NP-MRD: Showing NP-Card for [(1s,4as,10as)-7-(2-hydroxypropan-2-yl)-1,4a-dimethyl-2,3,4,9,10,10a-hexahydrophenanthren-1-yl]acetic acid (NP0311657)

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Record Information

Version

2.0

Created at

2022-09-11 07:47:46 UTC

Updated at

2022-09-11 07:47:46 UTC

NP-MRD ID

NP0311657

Secondary Accession Numbers

None

Natural Product Identification

Common Name

[(1s,4as,10as)-7-(2-hydroxypropan-2-yl)-1,4a-dimethyl-2,3,4,9,10,10a-hexahydrophenanthren-1-yl]acetic acid

Description

CHEMBL491539 belongs to the class of organic compounds known as diterpenoids. These are terpene compounds formed by four isoprene units. [(1s,4as,10as)-7-(2-hydroxypropan-2-yl)-1,4a-dimethyl-2,3,4,9,10,10a-hexahydrophenanthren-1-yl]acetic acid is found in Pinus luchuensis. Based on a literature review very few articles have been published on CHEMBL491539.

Structure

MOL 3D MOL SDF PDB SMILES InChI

     RDKit          3D

 54 56  0  0  0  0  0  0  0  0999 V2000
    5.6239   -1.2717    0.0581 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8586   -0.4864   -0.9880 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6131    0.7954   -1.2316 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8064   -1.2482   -2.1626 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.4567   -0.2405   -0.5794 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1601    0.8726    0.1765 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8641    1.1247    0.5676 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8229    0.2738    0.2169 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0967   -0.8434   -0.5371 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4149   -1.0718   -0.9181 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0446   -1.8272   -0.9647 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1429   -1.6372   -0.0455 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5226   -0.1841   -0.1343 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.9710    0.0507    0.1420 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.5037   -0.8539    1.2430 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7119   -0.3730   -1.1447 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1677   -0.1910   -1.0031 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6728    0.9629   -1.0851 O   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0391   -1.2561   -0.7781 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3199    1.4859    0.3565 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2722    2.3165    0.9946 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8790    2.0645    0.4624 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5635    0.6158    0.6756 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.6103    0.3224    2.1518 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.7110   -1.0787   -0.1554 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.4383   -2.3610   -0.0275 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.4115   -0.8562    1.0469 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.4762    0.5712   -1.8906 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.9728    1.5734   -1.7044 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.0249    1.1218   -0.2484 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.2731   -0.7249   -2.8216 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.9793    1.5523    0.4573 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6614    2.0070    1.1642 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6615   -1.9432   -1.5161 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2832   -1.6030   -2.0100 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4420   -2.8642   -0.9181 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8396   -1.9441    0.9786 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9331   -2.3245   -0.3888 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3472    0.1207   -1.2078 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0566   -0.2527    2.0150 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2660   -1.5809    0.8636 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7058   -1.4830    1.6934 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2973    0.1688   -2.0124 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5310   -1.4554   -1.3064 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.7438   -1.1183   -0.0543 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6109    1.9909   -0.6085 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2386    1.5279    0.9851 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2544    2.2798    2.1091 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4956    3.3950    0.7550 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2031    2.7487    0.9640 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9054    2.2672   -0.6520 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0506    1.0950    2.6414 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1913   -0.6553    2.4255 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5855    0.4252    2.6147 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  2  4  1  0
  2  5  1  0
  5  6  2  0
  6  7  1  0
  7  8  2  0
  8  9  1  0
  9 11  1  0
 11 12  1  0
 12 13  1  0
 13 14  1  0
 14 15  1  1
 14 16  1  0
 16 17  1  0
 17 19  1  0
 17 18  2  0
 14 20  1  0
 20 21  1  0
 21 22  1  0
 22 23  1  0
 23 24  1  1
  9 10  2  0
 10  5  1  0
 23  8  1  0
 23 13  1  0
  1 25  1  0
  1 26  1  0
  1 27  1  0
  3 28  1  0
  3 29  1  0
  3 30  1  0
  4 31  1  0
  6 32  1  0
  7 33  1  0
 11 35  1  0
 11 36  1  0
 12 37  1  0
 12 38  1  0
 13 39  1  6
 15 40  1  0
 15 41  1  0
 15 42  1  0
 16 43  1  0
 16 44  1  0
 19 45  1  0
 20 46  1  0
 20 47  1  0
 21 48  1  0
 21 49  1  0
 22 50  1  0
 22 51  1  0
 24 52  1  0
 24 53  1  0
 24 54  1  0
 10 34  1  0
M  END


  Mrv1652309112209472D          

 24 26  0  0  1  0            999 V2000
    5.6645    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
    4.8395    1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8395   -0.4125    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    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
    3.6020   -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  2  0  0  0  0  0  0  0  0  0
    0.4452   -1.1144    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4733   -0.5841    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1053   -0.0538    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8805   -0.3360    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9620    0.7586    0.0000 O   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
    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
  2  4  1  0  0  0  0
  2  5  1  0  0  0  0
  5  6  2  0  0  0  0
  6  7  1  0  0  0  0
  7  8  2  0  0  0  0
  8  9  1  0  0  0  0
  9 10  2  0  0  0  0
  5 10  1  0  0  0  0
  9 11  1  0  0  0  0
 11 12  1  0  0  0  0
 13 12  1  1  0  0  0
 13 14  1  0  0  0  0
 14 15  1  1  0  0  0
 14 16  1  6  0  0  0
 16 17  1  0  0  0  0
 17 18  2  0  0  0  0
 17 19  1  0  0  0  0
 14 20  1  0  0  0  0
 20 21  1  0  0  0  0
 21 22  1  0  0  0  0
 22 23  1  0  0  0  0
  8 23  1  0  0  0  0
 13 23  1  0  0  0  0
 23 24  1  1  0  0  0
M  END
> <DATABASE_ID>
NP0311657

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC(C)(O)C1=CC=C2C(CC[C@H]3[C@](C)(CC(O)=O)CCC[C@]23C)=C1

> <INCHI_IDENTIFIER>
InChI=1S/C21H30O3/c1-19(2,24)15-7-8-16-14(12-15)6-9-17-20(3,13-18(22)23)10-5-11-21(16,17)4/h7-8,12,17,24H,5-6,9-11,13H2,1-4H3,(H,22,23)/t17-,20-,21+/m0/s1

> <INCHI_KEY>
QMTZBWPBIQZLBJ-DZFGPLHGSA-N

> <FORMULA>
C21H30O3

> <MOLECULAR_WEIGHT>
330.468

> <EXACT_MASS>
330.219494826

> <JCHEM_ACCEPTOR_COUNT>
3

> <JCHEM_ATOM_COUNT>
54

> <JCHEM_AVERAGE_POLARIZABILITY>
38.71678016298903

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
2-[(1S,4aS,10aS)-7-(2-hydroxypropan-2-yl)-1,4a-dimethyl-1,2,3,4,4a,9,10,10a-octahydrophenanthren-1-yl]acetic acid

> <JCHEM_LOGP>
4.3661918040000005

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
-1

> <JCHEM_PKA>
14.634511823881386

> <JCHEM_PKA_STRONGEST_ACIDIC>
4.709094417788643

> <JCHEM_PKA_STRONGEST_BASIC>
-2.958669559671124

> <JCHEM_POLAR_SURFACE_AREA>
57.53

> <JCHEM_REFRACTIVITY>
95.67529999999998

> <JCHEM_ROTATABLE_BOND_COUNT>
3

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
[(1S,4aS,10aS)-7-(2-hydroxypropan-2-yl)-1,4a-dimethyl-2,3,4,9,10,10a-hexahydrophenanthren-1-yl]acetic acid

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 11-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   11-SEP-22         0                                  
HETATM    1  C   UNK     0      10.574   0.770   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       9.034   0.770   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       9.034   2.310   0.000  0.00  0.00           C+0
HETATM    4  O   UNK     0       9.034  -0.770   0.000  0.00  0.00           O+0
HETATM    5  C   UNK     0       7.494   0.770   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       6.724   2.104   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       5.184   2.104   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       4.414   0.770   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       5.184  -0.564   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       6.724  -0.564   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       4.414  -1.897   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       2.874  -1.897   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       2.104  -0.564   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       0.564  -0.564   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       0.831  -2.080   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      -0.883  -1.090   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      -2.063  -0.100   0.000  0.00  0.00           C+0
HETATM   18  O   UNK     0      -3.510  -0.627   0.000  0.00  0.00           O+0
HETATM   19  O   UNK     0      -1.796   1.416   0.000  0.00  0.00           O+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       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    4    5                                             
CONECT    3    2                                                            
CONECT    4    2                                                            
CONECT    5    2    6   10                                                  
CONECT    6    5    7                                                       
CONECT    7    6    8                                                       
CONECT    8    7    9   23                                                  
CONECT    9    8   10   11                                                  
CONECT   10    9    5                                                       
CONECT   11    9   12                                                       
CONECT   12   11   13                                                       
CONECT   13   12   14   23                                                  
CONECT   14   13   15   16   20                                             
CONECT   15   14                                                            
CONECT   16   14   17                                                       
CONECT   17   16   18   19                                                  
CONECT   18   17                                                            
CONECT   19   17                                                            
CONECT   20   14   21                                                       
CONECT   21   20   22                                                       
CONECT   22   21   23                                                       
CONECT   23   22    8   13   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

C₂₁H₃₀O₃

Average Mass

330.4680 Da

Monoisotopic Mass

330.21949 Da

IUPAC Name

2-[(1S,4aS,10aS)-7-(2-hydroxypropan-2-yl)-1,4a-dimethyl-1,2,3,4,4a,9,10,10a-octahydrophenanthren-1-yl]acetic acid

Traditional Name

[(1S,4aS,10aS)-7-(2-hydroxypropan-2-yl)-1,4a-dimethyl-2,3,4,9,10,10a-hexahydrophenanthren-1-yl]acetic acid

CAS Registry Number

Not Available

SMILES

CC(C)(O)C1=CC=C2C(CC[C@H]3[C@](C)(CC(O)=O)CCC[C@]23C)=C1

InChI Identifier

InChI=1S/C21H30O3/c1-19(2,24)15-7-8-16-14(12-15)6-9-17-20(3,13-18(22)23)10-5-11-21(16,17)4/h7-8,12,17,24H,5-6,9-11,13H2,1-4H3,(H,22,23)/t17-,20-,21+/m0/s1

InChI Key

QMTZBWPBIQZLBJ-DZFGPLHGSA-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
Pinus luchuensis	LOTUS Database	35616633

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

Abietane diterpenoid
Diterpenoid
Phenanthrene
Hydrophenanthrene
Tetralin
Benzenoid
Tertiary alcohol
Carboxylic acid derivative
Carboxylic acid
Monocarboxylic acid or derivatives
Alcohol
Organooxygen compound
Aromatic alcohol
Hydrocarbon derivative
Organic oxide
Organic oxygen 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	4.37	ChemAxon
pKa (Strongest Acidic)	4.71	ChemAxon
pKa (Strongest Basic)	-3	ChemAxon
Physiological Charge	-1	ChemAxon
Hydrogen Acceptor Count	3	ChemAxon
Hydrogen Donor Count	2	ChemAxon
Polar Surface Area	57.53 Å²	ChemAxon
Rotatable Bond Count	3	ChemAxon
Refractivity	95.68 m³·mol⁻¹	ChemAxon
Polarizability	38.72 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

Not Available

Chemspider ID

23338854

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

44566201

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for [(1s,4as,10as)-7-(2-hydroxypropan-2-yl)-1,4a-dimethyl-2,3,4,9,10,10a-hexahydrophenanthren-1-yl]acetic acid (NP0311657)

MOL for NP0311657 ([(1s,4as,10as)-7-(2-hydroxypropan-2-yl)-1,4a-dimethyl-2,3,4,9,10,10a-hexahydrophenanthren-1-yl]acetic acid)

3D MOL for NP0311657 ([(1s,4as,10as)-7-(2-hydroxypropan-2-yl)-1,4a-dimethyl-2,3,4,9,10,10a-hexahydrophenanthren-1-yl]acetic acid)

3D SDF for NP0311657 ([(1s,4as,10as)-7-(2-hydroxypropan-2-yl)-1,4a-dimethyl-2,3,4,9,10,10a-hexahydrophenanthren-1-yl]acetic acid)

3D-SDF for NP0311657 ([(1s,4as,10as)-7-(2-hydroxypropan-2-yl)-1,4a-dimethyl-2,3,4,9,10,10a-hexahydrophenanthren-1-yl]acetic acid)

PDB for NP0311657 ([(1s,4as,10as)-7-(2-hydroxypropan-2-yl)-1,4a-dimethyl-2,3,4,9,10,10a-hexahydrophenanthren-1-yl]acetic acid)

3D PDB for NP0311657 ([(1s,4as,10as)-7-(2-hydroxypropan-2-yl)-1,4a-dimethyl-2,3,4,9,10,10a-hexahydrophenanthren-1-yl]acetic acid)

SMILES for NP0311657 ([(1s,4as,10as)-7-(2-hydroxypropan-2-yl)-1,4a-dimethyl-2,3,4,9,10,10a-hexahydrophenanthren-1-yl]acetic acid)

INCHI for NP0311657 ([(1s,4as,10as)-7-(2-hydroxypropan-2-yl)-1,4a-dimethyl-2,3,4,9,10,10a-hexahydrophenanthren-1-yl]acetic acid)

Structure for NP0311657 ([(1s,4as,10as)-7-(2-hydroxypropan-2-yl)-1,4a-dimethyl-2,3,4,9,10,10a-hexahydrophenanthren-1-yl]acetic acid)

3D Structure for NP0311657 ([(1s,4as,10as)-7-(2-hydroxypropan-2-yl)-1,4a-dimethyl-2,3,4,9,10,10a-hexahydrophenanthren-1-yl]acetic acid)