7}]trideca-2(7),3,5-trien-4-yl acetate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 10-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   10-SEP-22         0                                  
HETATM    1  C   UNK     0       7.064  -2.495   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       8.449  -1.823   0.000  0.00  0.00           C+0
HETATM    3  O   UNK     0       9.724  -2.686   0.000  0.00  0.00           O+0
HETATM    4  O   UNK     0       8.560  -0.287   0.000  0.00  0.00           O+0
HETATM    5  C   UNK     0       7.285   0.577   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       5.899  -0.096   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       4.624   0.768   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       4.735   2.304   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       6.120   2.977   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       7.395   2.113   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       8.781   2.785   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      10.056   1.922   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       8.891   4.321   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       3.727   3.468   0.000  0.00  0.00           C+0
HETATM   15  O   UNK     0       4.417   4.845   0.000  0.00  0.00           O+0
HETATM   16  C   UNK     0       5.954   4.936   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       6.801   3.650   0.000  0.00  0.00           C+0
HETATM   18  O   UNK     0       6.644   6.313   0.000  0.00  0.00           O+0
HETATM   19  C   UNK     0       2.191   3.579   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       3.303   1.828   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       3.460  -0.240   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       3.946  -1.701   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       1.924  -0.129   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       1.234  -1.506   0.000  0.00  0.00           C+0
HETATM   25  O   UNK     0      -0.303  -1.597   0.000  0.00  0.00           O+0
HETATM   26  C   UNK     0       0.916   1.035   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0       0.052  -0.240   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0      -0.539   1.539   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0       1.026   2.571   0.000  0.00  0.00           C+0
HETATM   30  O   UNK     0      -0.350   3.261   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3    4                                                  
CONECT    3    2                                                            
CONECT    4    2    5                                                       
CONECT    5    4    6   10                                                  
CONECT    6    5    7                                                       
CONECT    7    6    8   21                                                  
CONECT    8    7    9   14                                                  
CONECT    9    8   10                                                       
CONECT   10    9    5   11                                                  
CONECT   11   10   12   13                                                  
CONECT   12   11                                                            
CONECT   13   11                                                            
CONECT   14    8   15   19                                                  
CONECT   15   14   16                                                       
CONECT   16   15   17   18                                                  
CONECT   17   16                                                            
CONECT   18   16                                                            
CONECT   19   14   20   29                                                  
CONECT   20   19   21                                                       
CONECT   21   20    7   22   23                                             
CONECT   22   21                                                            
CONECT   23   21   24   26                                                  
CONECT   24   23   25                                                       
CONECT   25   24                                                            
CONECT   26   23   27   28   29                                             
CONECT   27   26                                                            
CONECT   28   26                                                            
CONECT   29   26   19   30                                                  
CONECT   30   29                                                            
MASTER        0    0    0    0    0    0    0    0   30    0   64    0
END

View in JSmol

Synonyms

Value	Source
(1S,8S,9S,12R)-8-(Acetyloxy)-12-formyl-1,11,11-trimethyl-10-oxo-5-(propan-2-yl)tricyclo[7.3.1.0,]trideca-2,4,6-trien-4-yl acetic acid	Generator

Chemical Formula

C₂₄H₃₀O₆

Average Mass

414.4980 Da

Monoisotopic Mass

414.20424 Da

IUPAC Name

Not Available

Traditional Name

Not Available

CAS Registry Number

Not Available

SMILES

CC(C)C1=CC2=C(C=C1OC(C)=O)[C@@]1(C)C[C@@H]([C@@H]2OC(C)=O)C(=O)C(C)(C)[C@@H]1C=O

InChI Identifier

InChI=1S/C24H30O6/c1-12(2)15-8-16-18(9-19(15)29-13(3)26)24(7)10-17(21(16)30-14(4)27)22(28)23(5,6)20(24)11-25/h8-9,11-12,17,20-21H,10H2,1-7H3/t17-,20-,21+,24+/m0/s1

InChI Key

WPFFFCFKBSDSFI-CTLLREPQSA-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
Chamaecyparis obtusa	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as tetralins. These are polycyclic aromatic compounds containing a tetralin moiety, which consists of a benzene fused to a cyclohexane.

Kingdom

Organic compounds

Super Class

Benzenoids

Class

Tetralins

Sub Class

Not Available

Direct Parent

Tetralins

Alternative Parents

Substituents

Tetralin
Dicarboxylic acid or derivatives
Ketone
Carboxylic acid ester
Carboxylic acid derivative
Organic oxygen compound
Organic oxide
Hydrocarbon derivative
Organooxygen compound
Carbonyl group
Aldehyde
Aromatic homopolycyclic compound

Molecular Framework

Aromatic 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

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

162931572

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for (1s,8s,9s,12r)-8-(acetyloxy)-12-formyl-5-isopropyl-1,11,11-trimethyl-10-oxotricyclo[7.3.1.0²,⁷]trideca-2(7),3,5-trien-4-yl acetate (NP0294686)

MOL for NP0294686 ((1s,8s,9s,12r)-8-(acetyloxy)-12-formyl-5-isopropyl-1,11,11-trimethyl-10-oxotricyclo[7.3.1.0²,⁷]trideca-2(7),3,5-trien-4-yl acetate)

3D MOL for NP0294686 ((1s,8s,9s,12r)-8-(acetyloxy)-12-formyl-5-isopropyl-1,11,11-trimethyl-10-oxotricyclo[7.3.1.0²,⁷]trideca-2(7),3,5-trien-4-yl acetate)

3D SDF for NP0294686 ((1s,8s,9s,12r)-8-(acetyloxy)-12-formyl-5-isopropyl-1,11,11-trimethyl-10-oxotricyclo[7.3.1.0²,⁷]trideca-2(7),3,5-trien-4-yl acetate)

3D-SDF for NP0294686 ((1s,8s,9s,12r)-8-(acetyloxy)-12-formyl-5-isopropyl-1,11,11-trimethyl-10-oxotricyclo[7.3.1.0²,⁷]trideca-2(7),3,5-trien-4-yl acetate)

PDB for NP0294686 ((1s,8s,9s,12r)-8-(acetyloxy)-12-formyl-5-isopropyl-1,11,11-trimethyl-10-oxotricyclo[7.3.1.0²,⁷]trideca-2(7),3,5-trien-4-yl acetate)

3D PDB for NP0294686 ((1s,8s,9s,12r)-8-(acetyloxy)-12-formyl-5-isopropyl-1,11,11-trimethyl-10-oxotricyclo[7.3.1.0²,⁷]trideca-2(7),3,5-trien-4-yl acetate)

SMILES for NP0294686 ((1s,8s,9s,12r)-8-(acetyloxy)-12-formyl-5-isopropyl-1,11,11-trimethyl-10-oxotricyclo[7.3.1.0²,⁷]trideca-2(7),3,5-trien-4-yl acetate)

INCHI for NP0294686 ((1s,8s,9s,12r)-8-(acetyloxy)-12-formyl-5-isopropyl-1,11,11-trimethyl-10-oxotricyclo[7.3.1.0²,⁷]trideca-2(7),3,5-trien-4-yl acetate)

Structure for NP0294686 ((1s,8s,9s,12r)-8-(acetyloxy)-12-formyl-5-isopropyl-1,11,11-trimethyl-10-oxotricyclo[7.3.1.0²,⁷]trideca-2(7),3,5-trien-4-yl acetate)

3D Structure for NP0294686 ((1s,8s,9s,12r)-8-(acetyloxy)-12-formyl-5-isopropyl-1,11,11-trimethyl-10-oxotricyclo[7.3.1.0²,⁷]trideca-2(7),3,5-trien-4-yl acetate)