NP-MRD: Showing NP-Card for methyl 7,8-dihydroxy-6-(hydroxymethyl)-2,6,10,17,17-pentamethylhexacyclo[12.8.1.0¹,¹⁴.0²,¹¹.0⁵,¹⁰.0¹⁵,²⁰]tricos-12-ene-20-carboxylate (NP0324919)

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Record Information

Version

2.0

Created at

2022-09-12 05:17:10 UTC

Updated at

2022-09-12 05:17:11 UTC

NP-MRD ID

NP0324919

Secondary Accession Numbers

None

Natural Product Identification

Common Name

methyl 7,8-dihydroxy-6-(hydroxymethyl)-2,6,10,17,17-pentamethylhexacyclo[12.8.1.0¹,¹⁴.0²,¹¹.0⁵,¹⁰.0¹⁵,²⁰]tricos-12-ene-20-carboxylate

Description

Methyl 7,8-dihydroxy-6-(hydroxymethyl)-2,6,10,17,17-pentamethylhexacyclo[12.8.1.0¹,¹⁴.0²,¹¹.0⁵,¹⁰.0¹⁵,²⁰]Tricos-12-ene-20-carboxylate belongs to the class of organic compounds known as scalarane sesterterpenoids. These are sesterterpenoids with a structure based on the scalarane backbone. Scalarane is a tetracyclic compound, which is similar the homoandrostane with five methyl groups at the 4-, 4-, 8-, 17-, 17a-positions. methyl 7,8-dihydroxy-6-(hydroxymethyl)-2,6,10,17,17-pentamethylhexacyclo[12.8.1.0¹,¹⁴.0²,¹¹.0⁵,¹⁰.0¹⁵,²⁰]tricos-12-ene-20-carboxylate is found in Prunella vulgaris. Methyl 7,8-dihydroxy-6-(hydroxymethyl)-2,6,10,17,17-pentamethylhexacyclo[12.8.1.0¹,¹⁴.0²,¹¹.0⁵,¹⁰.0¹⁵,²⁰]Tricos-12-ene-20-carboxylate is an extremely weak basic (essentially neutral) compound (based on its pKa).

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1533004241516022D          

 36 41  0  0  0  0            999 V2000
   -1.2375   -2.9684    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8250   -2.2539    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000   -2.2539    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4125   -2.9684    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.4125   -1.5395    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4125   -1.5395    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8250   -0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4125   -0.1105    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1877    0.1716    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2692    0.7019    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4125   -0.1105    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8250   -0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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    2.4750   -0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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    4.5375   -1.5395    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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    3.3000   -0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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    2.0625   -0.1105    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
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  8 10  1  0  0  0  0
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 25 26  1  0  0  0  0
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 31 32  1  0  0  0  0
 22 32  1  0  0  0  0
 32 33  1  0  0  0  0
 32 34  1  0  0  0  0
 18 34  1  0  0  0  0
 34 35  1  0  0  0  0
 35 36  2  0  0  0  0
 13 36  1  0  0  0  0
M  END

     RDKit          3D

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  6 40  1  0
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M  END


  Mrv1533004241516022D          

 36 41  0  0  0  0            999 V2000
   -1.2375   -2.9684    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8250   -2.2539    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
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    4.1250   -2.2539    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5375   -1.5395    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3625   -1.5395    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2192   -2.3519    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1377   -1.8216    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.2810   -2.6341    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.7750   -0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.6000   -0.8250    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.3625   -0.1105    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7750    0.6039    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.5375   -0.1105    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1250   -0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7125   -0.1105    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3000   -0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8875   -0.1105    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0625   -0.1105    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
  3  5  1  0  0  0  0
  5  6  1  0  0  0  0
  6  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  1  0  0  0  0
  8 10  1  0  0  0  0
  8 11  1  0  0  0  0
 11 12  1  0  0  0  0
  5 12  1  0  0  0  0
 12 13  1  0  0  0  0
 13 14  1  0  0  0  0
 14 15  1  0  0  0  0
 13 15  1  0  0  0  0
 15 16  1  0  0  0  0
 16 17  1  0  0  0  0
  5 17  1  0  0  0  0
 15 18  1  0  0  0  0
 18 19  1  0  0  0  0
 18 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
 23 24  1  0  0  0  0
 23 25  1  0  0  0  0
 25 26  1  0  0  0  0
 23 27  1  0  0  0  0
 27 28  1  0  0  0  0
 27 29  1  0  0  0  0
 29 30  1  0  0  0  0
 29 31  1  0  0  0  0
 31 32  1  0  0  0  0
 22 32  1  0  0  0  0
 32 33  1  0  0  0  0
 32 34  1  0  0  0  0
 18 34  1  0  0  0  0
 34 35  1  0  0  0  0
 35 36  2  0  0  0  0
 13 36  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0324919

> <DATABASE_NAME>
NP-MRD

> <SMILES>
COC(=O)C12CCC34CC3(C=CC3C5(C)CC(O)C(O)C(C)(CO)C5CCC43C)C1CC(C)(C)CC2

> <INCHI_IDENTIFIER>
InChI=1S/C31H48O5/c1-25(2)11-12-29(24(35)36-6)13-14-31-17-30(31,22(29)16-25)10-8-21-26(3)15-19(33)23(34)27(4,18-32)20(26)7-9-28(21,31)5/h8,10,19-23,32-34H,7,9,11-18H2,1-6H3

> <INCHI_KEY>
ZGWCAZMHNIWYIX-UHFFFAOYSA-N

> <FORMULA>
C31H48O5

> <MOLECULAR_WEIGHT>
500.72

> <EXACT_MASS>
500.350174646

> <JCHEM_ACCEPTOR_COUNT>
4

> <JCHEM_ATOM_COUNT>
84

> <JCHEM_AVERAGE_POLARIZABILITY>
57.28846796244267

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
3

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
methyl 7,8-dihydroxy-6-(hydroxymethyl)-2,6,10,17,17-pentamethylhexacyclo[12.8.1.0¹,¹⁴.0²,¹¹.0⁵,¹⁰.0¹⁵,²⁰]tricos-12-ene-20-carboxylate

> <ALOGPS_LOGP>
4.28

> <JCHEM_LOGP>
3.820463102666668

> <ALOGPS_LOGS>
-5.25

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
6

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
14.827165288263874

> <JCHEM_PKA_STRONGEST_ACIDIC>
13.553641208625205

> <JCHEM_PKA_STRONGEST_BASIC>
-2.787489125850046

> <JCHEM_POLAR_SURFACE_AREA>
86.99000000000001

> <JCHEM_REFRACTIVITY>
139.86829999999998

> <JCHEM_ROTATABLE_BOND_COUNT>
3

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
2.82e-03 g/l

> <JCHEM_TRADITIONAL_IUPAC>
methyl 7,8-dihydroxy-6-(hydroxymethyl)-2,6,10,17,17-pentamethylhexacyclo[12.8.1.0¹,¹⁴.0²,¹¹.0⁵,¹⁰.0¹⁵,²⁰]tricos-12-ene-20-carboxylate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 24-APR-15   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   24-APR-15         0                                  
HETATM    1  C   UNK     0      -2.310  -5.541   0.000  0.00  0.00           C+0
HETATM    2  O   UNK     0      -1.540  -4.207   0.000  0.00  0.00           O+0
HETATM    3  C   UNK     0       0.000  -4.207   0.000  0.00  0.00           C+0
HETATM    4  O   UNK     0       0.770  -5.541   0.000  0.00  0.00           O+0
HETATM    5  C   UNK     0       0.770  -2.874   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      -0.770  -2.874   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      -1.540  -1.540   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      -0.770  -0.206   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      -2.217   0.320   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      -0.503   1.310   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       0.770  -0.206   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       1.540  -1.540   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       3.080  -1.540   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       4.620  -1.540   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       3.850  -2.874   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       3.080  -4.207   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       1.540  -4.207   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       5.390  -2.874   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       4.620  -4.207   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       6.160  -4.207   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       7.700  -4.207   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       8.470  -2.874   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0      10.010  -2.874   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       9.743  -4.390   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0      11.457  -3.400   0.000  0.00  0.00           C+0
HETATM   26  O   UNK     0      11.725  -4.917   0.000  0.00  0.00           O+0
HETATM   27  C   UNK     0      10.780  -1.540   0.000  0.00  0.00           C+0
HETATM   28  O   UNK     0      12.320  -1.540   0.000  0.00  0.00           O+0
HETATM   29  C   UNK     0      10.010  -0.206   0.000  0.00  0.00           C+0
HETATM   30  O   UNK     0      10.780   1.127   0.000  0.00  0.00           O+0
HETATM   31  C   UNK     0       8.470  -0.206   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0       7.700  -1.540   0.000  0.00  0.00           C+0
HETATM   33  C   UNK     0       6.930  -0.206   0.000  0.00  0.00           C+0
HETATM   34  C   UNK     0       6.160  -1.540   0.000  0.00  0.00           C+0
HETATM   35  C   UNK     0       5.390  -0.206   0.000  0.00  0.00           C+0
HETATM   36  C   UNK     0       3.850  -0.206   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4    5                                                  
CONECT    4    3                                                            
CONECT    5    3    6   12   17                                             
CONECT    6    5    7                                                       
CONECT    7    6    8                                                       
CONECT    8    7    9   10   11                                             
CONECT    9    8                                                            
CONECT   10    8                                                            
CONECT   11    8   12                                                       
CONECT   12   11    5   13                                                  
CONECT   13   12   14   15   36                                             
CONECT   14   13   15                                                       
CONECT   15   14   13   16   18                                             
CONECT   16   15   17                                                       
CONECT   17   16    5                                                       
CONECT   18   15   19   20   34                                             
CONECT   19   18                                                            
CONECT   20   18   21                                                       
CONECT   21   20   22                                                       
CONECT   22   21   23   32                                                  
CONECT   23   22   24   25   27                                             
CONECT   24   23                                                            
CONECT   25   23   26                                                       
CONECT   26   25                                                            
CONECT   27   23   28   29                                                  
CONECT   28   27                                                            
CONECT   29   27   30   31                                                  
CONECT   30   29                                                            
CONECT   31   29   32                                                       
CONECT   32   31   22   33   34                                             
CONECT   33   32                                                            
CONECT   34   32   18   35                                                  
CONECT   35   34   36                                                       
CONECT   36   35   13                                                       
MASTER        0    0    0    0    0    0    0    0   36    0   82    0
END

View in JSmol

Synonyms

Value	Source
Methyl 7,8-dihydroxy-6-(hydroxymethyl)-2,6,10,17,17-pentamethylhexacyclo[12.8.1.0,.0,.0,.0,]tricos-12-ene-20-carboxylic acid	Generator
Methyl 7,8-dihydroxy-6-(hydroxymethyl)-2,6,10,17,17-pentamethylhexacyclo[12.8.1.0¹,¹⁴.0²,¹¹.0⁵,¹⁰.0¹⁵,²⁰]tricos-12-ene-20-carboxylic acid	Generator

Chemical Formula

C₃₁H₄₈O₅

Average Mass

500.7200 Da

Monoisotopic Mass

500.35017 Da

IUPAC Name

methyl 7,8-dihydroxy-6-(hydroxymethyl)-2,6,10,17,17-pentamethylhexacyclo[12.8.1.0¹,¹⁴.0²,¹¹.0⁵,¹⁰.0¹⁵,²⁰]tricos-12-ene-20-carboxylate

Traditional Name

methyl 7,8-dihydroxy-6-(hydroxymethyl)-2,6,10,17,17-pentamethylhexacyclo[12.8.1.0¹,¹⁴.0²,¹¹.0⁵,¹⁰.0¹⁵,²⁰]tricos-12-ene-20-carboxylate

CAS Registry Number

Not Available

SMILES

COC(=O)C12CCC34CC3(C=CC3C5(C)CC(O)C(O)C(C)(CO)C5CCC43C)C1CC(C)(C)CC2

InChI Identifier

InChI=1S/C31H48O5/c1-25(2)11-12-29(24(35)36-6)13-14-31-17-30(31,22(29)16-25)10-8-21-26(3)15-19(33)23(34)27(4,18-32)20(26)7-9-28(21,31)5/h8,10,19-23,32-34H,7,9,11-18H2,1-6H3

InChI Key

ZGWCAZMHNIWYIX-UHFFFAOYSA-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
Prunella vulgaris	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as scalarane sesterterpenoids. These are sesterterpenoids with a structure based on the scalarane backbone. Scalarane is a tetracyclic compound, which is similar the homoandrostane with five methyl groups at the 4-, 4-, 8-, 17-, 17a-positions.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Prenol lipids

Sub Class

Sesterterpenoids

Direct Parent

Scalarane sesterterpenoids

Alternative Parents

Substituents

Scalarane sesterterpenoid
12-hydroxysteroid
Hydroxysteroid
Steroid
Cyclic alcohol
Methyl ester
Carboxylic acid ester
Secondary alcohol
Monocarboxylic acid or derivatives
Carboxylic acid derivative
Organooxygen compound
Hydrocarbon derivative
Organic oxide
Organic oxygen compound
Alcohol
Carbonyl group
Primary alcohol
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	4.28	ALOGPS
logP	3.82	ChemAxon
logS	-5.2	ALOGPS
pKa (Strongest Acidic)	13.55	ChemAxon
pKa (Strongest Basic)	-2.8	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	4	ChemAxon
Hydrogen Donor Count	3	ChemAxon
Polar Surface Area	86.99 Å²	ChemAxon
Rotatable Bond Count	3	ChemAxon
Refractivity	139.87 m³·mol⁻¹	ChemAxon
Polarizability	57.29 Å³	ChemAxon
Number of Rings	6	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	No	ChemAxon
Ghose Filter	No	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

Not Available

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for methyl 7,8-dihydroxy-6-(hydroxymethyl)-2,6,10,17,17-pentamethylhexacyclo[12.8.1.0¹,¹⁴.0²,¹¹.0⁵,¹⁰.0¹⁵,²⁰]tricos-12-ene-20-carboxylate (NP0324919)

MOL for NP0324919 (methyl 7,8-dihydroxy-6-(hydroxymethyl)-2,6,10,17,17-pentamethylhexacyclo[12.8.1.0¹,¹⁴.0²,¹¹.0⁵,¹⁰.0¹⁵,²⁰]tricos-12-ene-20-carboxylate)

3D MOL for NP0324919 (methyl 7,8-dihydroxy-6-(hydroxymethyl)-2,6,10,17,17-pentamethylhexacyclo[12.8.1.0¹,¹⁴.0²,¹¹.0⁵,¹⁰.0¹⁵,²⁰]tricos-12-ene-20-carboxylate)

3D SDF for NP0324919 (methyl 7,8-dihydroxy-6-(hydroxymethyl)-2,6,10,17,17-pentamethylhexacyclo[12.8.1.0¹,¹⁴.0²,¹¹.0⁵,¹⁰.0¹⁵,²⁰]tricos-12-ene-20-carboxylate)

3D-SDF for NP0324919 (methyl 7,8-dihydroxy-6-(hydroxymethyl)-2,6,10,17,17-pentamethylhexacyclo[12.8.1.0¹,¹⁴.0²,¹¹.0⁵,¹⁰.0¹⁵,²⁰]tricos-12-ene-20-carboxylate)

PDB for NP0324919 (methyl 7,8-dihydroxy-6-(hydroxymethyl)-2,6,10,17,17-pentamethylhexacyclo[12.8.1.0¹,¹⁴.0²,¹¹.0⁵,¹⁰.0¹⁵,²⁰]tricos-12-ene-20-carboxylate)

3D PDB for NP0324919 (methyl 7,8-dihydroxy-6-(hydroxymethyl)-2,6,10,17,17-pentamethylhexacyclo[12.8.1.0¹,¹⁴.0²,¹¹.0⁵,¹⁰.0¹⁵,²⁰]tricos-12-ene-20-carboxylate)

SMILES for NP0324919 (methyl 7,8-dihydroxy-6-(hydroxymethyl)-2,6,10,17,17-pentamethylhexacyclo[12.8.1.0¹,¹⁴.0²,¹¹.0⁵,¹⁰.0¹⁵,²⁰]tricos-12-ene-20-carboxylate)

INCHI for NP0324919 (methyl 7,8-dihydroxy-6-(hydroxymethyl)-2,6,10,17,17-pentamethylhexacyclo[12.8.1.0¹,¹⁴.0²,¹¹.0⁵,¹⁰.0¹⁵,²⁰]tricos-12-ene-20-carboxylate)

Structure for NP0324919 (methyl 7,8-dihydroxy-6-(hydroxymethyl)-2,6,10,17,17-pentamethylhexacyclo[12.8.1.0¹,¹⁴.0²,¹¹.0⁵,¹⁰.0¹⁵,²⁰]tricos-12-ene-20-carboxylate)

3D Structure for NP0324919 (methyl 7,8-dihydroxy-6-(hydroxymethyl)-2,6,10,17,17-pentamethylhexacyclo[12.8.1.0¹,¹⁴.0²,¹¹.0⁵,¹⁰.0¹⁵,²⁰]tricos-12-ene-20-carboxylate)