NP-MRD: Showing NP-Card for (5ar,5br,7s,7ar,9s,11ar,11br,13as,13br)-3-isopropyl-5a,5b,8,8,11a,13b-hexamethyl-1h,2h,6h,7h,7ah,9h,10h,11h,11bh,12h,13h,13ah-cyclopenta[a]chrysene-7,9-diol (NP0235204)

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Record Information

Version

2.0

Created at

2022-09-06 17:42:12 UTC

Updated at

2022-09-06 17:42:12 UTC

NP-MRD ID

NP0235204

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(5ar,5br,7s,7ar,9s,11ar,11br,13as,13br)-3-isopropyl-5a,5b,8,8,11a,13b-hexamethyl-1h,2h,6h,7h,7ah,9h,10h,11h,11bh,12h,13h,13ah-cyclopenta[a]chrysene-7,9-diol

Description

(1R,2R,9R,10S,13R,14R,17S,19R,20S)-1,2,9,14,18,18-hexamethyl-6-(propan-2-yl)pentacyclo[11.8.0.0²,¹⁰.0⁵,⁹.0¹⁴,¹⁹]Henicosa-3,5-diene-17,20-diol belongs to the class of organic compounds known as hopanoids. These are terpenoids containing hopane skeleton(A'-Neogammacerane), a pentacyclic structure with four cyclohexane rings and one cyclopentane ring (and often, a side chain emerging from C30). (5ar,5br,7s,7ar,9s,11ar,11br,13as,13br)-3-isopropyl-5a,5b,8,8,11a,13b-hexamethyl-1h,2h,6h,7h,7ah,9h,10h,11h,11bh,12h,13h,13ah-cyclopenta[a]chrysene-7,9-diol is found in Trigastrotheca pentaphylla. Based on a literature review very few articles have been published on (1R,2R,9R,10S,13R,14R,17S,19R,20S)-1,2,9,14,18,18-hexamethyl-6-(propan-2-yl)pentacyclo[11.8.0.0²,¹⁰.0⁵,⁹.0¹⁴,¹⁹]Henicosa-3,5-diene-17,20-diol.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309062219422D          

 32 36  0  0  1  0            999 V2000
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M  END

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M  END


  Mrv1652309062219422D          

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    1.4868   -4.3477    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.8338   -3.5992    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9442   -3.7263    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1855   -4.0503    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  2  0  0  0  0
  5  6  1  0  0  0  0
  6  7  2  0  0  0  0
  7  8  1  0  0  0  0
  8  9  1  1  0  0  0
  8 10  1  0  0  0  0
 10 11  1  6  0  0  0
 11 12  1  0  0  0  0
 13 12  1  6  0  0  0
 13 14  1  0  0  0  0
 14 15  1  6  0  0  0
 14 16  1  0  0  0  0
 16 17  1  0  0  0  0
 17 18  1  0  0  0  0
 18 19  1  6  0  0  0
 18 20  1  0  0  0  0
 20 21  1  0  0  0  0
 20 22  1  0  0  0  0
 23 20  1  6  0  0  0
 14 23  1  0  0  0  0
 23 24  1  0  0  0  0
 24 25  1  1  0  0  0
 24 26  1  0  0  0  0
 26 27  1  0  0  0  0
 13 27  1  0  0  0  0
  8 27  1  0  0  0  0
 27 28  1  6  0  0  0
 10 29  1  0  0  0  0
  5 29  1  0  0  0  0
 29 30  1  1  0  0  0
 29 31  1  0  0  0  0
 31 32  1  0  0  0  0
  4 32  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0235204

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC(C)C1=C2C=C[C@]3(C)[C@@H](CC[C@@H]4[C@@]5(C)CC[C@H](O)C(C)(C)[C@@H]5[C@@H](O)C[C@@]34C)[C@@]2(C)CC1

> <INCHI_IDENTIFIER>
InChI=1S/C30H48O2/c1-18(2)19-11-14-27(5)20(19)12-16-29(7)22(27)9-10-23-28(6)15-13-24(32)26(3,4)25(28)21(31)17-30(23,29)8/h12,16,18,21-25,31-32H,9-11,13-15,17H2,1-8H3/t21-,22-,23+,24-,25-,27-,28+,29+,30+/m0/s1

> <INCHI_KEY>
VUBKTAWHNLXBDM-XFFVLEOYSA-N

> <FORMULA>
C30H48O2

> <MOLECULAR_WEIGHT>
440.712

> <EXACT_MASS>
440.365430786

> <JCHEM_ACCEPTOR_COUNT>
2

> <JCHEM_ATOM_COUNT>
80

> <JCHEM_AVERAGE_POLARIZABILITY>
53.72880910475955

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(1R,2R,9R,10S,13R,14R,17S,19R,20S)-1,2,9,14,18,18-hexamethyl-6-(propan-2-yl)pentacyclo[11.8.0.0^{2,10}.0^{5,9}.0^{14,19}]henicosa-3,5-diene-17,20-diol

> <JCHEM_LOGP>
5.6757685323333344

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
5

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
15.11636610331756

> <JCHEM_PKA_STRONGEST_ACIDIC>
14.48824379645157

> <JCHEM_PKA_STRONGEST_BASIC>
-2.84567562164344

> <JCHEM_POLAR_SURFACE_AREA>
40.46

> <JCHEM_REFRACTIVITY>
134.4233

> <JCHEM_ROTATABLE_BOND_COUNT>
1

> <JCHEM_RULE_OF_FIVE>
0

> <JCHEM_TRADITIONAL_IUPAC>
(1R,2R,9R,10S,13R,14R,17S,19R,20S)-6-isopropyl-1,2,9,14,18,18-hexamethylpentacyclo[11.8.0.0^{2,10}.0^{5,9}.0^{14,19}]henicosa-3,5-diene-17,20-diol

> <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      -2.133  -9.609   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      -0.676 -10.107   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      -0.379 -11.618   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       0.484  -9.094   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       1.985  -9.438   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       2.735 -10.783   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       4.275 -10.806   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       5.065  -9.484   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       5.814 -10.830   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       4.315  -8.139   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       5.105  -6.817   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       6.645  -6.841   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       7.395  -8.186   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       8.935  -8.209   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       8.185  -6.864   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       9.725  -6.888   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      11.265  -6.911   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      12.014  -8.256   0.000  0.00  0.00           C+0
HETATM   19  O   UNK     0      13.554  -8.280   0.000  0.00  0.00           O+0
HETATM   20  C   UNK     0      11.224  -9.578   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0      12.663 -10.127   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0      10.934 -11.090   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       9.684  -9.555   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       8.894 -10.876   0.000  0.00  0.00           C+0
HETATM   25  O   UNK     0       9.644 -12.222   0.000  0.00  0.00           O+0
HETATM   26  C   UNK     0       7.354 -10.853   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0       6.605  -9.508   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0       6.742 -11.042   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0       2.775  -8.116   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0       3.423  -6.719   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0       1.762  -6.956   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0       0.346  -7.561   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3    4                                                  
CONECT    3    2                                                            
CONECT    4    2    5   32                                                  
CONECT    5    4    6   29                                                  
CONECT    6    5    7                                                       
CONECT    7    6    8                                                       
CONECT    8    7    9   10   27                                             
CONECT    9    8                                                            
CONECT   10    8   11   29                                                  
CONECT   11   10   12                                                       
CONECT   12   11   13                                                       
CONECT   13   12   14   27                                                  
CONECT   14   13   15   16   23                                             
CONECT   15   14                                                            
CONECT   16   14   17                                                       
CONECT   17   16   18                                                       
CONECT   18   17   19   20                                                  
CONECT   19   18                                                            
CONECT   20   18   21   22   23                                             
CONECT   21   20                                                            
CONECT   22   20                                                            
CONECT   23   20   14   24                                                  
CONECT   24   23   25   26                                                  
CONECT   25   24                                                            
CONECT   26   24   27                                                       
CONECT   27   26   13    8   28                                             
CONECT   28   27                                                            
CONECT   29   10    5   30   31                                             
CONECT   30   29                                                            
CONECT   31   29   32                                                       
CONECT   32   31    4                                                       
MASTER        0    0    0    0    0    0    0    0   32    0   72    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₃₀H₄₈O₂

Average Mass

440.7120 Da

Monoisotopic Mass

440.36543 Da

IUPAC Name

Not Available

Traditional Name

Not Available

CAS Registry Number

Not Available

SMILES

CC(C)C1=C2C=C[C@]3(C)[C@@H](CC[C@@H]4[C@@]5(C)CC[C@H](O)C(C)(C)[C@@H]5[C@@H](O)C[C@@]34C)[C@@]2(C)CC1

InChI Identifier

InChI=1S/C30H48O2/c1-18(2)19-11-14-27(5)20(19)12-16-29(7)22(27)9-10-23-28(6)15-13-24(32)26(3,4)25(28)21(31)17-30(23,29)8/h12,16,18,21-25,31-32H,9-11,13-15,17H2,1-8H3/t21-,22-,23+,24-,25-,27-,28+,29+,30+/m0/s1

InChI Key

VUBKTAWHNLXBDM-XFFVLEOYSA-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
Mollugo pentaphylla	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as hopanoids. These are terpenoids containing hopane skeleton(A'-Neogammacerane), a pentacyclic structure with four cyclohexane rings and one cyclopentane ring (and often, a side chain emerging from C30).

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Prenol lipids

Sub Class

Hopanoids

Direct Parent

Hopanoids

Alternative Parents

Substituents

Triterpenoid
Hopane-skeleton
Hydroxysteroid
2-hydroxysteroid
Steroid
Cyclic alcohol
Secondary alcohol
Organic oxygen compound
Hydrocarbon derivative
Organooxygen compound
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

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

162961777

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for (5ar,5br,7s,7ar,9s,11ar,11br,13as,13br)-3-isopropyl-5a,5b,8,8,11a,13b-hexamethyl-1h,2h,6h,7h,7ah,9h,10h,11h,11bh,12h,13h,13ah-cyclopenta[a]chrysene-7,9-diol (NP0235204)

MOL for NP0235204 ((5ar,5br,7s,7ar,9s,11ar,11br,13as,13br)-3-isopropyl-5a,5b,8,8,11a,13b-hexamethyl-1h,2h,6h,7h,7ah,9h,10h,11h,11bh,12h,13h,13ah-cyclopenta[a]chrysene-7,9-diol)

3D MOL for NP0235204 ((5ar,5br,7s,7ar,9s,11ar,11br,13as,13br)-3-isopropyl-5a,5b,8,8,11a,13b-hexamethyl-1h,2h,6h,7h,7ah,9h,10h,11h,11bh,12h,13h,13ah-cyclopenta[a]chrysene-7,9-diol)

3D SDF for NP0235204 ((5ar,5br,7s,7ar,9s,11ar,11br,13as,13br)-3-isopropyl-5a,5b,8,8,11a,13b-hexamethyl-1h,2h,6h,7h,7ah,9h,10h,11h,11bh,12h,13h,13ah-cyclopenta[a]chrysene-7,9-diol)

3D-SDF for NP0235204 ((5ar,5br,7s,7ar,9s,11ar,11br,13as,13br)-3-isopropyl-5a,5b,8,8,11a,13b-hexamethyl-1h,2h,6h,7h,7ah,9h,10h,11h,11bh,12h,13h,13ah-cyclopenta[a]chrysene-7,9-diol)

PDB for NP0235204 ((5ar,5br,7s,7ar,9s,11ar,11br,13as,13br)-3-isopropyl-5a,5b,8,8,11a,13b-hexamethyl-1h,2h,6h,7h,7ah,9h,10h,11h,11bh,12h,13h,13ah-cyclopenta[a]chrysene-7,9-diol)

3D PDB for NP0235204 ((5ar,5br,7s,7ar,9s,11ar,11br,13as,13br)-3-isopropyl-5a,5b,8,8,11a,13b-hexamethyl-1h,2h,6h,7h,7ah,9h,10h,11h,11bh,12h,13h,13ah-cyclopenta[a]chrysene-7,9-diol)

SMILES for NP0235204 ((5ar,5br,7s,7ar,9s,11ar,11br,13as,13br)-3-isopropyl-5a,5b,8,8,11a,13b-hexamethyl-1h,2h,6h,7h,7ah,9h,10h,11h,11bh,12h,13h,13ah-cyclopenta[a]chrysene-7,9-diol)

INCHI for NP0235204 ((5ar,5br,7s,7ar,9s,11ar,11br,13as,13br)-3-isopropyl-5a,5b,8,8,11a,13b-hexamethyl-1h,2h,6h,7h,7ah,9h,10h,11h,11bh,12h,13h,13ah-cyclopenta[a]chrysene-7,9-diol)

Structure for NP0235204 ((5ar,5br,7s,7ar,9s,11ar,11br,13as,13br)-3-isopropyl-5a,5b,8,8,11a,13b-hexamethyl-1h,2h,6h,7h,7ah,9h,10h,11h,11bh,12h,13h,13ah-cyclopenta[a]chrysene-7,9-diol)

3D Structure for NP0235204 ((5ar,5br,7s,7ar,9s,11ar,11br,13as,13br)-3-isopropyl-5a,5b,8,8,11a,13b-hexamethyl-1h,2h,6h,7h,7ah,9h,10h,11h,11bh,12h,13h,13ah-cyclopenta[a]chrysene-7,9-diol)