NP-MRD: Showing NP-Card for cis-p-menth-2-ene-1alpha,7,8-triol (NP0025699)

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Record Information

Version

1.0

Created at

2021-06-19 17:45:22 UTC

Updated at

2021-06-29 23:50:48 UTC

NP-MRD ID

NP0025699

Secondary Accession Numbers

None

Natural Product Identification

Common Name

cis-p-menth-2-ene-1alpha,7,8-triol

Provided By

JEOL Database JEOL Logo

Description

cis-p-menth-2-ene-1alpha,7,8-triol is found in Glehnia littoralis and Glehnia littoralis fruit. It was first documented in 2013 (PMID: 24077171). Based on a literature review very few articles have been published on (1R,4R)-p-Mentha-2-ene-1beta,7,8-triol (PMID: 26797293).

Structure

MOL 3D MOL SDF 3D SDF PDB SMILES InChI


  Mrv1652306192119453D          

 31 31  0  0  0  0            999 V2000
   -0.9827   -0.3510    2.5781 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4701    0.1448    1.2190 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.6155    0.8983    0.5213 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5659    1.0931    1.4956 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0768   -1.0328    0.3358 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.5569   -0.5544   -1.0228 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8451   -0.5305   -1.3996 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9955   -0.9701   -0.5287 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.4990   -2.1797   -1.1202 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.1571    0.0498   -0.5435 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.7285    0.1412   -1.8537 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.5715   -1.2622    0.9220 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.1789   -1.8934    1.0004 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.7173   -1.1544    2.4630 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4549    0.4660    3.1372 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1661   -0.7015    3.2171 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2736    1.4083   -0.3855 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0121    1.6888    1.1695 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4373    0.2244    0.2583 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8489    1.4740    0.6452 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7684   -1.7113    0.1505 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2008   -0.2298   -1.7338 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0982   -0.1887   -2.4024 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7378   -2.7755   -1.2338 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.9614   -0.2732    0.1267 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.8279    1.0481   -0.2373 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.8010   -0.7887   -2.1505 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2894   -1.9505    1.3861 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.5863   -0.3442    1.5195 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9369   -2.1248    2.0414 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2116   -2.8669    0.4913 H   0  0  0  0  0  0  0  0  0  0  0  0
  5  2  1  0  0  0  0
 12 13  1  0  0  0  0
  2  1  1  0  0  0  0
 12  8  1  0  0  0  0
  2  3  1  0  0  0  0
 13  5  1  0  0  0  0
  2  4  1  1  0  0  0
  5  6  1  0  0  0  0
  8 10  1  0  0  0  0
  6  7  2  0  0  0  0
  8  9  1  6  0  0  0
  7  8  1  0  0  0  0
 10 11  1  0  0  0  0
 12 28  1  0  0  0  0
 12 29  1  0  0  0  0
 13 30  1  0  0  0  0
 13 31  1  0  0  0  0
  5 21  1  6  0  0  0
  6 22  1  0  0  0  0
  7 23  1  0  0  0  0
  1 14  1  0  0  0  0
  1 15  1  0  0  0  0
  1 16  1  0  0  0  0
  3 17  1  0  0  0  0
  3 18  1  0  0  0  0
  3 19  1  0  0  0  0
  4 20  1  0  0  0  0
 10 25  1  0  0  0  0
 10 26  1  0  0  0  0
  9 24  1  0  0  0  0
 11 27  1  0  0  0  0
M  END

     RDKit          3D

 31 31  0  0  0  0  0  0  0  0999 V2000
   -0.9827   -0.3510    2.5781 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4701    0.1448    1.2190 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.6155    0.8983    0.5213 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5659    1.0931    1.4956 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0768   -1.0328    0.3358 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.5569   -0.5544   -1.0228 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8451   -0.5305   -1.3996 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9955   -0.9701   -0.5287 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.4990   -2.1797   -1.1202 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.1571    0.0498   -0.5435 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7285    0.1412   -1.8537 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.5715   -1.2622    0.9220 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1789   -1.8934    1.0004 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7173   -1.1544    2.4630 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4549    0.4660    3.1372 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1661   -0.7015    3.2171 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2736    1.4083   -0.3855 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0121    1.6888    1.1695 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4373    0.2244    0.2583 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8489    1.4740    0.6452 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7684   -1.7113    0.1505 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2008   -0.2298   -1.7338 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0982   -0.1887   -2.4024 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7378   -2.7755   -1.2338 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.9614   -0.2732    0.1267 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.8279    1.0481   -0.2373 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.8010   -0.7887   -2.1505 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2894   -1.9505    1.3861 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.5863   -0.3442    1.5195 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9369   -2.1248    2.0414 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2116   -2.8669    0.4913 H   0  0  0  0  0  0  0  0  0  0  0  0
  5  2  1  0
 12 13  1  0
  2  1  1  0
 12  8  1  0
  2  3  1  0
 13  5  1  0
  2  4  1  1
  5  6  1  0
  8 10  1  0
  6  7  2  0
  8  9  1  6
  7  8  1  0
 10 11  1  0
 12 28  1  0
 12 29  1  0
 13 30  1  0
 13 31  1  0
  5 21  1  6
  6 22  1  0
  7 23  1  0
  1 14  1  0
  1 15  1  0
  1 16  1  0
  3 17  1  0
  3 18  1  0
  3 19  1  0
  4 20  1  0
 10 25  1  0
 10 26  1  0
  9 24  1  0
 11 27  1  0
M  END


  Mrv1652306192119453D          

 31 31  0  0  0  0            999 V2000
   -0.9827   -0.3510    2.5781 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4701    0.1448    1.2190 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.6155    0.8983    0.5213 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5659    1.0931    1.4956 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0768   -1.0328    0.3358 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.5569   -0.5544   -1.0228 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8451   -0.5305   -1.3996 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9955   -0.9701   -0.5287 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.4990   -2.1797   -1.1202 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.1571    0.0498   -0.5435 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.7285    0.1412   -1.8537 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.5715   -1.2622    0.9220 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.1789   -1.8934    1.0004 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.7173   -1.1544    2.4630 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4549    0.4660    3.1372 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1661   -0.7015    3.2171 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2736    1.4083   -0.3855 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0121    1.6888    1.1695 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4373    0.2244    0.2583 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8489    1.4740    0.6452 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7684   -1.7113    0.1505 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2008   -0.2298   -1.7338 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0982   -0.1887   -2.4024 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7378   -2.7755   -1.2338 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.9614   -0.2732    0.1267 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.8279    1.0481   -0.2373 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.8010   -0.7887   -2.1505 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2894   -1.9505    1.3861 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.5863   -0.3442    1.5195 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9369   -2.1248    2.0414 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2116   -2.8669    0.4913 H   0  0  0  0  0  0  0  0  0  0  0  0
  5  2  1  0  0  0  0
 12 13  1  0  0  0  0
  2  1  1  0  0  0  0
 12  8  1  0  0  0  0
  2  3  1  0  0  0  0
 13  5  1  0  0  0  0
  2  4  1  1  0  0  0
  5  6  1  0  0  0  0
  8 10  1  0  0  0  0
  6  7  2  0  0  0  0
  8  9  1  6  0  0  0
  7  8  1  0  0  0  0
 10 11  1  0  0  0  0
 12 28  1  0  0  0  0
 12 29  1  0  0  0  0
 13 30  1  0  0  0  0
 13 31  1  0  0  0  0
  5 21  1  6  0  0  0
  6 22  1  0  0  0  0
  7 23  1  0  0  0  0
  1 14  1  0  0  0  0
  1 15  1  0  0  0  0
  1 16  1  0  0  0  0
  3 17  1  0  0  0  0
  3 18  1  0  0  0  0
  3 19  1  0  0  0  0
  4 20  1  0  0  0  0
 10 25  1  0  0  0  0
 10 26  1  0  0  0  0
  9 24  1  0  0  0  0
 11 27  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0025699

> <DATABASE_NAME>
NP-MRD

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

> <INCHI_IDENTIFIER>
InChI=1S/C10H18O3/c1-9(2,12)8-3-5-10(13,7-11)6-4-8/h3,5,8,11-13H,4,6-7H2,1-2H3/t8-,10-/m0/s1

> <INCHI_KEY>
QDURJIJAJVINHQ-WPRPVWTQSA-N

> <FORMULA>
C10H18O3

> <MOLECULAR_WEIGHT>
186.251

> <EXACT_MASS>
186.12559444

> <JCHEM_ACCEPTOR_COUNT>
3

> <JCHEM_ATOM_COUNT>
31

> <JCHEM_AVERAGE_POLARIZABILITY>
20.24084736535299

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
3

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(1R,4R)-1-(hydroxymethyl)-4-(2-hydroxypropan-2-yl)cyclohex-2-en-1-ol

> <ALOGPS_LOGP>
0.19

> <JCHEM_LOGP>
-0.0662081293333334

> <ALOGPS_LOGS>
-0.99

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
1

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
15.257029653388908

> <JCHEM_PKA_STRONGEST_ACIDIC>
13.571168540555984

> <JCHEM_PKA_STRONGEST_BASIC>
-0.9485159171022802

> <JCHEM_POLAR_SURFACE_AREA>
60.69

> <JCHEM_REFRACTIVITY>
51.8773

> <JCHEM_ROTATABLE_BOND_COUNT>
2

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
1.90e+01 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(1R,4R)-1-(hydroxymethyl)-4-(2-hydroxypropan-2-yl)cyclohex-2-en-1-ol

> <JCHEM_VEBER_RULE>
0

$$$$

     RDKit          3D

 31 31  0  0  0  0  0  0  0  0999 V2000
   -0.9827   -0.3510    2.5781 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4701    0.1448    1.2190 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.6155    0.8983    0.5213 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5659    1.0931    1.4956 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0768   -1.0328    0.3358 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.5569   -0.5544   -1.0228 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8451   -0.5305   -1.3996 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9955   -0.9701   -0.5287 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.4990   -2.1797   -1.1202 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.1571    0.0498   -0.5435 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7285    0.1412   -1.8537 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.5715   -1.2622    0.9220 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1789   -1.8934    1.0004 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7173   -1.1544    2.4630 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4549    0.4660    3.1372 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1661   -0.7015    3.2171 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2736    1.4083   -0.3855 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0121    1.6888    1.1695 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4373    0.2244    0.2583 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8489    1.4740    0.6452 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7684   -1.7113    0.1505 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2008   -0.2298   -1.7338 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0982   -0.1887   -2.4024 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7378   -2.7755   -1.2338 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.9614   -0.2732    0.1267 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.8279    1.0481   -0.2373 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.8010   -0.7887   -2.1505 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2894   -1.9505    1.3861 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.5863   -0.3442    1.5195 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9369   -2.1248    2.0414 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2116   -2.8669    0.4913 H   0  0  0  0  0  0  0  0  0  0  0  0
  5  2  1  0
 12 13  1  0
  2  1  1  0
 12  8  1  0
  2  3  1  0
 13  5  1  0
  2  4  1  1
  5  6  1  0
  8 10  1  0
  6  7  2  0
  8  9  1  6
  7  8  1  0
 10 11  1  0
 12 28  1  0
 12 29  1  0
 13 30  1  0
 13 31  1  0
  5 21  1  6
  6 22  1  0
  7 23  1  0
  1 14  1  0
  1 15  1  0
  1 16  1  0
  3 17  1  0
  3 18  1  0
  3 19  1  0
  4 20  1  0
 10 25  1  0
 10 26  1  0
  9 24  1  0
 11 27  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      -0.983  -0.351   2.578  0.00  0.00           C+0
HETATM    2  C   UNK     0      -0.470   0.145   1.219  0.00  0.00           C+0
HETATM    3  C   UNK     0      -1.615   0.898   0.521  0.00  0.00           C+0
HETATM    4  O   UNK     0       0.566   1.093   1.496  0.00  0.00           O+0
HETATM    5  C   UNK     0       0.077  -1.033   0.336  0.00  0.00           C+0
HETATM    6  C   UNK     0       0.557  -0.554  -1.023  0.00  0.00           C+0
HETATM    7  C   UNK     0       1.845  -0.531  -1.400  0.00  0.00           C+0
HETATM    8  C   UNK     0       2.995  -0.970  -0.529  0.00  0.00           C+0
HETATM    9  O   UNK     0       3.499  -2.180  -1.120  0.00  0.00           O+0
HETATM   10  C   UNK     0       4.157   0.050  -0.544  0.00  0.00           C+0
HETATM   11  O   UNK     0       4.729   0.141  -1.854  0.00  0.00           O+0
HETATM   12  C   UNK     0       2.571  -1.262   0.922  0.00  0.00           C+0
HETATM   13  C   UNK     0       1.179  -1.893   1.000  0.00  0.00           C+0
HETATM   14  H   UNK     0      -1.717  -1.154   2.463  0.00  0.00           H+0
HETATM   15  H   UNK     0      -1.455   0.466   3.137  0.00  0.00           H+0
HETATM   16  H   UNK     0      -0.166  -0.702   3.217  0.00  0.00           H+0
HETATM   17  H   UNK     0      -1.274   1.408  -0.386  0.00  0.00           H+0
HETATM   18  H   UNK     0      -2.012   1.689   1.169  0.00  0.00           H+0
HETATM   19  H   UNK     0      -2.437   0.224   0.258  0.00  0.00           H+0
HETATM   20  H   UNK     0       0.849   1.474   0.645  0.00  0.00           H+0
HETATM   21  H   UNK     0      -0.768  -1.711   0.151  0.00  0.00           H+0
HETATM   22  H   UNK     0      -0.201  -0.230  -1.734  0.00  0.00           H+0
HETATM   23  H   UNK     0       2.098  -0.189  -2.402  0.00  0.00           H+0
HETATM   24  H   UNK     0       2.738  -2.776  -1.234  0.00  0.00           H+0
HETATM   25  H   UNK     0       4.961  -0.273   0.127  0.00  0.00           H+0
HETATM   26  H   UNK     0       3.828   1.048  -0.237  0.00  0.00           H+0
HETATM   27  H   UNK     0       4.801  -0.789  -2.151  0.00  0.00           H+0
HETATM   28  H   UNK     0       3.289  -1.950   1.386  0.00  0.00           H+0
HETATM   29  H   UNK     0       2.586  -0.344   1.520  0.00  0.00           H+0
HETATM   30  H   UNK     0       0.937  -2.125   2.041  0.00  0.00           H+0
HETATM   31  H   UNK     0       1.212  -2.867   0.491  0.00  0.00           H+0
CONECT    1    2   14   15   16                                             
CONECT    2    5    1    3    4                                             
CONECT    3    2   17   18   19                                             
CONECT    4    2   20                                                       
CONECT    5    2   13    6   21                                             
CONECT    6    5    7   22                                                  
CONECT    7    6    8   23                                                  
CONECT    8   12   10    9    7                                             
CONECT    9    8   24                                                       
CONECT   10    8   11   25   26                                             
CONECT   11   10   27                                                       
CONECT   12   13    8   28   29                                             
CONECT   13   12    5   30   31                                             
CONECT   14    1                                                            
CONECT   15    1                                                            
CONECT   16    1                                                            
CONECT   17    3                                                            
CONECT   18    3                                                            
CONECT   19    3                                                            
CONECT   20    4                                                            
CONECT   21    5                                                            
CONECT   22    6                                                            
CONECT   23    7                                                            
CONECT   24    9                                                            
CONECT   25   10                                                            
CONECT   26   10                                                            
CONECT   27   11                                                            
CONECT   28   12                                                            
CONECT   29   12                                                            
CONECT   30   13                                                            
CONECT   31   13                                                            
MASTER        0    0    0    0    0    0    0    0   31    0   62    0
END

RDKit          3D

31 31  0  0  0  0  0  0  0  0999 V2000
   -0.9827   -0.3510    2.5781 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4701    0.1448    1.2190 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.6155    0.8983    0.5213 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5659    1.0931    1.4956 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0768   -1.0328    0.3358 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.5569   -0.5544   -1.0228 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8451   -0.5305   -1.3996 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9955   -0.9701   -0.5287 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.4990   -2.1797   -1.1202 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.1571    0.0498   -0.5435 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7285    0.1412   -1.8537 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.5715   -1.2622    0.9220 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1789   -1.8934    1.0004 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7173   -1.1544    2.4630 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4549    0.4660    3.1372 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1661   -0.7015    3.2171 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2736    1.4083   -0.3855 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0121    1.6888    1.1695 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4373    0.2244    0.2583 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8489    1.4740    0.6452 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7684   -1.7113    0.1505 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2008   -0.2298   -1.7338 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0982   -0.1887   -2.4024 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7378   -2.7755   -1.2338 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.9614   -0.2732    0.1267 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.8279    1.0481   -0.2373 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.8010   -0.7887   -2.1505 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2894   -1.9505    1.3861 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.5863   -0.3442    1.5195 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9369   -2.1248    2.0414 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2116   -2.8669    0.4913 H   0  0  0  0  0  0  0  0  0  0  0  0
  5  2  1  0
 12 13  1  0
  2  1  1  0
 12  8  1  0
  2  3  1  0
 13  5  1  0
  2  4  1  1
  5  6  1  0
  8 10  1  0
  6  7  2  0
  8  9  1  6
  7  8  1  0
 10 11  1  0
 12 28  1  0
 12 29  1  0
 13 30  1  0
 13 31  1  0
  5 21  1  6
  6 22  1  0
  7 23  1  0
  1 14  1  0
  1 15  1  0
  1 16  1  0
  3 17  1  0
  3 18  1  0
  3 19  1  0
  4 20  1  0
 10 25  1  0
 10 26  1  0
  9 24  1  0
 11 27  1  0
M  END

View in JSmol

Synonyms

Value	Source
(1R,4R)-p-Mentha-2-ene-1b,7,8-triol	Generator
(1R,4R)-p-Mentha-2-ene-1β,7,8-triol	Generator

Chemical Formula

C₁₀H₁₈O₃

Average Mass

186.2510 Da

Monoisotopic Mass

186.12559 Da

IUPAC Name

(1R,4R)-1-(hydroxymethyl)-4-(2-hydroxypropan-2-yl)cyclohex-2-en-1-ol

Traditional Name

(1R,4R)-1-(hydroxymethyl)-4-(2-hydroxypropan-2-yl)cyclohex-2-en-1-ol

CAS Registry Number

Not Available

SMILES

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

InChI Identifier

InChI=1S/C10H18O3/c1-9(2,12)8-3-5-10(13,7-11)6-4-8/h3,5,8,11-13H,4,6-7H2,1-2H3/t8-,10-/m0/s1

InChI Key

QDURJIJAJVINHQ-WPRPVWTQSA-N

Experimental Spectra

Spectrum Type	Description	Depositor Email	Depositor Organization	Depositor	Deposition Date	View
1D NMR	¹³C NMR Spectrum (1D, 500 MHz, C₅D₅N, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 500 MHz, C₅D₅N, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 100 MHz, C₅D₅N, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 100 MHz, C₅D₅N, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 200 MHz, C₅D₅N, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 200 MHz, C₅D₅N, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 300 MHz, C₅D₅N, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 300 MHz, C₅D₅N, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 400 MHz, C₅D₅N, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, C₅D₅N, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 600 MHz, C₅D₅N, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 600 MHz, C₅D₅N, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 700 MHz, C₅D₅N, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 700 MHz, C₅D₅N, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 800 MHz, C₅D₅N, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 800 MHz, C₅D₅N, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 900 MHz, C₅D₅N, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 900 MHz, C₅D₅N, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 1000 MHz, C₅D₅N, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 1000 MHz, C₅D₅N, 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
Glehnia littoralis	LOTUS Database	35616633
Glehnia littoralis fruit	JEOL database	Ishikawa, T., et al, Chem. Pharm. Bull. 49, 584 (2001)

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as menthane monoterpenoids. These are monoterpenoids with a structure based on the o-, m-, or p-menthane backbone. P-menthane consists of the cyclohexane ring with a methyl group and a (2-methyl)-propyl group at the 1 and 4 ring position, respectively. The o- and m- menthanes are much rarer, and presumably arise by alkyl migration of p-menthanes.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Prenol lipids

Sub Class

Monoterpenoids

Direct Parent

Menthane monoterpenoids

Alternative Parents

Substituents

P-menthane monoterpenoid
Monocyclic monoterpenoid
Tertiary alcohol
Organic oxygen compound
Hydrocarbon derivative
Primary alcohol
Organooxygen compound
Alcohol
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	0.19	ALOGPS
logP	-0.066	ChemAxon
logS	-0.99	ALOGPS
pKa (Strongest Acidic)	13.57	ChemAxon
pKa (Strongest Basic)	-0.95	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	3	ChemAxon
Hydrogen Donor Count	3	ChemAxon
Polar Surface Area	60.69 Å²	ChemAxon
Rotatable Bond Count	2	ChemAxon
Refractivity	51.88 m³·mol⁻¹	ChemAxon
Polarizability	20.24 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

HMDB ID

Not Available

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FoodDB ID

Not Available

KNApSAcK ID

Not Available

Chemspider ID

8925373

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

10750048

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Julio LF, Barrero AF, Herrador del Pino MM, Arteaga JF, Burillo J, Andres MF, Diaz CE, Gonzalez-Coloma A: Phytotoxic and Nematicidal Components of Lavandula luisieri. J Nat Prod. 2016 Feb 26;79(2):261-6. doi: 10.1021/acs.jnatprod.5b00501. Epub 2016 Jan 22. [PubMed:26797293 ]
Liu JF, Li HJ, Wang LX, Liu MQ, Bi YF, Zhang YB: Two new monoterpenes from the fruits of Illicium lanceolatum. Molecules. 2013 Sep 26;18(10):11866-72. doi: 10.3390/molecules181011866. [PubMed:24077171 ]
Ishikawa, T., et al. (2001). Ishikawa, T., et al, Chem. Pharm. Bull. 49, 584 (2001). Chem. Pharm. Bull..

Showing NP-Card for cis-p-menth-2-ene-1alpha,7,8-triol (NP0025699)

MOL for NP0025699 (cis-p-menth-2-ene-1alpha,7,8-triol)

3D MOL for NP0025699 (cis-p-menth-2-ene-1alpha,7,8-triol)

3D SDF for NP0025699 (cis-p-menth-2-ene-1alpha,7,8-triol)

3D-SDF for NP0025699 (cis-p-menth-2-ene-1alpha,7,8-triol)

PDB for NP0025699 (cis-p-menth-2-ene-1alpha,7,8-triol)

3D PDB for NP0025699 (cis-p-menth-2-ene-1alpha,7,8-triol)

SMILES for NP0025699 (cis-p-menth-2-ene-1alpha,7,8-triol)

INCHI for NP0025699 (cis-p-menth-2-ene-1alpha,7,8-triol)

Structure for NP0025699 (cis-p-menth-2-ene-1alpha,7,8-triol)

3D Structure for NP0025699 (cis-p-menth-2-ene-1alpha,7,8-triol)