NP-MRD: Showing NP-Card for Aspergiterpenoid A (NP0010662)

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Record Information

Version

2.0

Created at

2021-01-05 20:06:22 UTC

Updated at

2021-07-15 17:06:43 UTC

NP-MRD ID

NP0010662

Secondary Accession Numbers

None

Natural Product Identification

Common Name

Aspergiterpenoid A

Provided By

NPAtlas

Description

Aspergiterpenoid A is found in Aspergillus sp. Aspergiterpenoid A was first documented in 2012 (PMID: 22363233). Based on a literature review very few articles have been published on 2-[4-(hydroxymethyl)phenyl]-6-methylheptan-2-ol.

Structure

MOL 3D MOL SDF 3D SDF PDB SMILES InChI


  Mrv1652306242107403D          

 41 41  0  0  0  0            999 V2000
   -4.8434   -0.3726   -0.6538 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9097    0.0256    0.5108 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.5660    1.4415    0.3131 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8659   -1.0166    0.6652 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.9216   -1.2452   -0.4414 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.7129   -0.4085   -0.5418 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.2949   -0.7432    0.5671 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.6903   -2.2202    0.4185 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1527   -0.4115    1.8228 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.5537   -0.0065    0.2692 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6779    0.9520   -0.7082 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8565    1.6117   -0.9929 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9691    1.2934   -0.2593 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2474    2.0231   -0.5827 C   0  0  1  0  0  0  0  0  0  0  0  0
    6.3485    1.1637   -0.4663 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.9096    0.3340    0.7394 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7069   -0.3025    0.9936 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8502    0.3916   -1.4341 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9090   -0.4798   -0.2838 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5621   -1.3754   -1.0242 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5722   -0.0409    1.4351 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4612    2.0250    1.2750 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5362    1.9473   -0.1121 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8452    1.7136   -0.4505 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3684   -0.8058    1.6503 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4090   -1.9860    0.8718 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6441   -2.3368   -0.5389 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4658   -1.0926   -1.4598 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1836   -0.6122   -1.5009 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9348    0.6495   -0.3999 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1322   -2.3488   -0.5839 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4476   -2.4363    1.1948 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1387   -2.9129    0.5857 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1623   -1.2250    2.4286 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7966    1.2104   -1.2921 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9067    2.3721   -1.7696 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.2132    2.3297   -1.6649 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.3444    2.9270    0.0303 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.4938    0.9085    0.4777 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.8034    0.1094    1.2756 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6218   -1.0499    1.7671 H   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
  2  4  1  0  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  6  7  1  0  0  0  0
  7  8  1  0  0  0  0
  7  9  1  1  0  0  0
  7 10  1  0  0  0  0
 10 11  2  0  0  0  0
 11 12  1  0  0  0  0
 12 13  2  0  0  0  0
 13 14  1  0  0  0  0
 14 15  1  0  0  0  0
 13 16  1  0  0  0  0
 16 17  2  0  0  0  0
 17 10  1  0  0  0  0
  1 18  1  0  0  0  0
  1 19  1  0  0  0  0
  1 20  1  0  0  0  0
  2 21  1  1  0  0  0
  3 22  1  0  0  0  0
  3 23  1  0  0  0  0
  3 24  1  0  0  0  0
  4 25  1  0  0  0  0
  4 26  1  0  0  0  0
  5 27  1  0  0  0  0
  5 28  1  0  0  0  0
  6 29  1  0  0  0  0
  6 30  1  0  0  0  0
  8 31  1  0  0  0  0
  8 32  1  0  0  0  0
  8 33  1  0  0  0  0
  9 34  1  0  0  0  0
 11 35  1  0  0  0  0
 12 36  1  0  0  0  0
 14 37  1  0  0  0  0
 14 38  1  0  0  0  0
 15 39  1  0  0  0  0
 16 40  1  0  0  0  0
 17 41  1  0  0  0  0
M  END

     RDKit          3D

 41 41  0  0  0  0  0  0  0  0999 V2000
   -4.8434   -0.3726   -0.6538 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9097    0.0256    0.5108 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.5660    1.4415    0.3131 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8659   -1.0166    0.6652 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9216   -1.2452   -0.4414 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7129   -0.4085   -0.5418 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2949   -0.7432    0.5671 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.6903   -2.2202    0.4185 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1527   -0.4115    1.8228 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.5537   -0.0065    0.2692 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6779    0.9520   -0.7082 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8565    1.6117   -0.9929 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9691    1.2934   -0.2593 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2474    2.0231   -0.5827 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.3485    1.1637   -0.4663 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.9096    0.3340    0.7394 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7069   -0.3025    0.9936 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8502    0.3916   -1.4341 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9090   -0.4798   -0.2838 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5621   -1.3754   -1.0242 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5722   -0.0409    1.4351 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4612    2.0250    1.2750 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5362    1.9473   -0.1121 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8452    1.7136   -0.4505 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3684   -0.8058    1.6503 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4090   -1.9860    0.8718 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6441   -2.3368   -0.5389 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4658   -1.0926   -1.4598 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1836   -0.6122   -1.5009 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9348    0.6495   -0.3999 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1322   -2.3488   -0.5839 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4476   -2.4363    1.1948 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1387   -2.9129    0.5857 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1623   -1.2250    2.4286 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7966    1.2104   -1.2921 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9067    2.3721   -1.7696 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.2132    2.3297   -1.6649 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.3444    2.9270    0.0303 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.4938    0.9085    0.4777 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.8034    0.1094    1.2756 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6218   -1.0499    1.7671 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  2  4  1  0
  4  5  1  0
  5  6  1  0
  6  7  1  0
  7  8  1  0
  7  9  1  1
  7 10  1  0
 10 11  2  0
 11 12  1  0
 12 13  2  0
 13 14  1  0
 14 15  1  0
 13 16  1  0
 16 17  2  0
 17 10  1  0
  1 18  1  0
  1 19  1  0
  1 20  1  0
  2 21  1  1
  3 22  1  0
  3 23  1  0
  3 24  1  0
  4 25  1  0
  4 26  1  0
  5 27  1  0
  5 28  1  0
  6 29  1  0
  6 30  1  0
  8 31  1  0
  8 32  1  0
  8 33  1  0
  9 34  1  0
 11 35  1  0
 12 36  1  0
 14 37  1  0
 14 38  1  0
 15 39  1  0
 16 40  1  0
 17 41  1  0
M  END


  Mrv1652306242107403D          

 41 41  0  0  0  0            999 V2000
   -4.8434   -0.3726   -0.6538 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9097    0.0256    0.5108 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.5660    1.4415    0.3131 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8659   -1.0166    0.6652 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.9216   -1.2452   -0.4414 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.7129   -0.4085   -0.5418 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.2949   -0.7432    0.5671 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.6903   -2.2202    0.4185 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1527   -0.4115    1.8228 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.5537   -0.0065    0.2692 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6779    0.9520   -0.7082 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8565    1.6117   -0.9929 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9691    1.2934   -0.2593 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2474    2.0231   -0.5827 C   0  0  1  0  0  0  0  0  0  0  0  0
    6.3485    1.1637   -0.4663 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.9096    0.3340    0.7394 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7069   -0.3025    0.9936 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8502    0.3916   -1.4341 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9090   -0.4798   -0.2838 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5621   -1.3754   -1.0242 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5722   -0.0409    1.4351 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4612    2.0250    1.2750 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5362    1.9473   -0.1121 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8452    1.7136   -0.4505 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3684   -0.8058    1.6503 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4090   -1.9860    0.8718 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6441   -2.3368   -0.5389 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4658   -1.0926   -1.4598 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1836   -0.6122   -1.5009 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9348    0.6495   -0.3999 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1322   -2.3488   -0.5839 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4476   -2.4363    1.1948 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1387   -2.9129    0.5857 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1623   -1.2250    2.4286 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7966    1.2104   -1.2921 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9067    2.3721   -1.7696 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.2132    2.3297   -1.6649 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.3444    2.9270    0.0303 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.4938    0.9085    0.4777 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.8034    0.1094    1.2756 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6218   -1.0499    1.7671 H   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
  2  4  1  0  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  6  7  1  0  0  0  0
  7  8  1  0  0  0  0
  7  9  1  1  0  0  0
  7 10  1  0  0  0  0
 10 11  2  0  0  0  0
 11 12  1  0  0  0  0
 12 13  2  0  0  0  0
 13 14  1  0  0  0  0
 14 15  1  0  0  0  0
 13 16  1  0  0  0  0
 16 17  2  0  0  0  0
 17 10  1  0  0  0  0
  1 18  1  0  0  0  0
  1 19  1  0  0  0  0
  1 20  1  0  0  0  0
  2 21  1  1  0  0  0
  3 22  1  0  0  0  0
  3 23  1  0  0  0  0
  3 24  1  0  0  0  0
  4 25  1  0  0  0  0
  4 26  1  0  0  0  0
  5 27  1  0  0  0  0
  5 28  1  0  0  0  0
  6 29  1  0  0  0  0
  6 30  1  0  0  0  0
  8 31  1  0  0  0  0
  8 32  1  0  0  0  0
  8 33  1  0  0  0  0
  9 34  1  0  0  0  0
 11 35  1  0  0  0  0
 12 36  1  0  0  0  0
 14 37  1  0  0  0  0
 14 38  1  0  0  0  0
 15 39  1  0  0  0  0
 16 40  1  0  0  0  0
 17 41  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0010662

> <DATABASE_NAME>
NP-MRD

> <SMILES>
[H]OC([H])([H])C1=C([H])C([H])=C(C([H])=C1[H])[C@](O[H])(C([H])([H])[H])C([H])([H])C([H])([H])C([H])([H])C([H])(C([H])([H])[H])C([H])([H])[H]

> <INCHI_IDENTIFIER>
InChI=1S/C15H24O2/c1-12(2)5-4-10-15(3,17)14-8-6-13(11-16)7-9-14/h6-9,12,16-17H,4-5,10-11H2,1-3H3/t15-/m0/s1

> <INCHI_KEY>
VWMRQVRLVIZTJQ-UHFFFAOYSA-N

> <FORMULA>
C15H24O2

> <MOLECULAR_WEIGHT>
236.355

> <EXACT_MASS>
236.177630013

> <JCHEM_ACCEPTOR_COUNT>
2

> <JCHEM_ATOM_COUNT>
41

> <JCHEM_AVERAGE_POLARIZABILITY>
28.612922974883364

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(2S)-2-[4-(hydroxymethyl)phenyl]-6-methylheptan-2-ol

> <ALOGPS_LOGP>
3.38

> <JCHEM_LOGP>
3.2789454606666664

> <ALOGPS_LOGS>
-3.27

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
1

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
15.091615341636771

> <JCHEM_PKA_STRONGEST_ACIDIC>
14.228520525050133

> <JCHEM_PKA_STRONGEST_BASIC>
-2.7995364794173456

> <JCHEM_POLAR_SURFACE_AREA>
40.46

> <JCHEM_REFRACTIVITY>
71.62240000000001

> <JCHEM_ROTATABLE_BOND_COUNT>
6

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
1.27e-01 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(2S)-2-[4-(hydroxymethyl)phenyl]-6-methylheptan-2-ol

> <JCHEM_VEBER_RULE>
0

$$$$

     RDKit          3D

 41 41  0  0  0  0  0  0  0  0999 V2000
   -4.8434   -0.3726   -0.6538 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9097    0.0256    0.5108 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.5660    1.4415    0.3131 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8659   -1.0166    0.6652 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9216   -1.2452   -0.4414 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7129   -0.4085   -0.5418 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2949   -0.7432    0.5671 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.6903   -2.2202    0.4185 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1527   -0.4115    1.8228 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.5537   -0.0065    0.2692 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6779    0.9520   -0.7082 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8565    1.6117   -0.9929 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9691    1.2934   -0.2593 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2474    2.0231   -0.5827 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.3485    1.1637   -0.4663 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.9096    0.3340    0.7394 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7069   -0.3025    0.9936 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8502    0.3916   -1.4341 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9090   -0.4798   -0.2838 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5621   -1.3754   -1.0242 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5722   -0.0409    1.4351 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4612    2.0250    1.2750 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5362    1.9473   -0.1121 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8452    1.7136   -0.4505 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3684   -0.8058    1.6503 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4090   -1.9860    0.8718 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6441   -2.3368   -0.5389 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4658   -1.0926   -1.4598 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1836   -0.6122   -1.5009 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9348    0.6495   -0.3999 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1322   -2.3488   -0.5839 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4476   -2.4363    1.1948 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1387   -2.9129    0.5857 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1623   -1.2250    2.4286 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7966    1.2104   -1.2921 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9067    2.3721   -1.7696 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.2132    2.3297   -1.6649 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.3444    2.9270    0.0303 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.4938    0.9085    0.4777 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.8034    0.1094    1.2756 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6218   -1.0499    1.7671 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  2  4  1  0
  4  5  1  0
  5  6  1  0
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  7  9  1  1
  7 10  1  0
 10 11  2  0
 11 12  1  0
 12 13  2  0
 13 14  1  0
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 16 17  2  0
 17 10  1  0
  1 18  1  0
  1 19  1  0
  1 20  1  0
  2 21  1  1
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 11 35  1  0
 12 36  1  0
 14 37  1  0
 14 38  1  0
 15 39  1  0
 16 40  1  0
 17 41  1  0
M  END

HEADER    PROTEIN                                 24-JUN-21   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   24-JUN-21         0                                  
HETATM    1  C   UNK     0      -4.843  -0.373  -0.654  0.00  0.00           C+0
HETATM    2  C   UNK     0      -3.910   0.026   0.511  0.00  0.00           C+0
HETATM    3  C   UNK     0      -3.566   1.442   0.313  0.00  0.00           C+0
HETATM    4  C   UNK     0      -2.866  -1.017   0.665  0.00  0.00           C+0
HETATM    5  C   UNK     0      -1.922  -1.245  -0.441  0.00  0.00           C+0
HETATM    6  C   UNK     0      -0.713  -0.409  -0.542  0.00  0.00           C+0
HETATM    7  C   UNK     0       0.295  -0.743   0.567  0.00  0.00           C+0
HETATM    8  C   UNK     0       0.690  -2.220   0.419  0.00  0.00           C+0
HETATM    9  O   UNK     0      -0.153  -0.412   1.823  0.00  0.00           O+0
HETATM   10  C   UNK     0       1.554  -0.007   0.269  0.00  0.00           C+0
HETATM   11  C   UNK     0       1.678   0.952  -0.708  0.00  0.00           C+0
HETATM   12  C   UNK     0       2.857   1.612  -0.993  0.00  0.00           C+0
HETATM   13  C   UNK     0       3.969   1.293  -0.259  0.00  0.00           C+0
HETATM   14  C   UNK     0       5.247   2.023  -0.583  0.00  0.00           C+0
HETATM   15  O   UNK     0       6.348   1.164  -0.466  0.00  0.00           O+0
HETATM   16  C   UNK     0       3.910   0.334   0.739  0.00  0.00           C+0
HETATM   17  C   UNK     0       2.707  -0.303   0.994  0.00  0.00           C+0
HETATM   18  H   UNK     0      -4.850   0.392  -1.434  0.00  0.00           H+0
HETATM   19  H   UNK     0      -5.909  -0.480  -0.284  0.00  0.00           H+0
HETATM   20  H   UNK     0      -4.562  -1.375  -1.024  0.00  0.00           H+0
HETATM   21  H   UNK     0      -4.572  -0.041   1.435  0.00  0.00           H+0
HETATM   22  H   UNK     0      -3.461   2.025   1.275  0.00  0.00           H+0
HETATM   23  H   UNK     0      -4.536   1.947  -0.112  0.00  0.00           H+0
HETATM   24  H   UNK     0      -2.845   1.714  -0.451  0.00  0.00           H+0
HETATM   25  H   UNK     0      -2.368  -0.806   1.650  0.00  0.00           H+0
HETATM   26  H   UNK     0      -3.409  -1.986   0.872  0.00  0.00           H+0
HETATM   27  H   UNK     0      -1.644  -2.337  -0.539  0.00  0.00           H+0
HETATM   28  H   UNK     0      -2.466  -1.093  -1.460  0.00  0.00           H+0
HETATM   29  H   UNK     0      -0.184  -0.612  -1.501  0.00  0.00           H+0
HETATM   30  H   UNK     0      -0.935   0.650  -0.400  0.00  0.00           H+0
HETATM   31  H   UNK     0       1.132  -2.349  -0.584  0.00  0.00           H+0
HETATM   32  H   UNK     0       1.448  -2.436   1.195  0.00  0.00           H+0
HETATM   33  H   UNK     0      -0.139  -2.913   0.586  0.00  0.00           H+0
HETATM   34  H   UNK     0      -0.162  -1.225   2.429  0.00  0.00           H+0
HETATM   35  H   UNK     0       0.797   1.210  -1.292  0.00  0.00           H+0
HETATM   36  H   UNK     0       2.907   2.372  -1.770  0.00  0.00           H+0
HETATM   37  H   UNK     0       5.213   2.330  -1.665  0.00  0.00           H+0
HETATM   38  H   UNK     0       5.344   2.927   0.030  0.00  0.00           H+0
HETATM   39  H   UNK     0       6.494   0.909   0.478  0.00  0.00           H+0
HETATM   40  H   UNK     0       4.803   0.109   1.276  0.00  0.00           H+0
HETATM   41  H   UNK     0       2.622  -1.050   1.767  0.00  0.00           H+0
CONECT    1    2   18   19   20                                             
CONECT    2    1    3    4   21                                             
CONECT    3    2   22   23   24                                             
CONECT    4    2    5   25   26                                             
CONECT    5    4    6   27   28                                             
CONECT    6    5    7   29   30                                             
CONECT    7    6    8    9   10                                             
CONECT    8    7   31   32   33                                             
CONECT    9    7   34                                                       
CONECT   10    7   11   17                                                  
CONECT   11   10   12   35                                                  
CONECT   12   11   13   36                                                  
CONECT   13   12   14   16                                                  
CONECT   14   13   15   37   38                                             
CONECT   15   14   39                                                       
CONECT   16   13   17   40                                                  
CONECT   17   16   10   41                                                  
CONECT   18    1                                                            
CONECT   19    1                                                            
CONECT   20    1                                                            
CONECT   21    2                                                            
CONECT   22    3                                                            
CONECT   23    3                                                            
CONECT   24    3                                                            
CONECT   25    4                                                            
CONECT   26    4                                                            
CONECT   27    5                                                            
CONECT   28    5                                                            
CONECT   29    6                                                            
CONECT   30    6                                                            
CONECT   31    8                                                            
CONECT   32    8                                                            
CONECT   33    8                                                            
CONECT   34    9                                                            
CONECT   35   11                                                            
CONECT   36   12                                                            
CONECT   37   14                                                            
CONECT   38   14                                                            
CONECT   39   15                                                            
CONECT   40   16                                                            
CONECT   41   17                                                            
MASTER        0    0    0    0    0    0    0    0   41    0   82    0
END

RDKit          3D

41 41  0  0  0  0  0  0  0  0999 V2000
   -4.8434   -0.3726   -0.6538 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9097    0.0256    0.5108 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.5660    1.4415    0.3131 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8659   -1.0166    0.6652 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9216   -1.2452   -0.4414 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7129   -0.4085   -0.5418 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2949   -0.7432    0.5671 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.6903   -2.2202    0.4185 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1527   -0.4115    1.8228 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.5537   -0.0065    0.2692 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6779    0.9520   -0.7082 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8565    1.6117   -0.9929 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9691    1.2934   -0.2593 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2474    2.0231   -0.5827 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.3485    1.1637   -0.4663 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.9096    0.3340    0.7394 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7069   -0.3025    0.9936 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8502    0.3916   -1.4341 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9090   -0.4798   -0.2838 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5621   -1.3754   -1.0242 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5722   -0.0409    1.4351 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4612    2.0250    1.2750 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5362    1.9473   -0.1121 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8452    1.7136   -0.4505 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3684   -0.8058    1.6503 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4090   -1.9860    0.8718 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6441   -2.3368   -0.5389 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4658   -1.0926   -1.4598 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1836   -0.6122   -1.5009 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9348    0.6495   -0.3999 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1322   -2.3488   -0.5839 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4476   -2.4363    1.1948 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1387   -2.9129    0.5857 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1623   -1.2250    2.4286 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7966    1.2104   -1.2921 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9067    2.3721   -1.7696 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.2132    2.3297   -1.6649 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.3444    2.9270    0.0303 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.4938    0.9085    0.4777 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.8034    0.1094    1.2756 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6218   -1.0499    1.7671 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  2  4  1  0
  4  5  1  0
  5  6  1  0
  6  7  1  0
  7  8  1  0
  7  9  1  1
  7 10  1  0
 10 11  2  0
 11 12  1  0
 12 13  2  0
 13 14  1  0
 14 15  1  0
 13 16  1  0
 16 17  2  0
 17 10  1  0
  1 18  1  0
  1 19  1  0
  1 20  1  0
  2 21  1  1
  3 22  1  0
  3 23  1  0
  3 24  1  0
  4 25  1  0
  4 26  1  0
  5 27  1  0
  5 28  1  0
  6 29  1  0
  6 30  1  0
  8 31  1  0
  8 32  1  0
  8 33  1  0
  9 34  1  0
 11 35  1  0
 12 36  1  0
 14 37  1  0
 14 38  1  0
 15 39  1  0
 16 40  1  0
 17 41  1  0
M  END

View in JSmol View NMR Assignments

Synonyms

Not Available

Chemical Formula

C₁₅H₂₄O₂

Average Mass

236.3550 Da

Monoisotopic Mass

236.17763 Da

IUPAC Name

(2S)-2-[4-(hydroxymethyl)phenyl]-6-methylheptan-2-ol

Traditional Name

(2S)-2-[4-(hydroxymethyl)phenyl]-6-methylheptan-2-ol

CAS Registry Number

Not Available

SMILES

CC(C)CCCC(C)(O)C1=CC=C(CO)C=C1

InChI Identifier

InChI=1S/C15H24O2/c1-12(2)5-4-10-15(3,17)14-8-6-13(11-16)7-9-14/h6-9,12,16-17H,4-5,10-11H2,1-3H3

InChI Key

VWMRQVRLVIZTJQ-UHFFFAOYSA-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
Aspergillus sp.	NPAtlas	22363233

Chemical Taxonomy

Classification

Not classified

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	3.38	ALOGPS
logP	3.28	ChemAxon
logS	-3.3	ALOGPS
pKa (Strongest Acidic)	14.23	ChemAxon
pKa (Strongest Basic)	-2.8	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	2	ChemAxon
Hydrogen Donor Count	2	ChemAxon
Polar Surface Area	40.46 Å²	ChemAxon
Rotatable Bond Count	6	ChemAxon
Refractivity	71.62 m³·mol⁻¹	ChemAxon
Polarizability	28.61 Å³	ChemAxon
Number of Rings	1	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

NPAtlas ID

NPA018127

HMDB ID

Not Available

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FoodDB ID

Not Available

KNApSAcK ID

Not Available

Chemspider ID

78435744

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

139588138

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Li D, Xu Y, Shao CL, Yang RY, Zheng CJ, Chen YY, Fu XM, Qian PY, She ZG, de Voogd NJ, Wang CY: Antibacterial bisabolane-type sesquiterpenoids from the sponge-derived fungus Aspergillus sp. Mar Drugs. 2012 Jan;10(1):234-41. doi: 10.3390/md10010234. Epub 2012 Jan 19. [PubMed:22363233 ]

Showing NP-Card for Aspergiterpenoid A (NP0010662)

MOL for NP0010662 (Aspergiterpenoid A)

3D MOL for NP0010662 (Aspergiterpenoid A)

3D SDF for NP0010662 (Aspergiterpenoid A)

3D-SDF for NP0010662 (Aspergiterpenoid A)

PDB for NP0010662 (Aspergiterpenoid A)

3D PDB for NP0010662 (Aspergiterpenoid A)

SMILES for NP0010662 (Aspergiterpenoid A)

INCHI for NP0010662 (Aspergiterpenoid A)

Structure for NP0010662 (Aspergiterpenoid A)

3D Structure for NP0010662 (Aspergiterpenoid A)