NP-MRD: Showing NP-Card for Scopadulcic acid C (NP0071818)

Jump To Section:

Identification Spectra BioTaxonomy ChemoTaxonomy Physical properties Links References XML

Record Information

Version

2.0

Created at

2022-04-28 17:10:00 UTC

Updated at

2022-04-28 17:10:00 UTC

NP-MRD ID

NP0071818

Secondary Accession Numbers

None

Natural Product Identification

Common Name

Scopadulcic acid C

Description

(1R,2S,6S,7R,8S,10S,13R)-6-(hydroxymethyl)-2,6-dimethyl-12-oxotetracyclo[11.2.1.0¹,¹⁰.0²,⁷]Hexadecan-8-yl benzoate belongs to the class of organic compounds known as benzoic acid esters. These are ester derivatives of benzoic acid. Scopadulcic acid C is found in Scoparia dulcis L. . Based on a literature review very few articles have been published on (1R,2S,6S,7R,8S,10S,13R)-6-(hydroxymethyl)-2,6-dimethyl-12-oxotetracyclo[11.2.1.0¹,¹⁰.0²,⁷]Hexadecan-8-yl benzoate.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652304282219102D          

 30 34  0  0  1  0            999 V2000
    1.0833   -0.9483    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4812   -0.3262    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.0620    0.4328    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7629    0.4441    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.4959    1.1699    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3618    1.1013    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.7907    0.3302    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.8691   -0.5661    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6377    0.4266    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.0224    1.1564    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.5818    1.8646    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.7544    1.8379    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9707    2.5921    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.5352    3.2927    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7106    3.2658    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.9241    4.0203    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4886    4.7209    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8775    5.4485    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7021    5.4754    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1377    4.7747    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7487    4.0472    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8468    1.1881    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.2864    0.4900    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9017   -0.2398    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0773   -0.2715    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8439    2.0131    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5292    1.6518    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2719    1.2927    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.2805   -0.3171    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1248    0.0419    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  1  0  0  0  0
  3  4  2  0  0  0  0
  3  5  1  0  0  0  0
  6  5  1  6  0  0  0
  6  7  1  0  0  0  0
  7  8  1  0  0  0  0
  1  8  1  0  0  0  0
  7  9  1  0  0  0  0
 10  9  1  1  0  0  0
 10 11  1  0  0  0  0
 11 12  1  0  0  0  0
  6 12  1  0  0  0  0
 11 13  1  6  0  0  0
 13 14  1  0  0  0  0
 14 15  2  0  0  0  0
 14 16  1  0  0  0  0
 16 17  2  0  0  0  0
 17 18  1  0  0  0  0
 18 19  2  0  0  0  0
 19 20  1  0  0  0  0
 20 21  2  0  0  0  0
 16 21  1  0  0  0  0
 10 22  1  0  0  0  0
 22 23  1  0  0  0  0
 23 24  1  0  0  0  0
 24 25  1  0  0  0  0
  9 25  1  0  0  0  0
 22 26  1  6  0  0  0
 22 27  1  1  0  0  0
 27 28  1  0  0  0  0
  9 29  1  1  0  0  0
  7 30  1  6  0  0  0
  2 30  1  6  0  0  0
M  END

     RDKit          3D

 64 68  0  0  0  0  0  0  0  0999 V2000
    0.9265   -2.6117   -0.6357 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3897   -2.1281    0.0292 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.2487   -2.5094    1.4643 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8250   -1.9518    2.1421 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4791   -2.9132   -0.6695 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6036   -2.1992   -1.2613 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5977   -0.7262   -1.3972 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8257   -0.0892   -0.2146 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.6680   -0.5522    0.9662 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4772   -0.6996   -0.3327 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.5982    0.2226    0.0404 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.9198   -0.2531   -0.0072 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8280    0.0741    0.9662 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4149    0.8166    1.8944 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.2011   -0.3713    0.9919 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7150   -1.1850    0.0062 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0354   -1.6170    0.0251 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.8576   -1.2166    1.0665 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.3683   -0.4037    2.0637 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0400    0.0107    2.0136 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4800    1.3746   -1.0180 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7602    2.1384   -0.7747 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.1305    2.8144   -2.1072 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1680    3.8200   -1.7398 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2251    4.9333   -2.2099 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1568    3.3201   -0.7137 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.6421    3.4295    0.6768 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2309    2.0182    1.1260 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9150    1.3868   -0.2190 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.1897    1.8012   -0.9500 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1724   -2.0017   -1.5212 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7599   -2.5827    0.0550 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8037   -3.6613   -0.9924 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1229   -2.3017    2.1137 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0119   -3.6385    1.5373 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0680   -2.4921    2.9170 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8824   -3.6165    0.1240 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0592   -3.6456   -1.4151 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7925   -2.5833   -2.3179 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5903   -2.4828   -0.7756 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9948   -0.4637   -2.3075 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6141   -0.3488   -1.4652 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6834   -0.0679    0.7590 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2854   -0.2740    1.9370 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9353   -1.6182    0.9335 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3379   -0.7738   -1.5092 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4604    0.7663    0.9836 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.0663   -1.4848   -0.7907 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.4171   -2.2492   -0.7499 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.8955   -1.5630    1.0707 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.0123   -0.0976    2.8677 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.7172    0.6531    2.8347 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3944    1.9736   -0.9527 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3740    0.8323   -1.9791 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4574    3.0223   -0.1332 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2298    3.3797   -2.4408 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4283    2.1074   -2.8760 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1486    3.7645   -0.8818 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4986    3.7962    1.3168 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8404    4.1615    0.8309 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3461    2.0973    1.7873 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0916    1.6143    1.6422 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1803    1.5611   -2.0138 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1118    1.4843   -0.4257 H   0  0  0  0  0  0  0  0  0  0  0  0
  2  1  1  6
  2  3  1  0
  3  4  1  0
  2  5  1  0
  5  6  1  0
  6  7  1  0
  7  8  1  0
  8  9  1  1
  8 10  1  0
 10 11  1  0
 11 21  1  0
 21 22  1  0
 22 23  1  0
 23 24  1  0
 24 25  2  0
 24 26  1  0
 26 27  1  0
 27 28  1  0
 29 28  1  1
 29 30  1  0
 11 12  1  0
 12 13  1  0
 13 14  2  0
 13 15  1  0
 15 16  2  0
 16 17  1  0
 17 18  2  0
 18 19  1  0
 19 20  2  0
 10  2  1  0
 29 22  1  0
 20 15  1  0
 29  8  1  0
 30 26  1  0
  1 31  1  0
  1 32  1  0
  1 33  1  0
  3 34  1  0
  3 35  1  0
  4 36  1  0
  5 37  1  0
  5 38  1  0
  6 39  1  0
  6 40  1  0
  7 41  1  0
  7 42  1  0
  9 43  1  0
  9 44  1  0
  9 45  1  0
 10 46  1  6
 11 47  1  1
 21 53  1  0
 21 54  1  0
 22 55  1  1
 23 56  1  0
 23 57  1  0
 26 58  1  1
 27 59  1  0
 27 60  1  0
 28 61  1  0
 28 62  1  0
 30 63  1  0
 30 64  1  0
 16 48  1  0
 17 49  1  0
 18 50  1  0
 19 51  1  0
 20 52  1  0
M  END


  Mrv1652304282219102D          

 30 34  0  0  1  0            999 V2000
    1.0833   -0.9483    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4812   -0.3262    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.0620    0.4328    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7629    0.4441    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.4959    1.1699    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3618    1.1013    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.7907    0.3302    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.8691   -0.5661    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6377    0.4266    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.0224    1.1564    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.5818    1.8646    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.7544    1.8379    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9707    2.5921    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.5352    3.2927    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7106    3.2658    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.9241    4.0203    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4886    4.7209    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8775    5.4485    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7021    5.4754    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1377    4.7747    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7487    4.0472    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8468    1.1881    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.2864    0.4900    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9017   -0.2398    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0773   -0.2715    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8439    2.0131    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5292    1.6518    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2719    1.2927    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.2805   -0.3171    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1248    0.0419    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  1  0  0  0  0
  3  4  2  0  0  0  0
  3  5  1  0  0  0  0
  6  5  1  6  0  0  0
  6  7  1  0  0  0  0
  7  8  1  0  0  0  0
  1  8  1  0  0  0  0
  7  9  1  0  0  0  0
 10  9  1  1  0  0  0
 10 11  1  0  0  0  0
 11 12  1  0  0  0  0
  6 12  1  0  0  0  0
 11 13  1  6  0  0  0
 13 14  1  0  0  0  0
 14 15  2  0  0  0  0
 14 16  1  0  0  0  0
 16 17  2  0  0  0  0
 17 18  1  0  0  0  0
 18 19  2  0  0  0  0
 19 20  1  0  0  0  0
 20 21  2  0  0  0  0
 16 21  1  0  0  0  0
 10 22  1  0  0  0  0
 22 23  1  0  0  0  0
 23 24  1  0  0  0  0
 24 25  1  0  0  0  0
  9 25  1  0  0  0  0
 22 26  1  6  0  0  0
 22 27  1  1  0  0  0
 27 28  1  0  0  0  0
  9 29  1  1  0  0  0
  7 30  1  6  0  0  0
  2 30  1  6  0  0  0
M  END
> <DATABASE_ID>
NP0071818

> <DATABASE_NAME>
NP-MRD

> <SMILES>
C[C@]1(CO)CCC[C@@]2(C)[C@H]1[C@H](C[C@H]1CC(=O)[C@@H]3CC[C@]21C3)OC(=O)C1=CC=CC=C1

> <INCHI_IDENTIFIER>
InChI=1S/C26H34O4/c1-24(16-27)10-6-11-25(2)22(24)21(30-23(29)17-7-4-3-5-8-17)14-19-13-20(28)18-9-12-26(19,25)15-18/h3-5,7-8,18-19,21-22,27H,6,9-16H2,1-2H3/t18-,19-,21+,22+,24-,25+,26-/m1/s1

> <INCHI_KEY>
FNQZMWFGVBMQLB-QJDKAJMLSA-N

> <FORMULA>
C26H34O4

> <MOLECULAR_WEIGHT>
410.554

> <EXACT_MASS>
410.245709575

> <JCHEM_ACCEPTOR_COUNT>
3

> <JCHEM_ATOM_COUNT>
64

> <JCHEM_AVERAGE_POLARIZABILITY>
45.77893378703948

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(1R,2S,6S,7R,8S,10S,13R)-6-(hydroxymethyl)-2,6-dimethyl-12-oxotetracyclo[11.2.1.0^{1,10}.0^{2,7}]hexadecan-8-yl benzoate

> <ALOGPS_LOGP>
3.90

> <JCHEM_LOGP>
4.659278231666667

> <ALOGPS_LOGS>
-5.14

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
5

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_ACIDIC>
15.104670569617412

> <JCHEM_PKA_STRONGEST_BASIC>
-2.753015088597092

> <JCHEM_POLAR_SURFACE_AREA>
63.60000000000001

> <JCHEM_REFRACTIVITY>
115.1768

> <JCHEM_ROTATABLE_BOND_COUNT>
4

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
2.99e-03 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(1R,2S,6S,7R,8S,10S,13R)-6-(hydroxymethyl)-2,6-dimethyl-12-oxotetracyclo[11.2.1.0^{1,10}.0^{2,7}]hexadecan-8-yl benzoate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 28-APR-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   28-APR-22         0                                  
HETATM    1  C   UNK     0       2.022  -1.770   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       0.898  -0.609   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       0.116   0.808   0.000  0.00  0.00           C+0
HETATM    4  O   UNK     0      -1.424   0.829   0.000  0.00  0.00           O+0
HETATM    5  C   UNK     0       0.926   2.184   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       2.542   2.056   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       3.343   0.616   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       3.489  -1.057   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       4.924   0.796   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       5.642   2.159   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       4.819   3.481   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       3.275   3.431   0.000  0.00  0.00           C+0
HETATM   13  O   UNK     0       5.545   4.839   0.000  0.00  0.00           O+0
HETATM   14  C   UNK     0       4.732   6.146   0.000  0.00  0.00           C+0
HETATM   15  O   UNK     0       3.193   6.096   0.000  0.00  0.00           O+0
HETATM   16  C   UNK     0       5.458   7.505   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       4.645   8.812   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       5.371  10.170   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       6.911  10.221   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       7.724   8.913   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       6.998   7.555   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       7.181   2.218   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       8.001   0.915   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       7.283  -0.448   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       5.744  -0.507   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       7.175   3.758   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0       8.454   3.083   0.000  0.00  0.00           C+0
HETATM   28  O   UNK     0       9.841   2.413   0.000  0.00  0.00           O+0
HETATM   29  C   UNK     0       4.257  -0.592   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0       2.100   0.078   0.000  0.00  0.00           C+0
CONECT    1    2    8                                                       
CONECT    2    1    3   30                                                  
CONECT    3    2    4    5                                                  
CONECT    4    3                                                            
CONECT    5    3    6                                                       
CONECT    6    5    7   12                                                  
CONECT    7    6    8    9   30                                             
CONECT    8    7    1                                                       
CONECT    9    7   10   25   29                                             
CONECT   10    9   11   22                                                  
CONECT   11   10   12   13                                                  
CONECT   12   11    6                                                       
CONECT   13   11   14                                                       
CONECT   14   13   15   16                                                  
CONECT   15   14                                                            
CONECT   16   14   17   21                                                  
CONECT   17   16   18                                                       
CONECT   18   17   19                                                       
CONECT   19   18   20                                                       
CONECT   20   19   21                                                       
CONECT   21   20   16                                                       
CONECT   22   10   23   26   27                                             
CONECT   23   22   24                                                       
CONECT   24   23   25                                                       
CONECT   25   24    9                                                       
CONECT   26   22                                                            
CONECT   27   22   28                                                       
CONECT   28   27                                                            
CONECT   29    9                                                            
CONECT   30    7    2                                                       
MASTER        0    0    0    0    0    0    0    0   30    0   68    0
END

View in JSmol

Synonyms

Value	Source
(1R,2S,6S,7R,8S,10S,13R)-6-(Hydroxymethyl)-2,6-dimethyl-12-oxotetracyclo[11.2.1.0,.0,]hexadecan-8-yl benzoic acid	Generator

Chemical Formula

C₂₆H₃₄O₄

Average Mass

410.5540 Da

Monoisotopic Mass

410.24571 Da

IUPAC Name

(1R,2S,6S,7R,8S,10S,13R)-6-(hydroxymethyl)-2,6-dimethyl-12-oxotetracyclo[11.2.1.0^{1,10}.0^{2,7}]hexadecan-8-yl benzoate

Traditional Name

(1R,2S,6S,7R,8S,10S,13R)-6-(hydroxymethyl)-2,6-dimethyl-12-oxotetracyclo[11.2.1.0^{1,10}.0^{2,7}]hexadecan-8-yl benzoate

CAS Registry Number

Not Available

SMILES

C[C@]1(CO)CCC[C@@]2(C)[C@H]1[C@H](C[C@H]1CC(=O)[C@@H]3CC[C@]21C3)OC(=O)C1=CC=CC=C1

InChI Identifier

InChI=1S/C26H34O4/c1-24(16-27)10-6-11-25(2)22(24)21(30-23(29)17-7-4-3-5-8-17)14-19-13-20(28)18-9-12-26(19,25)15-18/h3-5,7-8,18-19,21-22,27H,6,9-16H2,1-2H3/t18-,19-,21+,22+,24-,25+,26-/m1/s1

InChI Key

FNQZMWFGVBMQLB-QJDKAJMLSA-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, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 100 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 252 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 1000 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 50 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 200 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 75 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 300 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 101 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 126 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 500 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 151 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 600 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 176 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 700 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 201 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 800 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 226 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 900 MHz, D₂O, 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
Scoparia dulcis	Plant	KNApSAcK

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as benzoic acid esters. These are ester derivatives of benzoic acid.

Kingdom

Organic compounds

Super Class

Benzenoids

Class

Benzene and substituted derivatives

Sub Class

Benzoic acids and derivatives

Direct Parent

Benzoic acid esters

Alternative Parents

Substituents

Benzoate ester
Benzoyl
Ketone
Carboxylic acid ester
Monocarboxylic acid or derivatives
Carboxylic acid derivative
Organic oxygen compound
Organic oxide
Hydrocarbon derivative
Primary alcohol
Organooxygen compound
Carbonyl group
Alcohol
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
logP	3.9	ALOGPS
logP	4.66	ChemAxon
logS	-5.1	ALOGPS
pKa (Strongest Acidic)	15.1	ChemAxon
pKa (Strongest Basic)	-2.8	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	3	ChemAxon
Hydrogen Donor Count	1	ChemAxon
Polar Surface Area	63.6 Å²	ChemAxon
Rotatable Bond Count	4	ChemAxon
Refractivity	115.18 m³·mol⁻¹	ChemAxon
Polarizability	45.78 Å³	ChemAxon
Number of Rings	5	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

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

154497445

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Not Available

Showing NP-Card for Scopadulcic acid C (NP0071818)

MOL for NP0071818 (Scopadulcic acid C)

3D MOL for NP0071818 (Scopadulcic acid C)

3D SDF for NP0071818 (Scopadulcic acid C)

3D-SDF for NP0071818 (Scopadulcic acid C)

PDB for NP0071818 (Scopadulcic acid C)

3D PDB for NP0071818 (Scopadulcic acid C)

SMILES for NP0071818 (Scopadulcic acid C)

INCHI for NP0071818 (Scopadulcic acid C)

Structure for NP0071818 (Scopadulcic acid C)

3D Structure for NP0071818 (Scopadulcic acid C)