NP-MRD: Showing NP-Card for Viperidone (NP0078804)

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Record Information

Version

2.0

Created at

2022-04-28 23:52:33 UTC

Updated at

2022-04-28 23:52:33 UTC

NP-MRD ID

NP0078804

Secondary Accession Numbers

None

Natural Product Identification

Common Name

Viperidone

Description

CHEMBL470041 belongs to the class of organic compounds known as cholesterols and derivatives. Cholesterols and derivatives are compounds containing a 3-hydroxylated cholestane core. Viperidone is found in Leptocereus quadricostatus and Peniocereus viperinus. Based on a literature review very few articles have been published on CHEMBL470041.

Structure

MOL 3D MOL SDF PDB SMILES InChI

  Mrv1652304292201532D          

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M  END

     RDKit          3D

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M  END

  Mrv1652304292201532D          

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M  END
> <DATABASE_ID>
NP0078804

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC(C)CCC[C@@H](C)[C@H]1CC[C@H]2C3=CC(=O)[C@H]4C[C@@H](O)CC[C@]4(C)[C@@]3(O)CC[C@]12C

> <INCHI_IDENTIFIER>
InChI=1S/C27H44O3/c1-17(2)7-6-8-18(3)20-9-10-21-22-16-24(29)23-15-19(28)11-12-26(23,5)27(22,30)14-13-25(20,21)4/h16-21,23,28,30H,6-15H2,1-5H3/t18-,19+,20-,21+,23-,25-,26+,27-/m1/s1

> <INCHI_KEY>
HGCLEPLEUUJGID-REBIDWDSSA-N

> <FORMULA>
C27H44O3

> <MOLECULAR_WEIGHT>
416.646

> <EXACT_MASS>
416.329045277

> <JCHEM_ACCEPTOR_COUNT>
3

> <JCHEM_ATOM_COUNT>
74

> <JCHEM_AVERAGE_POLARIZABILITY>
51.40763569242839

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(1S,2S,5S,7S,11R,14R,15R)-1,5-dihydroxy-2,15-dimethyl-14-[(2R)-6-methylheptan-2-yl]tetracyclo[8.7.0.0^{2,7}.0^{11,15}]heptadec-9-en-8-one

> <ALOGPS_LOGP>
5.43

> <JCHEM_LOGP>
5.545991328666666

> <ALOGPS_LOGS>
-5.14

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
15.246806753423435

> <JCHEM_PKA_STRONGEST_ACIDIC>
13.750036452688121

> <JCHEM_PKA_STRONGEST_BASIC>
-2.696720365281294

> <JCHEM_POLAR_SURFACE_AREA>
57.53

> <JCHEM_REFRACTIVITY>
122.63459999999998

> <JCHEM_ROTATABLE_BOND_COUNT>
5

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
3.03e-03 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(1S,2S,5S,7S,11R,14R,15R)-1,5-dihydroxy-2,15-dimethyl-14-[(2R)-6-methylheptan-2-yl]tetracyclo[8.7.0.0^{2,7}.0^{11,15}]heptadec-9-en-8-one

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 29-APR-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   29-APR-22         0                                  
HETATM    1  C   UNK     0     -11.375  -4.661   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0     -12.405  -3.517   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0     -11.929  -2.052   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0     -12.960  -0.908   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0     -14.466  -1.228   0.000  0.00  0.00           C+0
HETATM    6  O   UNK     0     -15.496  -0.084   0.000  0.00  0.00           O+0
HETATM    7  C   UNK     0     -14.942  -2.693   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0     -13.911  -3.837   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0     -14.387  -5.302   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0     -15.894  -5.622   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0     -16.924  -4.478   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0     -16.448  -3.013   0.000  0.00  0.00           C+0
HETATM   13  O   UNK     0     -18.430  -4.798   0.000  0.00  0.00           O+0
HETATM   14  C   UNK     0     -12.881  -4.982   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0     -10.423  -1.732   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      -9.392  -2.877   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      -9.868  -4.341   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      -7.986  -2.250   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0      -8.146  -0.719   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0      -9.653  -0.399   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0      -6.652  -3.020   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0      -6.652  -4.560   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0      -5.318  -2.250   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0      -3.984  -3.020   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0      -2.651  -2.250   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0      -1.317  -3.020   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0       0.017  -2.250   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0      -1.317  -4.560   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0      -8.248  -3.907   0.000  0.00  0.00           C+0
HETATM   30  O   UNK     0     -11.929  -4.982   0.000  0.00  0.00           O+0
CONECT    1    2   17                                                       
CONECT    2    1    3    8   30                                             
CONECT    3    2    4   15                                                  
CONECT    4    3    5                                                       
CONECT    5    4    6    7                                                  
CONECT    6    5                                                            
CONECT    7    5    8   12                                                  
CONECT    8    7    2    9   14                                             
CONECT    9    8   10                                                       
CONECT   10    9   11                                                       
CONECT   11   10   12   13                                                  
CONECT   12   11    7                                                       
CONECT   13   11                                                            
CONECT   14    8                                                            
CONECT   15    3   16   20                                                  
CONECT   16   15   17   18   29                                             
CONECT   17   16    1                                                       
CONECT   18   16   19   21                                                  
CONECT   19   18   20                                                       
CONECT   20   19   15                                                       
CONECT   21   18   22   23                                                  
CONECT   22   21                                                            
CONECT   23   21   24                                                       
CONECT   24   23   25                                                       
CONECT   25   24   26                                                       
CONECT   26   25   27   28                                                  
CONECT   27   26                                                            
CONECT   28   26                                                            
CONECT   29   16                                                            
CONECT   30    2                                                            
MASTER        0    0    0    0    0    0    0    0   30    0   66    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₇H₄₄O₃

Average Mass

416.6460 Da

Monoisotopic Mass

416.32905 Da

IUPAC Name

(1S,2S,5S,7S,11R,14R,15R)-1,5-dihydroxy-2,15-dimethyl-14-[(2R)-6-methylheptan-2-yl]tetracyclo[8.7.0.0^{2,7}.0^{11,15}]heptadec-9-en-8-one

Traditional Name

(1S,2S,5S,7S,11R,14R,15R)-1,5-dihydroxy-2,15-dimethyl-14-[(2R)-6-methylheptan-2-yl]tetracyclo[8.7.0.0^{2,7}.0^{11,15}]heptadec-9-en-8-one

CAS Registry Number

Not Available

SMILES

CC(C)CCC[C@@H](C)[C@H]1CC[C@H]2C3=CC(=O)[C@H]4C[C@@H](O)CC[C@]4(C)[C@@]3(O)CC[C@]12C

InChI Identifier

InChI=1S/C27H44O3/c1-17(2)7-6-8-18(3)20-9-10-21-22-16-24(29)23-15-19(28)11-12-26(23,5)27(22,30)14-13-25(20,21)4/h16-21,23,28,30H,6-15H2,1-5H3/t18-,19+,20-,21+,23-,25-,26+,27-/m1/s1

InChI Key

HGCLEPLEUUJGID-REBIDWDSSA-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, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 100 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 252 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 1000 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 50 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 200 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 75 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 300 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 101 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 126 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 500 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 151 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 600 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 176 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 700 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 201 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 800 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 226 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 900 MHz, D₂O, 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
Leptocereus quadricostatus	Plant	KNApSAcK
Peniocereus viperinus	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as cholesterols and derivatives. Cholesterols and derivatives are compounds containing a 3-hydroxylated cholestane core.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Steroids and steroid derivatives

Sub Class

Cholestane steroids

Direct Parent

Cholesterols and derivatives

Alternative Parents

Substituents

Cholesterol
Cholesterol-skeleton
Ecdysteroid
3-hydroxy-delta-7-steroid
3-hydroxysteroid
Hydroxysteroid
Oxosteroid
3-beta-hydroxysteroid
6-oxosteroid
Delta-7-steroid
Cyclohexenone
Cyclic alcohol
Tertiary alcohol
Ketone
Secondary alcohol
Organooxygen compound
Alcohol
Organic oxide
Carbonyl group
Organic oxygen compound
Hydrocarbon derivative
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	5.43	ALOGPS
logP	5.55	ChemAxon
logS	-5.1	ALOGPS
pKa (Strongest Acidic)	13.75	ChemAxon
pKa (Strongest Basic)	-2.7	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	3	ChemAxon
Hydrogen Donor Count	2	ChemAxon
Polar Surface Area	57.53 Å²	ChemAxon
Rotatable Bond Count	5	ChemAxon
Refractivity	122.63 m³·mol⁻¹	ChemAxon
Polarizability	51.41 Å³	ChemAxon
Number of Rings	4	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

10217081

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

21593998

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Not Available

Showing NP-Card for Viperidone (NP0078804)

MOL for NP0078804 (Viperidone)

3D MOL for NP0078804 (Viperidone)

3D SDF for NP0078804 (Viperidone)

3D-SDF for NP0078804 (Viperidone)

PDB for NP0078804 (Viperidone)

3D PDB for NP0078804 (Viperidone)

SMILES for NP0078804 (Viperidone)

INCHI for NP0078804 (Viperidone)

Structure for NP0078804 (Viperidone)

3D Structure for NP0078804 (Viperidone)