NP-MRD: Showing NP-Card for methyl (2s,5s)-2-[(1s,3as,5ar,7r,9as,11as)-7-hydroxy-3a,6,6,9a,11a-pentamethyl-1h,2h,3h,4h,5h,5ah,7h,8h,9h,10h,11h-cyclopenta[a]phenanthren-1-yl]-5-hydroxy-6-methylhept-6-enoate (NP0155671)

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Record Information

Version

2.0

Created at

2022-09-02 12:46:27 UTC

Updated at

2022-09-02 12:46:27 UTC

NP-MRD ID

NP0155671

Secondary Accession Numbers

None

Natural Product Identification

Common Name

methyl (2s,5s)-2-[(1s,3as,5ar,7r,9as,11as)-7-hydroxy-3a,6,6,9a,11a-pentamethyl-1h,2h,3h,4h,5h,5ah,7h,8h,9h,10h,11h-cyclopenta[a]phenanthren-1-yl]-5-hydroxy-6-methylhept-6-enoate

Description

Methyl (2S,5S)-5-hydroxy-2-[(2S,5R,7R,11S,14S,15S)-5-hydroxy-2,6,6,11,15-pentamethyltetracyclo[8.7.0.0²,⁷.0¹¹,¹⁵]Heptadec-1(10)-en-14-yl]-6-methylhept-6-enoate belongs to the class of organic compounds known as triterpenoids. These are terpene molecules containing six isoprene units. methyl (2s,5s)-2-[(1s,3as,5ar,7r,9as,11as)-7-hydroxy-3a,6,6,9a,11a-pentamethyl-1h,2h,3h,4h,5h,5ah,7h,8h,9h,10h,11h-cyclopenta[a]phenanthren-1-yl]-5-hydroxy-6-methylhept-6-enoate is found in Ozoroa insignis. Based on a literature review very few articles have been published on methyl (2S,5S)-5-hydroxy-2-[(2S,5R,7R,11S,14S,15S)-5-hydroxy-2,6,6,11,15-pentamethyltetracyclo[8.7.0.0²,⁷.0¹¹,¹⁵]Heptadec-1(10)-en-14-yl]-6-methylhept-6-enoate.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309022214462D          

 35 38  0  0  1  0            999 V2000
   -1.0852   -7.1030    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2602   -7.1030    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1523   -6.3885    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1523   -7.8175    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.2602   -8.5319    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.9773   -7.8175    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3898   -8.5319    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2148   -8.5319    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.6273   -7.8175    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4523   -7.8175    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.2148   -7.1030    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
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    2.2917  -10.0001    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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    3.7055  -10.9601    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4039  -10.3946    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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    6.4147   -9.5454    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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    8.1555  -10.8623    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.7578  -11.1594    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.4079  -11.6673    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.3705  -11.8878    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.9732  -10.9044    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    5.3601  -11.4565    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5754  -11.2015    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  0  0  0  0
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  2  4  1  0  0  0  0
  4  5  1  6  0  0  0
  4  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  2  0  0  0  0
  9 11  1  0  0  0  0
 11 12  1  0  0  0  0
 13  8  1  1  0  0  0
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 13 22  1  0  0  0  0
 16 22  1  0  0  0  0
 22 23  1  1  0  0  0
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 24 26  1  0  0  0  0
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 28 30  1  0  0  0  0
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 30 32  1  0  0  0  0
 30 33  1  0  0  0  0
 24 33  1  0  0  0  0
 33 34  1  6  0  0  0
 34 35  1  0  0  0  0
 18 35  1  0  0  0  0
M  END

     RDKit          3D

 85 88  0  0  0  0  0  0  0  0999 V2000
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M  END


  Mrv1652309022214462D          

 35 38  0  0  1  0            999 V2000
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    4.8455   -9.0356    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0609   -8.7806    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4478   -9.3326    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.1928   -8.5480    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8016  -10.0975    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    5.6301   -9.2905    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4147   -9.5454    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.1993   -9.8004    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.3709  -10.6073    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    8.1555  -10.8623    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.7578  -11.1594    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.4079  -11.6673    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.3705  -11.8878    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.9732  -10.9044    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    5.3601  -11.4565    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5754  -11.2015    0.0000 C   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
  2  4  1  0  0  0  0
  4  5  1  6  0  0  0
  4  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  2  0  0  0  0
  9 11  1  0  0  0  0
 11 12  1  0  0  0  0
 13  8  1  1  0  0  0
 13 14  1  0  0  0  0
 14 15  1  0  0  0  0
 15 16  1  0  0  0  0
 16 17  1  6  0  0  0
 16 18  1  0  0  0  0
 18 19  2  0  0  0  0
 19 20  1  0  0  0  0
 20 21  1  0  0  0  0
 21 22  1  0  0  0  0
 13 22  1  0  0  0  0
 16 22  1  0  0  0  0
 22 23  1  1  0  0  0
 19 24  1  0  0  0  0
 24 25  1  6  0  0  0
 24 26  1  0  0  0  0
 26 27  1  0  0  0  0
 27 28  1  0  0  0  0
 28 29  1  1  0  0  0
 28 30  1  0  0  0  0
 30 31  1  0  0  0  0
 30 32  1  0  0  0  0
 30 33  1  0  0  0  0
 24 33  1  0  0  0  0
 33 34  1  6  0  0  0
 34 35  1  0  0  0  0
 18 35  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0155671

> <DATABASE_NAME>
NP-MRD

> <SMILES>
COC(=O)[C@@H](CC[C@H](O)C(C)=C)[C@@H]1CC[C@]2(C)C3=C(CC[C@@]12C)[C@@]1(C)CC[C@@H](O)C(C)(C)[C@@H]1CC3

> <INCHI_IDENTIFIER>
InChI=1S/C31H50O4/c1-19(2)24(32)11-9-20(27(34)35-8)21-13-17-31(7)23-10-12-25-28(3,4)26(33)15-16-29(25,5)22(23)14-18-30(21,31)6/h20-21,24-26,32-33H,1,9-18H2,2-8H3/t20-,21-,24-,25-,26+,29+,30-,31+/m0/s1

> <INCHI_KEY>
DMBACTHBBJOGIN-DVFSKWCBSA-N

> <FORMULA>
C31H50O4

> <MOLECULAR_WEIGHT>
486.737

> <EXACT_MASS>
486.37091009

> <JCHEM_ACCEPTOR_COUNT>
3

> <JCHEM_ATOM_COUNT>
85

> <JCHEM_AVERAGE_POLARIZABILITY>
58.144730814552965

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
methyl (2S,5S)-5-hydroxy-2-[(2S,5R,7R,11S,14S,15S)-5-hydroxy-2,6,6,11,15-pentamethyltetracyclo[8.7.0.0^{2,7}.0^{11,15}]heptadec-1(10)-en-14-yl]-6-methylhept-6-enoate

> <ALOGPS_LOGP>
5.83

> <JCHEM_LOGP>
5.615414597333335

> <ALOGPS_LOGS>
-5.11

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
19.553786825962863

> <JCHEM_PKA_STRONGEST_ACIDIC>
18.066655345098532

> <JCHEM_PKA_STRONGEST_BASIC>
-0.7193235818181952

> <JCHEM_POLAR_SURFACE_AREA>
66.76

> <JCHEM_REFRACTIVITY>
141.4481

> <JCHEM_ROTATABLE_BOND_COUNT>
7

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
3.79e-03 g/l

> <JCHEM_TRADITIONAL_IUPAC>
methyl (2S,5S)-5-hydroxy-2-[(2S,5R,7R,11S,14S,15S)-5-hydroxy-2,6,6,11,15-pentamethyltetracyclo[8.7.0.0^{2,7}.0^{11,15}]heptadec-1(10)-en-14-yl]-6-methylhept-6-enoate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 02-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   02-SEP-22         0                                  
HETATM    1  C   UNK     0      -2.026 -13.259   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      -0.486 -13.259   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       0.284 -11.925   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       0.284 -14.593   0.000  0.00  0.00           C+0
HETATM    5  O   UNK     0      -0.486 -15.926   0.000  0.00  0.00           O+0
HETATM    6  C   UNK     0       1.824 -14.593   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       2.594 -15.926   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       4.134 -15.926   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       4.904 -14.593   0.000  0.00  0.00           C+0
HETATM   10  O   UNK     0       6.444 -14.593   0.000  0.00  0.00           O+0
HETATM   11  O   UNK     0       4.134 -13.259   0.000  0.00  0.00           O+0
HETATM   12  C   UNK     0       4.904 -11.925   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       4.904 -17.260   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       4.278 -18.667   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       5.422 -19.697   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       6.756 -18.927   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       6.917 -20.459   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       8.221 -19.403   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       9.365 -18.373   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       9.045 -16.866   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       7.580 -16.390   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       6.436 -17.421   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       5.960 -15.956   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0      10.830 -18.849   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0      10.510 -17.342   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0      11.974 -17.818   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0      13.439 -18.294   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0      13.759 -19.800   0.000  0.00  0.00           C+0
HETATM   29  O   UNK     0      15.224 -20.276   0.000  0.00  0.00           O+0
HETATM   30  C   UNK     0      12.615 -20.831   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0      13.828 -21.779   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0      11.892 -22.191   0.000  0.00  0.00           C+0
HETATM   33  C   UNK     0      11.150 -20.355   0.000  0.00  0.00           C+0
HETATM   34  C   UNK     0      10.005 -21.385   0.000  0.00  0.00           C+0
HETATM   35  C   UNK     0       8.541 -20.910   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3    4                                                  
CONECT    3    2                                                            
CONECT    4    2    5    6                                                  
CONECT    5    4                                                            
CONECT    6    4    7                                                       
CONECT    7    6    8                                                       
CONECT    8    7    9   13                                                  
CONECT    9    8   10   11                                                  
CONECT   10    9                                                            
CONECT   11    9   12                                                       
CONECT   12   11                                                            
CONECT   13    8   14   22                                                  
CONECT   14   13   15                                                       
CONECT   15   14   16                                                       
CONECT   16   15   17   18   22                                             
CONECT   17   16                                                            
CONECT   18   16   19   35                                                  
CONECT   19   18   20   24                                                  
CONECT   20   19   21                                                       
CONECT   21   20   22                                                       
CONECT   22   21   13   16   23                                             
CONECT   23   22                                                            
CONECT   24   19   25   26   33                                             
CONECT   25   24                                                            
CONECT   26   24   27                                                       
CONECT   27   26   28                                                       
CONECT   28   27   29   30                                                  
CONECT   29   28                                                            
CONECT   30   28   31   32   33                                             
CONECT   31   30                                                            
CONECT   32   30                                                            
CONECT   33   30   24   34                                                  
CONECT   34   33   35                                                       
CONECT   35   34   18                                                       
MASTER        0    0    0    0    0    0    0    0   35    0   76    0
END

View in JSmol

Synonyms

Value	Source
Methyl (2S,5S)-5-hydroxy-2-[(2S,5R,7R,11S,14S,15S)-5-hydroxy-2,6,6,11,15-pentamethyltetracyclo[8.7.0.0,.0,]heptadec-1(10)-en-14-yl]-6-methylhept-6-enoic acid	Generator

Chemical Formula

C₃₁H₅₀O₄

Average Mass

486.7370 Da

Monoisotopic Mass

486.37091 Da

IUPAC Name

methyl (2S,5S)-5-hydroxy-2-[(2S,5R,7R,11S,14S,15S)-5-hydroxy-2,6,6,11,15-pentamethyltetracyclo[8.7.0.0^{2,7}.0^{11,15}]heptadec-1(10)-en-14-yl]-6-methylhept-6-enoate

Traditional Name

methyl (2S,5S)-5-hydroxy-2-[(2S,5R,7R,11S,14S,15S)-5-hydroxy-2,6,6,11,15-pentamethyltetracyclo[8.7.0.0^{2,7}.0^{11,15}]heptadec-1(10)-en-14-yl]-6-methylhept-6-enoate

CAS Registry Number

Not Available

SMILES

COC(=O)[C@@H](CC[C@H](O)C(C)=C)[C@@H]1CC[C@]2(C)C3=C(CC[C@@]12C)[C@@]1(C)CC[C@@H](O)C(C)(C)[C@@H]1CC3

InChI Identifier

InChI=1S/C31H50O4/c1-19(2)24(32)11-9-20(27(34)35-8)21-13-17-31(7)23-10-12-25-28(3,4)26(33)15-16-29(25,5)22(23)14-18-30(21,31)6/h20-21,24-26,32-33H,1,9-18H2,2-8H3/t20-,21-,24-,25-,26+,29+,30-,31+/m0/s1

InChI Key

DMBACTHBBJOGIN-DVFSKWCBSA-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
Ozoroa insignis	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as triterpenoids. These are terpene molecules containing six isoprene units.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Prenol lipids

Sub Class

Triterpenoids

Direct Parent

Triterpenoids

Alternative Parents

Substituents

Triterpenoid
Dihydroxy bile acid, alcohol, or derivatives
24-hydroxysteroid
Hydroxy bile acid, alcohol, or derivatives
Bile acid, alcohol, or derivatives
3-hydroxysteroid
Hydroxysteroid
3-alpha-hydroxysteroid
Steroid
Methyl ester
Cyclic alcohol
Carboxylic acid ester
Secondary alcohol
Monocarboxylic acid or derivatives
Carboxylic acid derivative
Organooxygen compound
Alcohol
Hydrocarbon derivative
Organic oxide
Carbonyl group
Organic oxygen compound
Aliphatic homopolycyclic compound

Molecular Framework

Aliphatic 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	5.83	ALOGPS
logP	5.62	ChemAxon
logS	-5.1	ALOGPS
pKa (Strongest Acidic)	18.07	ChemAxon
pKa (Strongest Basic)	-0.72	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	3	ChemAxon
Hydrogen Donor Count	2	ChemAxon
Polar Surface Area	66.76 Å²	ChemAxon
Rotatable Bond Count	7	ChemAxon
Refractivity	141.45 m³·mol⁻¹	ChemAxon
Polarizability	58.14 Å³	ChemAxon
Number of Rings	4	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	No	ChemAxon
Ghose Filter	No	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	Yes	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

162944784

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for methyl (2s,5s)-2-[(1s,3as,5ar,7r,9as,11as)-7-hydroxy-3a,6,6,9a,11a-pentamethyl-1h,2h,3h,4h,5h,5ah,7h,8h,9h,10h,11h-cyclopenta[a]phenanthren-1-yl]-5-hydroxy-6-methylhept-6-enoate (NP0155671)

MOL for NP0155671 (methyl (2s,5s)-2-[(1s,3as,5ar,7r,9as,11as)-7-hydroxy-3a,6,6,9a,11a-pentamethyl-1h,2h,3h,4h,5h,5ah,7h,8h,9h,10h,11h-cyclopenta[a]phenanthren-1-yl]-5-hydroxy-6-methylhept-6-enoate)

3D MOL for NP0155671 (methyl (2s,5s)-2-[(1s,3as,5ar,7r,9as,11as)-7-hydroxy-3a,6,6,9a,11a-pentamethyl-1h,2h,3h,4h,5h,5ah,7h,8h,9h,10h,11h-cyclopenta[a]phenanthren-1-yl]-5-hydroxy-6-methylhept-6-enoate)

3D SDF for NP0155671 (methyl (2s,5s)-2-[(1s,3as,5ar,7r,9as,11as)-7-hydroxy-3a,6,6,9a,11a-pentamethyl-1h,2h,3h,4h,5h,5ah,7h,8h,9h,10h,11h-cyclopenta[a]phenanthren-1-yl]-5-hydroxy-6-methylhept-6-enoate)

3D-SDF for NP0155671 (methyl (2s,5s)-2-[(1s,3as,5ar,7r,9as,11as)-7-hydroxy-3a,6,6,9a,11a-pentamethyl-1h,2h,3h,4h,5h,5ah,7h,8h,9h,10h,11h-cyclopenta[a]phenanthren-1-yl]-5-hydroxy-6-methylhept-6-enoate)

PDB for NP0155671 (methyl (2s,5s)-2-[(1s,3as,5ar,7r,9as,11as)-7-hydroxy-3a,6,6,9a,11a-pentamethyl-1h,2h,3h,4h,5h,5ah,7h,8h,9h,10h,11h-cyclopenta[a]phenanthren-1-yl]-5-hydroxy-6-methylhept-6-enoate)

3D PDB for NP0155671 (methyl (2s,5s)-2-[(1s,3as,5ar,7r,9as,11as)-7-hydroxy-3a,6,6,9a,11a-pentamethyl-1h,2h,3h,4h,5h,5ah,7h,8h,9h,10h,11h-cyclopenta[a]phenanthren-1-yl]-5-hydroxy-6-methylhept-6-enoate)

SMILES for NP0155671 (methyl (2s,5s)-2-[(1s,3as,5ar,7r,9as,11as)-7-hydroxy-3a,6,6,9a,11a-pentamethyl-1h,2h,3h,4h,5h,5ah,7h,8h,9h,10h,11h-cyclopenta[a]phenanthren-1-yl]-5-hydroxy-6-methylhept-6-enoate)

INCHI for NP0155671 (methyl (2s,5s)-2-[(1s,3as,5ar,7r,9as,11as)-7-hydroxy-3a,6,6,9a,11a-pentamethyl-1h,2h,3h,4h,5h,5ah,7h,8h,9h,10h,11h-cyclopenta[a]phenanthren-1-yl]-5-hydroxy-6-methylhept-6-enoate)

Structure for NP0155671 (methyl (2s,5s)-2-[(1s,3as,5ar,7r,9as,11as)-7-hydroxy-3a,6,6,9a,11a-pentamethyl-1h,2h,3h,4h,5h,5ah,7h,8h,9h,10h,11h-cyclopenta[a]phenanthren-1-yl]-5-hydroxy-6-methylhept-6-enoate)

3D Structure for NP0155671 (methyl (2s,5s)-2-[(1s,3as,5ar,7r,9as,11as)-7-hydroxy-3a,6,6,9a,11a-pentamethyl-1h,2h,3h,4h,5h,5ah,7h,8h,9h,10h,11h-cyclopenta[a]phenanthren-1-yl]-5-hydroxy-6-methylhept-6-enoate)