NP-MRD: Showing NP-Card for (4as,10as)-7-isopropyl-8-methoxy-1,4a-dimethyl-4,9,10,10a-tetrahydro-3h-phenanthrene-2-carboxylic acid (NP0236558)

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Record Information

Version

2.0

Created at

2022-09-06 19:29:12 UTC

Updated at

2022-09-06 19:29:12 UTC

NP-MRD ID

NP0236558

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(4as,10as)-7-isopropyl-8-methoxy-1,4a-dimethyl-4,9,10,10a-tetrahydro-3h-phenanthrene-2-carboxylic acid

Description

C21H28O3 belongs to the class of organic compounds known as oxosteroids. These are steroid derivatives carrying a C=O group attached to steroid skeleton. (4as,10as)-7-isopropyl-8-methoxy-1,4a-dimethyl-4,9,10,10a-tetrahydro-3h-phenanthrene-2-carboxylic acid is found in Tripterygium hypoglaucum and Tripterygium wilfordii. Based on a literature review very few articles have been published on C21H28O3.

Structure

MOL 3D MOL SDF PDB SMILES InChI

     RDKit          3D

 52 54  0  0  0  0  0  0  0  0999 V2000
   -3.6443   -1.5165    1.5435 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9403   -0.3100    1.5666 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2076    0.1879    0.5011 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7481    1.0455   -0.4232 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1652    1.4653   -0.3029 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4591    2.6509   -1.2202 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0412    0.2920   -0.7445 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9691    1.5270   -1.4878 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6679    1.0917   -1.5368 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1263    0.2408   -0.6226 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8709   -0.2327    0.4138 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3560   -1.1620    1.4518 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1023   -1.4450    1.3517 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7816   -0.2626    0.6843 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.2331   -0.2222    0.8454 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7685   -0.3395    2.2417 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0332   -0.0688   -0.1945 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4681   -0.0539    0.0064 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0301   -0.1840    1.1228 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.3003    0.1147   -1.1042 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.5200    0.0775   -1.6051 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1371    0.7137   -1.5773 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2798   -0.1846   -0.7383 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.2534   -1.5435   -1.4072 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7045   -1.3303    1.8434 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6018   -2.0369    0.5787 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2122   -2.2170    2.3284 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4158    1.7603    0.7125 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5174    2.3153   -2.2806 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4328    3.0548   -0.8951 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6803    3.3933   -1.0392 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6572   -0.0309    0.1065 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4219   -0.5568   -1.0730 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6907    0.6122   -1.6042 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4338    2.1957   -2.1872 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0859    1.4860   -2.3790 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5461   -0.7177    2.4600 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0013   -2.0835    1.4134 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6043   -1.6059    2.3205 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3078   -2.3911    0.7671 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3707    0.6500    1.2101 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.3987   -1.2068    2.4067 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.3902    0.5740    2.4932 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9197   -0.2624    2.9638 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.2210   -0.3374   -1.1408 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5756   -0.8436   -2.1813 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.1911    0.8278   -2.0891 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2501    1.7249   -1.1293 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7953    0.7529   -2.6126 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1953   -2.0902   -1.3546 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0470   -1.3430   -2.4977 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4233   -2.1756   -1.0579 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  8  1  0
  8  9  2  0
  9 10  1  0
 10 11  2  0
 11 12  1  0
 12 13  1  0
 13 14  1  0
 14 15  1  0
 15 16  1  0
 15 17  2  0
 17 21  1  0
 21 22  1  0
 22 23  1  0
 23 24  1  6
 17 18  1  0
 18 20  1  0
 18 19  2  0
  4  5  1  0
  5  6  1  0
  5  7  1  0
 11  3  1  0
 23 14  1  0
 23 10  1  0
  1 25  1  0
  1 26  1  0
  1 27  1  0
  8 35  1  0
  9 36  1  0
 12 37  1  0
 12 38  1  0
 13 39  1  0
 13 40  1  0
 14 41  1  1
 16 42  1  0
 16 43  1  0
 16 44  1  0
 21 46  1  0
 21 47  1  0
 22 48  1  0
 22 49  1  0
 24 50  1  0
 24 51  1  0
 24 52  1  0
 20 45  1  0
  5 28  1  0
  6 29  1  0
  6 30  1  0
  6 31  1  0
  7 32  1  0
  7 33  1  0
  7 34  1  0
M  END


  Mrv1652309062221292D          

 24 26  0  0  1  0            999 V2000
    3.6020   -1.7309    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   -0.3020    0.0000 C   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
    4.8395    0.4125    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
    5.2520   -0.3020    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
    2.7770    1.1270    0.0000 C   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   -0.3020    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3645   -1.0164    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5395   -1.0164    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1270   -0.3020    0.0000 C   0  0  1  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   -1.0164    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
   -0.9355    0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3480   -0.3020    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3480    1.1270    0.0000 O   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
    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
    1.9520    1.1270    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  1  0  0  0  0
  3  4  2  0  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  5  7  1  0  0  0  0
  4  8  1  0  0  0  0
  8  9  2  0  0  0  0
  9 10  1  0  0  0  0
 10 11  2  0  0  0  0
  3 11  1  0  0  0  0
 11 12  1  0  0  0  0
 12 13  1  0  0  0  0
 14 13  1  1  0  0  0
 14 15  1  0  0  0  0
 15 16  1  0  0  0  0
 15 17  2  0  0  0  0
 17 18  1  0  0  0  0
 18 19  2  0  0  0  0
 18 20  1  0  0  0  0
 17 21  1  0  0  0  0
 21 22  1  0  0  0  0
 22 23  1  0  0  0  0
 10 23  1  0  0  0  0
 14 23  1  0  0  0  0
 23 24  1  1  0  0  0
M  END
> <DATABASE_ID>
NP0236558

> <DATABASE_NAME>
NP-MRD

> <SMILES>
COC1=C(C=CC2=C1CC[C@H]1C(C)=C(CC[C@]21C)C(O)=O)C(C)C

> <INCHI_IDENTIFIER>
InChI=1S/C21H28O3/c1-12(2)14-6-9-18-16(19(14)24-5)7-8-17-13(3)15(20(22)23)10-11-21(17,18)4/h6,9,12,17H,7-8,10-11H2,1-5H3,(H,22,23)/t17-,21-/m0/s1

> <INCHI_KEY>
UAEUNTXALQHLMF-UWJYYQICSA-N

> <FORMULA>
C21H28O3

> <MOLECULAR_WEIGHT>
328.452

> <EXACT_MASS>
328.203844762

> <JCHEM_ACCEPTOR_COUNT>
3

> <JCHEM_ATOM_COUNT>
52

> <JCHEM_AVERAGE_POLARIZABILITY>
38.301906908034155

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(4aS,10aS)-8-methoxy-1,4a-dimethyl-7-(propan-2-yl)-3,4,4a,9,10,10a-hexahydrophenanthrene-2-carboxylic acid

> <JCHEM_LOGP>
5.1288281326666665

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
-1

> <JCHEM_PKA_STRONGEST_ACIDIC>
4.389943568618073

> <JCHEM_PKA_STRONGEST_BASIC>
-4.825078379350319

> <JCHEM_POLAR_SURFACE_AREA>
46.53

> <JCHEM_REFRACTIVITY>
96.56409999999998

> <JCHEM_ROTATABLE_BOND_COUNT>
3

> <JCHEM_RULE_OF_FIVE>
0

> <JCHEM_TRADITIONAL_IUPAC>
(4aS,10aS)-7-isopropyl-8-methoxy-1,4a-dimethyl-4,9,10,10a-tetrahydro-3H-phenanthrene-2-carboxylic acid

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 06-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   06-SEP-22         0                                  
HETATM    1  C   UNK     0       6.724  -3.231   0.000  0.00  0.00           C+0
HETATM    2  O   UNK     0       7.494  -1.897   0.000  0.00  0.00           O+0
HETATM    3  C   UNK     0       6.724  -0.564   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       7.494   0.770   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       9.034   0.770   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       9.804   2.104   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       9.804  -0.564   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       6.724   2.104   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       5.184   2.104   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       4.414   0.770   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       5.184  -0.564   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       4.414  -1.897   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       2.874  -1.897   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       2.104  -0.564   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       0.564  -0.564   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      -0.206  -1.897   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      -0.206   0.770   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      -1.746   0.770   0.000  0.00  0.00           C+0
HETATM   19  O   UNK     0      -2.516  -0.564   0.000  0.00  0.00           O+0
HETATM   20  O   UNK     0      -2.516   2.104   0.000  0.00  0.00           O+0
HETATM   21  C   UNK     0       0.564   2.104   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       2.104   2.104   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       2.874   0.770   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       3.644   2.104   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4   11                                                  
CONECT    4    3    5    8                                                  
CONECT    5    4    6    7                                                  
CONECT    6    5                                                            
CONECT    7    5                                                            
CONECT    8    4    9                                                       
CONECT    9    8   10                                                       
CONECT   10    9   11   23                                                  
CONECT   11   10    3   12                                                  
CONECT   12   11   13                                                       
CONECT   13   12   14                                                       
CONECT   14   13   15   23                                                  
CONECT   15   14   16   17                                                  
CONECT   16   15                                                            
CONECT   17   15   18   21                                                  
CONECT   18   17   19   20                                                  
CONECT   19   18                                                            
CONECT   20   18                                                            
CONECT   21   17   22                                                       
CONECT   22   21   23                                                       
CONECT   23   22   10   14   24                                             
CONECT   24   23                                                            
MASTER        0    0    0    0    0    0    0    0   24    0   52    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₁H₂₈O₃

Average Mass

328.4520 Da

Monoisotopic Mass

328.20384 Da

IUPAC Name

(4aS,10aS)-8-methoxy-1,4a-dimethyl-7-(propan-2-yl)-3,4,4a,9,10,10a-hexahydrophenanthrene-2-carboxylic acid

Traditional Name

(4aS,10aS)-7-isopropyl-8-methoxy-1,4a-dimethyl-4,9,10,10a-tetrahydro-3H-phenanthrene-2-carboxylic acid

CAS Registry Number

Not Available

SMILES

COC1=C(C=CC2=C1CC[C@H]1C(C)=C(CC[C@]21C)C(O)=O)C(C)C

InChI Identifier

InChI=1S/C21H28O3/c1-12(2)14-6-9-18-16(19(14)24-5)7-8-17-13(3)15(20(22)23)10-11-21(17,18)4/h6,9,12,17H,7-8,10-11H2,1-5H3,(H,22,23)/t17-,21-/m0/s1

InChI Key

UAEUNTXALQHLMF-UWJYYQICSA-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
Tripterygium hypoglaucum	LOTUS Database	35616633
Tripterygium wilfordii	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as oxosteroids. These are steroid derivatives carrying a C=O group attached to steroid skeleton.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Steroids and steroid derivatives

Sub Class

Oxosteroids

Direct Parent

Oxosteroids

Alternative Parents

Substituents

Abietane diterpenoid
Diterpenoid
Oxosteroid
17-oxosteroid
Phenanthrene
Hydrophenanthrene
Tetralin
Cumene
Anisole
Phenol ether
Alkyl aryl ether
Benzenoid
Carboxylic acid derivative
Carboxylic acid
Monocarboxylic acid or derivatives
Ether
Organic oxide
Organic oxygen compound
Hydrocarbon derivative
Organooxygen compound
Carbonyl group
Aromatic homopolycyclic compound

Molecular Framework

Aromatic homopolycyclic 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	5.13	ChemAxon
pKa (Strongest Acidic)	4.39	ChemAxon
pKa (Strongest Basic)	-4.8	ChemAxon
Physiological Charge	-1	ChemAxon
Hydrogen Acceptor Count	3	ChemAxon
Hydrogen Donor Count	1	ChemAxon
Polar Surface Area	46.53 Å²	ChemAxon
Rotatable Bond Count	3	ChemAxon
Refractivity	96.56 m³·mol⁻¹	ChemAxon
Polarizability	38.3 Å³	ChemAxon
Number of Rings	3	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	No	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

C00003056

Chemspider ID

8624605

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

C21H28O3

METLIN ID

Not Available

PubChem Compound

10449188

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for (4as,10as)-7-isopropyl-8-methoxy-1,4a-dimethyl-4,9,10,10a-tetrahydro-3h-phenanthrene-2-carboxylic acid (NP0236558)

MOL for NP0236558 ((4as,10as)-7-isopropyl-8-methoxy-1,4a-dimethyl-4,9,10,10a-tetrahydro-3h-phenanthrene-2-carboxylic acid)

3D MOL for NP0236558 ((4as,10as)-7-isopropyl-8-methoxy-1,4a-dimethyl-4,9,10,10a-tetrahydro-3h-phenanthrene-2-carboxylic acid)

3D SDF for NP0236558 ((4as,10as)-7-isopropyl-8-methoxy-1,4a-dimethyl-4,9,10,10a-tetrahydro-3h-phenanthrene-2-carboxylic acid)

3D-SDF for NP0236558 ((4as,10as)-7-isopropyl-8-methoxy-1,4a-dimethyl-4,9,10,10a-tetrahydro-3h-phenanthrene-2-carboxylic acid)

PDB for NP0236558 ((4as,10as)-7-isopropyl-8-methoxy-1,4a-dimethyl-4,9,10,10a-tetrahydro-3h-phenanthrene-2-carboxylic acid)

3D PDB for NP0236558 ((4as,10as)-7-isopropyl-8-methoxy-1,4a-dimethyl-4,9,10,10a-tetrahydro-3h-phenanthrene-2-carboxylic acid)

SMILES for NP0236558 ((4as,10as)-7-isopropyl-8-methoxy-1,4a-dimethyl-4,9,10,10a-tetrahydro-3h-phenanthrene-2-carboxylic acid)

INCHI for NP0236558 ((4as,10as)-7-isopropyl-8-methoxy-1,4a-dimethyl-4,9,10,10a-tetrahydro-3h-phenanthrene-2-carboxylic acid)

Structure for NP0236558 ((4as,10as)-7-isopropyl-8-methoxy-1,4a-dimethyl-4,9,10,10a-tetrahydro-3h-phenanthrene-2-carboxylic acid)

3D Structure for NP0236558 ((4as,10as)-7-isopropyl-8-methoxy-1,4a-dimethyl-4,9,10,10a-tetrahydro-3h-phenanthrene-2-carboxylic acid)