NP-MRD: Showing NP-Card for {3-isopropyl-3a,5a,7a,8,13a-pentamethyl-1h,2h,3h,4h,5h,5bh,6h,7h,10h,11h,11ah,12h,13h,13bh-cyclopenta[a]chrysen-11b-yl}methanol (NP0318951)

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Record Information

Version

2.0

Created at

2022-09-11 19:44:19 UTC

Updated at

2022-09-11 19:44:19 UTC

NP-MRD ID

NP0318951

Secondary Accession Numbers

None

Natural Product Identification

Common Name

{3-isopropyl-3a,5a,7a,8,13a-pentamethyl-1h,2h,3h,4h,5h,5bh,6h,7h,10h,11h,11ah,12h,13h,13bh-cyclopenta[a]chrysen-11b-yl}methanol

Description

Filicenol B belongs to the class of organic compounds known as colensane and clerodane diterpenoids. These are diterpenoids with a structure based on the clerodane or the colensane skeleton. Clerodanes arise from labdanes by two methyl migrations. Filicenol B is an extremely weak basic (essentially neutral) compound (based on its pKa).

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1533004151519432D          

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M  END

     RDKit          3D

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M  END


  Mrv1533004151519432D          

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 17 19  1  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
 22 23  2  0  0  0  0
 17 23  1  0  0  0  0
 23 24  1  0  0  0  0
 19 25  1  0  0  0  0
 14 25  1  0  0  0  0
 25 26  1  0  0  0  0
 26 27  1  0  0  0  0
 25 28  1  0  0  0  0
 28 29  1  0  0  0  0
 29 30  1  0  0  0  0
  7 30  1  0  0  0  0
 12 30  1  0  0  0  0
 30 31  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0318951

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC(C)C1CCC2C1(C)CCC1(C)C3CCC4(C)C(CCC=C4C)C3(CO)CCC21C

> <INCHI_IDENTIFIER>
InChI=1S/C30H50O/c1-20(2)22-11-12-23-27(22,5)15-16-29(7)25-13-14-26(4)21(3)9-8-10-24(26)30(25,19-31)18-17-28(23,29)6/h9,20,22-25,31H,8,10-19H2,1-7H3

> <INCHI_KEY>
BBMOJJIXVZRNCE-UHFFFAOYSA-N

> <FORMULA>
C30H50O

> <MOLECULAR_WEIGHT>
426.729

> <EXACT_MASS>
426.38616623

> <JCHEM_ACCEPTOR_COUNT>
1

> <JCHEM_ATOM_COUNT>
81

> <JCHEM_AVERAGE_POLARIZABILITY>
54.389651635646146

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
[2,5,10,18,19-pentamethyl-6-(propan-2-yl)pentacyclo[11.8.0.0²,¹⁰.0⁵,⁹.0¹⁴,¹⁹]henicos-17-en-13-yl]methanol

> <ALOGPS_LOGP>
6.71

> <JCHEM_LOGP>
7.340152721

> <ALOGPS_LOGS>
-7.09

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
5

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_ACIDIC>
19.467346373984082

> <JCHEM_PKA_STRONGEST_BASIC>
-0.8447826960193615

> <JCHEM_POLAR_SURFACE_AREA>
20.23

> <JCHEM_REFRACTIVITY>
132.24

> <JCHEM_ROTATABLE_BOND_COUNT>
2

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
3.48e-05 g/l

> <JCHEM_TRADITIONAL_IUPAC>
{6-isopropyl-2,5,10,18,19-pentamethylpentacyclo[11.8.0.0²,¹⁰.0⁵,⁹.0¹⁴,¹⁹]henicos-17-en-13-yl}methanol

> <JCHEM_VEBER_RULE>
1

$$$$

HEADER    PROTEIN                                 15-APR-15   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   15-APR-15         0                                  
HETATM    1  C   UNK     0      -9.998  -5.226   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      -8.541  -5.725   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      -8.244  -7.236   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      -7.381  -4.712   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      -7.519  -3.178   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      -6.103  -2.573   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      -5.090  -3.733   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      -5.880  -5.055   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      -6.804  -6.287   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      -5.130  -6.400   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      -3.591  -6.423   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      -2.800  -5.102   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      -2.051  -6.447   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      -1.261  -5.125   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      -0.511  -6.470   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       1.029  -6.494   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       1.819  -5.172   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       2.569  -6.517   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       1.070  -3.827   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       1.860  -2.505   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       3.400  -2.528   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       4.149  -3.873   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       3.359  -5.195   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       4.109  -6.540   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0      -0.470  -3.803   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       0.320  -2.481   0.000  0.00  0.00           C+0
HETATM   27  O   UNK     0      -0.430  -1.136   0.000  0.00  0.00           O+0
HETATM   28  C   UNK     0      -1.220  -2.458   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0      -2.760  -2.435   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0      -3.550  -3.756   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0      -4.300  -2.411   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3    4                                                  
CONECT    3    2                                                            
CONECT    4    2    5    8                                                  
CONECT    5    4    6                                                       
CONECT    6    5    7                                                       
CONECT    7    6    8   30                                                  
CONECT    8    7    4    9   10                                             
CONECT    9    8                                                            
CONECT   10    8   11                                                       
CONECT   11   10   12                                                       
CONECT   12   11   13   14   30                                             
CONECT   13   12                                                            
CONECT   14   12   15   25                                                  
CONECT   15   14   16                                                       
CONECT   16   15   17                                                       
CONECT   17   16   18   19   23                                             
CONECT   18   17                                                            
CONECT   19   17   20   25                                                  
CONECT   20   19   21                                                       
CONECT   21   20   22                                                       
CONECT   22   21   23                                                       
CONECT   23   22   17   24                                                  
CONECT   24   23                                                            
CONECT   25   19   14   26   28                                             
CONECT   26   25   27                                                       
CONECT   27   26                                                            
CONECT   28   25   29                                                       
CONECT   29   28   30                                                       
CONECT   30   29    7   12   31                                             
CONECT   31   30                                                            
MASTER        0    0    0    0    0    0    0    0   31    0   70    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₃₀H₅₀O

Average Mass

426.7290 Da

Monoisotopic Mass

426.38617 Da

IUPAC Name

[2,5,10,18,19-pentamethyl-6-(propan-2-yl)pentacyclo[11.8.0.0²,¹⁰.0⁵,⁹.0¹⁴,¹⁹]henicos-17-en-13-yl]methanol

Traditional Name

{6-isopropyl-2,5,10,18,19-pentamethylpentacyclo[11.8.0.0²,¹⁰.0⁵,⁹.0¹⁴,¹⁹]henicos-17-en-13-yl}methanol

CAS Registry Number

Not Available

SMILES

CC(C)C1CCC2C1(C)CCC1(C)C3CCC4(C)C(CCC=C4C)C3(CO)CCC21C

InChI Identifier

InChI=1S/C30H50O/c1-20(2)22-11-12-23-27(22,5)15-16-29(7)25-13-14-26(4)21(3)9-8-10-24(26)30(25,19-31)18-17-28(23,29)6/h9,20,22-25,31H,8,10-19H2,1-7H3

InChI Key

BBMOJJIXVZRNCE-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

Not Available

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as colensane and clerodane diterpenoids. These are diterpenoids with a structure based on the clerodane or the colensane skeleton. Clerodanes arise from labdanes by two methyl migrations.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Prenol lipids

Sub Class

Diterpenoids

Direct Parent

Colensane and clerodane diterpenoids

Alternative Parents

Substituents

Clerodane diterpenoid
Steroid
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	6.71	ALOGPS
logP	7.34	ChemAxon
logS	-7.1	ALOGPS
pKa (Strongest Acidic)	19.47	ChemAxon
pKa (Strongest Basic)	-0.84	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	1	ChemAxon
Hydrogen Donor Count	1	ChemAxon
Polar Surface Area	20.23 Å²	ChemAxon
Rotatable Bond Count	2	ChemAxon
Refractivity	132.24 m³·mol⁻¹	ChemAxon
Polarizability	54.39 Å³	ChemAxon
Number of Rings	5	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	No	ChemAxon
Ghose Filter	No	ChemAxon
Veber's Rule	Yes	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

85096041

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for {3-isopropyl-3a,5a,7a,8,13a-pentamethyl-1h,2h,3h,4h,5h,5bh,6h,7h,10h,11h,11ah,12h,13h,13bh-cyclopenta[a]chrysen-11b-yl}methanol (NP0318951)

MOL for NP0318951 ({3-isopropyl-3a,5a,7a,8,13a-pentamethyl-1h,2h,3h,4h,5h,5bh,6h,7h,10h,11h,11ah,12h,13h,13bh-cyclopenta[a]chrysen-11b-yl}methanol)

3D MOL for NP0318951 ({3-isopropyl-3a,5a,7a,8,13a-pentamethyl-1h,2h,3h,4h,5h,5bh,6h,7h,10h,11h,11ah,12h,13h,13bh-cyclopenta[a]chrysen-11b-yl}methanol)

3D SDF for NP0318951 ({3-isopropyl-3a,5a,7a,8,13a-pentamethyl-1h,2h,3h,4h,5h,5bh,6h,7h,10h,11h,11ah,12h,13h,13bh-cyclopenta[a]chrysen-11b-yl}methanol)

3D-SDF for NP0318951 ({3-isopropyl-3a,5a,7a,8,13a-pentamethyl-1h,2h,3h,4h,5h,5bh,6h,7h,10h,11h,11ah,12h,13h,13bh-cyclopenta[a]chrysen-11b-yl}methanol)

PDB for NP0318951 ({3-isopropyl-3a,5a,7a,8,13a-pentamethyl-1h,2h,3h,4h,5h,5bh,6h,7h,10h,11h,11ah,12h,13h,13bh-cyclopenta[a]chrysen-11b-yl}methanol)

3D PDB for NP0318951 ({3-isopropyl-3a,5a,7a,8,13a-pentamethyl-1h,2h,3h,4h,5h,5bh,6h,7h,10h,11h,11ah,12h,13h,13bh-cyclopenta[a]chrysen-11b-yl}methanol)

SMILES for NP0318951 ({3-isopropyl-3a,5a,7a,8,13a-pentamethyl-1h,2h,3h,4h,5h,5bh,6h,7h,10h,11h,11ah,12h,13h,13bh-cyclopenta[a]chrysen-11b-yl}methanol)

INCHI for NP0318951 ({3-isopropyl-3a,5a,7a,8,13a-pentamethyl-1h,2h,3h,4h,5h,5bh,6h,7h,10h,11h,11ah,12h,13h,13bh-cyclopenta[a]chrysen-11b-yl}methanol)

Structure for NP0318951 ({3-isopropyl-3a,5a,7a,8,13a-pentamethyl-1h,2h,3h,4h,5h,5bh,6h,7h,10h,11h,11ah,12h,13h,13bh-cyclopenta[a]chrysen-11b-yl}methanol)

3D Structure for NP0318951 ({3-isopropyl-3a,5a,7a,8,13a-pentamethyl-1h,2h,3h,4h,5h,5bh,6h,7h,10h,11h,11ah,12h,13h,13bh-cyclopenta[a]chrysen-11b-yl}methanol)