NP-MRD: Showing NP-Card for 12-Methyl-5-dehydrohorminone (NP0078170)

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Record Information

Version

2.0

Created at

2022-04-28 23:17:46 UTC

Updated at

2022-04-28 23:17:46 UTC

NP-MRD ID

NP0078170

Secondary Accession Numbers

None

Natural Product Identification

Common Name

12-Methyl-5-dehydrohorminone

Description

12-Methyl-5-dehydrohorminone belongs to the class of organic compounds known as diterpenoids. These are terpene compounds formed by four isoprene units. 12-Methyl-5-dehydrohorminone is found in Salvia multicaulis, Salvia recognita and Salvia recognita Fisch.et Mey.. Based on a literature review very few articles have been published on 12-methyl-5-dehydrohorminone.

Structure

MOL 3D MOL SDF PDB SMILES InChI

     RDKit          3D

 53 55  0  0  0  0  0  0  0  0999 V2000
   -3.1220    3.2848   -0.3683 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4125    1.9505   -0.1001 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5032    0.9209   -0.0332 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9156   -0.2353    0.4402 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2674   -0.5430    0.9113 C   0  0  2  0  0  0  0  0  0  0  0  0
   -4.8520   -1.7232    0.1285 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2435    0.5706    0.8370 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9297   -1.3121    0.4999 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2498   -2.4644    0.9461 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5406   -1.1402    0.0605 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1286    0.0193   -0.4128 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1096    1.0940   -0.4739 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7739    2.2218   -0.9180 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.2712    0.1707   -0.8476 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.3628   -0.4665   -2.2403 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7107    1.6108   -0.9960 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2239    1.7109   -1.0558 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7172    1.2952    0.3142 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4977   -0.1641    0.5006 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.5020   -0.9996   -0.2823 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7347   -0.4967    1.9710 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1477   -0.5881    0.0516 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7230   -1.7621    0.5149 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4107   -2.3069    0.1484 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.1052   -3.1853    1.0927 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4362    3.7526    0.3534 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7441    3.3767   -1.4169 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1053    3.8393   -0.3709 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2024   -0.8759    1.9719 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6626   -2.6585    0.6707 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9181   -1.5500   -0.1189 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2678   -1.7795   -0.8163 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5006    0.9153   -0.1680 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.2118    0.1731    1.2669 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9698    1.3966    1.5446 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9877   -1.3921   -2.2126 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3847   -0.7275   -2.6437 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8613    0.2111   -2.9630 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3961    2.2592   -0.1636 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3107    2.0240   -1.9391 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.4723    2.7851   -1.1756 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.6673    1.1447   -1.8746 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.7482    1.5950    0.4962 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0820    1.8347    1.0519 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.1283   -2.0455   -0.2751 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.5235   -0.6936   -1.3567 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.5112   -0.9752    0.1776 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9155   -0.1627    2.6171 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.6437    0.0932    2.2678 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.0193   -1.5610    2.1112 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3447   -2.3647    1.1904 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4457   -2.8465   -0.8193 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4289   -3.2297    1.9057 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  2  0
  4  5  1  0
  5  6  1  0
  5  7  1  0
  4  8  1  0
  8  9  2  0
  8 10  1  0
 10 11  2  0
 11 12  1  0
 12 13  2  0
 11 14  1  0
 14 15  1  6
 14 16  1  0
 16 17  1  0
 17 18  1  0
 18 19  1  0
 19 20  1  6
 19 21  1  0
 19 22  1  0
 22 23  2  0
 23 24  1  0
 24 25  1  0
 12  3  1  0
 22 14  1  0
 24 10  1  0
  1 26  1  0
  1 27  1  0
  1 28  1  0
  5 29  1  1
  6 30  1  0
  6 31  1  0
  6 32  1  0
  7 33  1  0
  7 34  1  0
  7 35  1  0
 15 36  1  0
 15 37  1  0
 15 38  1  0
 16 39  1  0
 16 40  1  0
 17 41  1  0
 17 42  1  0
 18 43  1  0
 18 44  1  0
 20 45  1  0
 20 46  1  0
 20 47  1  0
 21 48  1  0
 21 49  1  0
 21 50  1  0
 23 51  1  0
 24 52  1  6
 25 53  1  0
M  END


  Mrv1652304292201172D          

 25 27  0  0  1  0            999 V2000
    2.7770   -0.3020    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3645   -1.0164    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.3645    0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7770    1.1270    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6020    1.1270    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0145    1.8414    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.0145    0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6020   -0.3020    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0145   -1.0164    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.6020   -1.7309    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8395    0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2520   -0.3020    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2520    1.1270    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3645    1.8414    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.5395    1.8414    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1270    1.1270    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5395    0.4125    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.1270   -0.3020    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3020   -0.3020    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1105    0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3020    1.1270    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3977    1.5642    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2732    1.9515    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9520   -0.3020    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7770    2.5559    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  0  0  0  0
  1  3  1  0  0  0  0
  3  4  2  0  0  0  0
  4  5  1  0  0  0  0
  5  6  2  0  0  0  0
  5  7  1  0  0  0  0
  7  8  2  0  0  0  0
  1  8  1  0  0  0  0
  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
  7 11  1  0  0  0  0
 11 12  1  0  0  0  0
 11 13  1  0  0  0  0
  4 14  1  0  0  0  0
 14 15  1  0  0  0  0
 15 16  2  0  0  0  0
 16 17  1  0  0  0  0
  3 17  1  0  0  0  0
 17 18  1  0  0  0  0
 18 19  1  0  0  0  0
 19 20  1  0  0  0  0
 20 21  1  0  0  0  0
 16 21  1  0  0  0  0
 21 22  1  0  0  0  0
 21 23  1  0  0  0  0
 17 24  1  6  0  0  0
 14 25  1  1  0  0  0
M  END
> <DATABASE_ID>
NP0078170

> <DATABASE_NAME>
NP-MRD

> <SMILES>
COC1=C(C(C)C)C(=O)C2=C(C1=O)[C@@]1(C)CCCC(C)(C)C1=C[C@H]2O

> <INCHI_IDENTIFIER>
InChI=1S/C21H28O4/c1-11(2)14-17(23)15-12(22)10-13-20(3,4)8-7-9-21(13,5)16(15)18(24)19(14)25-6/h10-12,22H,7-9H2,1-6H3/t12-,21+/m1/s1

> <INCHI_KEY>
RUONQJYGQKYSSL-GTJPDFRWSA-N

> <FORMULA>
C21H28O4

> <MOLECULAR_WEIGHT>
344.451

> <EXACT_MASS>
344.198759382

> <JCHEM_ACCEPTOR_COUNT>
4

> <JCHEM_ATOM_COUNT>
53

> <JCHEM_AVERAGE_POLARIZABILITY>
38.55708751579226

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(4bS,10R)-10-hydroxy-3-methoxy-4b,8,8-trimethyl-2-(propan-2-yl)-1,4,4b,5,6,7,8,10-octahydrophenanthrene-1,4-dione

> <ALOGPS_LOGP>
3.61

> <JCHEM_LOGP>
3.3680140439999997

> <ALOGPS_LOGS>
-4.21

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
19.587343544526405

> <JCHEM_PKA_STRONGEST_ACIDIC>
13.96126134822769

> <JCHEM_PKA_STRONGEST_BASIC>
-3.253063068552402

> <JCHEM_POLAR_SURFACE_AREA>
63.60000000000001

> <JCHEM_REFRACTIVITY>
99.57539999999997

> <JCHEM_ROTATABLE_BOND_COUNT>
2

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
2.10e-02 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(4bS,10R)-10-hydroxy-2-isopropyl-3-methoxy-4b,8,8-trimethyl-5,6,7,10-tetrahydrophenanthrene-1,4-dione

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 29-APR-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   29-APR-22         0                                  
HETATM    1  C   UNK     0       5.184  -0.564   0.000  0.00  0.00           C+0
HETATM    2  O   UNK     0       4.414  -1.897   0.000  0.00  0.00           O+0
HETATM    3  C   UNK     0       4.414   0.770   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       5.184   2.104   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       6.724   2.104   0.000  0.00  0.00           C+0
HETATM    6  O   UNK     0       7.494   3.437   0.000  0.00  0.00           O+0
HETATM    7  C   UNK     0       7.494   0.770   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       6.724  -0.564   0.000  0.00  0.00           C+0
HETATM    9  O   UNK     0       7.494  -1.897   0.000  0.00  0.00           O+0
HETATM   10  C   UNK     0       6.724  -3.231   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       9.034   0.770   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       9.804  -0.564   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       9.804   2.104   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       4.414   3.437   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       2.874   3.437   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       2.104   2.104   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       2.874   0.770   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       2.104  -0.564   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       0.564  -0.564   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0      -0.206   0.770   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       0.564   2.104   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0      -0.742   2.920   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       0.510   3.643   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       3.644  -0.564   0.000  0.00  0.00           C+0
HETATM   25  O   UNK     0       5.184   4.771   0.000  0.00  0.00           O+0
CONECT    1    2    3    8                                                  
CONECT    2    1                                                            
CONECT    3    1    4   17                                                  
CONECT    4    3    5   14                                                  
CONECT    5    4    6    7                                                  
CONECT    6    5                                                            
CONECT    7    5    8   11                                                  
CONECT    8    7    1    9                                                  
CONECT    9    8   10                                                       
CONECT   10    9                                                            
CONECT   11    7   12   13                                                  
CONECT   12   11                                                            
CONECT   13   11                                                            
CONECT   14    4   15   25                                                  
CONECT   15   14   16                                                       
CONECT   16   15   17   21                                                  
CONECT   17   16    3   18   24                                             
CONECT   18   17   19                                                       
CONECT   19   18   20                                                       
CONECT   20   19   21                                                       
CONECT   21   20   16   22   23                                             
CONECT   22   21                                                            
CONECT   23   21                                                            
CONECT   24   17                                                            
CONECT   25   14                                                            
MASTER        0    0    0    0    0    0    0    0   25    0   54    0
END

View in JSmol

Synonyms

Value	Source
(4BS,10R)-10-Hydroxy-3-methoxy-4b,8,8-trimethyl-2-propan-2-yl-5,6,7,10-tetrahydrophenanthrene-1,4-dione	ChEBI

Chemical Formula

C₂₁H₂₈O₄

Average Mass

344.4510 Da

Monoisotopic Mass

344.19876 Da

IUPAC Name

(4bS,10R)-10-hydroxy-3-methoxy-4b,8,8-trimethyl-2-(propan-2-yl)-1,4,4b,5,6,7,8,10-octahydrophenanthrene-1,4-dione

Traditional Name

(4bS,10R)-10-hydroxy-2-isopropyl-3-methoxy-4b,8,8-trimethyl-5,6,7,10-tetrahydrophenanthrene-1,4-dione

CAS Registry Number

Not Available

SMILES

COC1=C(C(C)C)C(=O)C2=C(C1=O)[C@@]1(C)CCCC(C)(C)C1=C[C@H]2O

InChI Identifier

InChI=1S/C21H28O4/c1-11(2)14-17(23)15-12(22)10-13-20(3,4)8-7-9-21(13,5)16(15)18(24)19(14)25-6/h10-12,22H,7-9H2,1-6H3/t12-,21+/m1/s1

InChI Key

RUONQJYGQKYSSL-GTJPDFRWSA-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
Salvia multicaulis	LOTUS Database	35616633
Salvia recognita	LOTUS Database	35616633
Salvia recognita Fisch.et Mey.	Plant	KNApSAcK

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as diterpenoids. These are terpene compounds formed by four isoprene units.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Prenol lipids

Sub Class

Diterpenoids

Direct Parent

Diterpenoids

Alternative Parents

Substituents

Diterpenoid
Abietane diterpenoid
Phenanthrene
Hydrophenanthrene
Vinylogous ester
Secondary alcohol
Ketone
Organic oxygen compound
Organic oxide
Hydrocarbon derivative
Organooxygen compound
Carbonyl group
Alcohol
Aliphatic homopolycyclic compound

Molecular Framework

Aliphatic homopolycyclic compounds

External Descriptors

secondary alcohol (CHEBI:66364 )
abietane diterpenoid (CHEBI:66364 )
quinone (CHEBI:66364 )
enol ether (CHEBI:66364 )

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	3.61	ALOGPS
logP	3.37	ChemAxon
logS	-4.2	ALOGPS
pKa (Strongest Acidic)	13.96	ChemAxon
pKa (Strongest Basic)	-3.3	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	4	ChemAxon
Hydrogen Donor Count	1	ChemAxon
Polar Surface Area	63.6 Å²	ChemAxon
Rotatable Bond Count	2	ChemAxon
Refractivity	99.58 m³·mol⁻¹	ChemAxon
Polarizability	38.56 Å³	ChemAxon
Number of Rings	3	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

C00042048

Chemspider ID

411021

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

467786

PDB ID

Not Available

ChEBI ID

66364

Good Scents ID

Not Available

References

General References

Showing NP-Card for 12-Methyl-5-dehydrohorminone (NP0078170)

MOL for NP0078170 (12-Methyl-5-dehydrohorminone)

3D MOL for NP0078170 (12-Methyl-5-dehydrohorminone)

3D SDF for NP0078170 (12-Methyl-5-dehydrohorminone)

3D-SDF for NP0078170 (12-Methyl-5-dehydrohorminone)

PDB for NP0078170 (12-Methyl-5-dehydrohorminone)

3D PDB for NP0078170 (12-Methyl-5-dehydrohorminone)

SMILES for NP0078170 (12-Methyl-5-dehydrohorminone)

INCHI for NP0078170 (12-Methyl-5-dehydrohorminone)

Structure for NP0078170 (12-Methyl-5-dehydrohorminone)

3D Structure for NP0078170 (12-Methyl-5-dehydrohorminone)