NP-MRD: Showing NP-Card for (1s,2s,3s,4s)-4-bromo-2-[(3s)-3-hydroxy-3-methylpent-4-en-1-yl]-3-[(2e)-4-hydroxy-4-methylpent-2-en-1-yl]-1,3-dimethylcyclohexan-1-ol (NP0171246)

Jump To Section:

Identification Spectra BioTaxonomy ChemoTaxonomy Physical properties Links References XML

Record Information

Version

2.0

Created at

2022-09-03 07:41:06 UTC

Updated at

2022-09-03 07:41:07 UTC

NP-MRD ID

NP0171246

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(1s,2s,3s,4s)-4-bromo-2-[(3s)-3-hydroxy-3-methylpent-4-en-1-yl]-3-[(2e)-4-hydroxy-4-methylpent-2-en-1-yl]-1,3-dimethylcyclohexan-1-ol

Description

(1S,2S,3S,4S)-4-bromo-2-[(3S)-3-hydroxy-3-methylpent-4-en-1-yl]-3-[(2E)-4-hydroxy-4-methylpent-2-en-1-yl]-1,3-dimethylcyclohexan-1-ol belongs to the class of organic compounds known as sesquiterpenoids. These are terpenes with three consecutive isoprene units. (1s,2s,3s,4s)-4-bromo-2-[(3s)-3-hydroxy-3-methylpent-4-en-1-yl]-3-[(2e)-4-hydroxy-4-methylpent-2-en-1-yl]-1,3-dimethylcyclohexan-1-ol is found in Laurencia decumbens. Based on a literature review very few articles have been published on (1S,2S,3S,4S)-4-bromo-2-[(3S)-3-hydroxy-3-methylpent-4-en-1-yl]-3-[(2E)-4-hydroxy-4-methylpent-2-en-1-yl]-1,3-dimethylcyclohexan-1-ol.

Structure

MOL 3D MOL SDF PDB SMILES InChI

     RDKit          3D

 59 59  0  0  0  0  0  0  0  0999 V2000
   -3.4654    3.8932   -1.0606 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0350    2.6484   -1.1626 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6174    1.5971   -0.3211 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.5401    1.9573    1.1272 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9906    1.4889   -0.6421 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0076    0.2579   -0.6393 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5424    0.1938   -0.2759 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9194   -1.1258   -0.5877 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.6539   -2.3420   -0.2630 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.3746   -2.2546    1.0572 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6942   -2.4949   -1.2286 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9143   -3.6372   -0.2976 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5525   -3.5541   -0.1014 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0719   -2.3788   -0.9155 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.8970   -2.5369   -1.3509 Br  0  0  0  0  0  0  0  0  0  0  0  0
    0.5943   -1.1599   -0.2110 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.6848   -1.1904    1.2930 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2419    0.1025   -0.6591 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6516    0.2745   -0.2529 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0198    1.3256    0.5307 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4377    1.4970    0.9383 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8172    2.9589    0.9084 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3711    0.7621   -0.0298 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6331    0.9325    2.2025 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0402    4.6678   -1.6768 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2481    4.1594   -0.3617 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2530    2.3948   -1.8640 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5522    2.4305    1.3131 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7503    1.1232    1.8053 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2997    2.7416    1.3284 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1605    1.6711   -1.5801 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0593    0.1579   -1.7640 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5601   -0.5818   -0.2364 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3466    0.5682    0.7445 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0825    0.9941   -0.9515 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8003   -1.0968   -1.7301 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4489   -2.5573    0.9946 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2286   -1.3184    1.6056 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9434   -3.0665    1.7192 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2639   -3.2521   -1.0263 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3015   -4.3473    0.4955 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0853   -4.2005   -1.2490 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0729   -4.4572   -0.5498 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8509   -3.5533    0.9425 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4901   -2.4829   -1.9003 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0680   -1.9258    1.7851 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3251   -0.1804    1.6357 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7308   -1.2506    1.6492 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2166    0.2173   -1.7833 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7004    1.0185   -0.2924 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.4849   -0.3516   -0.5162 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2629    2.0139    0.8380 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.9022    3.5598    1.0923 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.5819    3.1572    1.6843 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.2366    3.1776   -0.0932 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.3975    1.1616    0.0424 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.0261    0.8988   -1.0749 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.4142   -0.3172    0.1911 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.4456    1.6112    2.9096 H   0  0  0  0  0  0  0  0  0  0  0  0
 22 21  1  0
 21 23  1  0
 21 24  1  0
 21 20  1  0
 20 19  2  0
 19 18  1  0
 16 18  1  6
 16 17  1  0
 16 14  1  0
 14 15  1  0
 14 13  1  0
 13 12  1  0
 12  9  1  0
  9 10  1  0
  9 11  1  6
  9  8  1  0
  8  7  1  0
  7  6  1  0
  6  3  1  0
  3  4  1  0
  3  5  1  6
  3  2  1  0
  2  1  2  3
  8 16  1  0
 22 53  1  0
 22 54  1  0
 22 55  1  0
 23 56  1  0
 23 57  1  0
 23 58  1  0
 24 59  1  0
 20 52  1  0
 19 51  1  0
 18 49  1  0
 18 50  1  0
 17 46  1  0
 17 47  1  0
 17 48  1  0
 14 45  1  6
 13 43  1  0
 13 44  1  0
 12 41  1  0
 12 42  1  0
 10 37  1  0
 10 38  1  0
 10 39  1  0
 11 40  1  0
  8 36  1  6
  7 34  1  0
  7 35  1  0
  6 32  1  0
  6 33  1  0
  4 28  1  0
  4 29  1  0
  4 30  1  0
  5 31  1  0
  2 27  1  0
  1 25  1  0
  1 26  1  0
M  END


  Mrv1652309032209412D          

 24 24  0  0  1  0            999 V2000
    5.0013    1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868    1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724    1.2375    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.1599    1.9520    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9849    0.5230    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434    1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289    0.8250    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.4289   -0.0000    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.2414    0.1433    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7111   -0.7752    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000   -0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000    0.8250    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.7145    1.2375    0.0000 Br  0  0  0  0  0  0  0  0  0  0  0  0
    0.7145    1.2375    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.3272    1.9659    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1018    1.9659    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6646    2.6656    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0519    3.3940    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6147    4.0936    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1775    4.7933    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3144    4.5308    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0849    3.6565    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  0  0  0  0
  2  3  1  0  0  0  0
  3  4  1  6  0  0  0
  3  5  1  6  0  0  0
  3  6  1  0  0  0  0
  6  7  1  0  0  0  0
  8  7  1  6  0  0  0
  8  9  1  0  0  0  0
  9 10  1  6  0  0  0
  9 11  1  1  0  0  0
  9 12  1  0  0  0  0
 12 13  1  0  0  0  0
 13 14  1  0  0  0  0
 14 15  1  6  0  0  0
 14 16  1  0  0  0  0
  8 16  1  0  0  0  0
 16 17  1  6  0  0  0
 16 18  1  1  0  0  0
 18 19  1  0  0  0  0
 19 20  2  0  0  0  0
 20 21  1  0  0  0  0
 21 22  1  0  0  0  0
 21 23  1  0  0  0  0
 21 24  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0171246

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC(C)(O)\C=C\C[C@]1(C)[C@@H](Br)CC[C@](C)(O)[C@H]1CC[C@](C)(O)C=C

> <INCHI_IDENTIFIER>
InChI=1S/C20H35BrO3/c1-7-18(4,23)13-9-15-19(5,12-8-11-17(2,3)22)16(21)10-14-20(15,6)24/h7-8,11,15-16,22-24H,1,9-10,12-14H2,2-6H3/b11-8+/t15-,16-,18+,19-,20-/m0/s1

> <INCHI_KEY>
FKRGJYXGAOPGOH-AYMKAHHASA-N

> <FORMULA>
C20H35BrO3

> <MOLECULAR_WEIGHT>
403.401

> <EXACT_MASS>
402.176958

> <JCHEM_ACCEPTOR_COUNT>
3

> <JCHEM_ATOM_COUNT>
59

> <JCHEM_AVERAGE_POLARIZABILITY>
41.76473865919925

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
3

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(1S,2S,3S,4S)-4-bromo-2-[(3S)-3-hydroxy-3-methylpent-4-en-1-yl]-3-[(2E)-4-hydroxy-4-methylpent-2-en-1-yl]-1,3-dimethylcyclohexan-1-ol

> <ALOGPS_LOGP>
4.36

> <JCHEM_LOGP>
3.734802375333332

> <ALOGPS_LOGS>
-5.13

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
1

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
17.781309930990773

> <JCHEM_PKA_STRONGEST_ACIDIC>
14.769179425176137

> <JCHEM_PKA_STRONGEST_BASIC>
-1.1655316927258585

> <JCHEM_POLAR_SURFACE_AREA>
60.69

> <JCHEM_REFRACTIVITY>
105.3121

> <JCHEM_ROTATABLE_BOND_COUNT>
7

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
3.02e-03 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(1S,2S,3S,4S)-4-bromo-2-[(3S)-3-hydroxy-3-methylpent-4-en-1-yl]-3-[(2E)-4-hydroxy-4-methylpent-2-en-1-yl]-1,3-dimethylcyclohexan-1-ol

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 03-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   03-SEP-22         0                                  
HETATM    1  C   UNK     0       9.336   2.310   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       8.002   3.080   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       6.668   2.310   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       5.898   3.644   0.000  0.00  0.00           C+0
HETATM    5  O   UNK     0       7.438   0.976   0.000  0.00  0.00           O+0
HETATM    6  C   UNK     0       5.335   1.540   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       4.001   2.310   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       2.667   1.540   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       2.667  -0.000   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       4.184   0.267   0.000  0.00  0.00           C+0
HETATM   11  O   UNK     0       3.194  -1.447   0.000  0.00  0.00           O+0
HETATM   12  C   UNK     0       1.334  -0.770   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       0.000  -0.000   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       0.000   1.540   0.000  0.00  0.00           C+0
HETATM   15 Br   UNK     0      -1.334   2.310   0.000  0.00  0.00          Br+0
HETATM   16  C   UNK     0       1.334   2.310   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       0.611   3.670   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       2.057   3.670   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       1.241   4.976   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       1.964   6.335   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       1.148   7.641   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       0.331   8.947   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       2.453   8.458   0.000  0.00  0.00           C+0
HETATM   24  O   UNK     0      -0.158   6.825   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4    5    6                                             
CONECT    4    3                                                            
CONECT    5    3                                                            
CONECT    6    3    7                                                       
CONECT    7    6    8                                                       
CONECT    8    7    9   16                                                  
CONECT    9    8   10   11   12                                             
CONECT   10    9                                                            
CONECT   11    9                                                            
CONECT   12    9   13                                                       
CONECT   13   12   14                                                       
CONECT   14   13   15   16                                                  
CONECT   15   14                                                            
CONECT   16   14    8   17   18                                             
CONECT   17   16                                                            
CONECT   18   16   19                                                       
CONECT   19   18   20                                                       
CONECT   20   19   21                                                       
CONECT   21   20   22   23   24                                             
CONECT   22   21                                                            
CONECT   23   21                                                            
CONECT   24   21                                                            
MASTER        0    0    0    0    0    0    0    0   24    0   48    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₀H₃₅BrO₃

Average Mass

403.4010 Da

Monoisotopic Mass

402.17696 Da

IUPAC Name

(1S,2S,3S,4S)-4-bromo-2-[(3S)-3-hydroxy-3-methylpent-4-en-1-yl]-3-[(2E)-4-hydroxy-4-methylpent-2-en-1-yl]-1,3-dimethylcyclohexan-1-ol

Traditional Name

(1S,2S,3S,4S)-4-bromo-2-[(3S)-3-hydroxy-3-methylpent-4-en-1-yl]-3-[(2E)-4-hydroxy-4-methylpent-2-en-1-yl]-1,3-dimethylcyclohexan-1-ol

CAS Registry Number

Not Available

SMILES

CC(C)(O)\C=C\C[C@]1(C)[C@@H](Br)CC[C@](C)(O)[C@H]1CC[C@](C)(O)C=C

InChI Identifier

InChI=1S/C20H35BrO3/c1-7-18(4,23)13-9-15-19(5,12-8-11-17(2,3)22)16(21)10-14-20(15,6)24/h7-8,11,15-16,22-24H,1,9-10,12-14H2,2-6H3/b11-8+/t15-,16-,18+,19-,20-/m0/s1

InChI Key

FKRGJYXGAOPGOH-AYMKAHHASA-N

Experimental Spectra

Not Available

Predicted Spectra

Spectrum Type	Description	Depositor ID	Depositor Organization	Depositor	Deposition Date	View
1D NMR	¹³C NMR Spectrum (1D, 25 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 100 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 252 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 1000 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 50 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 200 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 75 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 300 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 101 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 126 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 500 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 151 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 600 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 176 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 700 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 201 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 800 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 226 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 900 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum

Chemical Shift Submissions

Not Available

Species

Species of Origin

Species Name	Source	Reference
Laurencia decumbens	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as sesquiterpenoids. These are terpenes with three consecutive isoprene units.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Prenol lipids

Sub Class

Sesquiterpenoids

Direct Parent

Sesquiterpenoids

Alternative Parents

Substituents

Sesquiterpenoid
Megastigmane sesquiterpenoid
Cyclofarsesane sesquiterpenoid
Cyclohexanol
Cyclohexyl halide
Cyclic alcohol
Tertiary alcohol
Organooxygen compound
Organobromide
Organohalogen compound
Organic oxygen compound
Alcohol
Alkyl halide
Alkyl bromide
Hydrocarbon derivative
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	4.36	ALOGPS
logP	3.73	ChemAxon
logS	-5.1	ALOGPS
pKa (Strongest Acidic)	14.77	ChemAxon
pKa (Strongest Basic)	-1.2	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	7	ChemAxon
Refractivity	105.31 m³·mol⁻¹	ChemAxon
Polarizability	41.76 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

Not Available

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

162923467

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for (1s,2s,3s,4s)-4-bromo-2-[(3s)-3-hydroxy-3-methylpent-4-en-1-yl]-3-[(2e)-4-hydroxy-4-methylpent-2-en-1-yl]-1,3-dimethylcyclohexan-1-ol (NP0171246)

MOL for NP0171246 ((1s,2s,3s,4s)-4-bromo-2-[(3s)-3-hydroxy-3-methylpent-4-en-1-yl]-3-[(2e)-4-hydroxy-4-methylpent-2-en-1-yl]-1,3-dimethylcyclohexan-1-ol)

3D MOL for NP0171246 ((1s,2s,3s,4s)-4-bromo-2-[(3s)-3-hydroxy-3-methylpent-4-en-1-yl]-3-[(2e)-4-hydroxy-4-methylpent-2-en-1-yl]-1,3-dimethylcyclohexan-1-ol)

3D SDF for NP0171246 ((1s,2s,3s,4s)-4-bromo-2-[(3s)-3-hydroxy-3-methylpent-4-en-1-yl]-3-[(2e)-4-hydroxy-4-methylpent-2-en-1-yl]-1,3-dimethylcyclohexan-1-ol)

3D-SDF for NP0171246 ((1s,2s,3s,4s)-4-bromo-2-[(3s)-3-hydroxy-3-methylpent-4-en-1-yl]-3-[(2e)-4-hydroxy-4-methylpent-2-en-1-yl]-1,3-dimethylcyclohexan-1-ol)

PDB for NP0171246 ((1s,2s,3s,4s)-4-bromo-2-[(3s)-3-hydroxy-3-methylpent-4-en-1-yl]-3-[(2e)-4-hydroxy-4-methylpent-2-en-1-yl]-1,3-dimethylcyclohexan-1-ol)

3D PDB for NP0171246 ((1s,2s,3s,4s)-4-bromo-2-[(3s)-3-hydroxy-3-methylpent-4-en-1-yl]-3-[(2e)-4-hydroxy-4-methylpent-2-en-1-yl]-1,3-dimethylcyclohexan-1-ol)

SMILES for NP0171246 ((1s,2s,3s,4s)-4-bromo-2-[(3s)-3-hydroxy-3-methylpent-4-en-1-yl]-3-[(2e)-4-hydroxy-4-methylpent-2-en-1-yl]-1,3-dimethylcyclohexan-1-ol)

INCHI for NP0171246 ((1s,2s,3s,4s)-4-bromo-2-[(3s)-3-hydroxy-3-methylpent-4-en-1-yl]-3-[(2e)-4-hydroxy-4-methylpent-2-en-1-yl]-1,3-dimethylcyclohexan-1-ol)

Structure for NP0171246 ((1s,2s,3s,4s)-4-bromo-2-[(3s)-3-hydroxy-3-methylpent-4-en-1-yl]-3-[(2e)-4-hydroxy-4-methylpent-2-en-1-yl]-1,3-dimethylcyclohexan-1-ol)

3D Structure for NP0171246 ((1s,2s,3s,4s)-4-bromo-2-[(3s)-3-hydroxy-3-methylpent-4-en-1-yl]-3-[(2e)-4-hydroxy-4-methylpent-2-en-1-yl]-1,3-dimethylcyclohexan-1-ol)