NP-MRD: Showing NP-Card for (1r,3s,3ar,5as,5bs,6s,7as,9s,13ar,13br)-3a-(hydroxymethyl)-3-isopropyl-5a,8,8,13a-tetramethyl-1h,2h,3h,4h,5h,5bh,6h,7h,7ah,9h,10h,13h,13bh-cyclopenta[a]chrysene-1,6,9-triol (NP0256487)

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Record Information

Version

2.0

Created at

2022-09-07 21:20:03 UTC

Updated at

2022-09-07 21:20:03 UTC

NP-MRD ID

NP0256487

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(1r,3s,3ar,5as,5bs,6s,7as,9s,13ar,13br)-3a-(hydroxymethyl)-3-isopropyl-5a,8,8,13a-tetramethyl-1h,2h,3h,4h,5h,5bh,6h,7h,7ah,9h,10h,13h,13bh-cyclopenta[a]chrysene-1,6,9-triol

Description

CHEMBL2063153 belongs to the class of organic compounds known as 1-hydroxysteroids. These are steroids carrying a hydroxyl group at the 1-position of the steroid backbone. (1r,3s,3ar,5as,5bs,6s,7as,9s,13ar,13br)-3a-(hydroxymethyl)-3-isopropyl-5a,8,8,13a-tetramethyl-1h,2h,3h,4h,5h,5bh,6h,7h,7ah,9h,10h,13h,13bh-cyclopenta[a]chrysene-1,6,9-triol is found in Bambusa emeiensis. Based on a literature review very few articles have been published on CHEMBL2063153.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309072223202D          

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M  END

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M  END


  Mrv1652309072223202D          

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  8  9  1  0  0  0  0
  4  9  1  0  0  0  0
  9 10  1  6  0  0  0
 10 11  1  0  0  0  0
  9 12  1  0  0  0  0
 12 13  1  0  0  0  0
 13 14  1  0  0  0  0
 14 15  1  1  0  0  0
 14 16  1  0  0  0  0
 16 17  1  1  0  0  0
 17 18  2  0  0  0  0
 18 19  1  0  0  0  0
 19 20  1  0  0  0  0
  8 20  1  0  0  0  0
 14 20  1  0  0  0  0
 20 21  1  6  0  0  0
 17 22  1  0  0  0  0
 22 23  2  0  0  0  0
 23 24  1  0  0  0  0
 24 25  1  0  0  0  0
 25 26  1  6  0  0  0
 25 27  1  0  0  0  0
 27 28  1  0  0  0  0
 27 29  1  0  0  0  0
 27 30  1  0  0  0  0
 30 22  1  1  0  0  0
 30 31  1  0  0  0  0
 31 32  1  0  0  0  0
 16 32  1  0  0  0  0
 32 33  1  6  0  0  0
M  END
> <DATABASE_ID>
NP0256487

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC(C)[C@@H]1C[C@@H](O)[C@H]2[C@@]1(CO)CC[C@@]1(C)[C@@H]3[C@@H](O)C[C@H]4C(=CC[C@H](O)C4(C)C)C3=CC[C@]21C

> <INCHI_IDENTIFIER>
InChI=1S/C29H46O4/c1-16(2)19-13-22(32)25-28(6)10-9-18-17-7-8-23(33)26(3,4)20(17)14-21(31)24(18)27(28,5)11-12-29(19,25)15-30/h7,9,16,19-25,30-33H,8,10-15H2,1-6H3/t19-,20-,21-,22+,23-,24-,25+,27-,28+,29+/m0/s1

> <INCHI_KEY>
QUGMJAYSRDUJID-WOSWGKDQSA-N

> <FORMULA>
C29H46O4

> <MOLECULAR_WEIGHT>
458.683

> <EXACT_MASS>
458.339609961

> <JCHEM_ACCEPTOR_COUNT>
4

> <JCHEM_ATOM_COUNT>
79

> <JCHEM_AVERAGE_POLARIZABILITY>
54.6728246539916

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
4

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(1S,2S,5R,6S,8R,9R,10R,17S,19S,21S)-5-(hydroxymethyl)-2,10,18,18-tetramethyl-6-(propan-2-yl)pentacyclo[11.8.0.0^{2,10}.0^{5,9}.0^{14,19}]henicosa-12,14-diene-8,17,21-triol

> <JCHEM_LOGP>
2.7861854586666657

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
5

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
15.310666689807512

> <JCHEM_PKA_STRONGEST_ACIDIC>
14.682468406106786

> <JCHEM_PKA_STRONGEST_BASIC>
-0.30621979645934616

> <JCHEM_POLAR_SURFACE_AREA>
80.92

> <JCHEM_REFRACTIVITY>
133.3154

> <JCHEM_ROTATABLE_BOND_COUNT>
2

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
(1S,2S,5R,6S,8R,9R,10R,17S,19S,21S)-5-(hydroxymethyl)-6-isopropyl-2,10,18,18-tetramethylpentacyclo[11.8.0.0^{2,10}.0^{5,9}.0^{14,19}]henicosa-12,14-diene-8,17,21-triol

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 07-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   07-SEP-22         0                                  
HETATM    1  C   UNK     0      13.941   2.146   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      12.484   2.645   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      12.187   4.156   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      11.324   1.632   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      11.462   0.098   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      10.046  -0.507   0.000  0.00  0.00           C+0
HETATM    7  O   UNK     0       9.703  -2.008   0.000  0.00  0.00           O+0
HETATM    8  C   UNK     0       9.033   0.653   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       9.823   1.975   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      10.747   3.207   0.000  0.00  0.00           C+0
HETATM   11  O   UNK     0      10.142   4.623   0.000  0.00  0.00           O+0
HETATM   12  C   UNK     0       9.073   3.320   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       7.534   3.343   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       6.743   2.022   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       5.994   3.367   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       5.204   2.045   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       4.413   0.723   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       5.163  -0.622   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       6.703  -0.645   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       7.493   0.676   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       8.243  -0.669   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       2.874   0.747   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       2.083  -0.575   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       0.543  -0.552   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0      -0.206   0.793   0.000  0.00  0.00           C+0
HETATM   26  O   UNK     0      -1.746   0.817   0.000  0.00  0.00           O+0
HETATM   27  C   UNK     0       0.584   2.115   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0      -0.855   2.664   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0       0.875   3.628   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0       2.124   2.092   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0       2.914   3.414   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0       4.454   3.390   0.000  0.00  0.00           C+0
HETATM   33  O   UNK     0       5.244   4.712   0.000  0.00  0.00           O+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   20                                                  
CONECT    9    8    4   10   12                                             
CONECT   10    9   11                                                       
CONECT   11   10                                                            
CONECT   12    9   13                                                       
CONECT   13   12   14                                                       
CONECT   14   13   15   16   20                                             
CONECT   15   14                                                            
CONECT   16   14   17   32                                                  
CONECT   17   16   18   22                                                  
CONECT   18   17   19                                                       
CONECT   19   18   20                                                       
CONECT   20   19    8   14   21                                             
CONECT   21   20                                                            
CONECT   22   17   23   30                                                  
CONECT   23   22   24                                                       
CONECT   24   23   25                                                       
CONECT   25   24   26   27                                                  
CONECT   26   25                                                            
CONECT   27   25   28   29   30                                             
CONECT   28   27                                                            
CONECT   29   27                                                            
CONECT   30   27   22   31                                                  
CONECT   31   30   32                                                       
CONECT   32   31   16   33                                                  
CONECT   33   32                                                            
MASTER        0    0    0    0    0    0    0    0   33    0   74    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₉H₄₆O₄

Average Mass

458.6830 Da

Monoisotopic Mass

458.33961 Da

IUPAC Name

(1S,2S,5R,6S,8R,9R,10R,17S,19S,21S)-5-(hydroxymethyl)-2,10,18,18-tetramethyl-6-(propan-2-yl)pentacyclo[11.8.0.0^{2,10}.0^{5,9}.0^{14,19}]henicosa-12,14-diene-8,17,21-triol

Traditional Name

(1S,2S,5R,6S,8R,9R,10R,17S,19S,21S)-5-(hydroxymethyl)-6-isopropyl-2,10,18,18-tetramethylpentacyclo[11.8.0.0^{2,10}.0^{5,9}.0^{14,19}]henicosa-12,14-diene-8,17,21-triol

CAS Registry Number

Not Available

SMILES

CC(C)[C@@H]1C[C@@H](O)[C@H]2[C@@]1(CO)CC[C@@]1(C)[C@@H]3[C@@H](O)C[C@H]4C(=CC[C@H](O)C4(C)C)C3=CC[C@]21C

InChI Identifier

InChI=1S/C29H46O4/c1-16(2)19-13-22(32)25-28(6)10-9-18-17-7-8-23(33)26(3,4)20(17)14-21(31)24(18)27(28,5)11-12-29(19,25)15-30/h7,9,16,19-25,30-33H,8,10-15H2,1-6H3/t19-,20-,21-,22+,23-,24-,25+,27-,28+,29+/m0/s1

InChI Key

QUGMJAYSRDUJID-WOSWGKDQSA-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
Bambusa emeiensis	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as 1-hydroxysteroids. These are steroids carrying a hydroxyl group at the 1-position of the steroid backbone.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Steroids and steroid derivatives

Sub Class

Hydroxysteroids

Direct Parent

1-hydroxysteroids

Alternative Parents

Substituents

18-hydroxysteroid
1-hydroxysteroid
Delta-5-steroid
Cyclic alcohol
Secondary alcohol
Polyol
Organic oxygen compound
Hydrocarbon derivative
Primary alcohol
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
logP	2.79	ChemAxon
pKa (Strongest Acidic)	14.68	ChemAxon
pKa (Strongest Basic)	-0.31	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	4	ChemAxon
Hydrogen Donor Count	4	ChemAxon
Polar Surface Area	80.92 Å²	ChemAxon
Rotatable Bond Count	2	ChemAxon
Refractivity	133.32 m³·mol⁻¹	ChemAxon
Polarizability	54.67 Å³	ChemAxon
Number of Rings	5	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	Yes	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

28519948

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

70682276

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for (1r,3s,3ar,5as,5bs,6s,7as,9s,13ar,13br)-3a-(hydroxymethyl)-3-isopropyl-5a,8,8,13a-tetramethyl-1h,2h,3h,4h,5h,5bh,6h,7h,7ah,9h,10h,13h,13bh-cyclopenta[a]chrysene-1,6,9-triol (NP0256487)

MOL for NP0256487 ((1r,3s,3ar,5as,5bs,6s,7as,9s,13ar,13br)-3a-(hydroxymethyl)-3-isopropyl-5a,8,8,13a-tetramethyl-1h,2h,3h,4h,5h,5bh,6h,7h,7ah,9h,10h,13h,13bh-cyclopenta[a]chrysene-1,6,9-triol)

3D MOL for NP0256487 ((1r,3s,3ar,5as,5bs,6s,7as,9s,13ar,13br)-3a-(hydroxymethyl)-3-isopropyl-5a,8,8,13a-tetramethyl-1h,2h,3h,4h,5h,5bh,6h,7h,7ah,9h,10h,13h,13bh-cyclopenta[a]chrysene-1,6,9-triol)

3D SDF for NP0256487 ((1r,3s,3ar,5as,5bs,6s,7as,9s,13ar,13br)-3a-(hydroxymethyl)-3-isopropyl-5a,8,8,13a-tetramethyl-1h,2h,3h,4h,5h,5bh,6h,7h,7ah,9h,10h,13h,13bh-cyclopenta[a]chrysene-1,6,9-triol)

3D-SDF for NP0256487 ((1r,3s,3ar,5as,5bs,6s,7as,9s,13ar,13br)-3a-(hydroxymethyl)-3-isopropyl-5a,8,8,13a-tetramethyl-1h,2h,3h,4h,5h,5bh,6h,7h,7ah,9h,10h,13h,13bh-cyclopenta[a]chrysene-1,6,9-triol)

PDB for NP0256487 ((1r,3s,3ar,5as,5bs,6s,7as,9s,13ar,13br)-3a-(hydroxymethyl)-3-isopropyl-5a,8,8,13a-tetramethyl-1h,2h,3h,4h,5h,5bh,6h,7h,7ah,9h,10h,13h,13bh-cyclopenta[a]chrysene-1,6,9-triol)

3D PDB for NP0256487 ((1r,3s,3ar,5as,5bs,6s,7as,9s,13ar,13br)-3a-(hydroxymethyl)-3-isopropyl-5a,8,8,13a-tetramethyl-1h,2h,3h,4h,5h,5bh,6h,7h,7ah,9h,10h,13h,13bh-cyclopenta[a]chrysene-1,6,9-triol)

SMILES for NP0256487 ((1r,3s,3ar,5as,5bs,6s,7as,9s,13ar,13br)-3a-(hydroxymethyl)-3-isopropyl-5a,8,8,13a-tetramethyl-1h,2h,3h,4h,5h,5bh,6h,7h,7ah,9h,10h,13h,13bh-cyclopenta[a]chrysene-1,6,9-triol)

INCHI for NP0256487 ((1r,3s,3ar,5as,5bs,6s,7as,9s,13ar,13br)-3a-(hydroxymethyl)-3-isopropyl-5a,8,8,13a-tetramethyl-1h,2h,3h,4h,5h,5bh,6h,7h,7ah,9h,10h,13h,13bh-cyclopenta[a]chrysene-1,6,9-triol)

Structure for NP0256487 ((1r,3s,3ar,5as,5bs,6s,7as,9s,13ar,13br)-3a-(hydroxymethyl)-3-isopropyl-5a,8,8,13a-tetramethyl-1h,2h,3h,4h,5h,5bh,6h,7h,7ah,9h,10h,13h,13bh-cyclopenta[a]chrysene-1,6,9-triol)

3D Structure for NP0256487 ((1r,3s,3ar,5as,5bs,6s,7as,9s,13ar,13br)-3a-(hydroxymethyl)-3-isopropyl-5a,8,8,13a-tetramethyl-1h,2h,3h,4h,5h,5bh,6h,7h,7ah,9h,10h,13h,13bh-cyclopenta[a]chrysene-1,6,9-triol)