NP-MRD: Showing NP-Card for striatenic acid (NP0029831)

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Record Information

Version

2.0

Created at

2021-06-19 21:21:22 UTC

Updated at

2021-06-29 23:57:27 UTC

NP-MRD ID

NP0029831

Secondary Accession Numbers

None

Natural Product Identification

Common Name

striatenic acid

Provided By

JEOL Database JEOL Logo

Description

Striatenic acid is also known as striatenate. striatenic acid is found in Cheilolejeunea serpentina. striatenic acid was first documented in 2000 (Tori, M., et al.). Based on a literature review very few articles have been published on Striatenic acid.

Structure

MOL 3D MOL SDF 3D SDF PDB SMILES InChI


  Mrv1652306192123213D          

 39 39  0  0  0  0            999 V2000
    4.8240    1.5804   -0.7136 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7602    0.9866   -0.1567 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5265    0.5895   -0.8347 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4397    0.8400   -2.3191 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5482    0.0220   -0.0970 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1872   -0.4627   -0.5450 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.0472    0.2047    0.1681 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.3264   -0.3182   -0.5365 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0251    1.7398    0.0322 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7058    2.3409   -1.2912 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8447    1.8080   -2.3775 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2021    3.5853   -1.2050 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3088    2.5741    1.0536 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7000    2.1342    2.4274 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.0619    0.6567    2.5045 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.0678   -0.1997    1.7017 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.3528   -1.6822    1.9794 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6878    1.8321   -0.1056 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.8773    1.8349   -1.7658 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.8147    0.7819    0.9125 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.4677    1.9152   -2.5280 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2756    0.3593   -2.8399 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5321    0.4474   -2.7798 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7419   -0.1392    0.9624 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0734   -0.3710   -1.6278 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1642   -1.5457   -0.3742 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2382    0.0781   -0.0778 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3553   -0.0387   -1.5950 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3826   -1.4115   -0.5095 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0188    3.8211   -2.1368 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2726    3.6530    0.9117 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8675    2.3486    3.1082 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5540    2.7289    2.7714 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0667    0.3507    3.5581 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0838    0.5042    2.1372 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0781    0.0071    2.1289 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6549   -2.3398    1.4555 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2455   -1.8928    3.0498 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3729   -1.9619    1.6984 H   0  0  0  0  0  0  0  0  0  0  0  0
 15 16  1  0  0  0  0
  5  3  2  0  0  0  0
 14 13  1  0  0  0  0
  3  2  1  0  0  0  0
 13  9  2  0  0  0  0
  2  1  2  0  0  0  0
  9  7  1  0  0  0  0
  3  4  1  0  0  0  0
  7 16  1  0  0  0  0
  9 10  1  0  0  0  0
 10 11  2  0  0  0  0
  7  6  1  6  0  0  0
 10 12  1  0  0  0  0
 15 14  1  0  0  0  0
 16 17  1  0  0  0  0
  6  5  1  0  0  0  0
  7  8  1  0  0  0  0
 15 34  1  0  0  0  0
 15 35  1  0  0  0  0
 14 32  1  0  0  0  0
 14 33  1  0  0  0  0
 13 31  1  0  0  0  0
 16 36  1  1  0  0  0
  6 25  1  0  0  0  0
  6 26  1  0  0  0  0
  5 24  1  0  0  0  0
  2 20  1  0  0  0  0
  1 18  1  0  0  0  0
  1 19  1  0  0  0  0
  4 21  1  0  0  0  0
  4 22  1  0  0  0  0
  4 23  1  0  0  0  0
 12 30  1  0  0  0  0
 17 37  1  0  0  0  0
 17 38  1  0  0  0  0
 17 39  1  0  0  0  0
  8 27  1  0  0  0  0
  8 28  1  0  0  0  0
  8 29  1  0  0  0  0
M  END

     RDKit          3D

 39 39  0  0  0  0  0  0  0  0999 V2000
    4.8240    1.5804   -0.7136 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7602    0.9866   -0.1567 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5265    0.5895   -0.8347 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4397    0.8400   -2.3191 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5482    0.0220   -0.0970 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1872   -0.4627   -0.5450 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0472    0.2047    0.1681 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.3264   -0.3182   -0.5365 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0251    1.7398    0.0322 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7058    2.3409   -1.2912 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8447    1.8080   -2.3775 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2021    3.5853   -1.2050 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3088    2.5741    1.0536 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7000    2.1342    2.4274 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0619    0.6567    2.5045 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0678   -0.1997    1.7017 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.3528   -1.6822    1.9794 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6878    1.8321   -0.1056 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.8773    1.8349   -1.7658 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.8147    0.7819    0.9125 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.4677    1.9152   -2.5280 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2756    0.3593   -2.8399 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5321    0.4474   -2.7798 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7419   -0.1392    0.9624 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0734   -0.3710   -1.6278 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1642   -1.5457   -0.3742 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2382    0.0781   -0.0778 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3553   -0.0387   -1.5950 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3826   -1.4115   -0.5095 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0188    3.8211   -2.1368 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2726    3.6530    0.9117 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8675    2.3486    3.1082 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5540    2.7289    2.7714 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0667    0.3507    3.5581 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0838    0.5042    2.1372 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0781    0.0071    2.1289 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6549   -2.3398    1.4555 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2455   -1.8928    3.0498 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3729   -1.9619    1.6984 H   0  0  0  0  0  0  0  0  0  0  0  0
 15 16  1  0
  5  3  2  0
 14 13  1  0
  3  2  1  0
 13  9  2  0
  2  1  2  0
  9  7  1  0
  3  4  1  0
  7 16  1  0
  9 10  1  0
 10 11  2  0
  7  6  1  6
 10 12  1  0
 15 14  1  0
 16 17  1  0
  6  5  1  0
  7  8  1  0
 15 34  1  0
 15 35  1  0
 14 32  1  0
 14 33  1  0
 13 31  1  0
 16 36  1  1
  6 25  1  0
  6 26  1  0
  5 24  1  0
  2 20  1  0
  1 18  1  0
  1 19  1  0
  4 21  1  0
  4 22  1  0
  4 23  1  0
 12 30  1  0
 17 37  1  0
 17 38  1  0
 17 39  1  0
  8 27  1  0
  8 28  1  0
  8 29  1  0
M  END


  Mrv1652306192123213D          

 39 39  0  0  0  0            999 V2000
    4.8240    1.5804   -0.7136 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7602    0.9866   -0.1567 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5265    0.5895   -0.8347 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4397    0.8400   -2.3191 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5482    0.0220   -0.0970 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1872   -0.4627   -0.5450 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.0472    0.2047    0.1681 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.3264   -0.3182   -0.5365 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0251    1.7398    0.0322 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7058    2.3409   -1.2912 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8447    1.8080   -2.3775 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2021    3.5853   -1.2050 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3088    2.5741    1.0536 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7000    2.1342    2.4274 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.0619    0.6567    2.5045 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.0678   -0.1997    1.7017 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.3528   -1.6822    1.9794 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6878    1.8321   -0.1056 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.8773    1.8349   -1.7658 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.8147    0.7819    0.9125 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.4677    1.9152   -2.5280 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2756    0.3593   -2.8399 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5321    0.4474   -2.7798 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7419   -0.1392    0.9624 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0734   -0.3710   -1.6278 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1642   -1.5457   -0.3742 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2382    0.0781   -0.0778 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3553   -0.0387   -1.5950 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3826   -1.4115   -0.5095 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0188    3.8211   -2.1368 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2726    3.6530    0.9117 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8675    2.3486    3.1082 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5540    2.7289    2.7714 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0667    0.3507    3.5581 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0838    0.5042    2.1372 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0781    0.0071    2.1289 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6549   -2.3398    1.4555 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2455   -1.8928    3.0498 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3729   -1.9619    1.6984 H   0  0  0  0  0  0  0  0  0  0  0  0
 15 16  1  0  0  0  0
  5  3  2  0  0  0  0
 14 13  1  0  0  0  0
  3  2  1  0  0  0  0
 13  9  2  0  0  0  0
  2  1  2  0  0  0  0
  9  7  1  0  0  0  0
  3  4  1  0  0  0  0
  7 16  1  0  0  0  0
  9 10  1  0  0  0  0
 10 11  2  0  0  0  0
  7  6  1  6  0  0  0
 10 12  1  0  0  0  0
 15 14  1  0  0  0  0
 16 17  1  0  0  0  0
  6  5  1  0  0  0  0
  7  8  1  0  0  0  0
 15 34  1  0  0  0  0
 15 35  1  0  0  0  0
 14 32  1  0  0  0  0
 14 33  1  0  0  0  0
 13 31  1  0  0  0  0
 16 36  1  1  0  0  0
  6 25  1  0  0  0  0
  6 26  1  0  0  0  0
  5 24  1  0  0  0  0
  2 20  1  0  0  0  0
  1 18  1  0  0  0  0
  1 19  1  0  0  0  0
  4 21  1  0  0  0  0
  4 22  1  0  0  0  0
  4 23  1  0  0  0  0
 12 30  1  0  0  0  0
 17 37  1  0  0  0  0
 17 38  1  0  0  0  0
 17 39  1  0  0  0  0
  8 27  1  0  0  0  0
  8 28  1  0  0  0  0
  8 29  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0029831

> <DATABASE_NAME>
NP-MRD

> <SMILES>
[H]OC(=O)C1=C([H])C([H])([H])C([H])([H])[C@@]([H])(C([H])([H])[H])[C@]1(C([H])([H])[H])C([H])([H])C(\[H])=C(\C([H])=C([H])[H])C([H])([H])[H]

> <INCHI_IDENTIFIER>
InChI=1S/C15H22O2/c1-5-11(2)9-10-15(4)12(3)7-6-8-13(15)14(16)17/h5,8-9,12H,1,6-7,10H2,2-4H3,(H,16,17)/b11-9+/t12-,15+/m1/s1

> <INCHI_KEY>
NHASXRPHDCXJBS-QSKJXDJHSA-N

> <FORMULA>
C15H22O2

> <MOLECULAR_WEIGHT>
234.339

> <EXACT_MASS>
234.161979948

> <JCHEM_ACCEPTOR_COUNT>
2

> <JCHEM_ATOM_COUNT>
39

> <JCHEM_AVERAGE_POLARIZABILITY>
27.174443432012907

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(5R,6S)-5,6-dimethyl-6-[(2E)-3-methylpenta-2,4-dien-1-yl]cyclohex-1-ene-1-carboxylic acid

> <ALOGPS_LOGP>
4.47

> <JCHEM_LOGP>
3.970355805333334

> <ALOGPS_LOGS>
-3.90

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
1

> <JCHEM_PHYSIOLOGICAL_CHARGE>
-1

> <JCHEM_PKA_STRONGEST_ACIDIC>
5.126042776772249

> <JCHEM_POLAR_SURFACE_AREA>
37.3

> <JCHEM_REFRACTIVITY>
72.1408

> <JCHEM_ROTATABLE_BOND_COUNT>
4

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
2.94e-02 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(5R,6S)-5,6-dimethyl-6-[(2E)-3-methylpenta-2,4-dien-1-yl]cyclohex-1-ene-1-carboxylic acid

> <JCHEM_VEBER_RULE>
1

$$$$

     RDKit          3D

 39 39  0  0  0  0  0  0  0  0999 V2000
    4.8240    1.5804   -0.7136 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7602    0.9866   -0.1567 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5265    0.5895   -0.8347 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4397    0.8400   -2.3191 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5482    0.0220   -0.0970 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1872   -0.4627   -0.5450 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0472    0.2047    0.1681 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.3264   -0.3182   -0.5365 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0251    1.7398    0.0322 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7058    2.3409   -1.2912 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8447    1.8080   -2.3775 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2021    3.5853   -1.2050 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3088    2.5741    1.0536 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7000    2.1342    2.4274 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0619    0.6567    2.5045 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0678   -0.1997    1.7017 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.3528   -1.6822    1.9794 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6878    1.8321   -0.1056 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.8773    1.8349   -1.7658 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.8147    0.7819    0.9125 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.4677    1.9152   -2.5280 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2756    0.3593   -2.8399 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5321    0.4474   -2.7798 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7419   -0.1392    0.9624 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0734   -0.3710   -1.6278 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1642   -1.5457   -0.3742 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2382    0.0781   -0.0778 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3553   -0.0387   -1.5950 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3826   -1.4115   -0.5095 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0188    3.8211   -2.1368 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2726    3.6530    0.9117 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8675    2.3486    3.1082 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5540    2.7289    2.7714 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0667    0.3507    3.5581 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0838    0.5042    2.1372 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0781    0.0071    2.1289 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6549   -2.3398    1.4555 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2455   -1.8928    3.0498 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3729   -1.9619    1.6984 H   0  0  0  0  0  0  0  0  0  0  0  0
 15 16  1  0
  5  3  2  0
 14 13  1  0
  3  2  1  0
 13  9  2  0
  2  1  2  0
  9  7  1  0
  3  4  1  0
  7 16  1  0
  9 10  1  0
 10 11  2  0
  7  6  1  6
 10 12  1  0
 15 14  1  0
 16 17  1  0
  6  5  1  0
  7  8  1  0
 15 34  1  0
 15 35  1  0
 14 32  1  0
 14 33  1  0
 13 31  1  0
 16 36  1  1
  6 25  1  0
  6 26  1  0
  5 24  1  0
  2 20  1  0
  1 18  1  0
  1 19  1  0
  4 21  1  0
  4 22  1  0
  4 23  1  0
 12 30  1  0
 17 37  1  0
 17 38  1  0
 17 39  1  0
  8 27  1  0
  8 28  1  0
  8 29  1  0
M  END

HEADER    PROTEIN                                 19-JUN-21   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   19-JUN-21         0                                  
HETATM    1  C   UNK     0       4.824   1.580  -0.714  0.00  0.00           C+0
HETATM    2  C   UNK     0       3.760   0.987  -0.157  0.00  0.00           C+0
HETATM    3  C   UNK     0       2.527   0.590  -0.835  0.00  0.00           C+0
HETATM    4  C   UNK     0       2.440   0.840  -2.319  0.00  0.00           C+0
HETATM    5  C   UNK     0       1.548   0.022  -0.097  0.00  0.00           C+0
HETATM    6  C   UNK     0       0.187  -0.463  -0.545  0.00  0.00           C+0
HETATM    7  C   UNK     0      -1.047   0.205   0.168  0.00  0.00           C+0
HETATM    8  C   UNK     0      -2.326  -0.318  -0.537  0.00  0.00           C+0
HETATM    9  C   UNK     0      -1.025   1.740   0.032  0.00  0.00           C+0
HETATM   10  C   UNK     0      -0.706   2.341  -1.291  0.00  0.00           C+0
HETATM   11  O   UNK     0      -0.845   1.808  -2.377  0.00  0.00           O+0
HETATM   12  O   UNK     0      -0.202   3.585  -1.205  0.00  0.00           O+0
HETATM   13  C   UNK     0      -1.309   2.574   1.054  0.00  0.00           C+0
HETATM   14  C   UNK     0      -1.700   2.134   2.427  0.00  0.00           C+0
HETATM   15  C   UNK     0      -2.062   0.657   2.505  0.00  0.00           C+0
HETATM   16  C   UNK     0      -1.068  -0.200   1.702  0.00  0.00           C+0
HETATM   17  C   UNK     0      -1.353  -1.682   1.979  0.00  0.00           C+0
HETATM   18  H   UNK     0       5.688   1.832  -0.106  0.00  0.00           H+0
HETATM   19  H   UNK     0       4.877   1.835  -1.766  0.00  0.00           H+0
HETATM   20  H   UNK     0       3.815   0.782   0.913  0.00  0.00           H+0
HETATM   21  H   UNK     0       2.468   1.915  -2.528  0.00  0.00           H+0
HETATM   22  H   UNK     0       3.276   0.359  -2.840  0.00  0.00           H+0
HETATM   23  H   UNK     0       1.532   0.447  -2.780  0.00  0.00           H+0
HETATM   24  H   UNK     0       1.742  -0.139   0.962  0.00  0.00           H+0
HETATM   25  H   UNK     0       0.073  -0.371  -1.628  0.00  0.00           H+0
HETATM   26  H   UNK     0       0.164  -1.546  -0.374  0.00  0.00           H+0
HETATM   27  H   UNK     0      -3.238   0.078  -0.078  0.00  0.00           H+0
HETATM   28  H   UNK     0      -2.355  -0.039  -1.595  0.00  0.00           H+0
HETATM   29  H   UNK     0      -2.383  -1.412  -0.509  0.00  0.00           H+0
HETATM   30  H   UNK     0      -0.019   3.821  -2.137  0.00  0.00           H+0
HETATM   31  H   UNK     0      -1.273   3.653   0.912  0.00  0.00           H+0
HETATM   32  H   UNK     0      -0.868   2.349   3.108  0.00  0.00           H+0
HETATM   33  H   UNK     0      -2.554   2.729   2.771  0.00  0.00           H+0
HETATM   34  H   UNK     0      -2.067   0.351   3.558  0.00  0.00           H+0
HETATM   35  H   UNK     0      -3.084   0.504   2.137  0.00  0.00           H+0
HETATM   36  H   UNK     0      -0.078   0.007   2.129  0.00  0.00           H+0
HETATM   37  H   UNK     0      -0.655  -2.340   1.456  0.00  0.00           H+0
HETATM   38  H   UNK     0      -1.246  -1.893   3.050  0.00  0.00           H+0
HETATM   39  H   UNK     0      -2.373  -1.962   1.698  0.00  0.00           H+0
CONECT    1    2   18   19                                                  
CONECT    2    3    1   20                                                  
CONECT    3    5    2    4                                                  
CONECT    4    3   21   22   23                                             
CONECT    5    3    6   24                                                  
CONECT    6    7    5   25   26                                             
CONECT    7    9   16    6    8                                             
CONECT    8    7   27   28   29                                             
CONECT    9   13    7   10                                                  
CONECT   10    9   11   12                                                  
CONECT   11   10                                                            
CONECT   12   10   30                                                       
CONECT   13   14    9   31                                                  
CONECT   14   13   15   32   33                                             
CONECT   15   16   14   34   35                                             
CONECT   16   15    7   17   36                                             
CONECT   17   16   37   38   39                                             
CONECT   18    1                                                            
CONECT   19    1                                                            
CONECT   20    2                                                            
CONECT   21    4                                                            
CONECT   22    4                                                            
CONECT   23    4                                                            
CONECT   24    5                                                            
CONECT   25    6                                                            
CONECT   26    6                                                            
CONECT   27    8                                                            
CONECT   28    8                                                            
CONECT   29    8                                                            
CONECT   30   12                                                            
CONECT   31   13                                                            
CONECT   32   14                                                            
CONECT   33   14                                                            
CONECT   34   15                                                            
CONECT   35   15                                                            
CONECT   36   16                                                            
CONECT   37   17                                                            
CONECT   38   17                                                            
CONECT   39   17                                                            
MASTER        0    0    0    0    0    0    0    0   39    0   78    0
END

RDKit          3D

39 39  0  0  0  0  0  0  0  0999 V2000
    4.8240    1.5804   -0.7136 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7602    0.9866   -0.1567 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5265    0.5895   -0.8347 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4397    0.8400   -2.3191 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5482    0.0220   -0.0970 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1872   -0.4627   -0.5450 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0472    0.2047    0.1681 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.3264   -0.3182   -0.5365 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0251    1.7398    0.0322 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7058    2.3409   -1.2912 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8447    1.8080   -2.3775 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2021    3.5853   -1.2050 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3088    2.5741    1.0536 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7000    2.1342    2.4274 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0619    0.6567    2.5045 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0678   -0.1997    1.7017 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.3528   -1.6822    1.9794 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6878    1.8321   -0.1056 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.8773    1.8349   -1.7658 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.8147    0.7819    0.9125 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.4677    1.9152   -2.5280 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2756    0.3593   -2.8399 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5321    0.4474   -2.7798 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7419   -0.1392    0.9624 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0734   -0.3710   -1.6278 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1642   -1.5457   -0.3742 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2382    0.0781   -0.0778 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3553   -0.0387   -1.5950 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3826   -1.4115   -0.5095 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0188    3.8211   -2.1368 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2726    3.6530    0.9117 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8675    2.3486    3.1082 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5540    2.7289    2.7714 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0667    0.3507    3.5581 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0838    0.5042    2.1372 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0781    0.0071    2.1289 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6549   -2.3398    1.4555 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2455   -1.8928    3.0498 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3729   -1.9619    1.6984 H   0  0  0  0  0  0  0  0  0  0  0  0
 15 16  1  0
  5  3  2  0
 14 13  1  0
  3  2  1  0
 13  9  2  0
  2  1  2  0
  9  7  1  0
  3  4  1  0
  7 16  1  0
  9 10  1  0
 10 11  2  0
  7  6  1  6
 10 12  1  0
 15 14  1  0
 16 17  1  0
  6  5  1  0
  7  8  1  0
 15 34  1  0
 15 35  1  0
 14 32  1  0
 14 33  1  0
 13 31  1  0
 16 36  1  1
  6 25  1  0
  6 26  1  0
  5 24  1  0
  2 20  1  0
  1 18  1  0
  1 19  1  0
  4 21  1  0
  4 22  1  0
  4 23  1  0
 12 30  1  0
 17 37  1  0
 17 38  1  0
 17 39  1  0
  8 27  1  0
  8 28  1  0
  8 29  1  0
M  END

View in JSmol

Synonyms

Value	Source
Striatenate	Generator

Chemical Formula

C₁₅H₂₂O₂

Average Mass

234.3390 Da

Monoisotopic Mass

234.16198 Da

IUPAC Name

(5R,6S)-5,6-dimethyl-6-[(2E)-3-methylpenta-2,4-dien-1-yl]cyclohex-1-ene-1-carboxylic acid

Traditional Name

(5R,6S)-5,6-dimethyl-6-[(2E)-3-methylpenta-2,4-dien-1-yl]cyclohex-1-ene-1-carboxylic acid

CAS Registry Number

Not Available

SMILES

[H]OC(=O)C1=C([H])C([H])([H])C([H])([H])[C@@]([H])(C([H])([H])[H])[C@]1(C([H])([H])[H])C([H])([H])C(\[H])=C(\C([H])=C([H])[H])C([H])([H])[H]

InChI Identifier

InChI=1S/C15H22O2/c1-5-11(2)9-10-15(4)12(3)7-6-8-13(15)14(16)17/h5,8-9,12H,1,6-7,10H2,2-4H3,(H,16,17)/b11-9+/t12-,15+/m1/s1

InChI Key

NHASXRPHDCXJBS-QSKJXDJHSA-N

Experimental Spectra

Spectrum Type	Description	Depositor Email	Depositor Organization	Depositor	Deposition Date	View
1D NMR	¹³C NMR Spectrum (1D, 400 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 100 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 100 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 200 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 200 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 300 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 300 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 500 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 500 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 600 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 600 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 700 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 700 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 800 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 800 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 900 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 900 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 1000 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 1000 MHz, CDCl₃, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum

Predicted Spectra

Not Available

Chemical Shift Submissions

Not Available

Species

Species of Origin

Species Name	Source	Reference
Cheilolejeunea serpentina	JEOL database	Tori, M., et al, Tetrahedron 56, 1655 (2000)

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as monocyclic monoterpenoids. These are monoterpenoids containing 1 ring in the isoprene chain.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Prenol lipids

Sub Class

Monoterpenoids

Direct Parent

Monocyclic monoterpenoids

Alternative Parents

Substituents

Monocyclic monoterpenoid
Monocarboxylic acid or derivatives
Carboxylic acid
Carboxylic acid derivative
Organic oxygen compound
Organic oxide
Hydrocarbon derivative
Organooxygen compound
Carbonyl group
Aliphatic homomonocyclic compound

Molecular Framework

Aliphatic homomonocyclic 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	4.47	ALOGPS
logP	3.97	ChemAxon
logS	-3.9	ALOGPS
pKa (Strongest Acidic)	5.13	ChemAxon
Physiological Charge	-1	ChemAxon
Hydrogen Acceptor Count	2	ChemAxon
Hydrogen Donor Count	1	ChemAxon
Polar Surface Area	37.3 Å²	ChemAxon
Rotatable Bond Count	4	ChemAxon
Refractivity	72.14 m³·mol⁻¹	ChemAxon
Polarizability	27.17 Å³	ChemAxon
Number of Rings	1	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	Yes	ChemAxon
Ghose Filter	Yes	ChemAxon
Veber's Rule	Yes	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

10245468

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

21608099

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Tori, M., et al. (2000). Tori, M., et al, Tetrahedron 56, 1655 (2000). Tetrahedron.

Showing NP-Card for striatenic acid (NP0029831)

MOL for NP0029831 (striatenic acid)

3D MOL for NP0029831 (striatenic acid)

3D SDF for NP0029831 (striatenic acid)

3D-SDF for NP0029831 (striatenic acid)

PDB for NP0029831 (striatenic acid)

3D PDB for NP0029831 (striatenic acid)

SMILES for NP0029831 (striatenic acid)

INCHI for NP0029831 (striatenic acid)

Structure for NP0029831 (striatenic acid)

3D Structure for NP0029831 (striatenic acid)