NP-MRD: Showing NP-Card for 1,6,9-trihydroxy-3-isopropyl-3a,5a,8,8,11a,13a-hexamethyl-1h,2h,3h,4h,5h,5bh,6h,7h,7ah,9h,10h,11h,13h,13bh-cyclopenta[a]chrysen-10-yl acetate (NP0320734)

Jump To Section:

Identification Spectra BioTaxonomy ChemoTaxonomy Physical properties Links References XML

Record Information

Version

2.0

Created at

2022-09-11 22:33:36 UTC

Updated at

2022-09-11 22:33:36 UTC

NP-MRD ID

NP0320734

Secondary Accession Numbers

None

Natural Product Identification

Common Name

1,6,9-trihydroxy-3-isopropyl-3a,5a,8,8,11a,13a-hexamethyl-1h,2h,3h,4h,5h,5bh,6h,7h,7ah,9h,10h,11h,13h,13bh-cyclopenta[a]chrysen-10-yl acetate

Description

8,17,21-Trihydroxy-2,5,10,14,18,18-hexamethyl-6-(propan-2-yl)pentacyclo[11.8.0.0²,¹⁰.0⁵,⁹.0¹⁴,¹⁹]Henicos-12-en-16-yl acetate belongs to the class of organic compounds known as triterpenoids. These are terpene molecules containing six isoprene units. 1,6,9-trihydroxy-3-isopropyl-3a,5a,8,8,11a,13a-hexamethyl-1h,2h,3h,4h,5h,5bh,6h,7h,7ah,9h,10h,11h,13h,13bh-cyclopenta[a]chrysen-10-yl acetate is found in Rubia oncotricha. 8,17,21-Trihydroxy-2,5,10,14,18,18-hexamethyl-6-(propan-2-yl)pentacyclo[11.8.0.0²,¹⁰.0⁵,⁹.0¹⁴,¹⁹]Henicos-12-en-16-yl acetate is an extremely weak basic (essentially neutral) compound (based on its pKa).

Structure

MOL SDF PDB SMILES InChI


  Mrv1533004261504422D          

 37 41  0  0  0  0            999 V2000
    2.9239   -1.3251    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7046   -1.0583    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8638   -0.2488    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3260   -1.6009    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2522   -2.4226    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0109   -2.7467    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1947   -3.5509    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.5536   -2.1252    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1302   -1.4171    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6352   -0.7571    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5318   -0.6965    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.3567   -0.6839    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.7801   -1.3920    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.1816   -0.6714    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.6050   -1.3795    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.0065   -0.6588    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.5832    0.0493    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.8314   -0.6463    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.2548   -1.3544    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.0797   -1.3418    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.9241   -0.5316    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.8505   -1.0479    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.5030   -2.0500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.3279   -2.0374    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   10.1014   -2.7706    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.2765   -2.7832    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.8532   -2.0750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.4516   -2.7957    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.0283   -2.0876    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.6267   -2.8083    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.8018   -2.8208    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.3785   -2.1127    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.9769   -2.8333    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.5247   -3.4787    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   10.1231   -4.1994    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.5465   -4.9075    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    9.2982   -4.2119    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
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  6  7  1  0  0  0  0
  6  8  1  0  0  0  0
  8  9  1  0  0  0  0
  4  9  1  0  0  0  0
  9 10  1  0  0  0  0
  9 11  1  0  0  0  0
 11 12  1  0  0  0  0
 12 13  1  0  0  0  0
 13 14  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
 16 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
 20 22  1  0  0  0  0
 20 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
 26 27  1  0  0  0  0
 19 27  1  0  0  0  0
 27 28  1  0  0  0  0
 27 29  1  0  0  0  0
 15 29  1  0  0  0  0
 29 30  2  0  0  0  0
 30 31  1  0  0  0  0
 31 32  1  0  0  0  0
  8 32  1  0  0  0  0
 13 32  1  0  0  0  0
 32 33  1  0  0  0  0
 25 34  1  0  0  0  0
 34 35  1  0  0  0  0
 35 36  2  0  0  0  0
 35 37  1  0  0  0  0
M  END


  Mrv1533004261504422D          

 37 41  0  0  0  0            999 V2000
    2.9239   -1.3251    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7046   -1.0583    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8638   -0.2488    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3260   -1.6009    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2522   -2.4226    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0109   -2.7467    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1947   -3.5509    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.5536   -2.1252    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1302   -1.4171    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6352   -0.7571    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5318   -0.6965    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.3567   -0.6839    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.7801   -1.3920    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.1816   -0.6714    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.6050   -1.3795    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.0065   -0.6588    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.5832    0.0493    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.8314   -0.6463    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.2548   -1.3544    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.0797   -1.3418    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.9241   -0.5316    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.8505   -1.0479    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.5030   -2.0500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.3279   -2.0374    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   10.1014   -2.7706    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.2765   -2.7832    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.8532   -2.0750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.4516   -2.7957    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.0283   -2.0876    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.6267   -2.8083    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.8018   -2.8208    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.3785   -2.1127    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.9769   -2.8333    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.5247   -3.4787    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   10.1231   -4.1994    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.5465   -4.9075    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    9.2982   -4.2119    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
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  6  7  1  0  0  0  0
  6  8  1  0  0  0  0
  8  9  1  0  0  0  0
  4  9  1  0  0  0  0
  9 10  1  0  0  0  0
  9 11  1  0  0  0  0
 11 12  1  0  0  0  0
 12 13  1  0  0  0  0
 13 14  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
 16 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
 20 22  1  0  0  0  0
 20 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
 26 27  1  0  0  0  0
 19 27  1  0  0  0  0
 27 28  1  0  0  0  0
 27 29  1  0  0  0  0
 15 29  1  0  0  0  0
 29 30  2  0  0  0  0
 30 31  1  0  0  0  0
 31 32  1  0  0  0  0
  8 32  1  0  0  0  0
 13 32  1  0  0  0  0
 32 33  1  0  0  0  0
 25 34  1  0  0  0  0
 34 35  1  0  0  0  0
 35 36  2  0  0  0  0
 35 37  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0320734

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC(C)C1CC(O)C2C1(C)CCC1(C)C3C(O)CC4C(C)(C)C(O)C(CC4(C)C3=CCC21C)OC(C)=O

> <INCHI_IDENTIFIER>
InChI=1S/C32H52O5/c1-17(2)20-14-22(35)26-29(20,6)12-13-31(8)25-19(10-11-32(26,31)9)30(7)16-23(37-18(3)33)27(36)28(4,5)24(30)15-21(25)34/h10,17,20-27,34-36H,11-16H2,1-9H3

> <INCHI_KEY>
QAAPYCILWKIPRZ-UHFFFAOYSA-N

> <FORMULA>
C32H52O5

> <MOLECULAR_WEIGHT>
516.763

> <EXACT_MASS>
516.381474774

> <JCHEM_ACCEPTOR_COUNT>
4

> <JCHEM_ATOM_COUNT>
89

> <JCHEM_AVERAGE_POLARIZABILITY>
61.0735408937853

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
3

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
8,17,21-trihydroxy-2,5,10,14,18,18-hexamethyl-6-(propan-2-yl)pentacyclo[11.8.0.0²,¹⁰.0⁵,⁹.0¹⁴,¹⁹]henicos-12-en-16-yl acetate

> <ALOGPS_LOGP>
4.86

> <JCHEM_LOGP>
4.138805019999999

> <ALOGPS_LOGS>
-5.02

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
5

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_ACIDIC>
13.73727599806972

> <JCHEM_PKA_STRONGEST_BASIC>
-0.1572462920881369

> <JCHEM_POLAR_SURFACE_AREA>
86.99000000000001

> <JCHEM_REFRACTIVITY>
145.6788

> <JCHEM_ROTATABLE_BOND_COUNT>
3

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
4.94e-03 g/l

> <JCHEM_TRADITIONAL_IUPAC>
8,17,21-trihydroxy-6-isopropyl-2,5,10,14,18,18-hexamethylpentacyclo[11.8.0.0²,¹⁰.0⁵,⁹.0¹⁴,¹⁹]henicos-12-en-16-yl acetate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 26-APR-15   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   26-APR-15         0                                  
HETATM    1  C   UNK     0       5.458  -2.474   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       6.915  -1.975   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       7.212  -0.464   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       8.075  -2.988   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       7.937  -4.522   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       9.354  -5.127   0.000  0.00  0.00           C+0
HETATM    7  O   UNK     0       9.697  -6.628   0.000  0.00  0.00           O+0
HETATM    8  C   UNK     0      10.367  -3.967   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       9.576  -2.645   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       8.652  -1.413   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      10.326  -1.300   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      11.866  -1.277   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      12.656  -2.598   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      13.406  -1.253   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      14.196  -2.575   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      14.946  -1.230   0.000  0.00  0.00           C+0
HETATM   17  O   UNK     0      14.155   0.092   0.000  0.00  0.00           O+0
HETATM   18  C   UNK     0      16.485  -1.206   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0      17.276  -2.528   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0      18.815  -2.505   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0      18.525  -0.992   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0      20.254  -1.956   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0      19.606  -3.827   0.000  0.00  0.00           C+0
HETATM   24  O   UNK     0      21.145  -3.803   0.000  0.00  0.00           O+0
HETATM   25  C   UNK     0      18.856  -5.172   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0      17.316  -5.195   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0      16.526  -3.873   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0      15.776  -5.219   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0      14.986  -3.897   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0      14.236  -5.242   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0      12.697  -5.265   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0      11.906  -3.944   0.000  0.00  0.00           C+0
HETATM   33  C   UNK     0      11.157  -5.289   0.000  0.00  0.00           C+0
HETATM   34  O   UNK     0      19.646  -6.494   0.000  0.00  0.00           O+0
HETATM   35  C   UNK     0      18.897  -7.839   0.000  0.00  0.00           C+0
HETATM   36  O   UNK     0      19.687  -9.161   0.000  0.00  0.00           O+0
HETATM   37  C   UNK     0      17.357  -7.862   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3    4                                                  
CONECT    3    2                                                            
CONECT    4    2    5    9                                                  
CONECT    5    4    6                                                       
CONECT    6    5    7    8                                                  
CONECT    7    6                                                            
CONECT    8    6    9   32                                                  
CONECT    9    8    4   10   11                                             
CONECT   10    9                                                            
CONECT   11    9   12                                                       
CONECT   12   11   13                                                       
CONECT   13   12   14   15   32                                             
CONECT   14   13                                                            
CONECT   15   13   16   29                                                  
CONECT   16   15   17   18                                                  
CONECT   17   16                                                            
CONECT   18   16   19                                                       
CONECT   19   18   20   27                                                  
CONECT   20   19   21   22   23                                             
CONECT   21   20                                                            
CONECT   22   20                                                            
CONECT   23   20   24   25                                                  
CONECT   24   23                                                            
CONECT   25   23   26   34                                                  
CONECT   26   25   27                                                       
CONECT   27   26   19   28   29                                             
CONECT   28   27                                                            
CONECT   29   27   15   30                                                  
CONECT   30   29   31                                                       
CONECT   31   30   32                                                       
CONECT   32   31    8   13   33                                             
CONECT   33   32                                                            
CONECT   34   25   35                                                       
CONECT   35   34   36   37                                                  
CONECT   36   35                                                            
CONECT   37   35                                                            
MASTER        0    0    0    0    0    0    0    0   37    0   82    0
END

View in JSmol

Synonyms

Value	Source
8,17,21-Trihydroxy-2,5,10,14,18,18-hexamethyl-6-(propan-2-yl)pentacyclo[11.8.0.0,.0,.0,]henicos-12-en-16-yl acetic acid	Generator
8,17,21-Trihydroxy-2,5,10,14,18,18-hexamethyl-6-(propan-2-yl)pentacyclo[11.8.0.0²,¹⁰.0⁵,⁹.0¹⁴,¹⁹]henicos-12-en-16-yl acetic acid	Generator

Chemical Formula

C₃₂H₅₂O₅

Average Mass

516.7630 Da

Monoisotopic Mass

516.38147 Da

IUPAC Name

8,17,21-trihydroxy-2,5,10,14,18,18-hexamethyl-6-(propan-2-yl)pentacyclo[11.8.0.0²,¹⁰.0⁵,⁹.0¹⁴,¹⁹]henicos-12-en-16-yl acetate

Traditional Name

8,17,21-trihydroxy-6-isopropyl-2,5,10,14,18,18-hexamethylpentacyclo[11.8.0.0²,¹⁰.0⁵,⁹.0¹⁴,¹⁹]henicos-12-en-16-yl acetate

CAS Registry Number

Not Available

SMILES

CC(C)C1CC(O)C2C1(C)CCC1(C)C3C(O)CC4C(C)(C)C(O)C(CC4(C)C3=CCC21C)OC(C)=O

InChI Identifier

InChI=1S/C32H52O5/c1-17(2)20-14-22(35)26-29(20,6)12-13-31(8)25-19(10-11-32(26,31)9)30(7)16-23(37-18(3)33)27(36)28(4,5)24(30)15-21(25)34/h10,17,20-27,34-36H,11-16H2,1-9H3

InChI Key

QAAPYCILWKIPRZ-UHFFFAOYSA-N

Experimental Spectra

Not Available

Predicted Spectra

Not Available

Chemical Shift Submissions

Not Available

Species

Species of Origin

Species Name	Source	Reference
Rubia oncotricha	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
1-hydroxysteroid
15-hydroxysteroid
Hydroxysteroid
Delta-5-steroid
Steroid
Cyclic alcohol
Carboxylic acid ester
Secondary alcohol
Monocarboxylic acid or derivatives
Carboxylic acid derivative
Polyol
Hydrocarbon derivative
Organic oxide
Organic oxygen compound
Alcohol
Carbonyl group
Organooxygen 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	4.86	ALOGPS
logP	4.14	ChemAxon
logS	-5	ALOGPS
pKa (Strongest Acidic)	13.74	ChemAxon
pKa (Strongest Basic)	-0.16	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	145.68 m³·mol⁻¹	ChemAxon
Polarizability	61.07 Å³	ChemAxon
Number of Rings	5	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

14608095

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for 1,6,9-trihydroxy-3-isopropyl-3a,5a,8,8,11a,13a-hexamethyl-1h,2h,3h,4h,5h,5bh,6h,7h,7ah,9h,10h,11h,13h,13bh-cyclopenta[a]chrysen-10-yl acetate (NP0320734)

MOL for NP0320734 (1,6,9-trihydroxy-3-isopropyl-3a,5a,8,8,11a,13a-hexamethyl-1h,2h,3h,4h,5h,5bh,6h,7h,7ah,9h,10h,11h,13h,13bh-cyclopenta[a]chrysen-10-yl acetate)

3D MOL for NP0320734 (1,6,9-trihydroxy-3-isopropyl-3a,5a,8,8,11a,13a-hexamethyl-1h,2h,3h,4h,5h,5bh,6h,7h,7ah,9h,10h,11h,13h,13bh-cyclopenta[a]chrysen-10-yl acetate)

3D SDF for NP0320734 (1,6,9-trihydroxy-3-isopropyl-3a,5a,8,8,11a,13a-hexamethyl-1h,2h,3h,4h,5h,5bh,6h,7h,7ah,9h,10h,11h,13h,13bh-cyclopenta[a]chrysen-10-yl acetate)

3D-SDF for NP0320734 (1,6,9-trihydroxy-3-isopropyl-3a,5a,8,8,11a,13a-hexamethyl-1h,2h,3h,4h,5h,5bh,6h,7h,7ah,9h,10h,11h,13h,13bh-cyclopenta[a]chrysen-10-yl acetate)

PDB for NP0320734 (1,6,9-trihydroxy-3-isopropyl-3a,5a,8,8,11a,13a-hexamethyl-1h,2h,3h,4h,5h,5bh,6h,7h,7ah,9h,10h,11h,13h,13bh-cyclopenta[a]chrysen-10-yl acetate)

3D PDB for NP0320734 (1,6,9-trihydroxy-3-isopropyl-3a,5a,8,8,11a,13a-hexamethyl-1h,2h,3h,4h,5h,5bh,6h,7h,7ah,9h,10h,11h,13h,13bh-cyclopenta[a]chrysen-10-yl acetate)

SMILES for NP0320734 (1,6,9-trihydroxy-3-isopropyl-3a,5a,8,8,11a,13a-hexamethyl-1h,2h,3h,4h,5h,5bh,6h,7h,7ah,9h,10h,11h,13h,13bh-cyclopenta[a]chrysen-10-yl acetate)

INCHI for NP0320734 (1,6,9-trihydroxy-3-isopropyl-3a,5a,8,8,11a,13a-hexamethyl-1h,2h,3h,4h,5h,5bh,6h,7h,7ah,9h,10h,11h,13h,13bh-cyclopenta[a]chrysen-10-yl acetate)

Structure for NP0320734 (1,6,9-trihydroxy-3-isopropyl-3a,5a,8,8,11a,13a-hexamethyl-1h,2h,3h,4h,5h,5bh,6h,7h,7ah,9h,10h,11h,13h,13bh-cyclopenta[a]chrysen-10-yl acetate)

3D Structure for NP0320734 (1,6,9-trihydroxy-3-isopropyl-3a,5a,8,8,11a,13a-hexamethyl-1h,2h,3h,4h,5h,5bh,6h,7h,7ah,9h,10h,11h,13h,13bh-cyclopenta[a]chrysen-10-yl acetate)