NP-MRD: Showing NP-Card for 5alpha-Stigmasta-7,24(28)-dien-3beta-ol (NP0044238)

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Record Information

Version

1.0

Created at

2022-02-14 20:33:33 UTC

Updated at

2022-03-10 22:17:43 UTC

NP-MRD ID

NP0044238

Secondary Accession Numbers

None

Natural Product Identification

Common Name

5alpha-Stigmasta-7,24(28)-dien-3beta-ol

Description

5Alpha-Stigmasta-7,24(28)-dien-3beta-ol is a steroid derivative characterized by a hydroxyl group in position C-3 of the steroid skeleton, and unsaturated bonds in position 7-8 the B ring, and position 24-25 in the alkyl substituent. It belongs to the class of organic compounds known as stigmastanes and derivatives. These are sterol-like molecules with a structure based on the stigmastane skeleton, which consists of a cholestane moiety bearing an ethyl group at the carbon atom C24 and a trans double bond in position C22. 5Alpha-Stigmasta-7,24(28)-dien-3beta-o lis a neutral, hydrophobic molecule that is insoluble in water. 5Alpha-Stigmasta-7,24(28)-dien-3beta-ol is a naturally occurring phytosterol found in plants. Phytosterols have a cholesterol-like structure consisting of four fused rings as a core structure and an acyclic side chain. Phytosterols differ only in carbon side chains and/or the presence or absence of a double bond. They play a similar role to cholesterol in stabilizing membrane lipids in plants. Phytosterols derive from the same biosynthetic precursor as the triterpenoids (2,3-oxidosqualene) and their biosynthesis also proceeds via the mevalonic acid pathway (MVA), mainly in the cytosol. In humans the intake of naturally occurring phytosterols ranges between ~200-300 mg/day depending on eating habits (PMID: 28702423 ). Phytosterols have cholesterol-lowering properties (reducing cholesterol absorption in intestines) and can reduce cholesterol in human subjects by up to 15% (PMID: 28702423 ). They may also have a role in cancer prevention and treatment (PMID: 26086253 ). Phytosterols naturally occur in small amount in vegetable oils, especially soybean oil. One such phytosterol complex, isolated from vegetable oil, is cholestatin, composed of campesterol, stigmasterol, and brassicasterol, and is marketed as a dietary supplement. 5Alpha-Stigmasta-7,24(28)-dien-3beta-ol is one of the phytosterols found in cannabis plants and oils (PMID: 6991645 ).

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652306262018362D          

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M  END

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M  END


  Mrv1652306262018362D          

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  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
 11 12  1  0  0  0  0
  9  3  1  1  0  0  0
 13 14  1  0  0  0  0
 13 18  1  0  0  0  0
 14 15  1  0  0  0  0
 15 16  1  0  0  0  0
 16 17  1  0  0  0  0
 17 18  2  0  0  0  0
 10 15  1  0  0  0  0
 15  6  1  6  0  0  0
  7 14  1  0  0  0  0
 14  2  1  1  0  0  0
 12 13  1  0  0  0  0
 13  4  1  6  0  0  0
 19 20  1  0  0  0  0
 20 21  1  0  0  0  0
 21 22  1  0  0  0  0
 23 24  1  0  0  0  0
 23 34  1  6  0  0  0
 24 25  1  0  0  0  0
 24 26  1  6  0  0  0
 25 27  1  0  0  0  0
 27 28  1  0  0  0  0
 28 29  1  0  0  0  0
 28 30  2  0  0  0  0
 29 31  1  0  0  0  0
 29 32  1  0  0  0  0
 30 33  1  0  0  0  0
 23 19  1  0  0  0  0
 23 22  1  0  0  0  0
 20  5  1  6  0  0  0
 18 20  1  0  0  0  0
 11 19  1  0  0  0  0
 19  1  1  1  0  0  0
M  END
> <DATABASE_ID>
NP0044238

> <DATABASE_NAME>
NP-MRD

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

> <INCHI_IDENTIFIER>
InChI=1S/C29H48O/c1-7-21(19(2)3)9-8-20(4)25-12-13-26-24-11-10-22-18-23(30)14-16-28(22,5)27(24)15-17-29(25,26)6/h7,11,19-20,22-23,25-27,30H,8-10,12-18H2,1-6H3/b21-7-/t20-,22+,23+,25-,26+,27+,28+,29-/m1/s1

> <INCHI_KEY>
MCWVPSBQQXUCTB-OQTIOYDCSA-N

> <FORMULA>
C29H48O

> <MOLECULAR_WEIGHT>
412.702

> <EXACT_MASS>
412.370516166

> <JCHEM_ACCEPTOR_COUNT>
1

> <JCHEM_ATOM_COUNT>
78

> <JCHEM_AVERAGE_POLARIZABILITY>
53.655273618026996

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(1R,2S,5S,7S,11R,14R,15R)-2,15-dimethyl-14-[(2R,5Z)-5-(propan-2-yl)hept-5-en-2-yl]tetracyclo[8.7.0.0^{2,7}.0^{11,15}]heptadec-9-en-5-ol

> <ALOGPS_LOGP>
7.62

> <JCHEM_LOGP>
7.4388973106666665

> <ALOGPS_LOGS>
-6.65

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_ACIDIC>
18.361777845540015

> <JCHEM_PKA_STRONGEST_BASIC>
-1.3283583703607977

> <JCHEM_POLAR_SURFACE_AREA>
20.23

> <JCHEM_REFRACTIVITY>
130.6161

> <JCHEM_ROTATABLE_BOND_COUNT>
5

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
9.25e-05 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(1R,2S,5S,7S,11R,14R,15R)-14-[(2R,5Z)-5-isopropylhept-5-en-2-yl]-2,15-dimethyltetracyclo[8.7.0.0^{2,7}.0^{11,15}]heptadec-9-en-5-ol

> <JCHEM_VEBER_RULE>
1

$$$$

HEADER    PROTEIN                                 26-JUN-20   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   26-JUN-20         0                                  
HETATM    1  C   UNK     0    8666.6228668.218   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0    8662.6338665.893   0.000  0.00  0.00           C+0
HETATM    3  O   UNK     0    8658.6368662.029   0.000  0.00  0.00           O+0
HETATM    4  H   UNK     0    8663.9638663.589   0.000  0.00  0.00           H+0
HETATM    5  H   UNK     0    8666.6228663.589   0.000  0.00  0.00           H+0
HETATM    6  H   UNK     0    8662.6338661.257   0.000  0.00  0.00           H+0
HETATM    7  C   UNK     0    8661.3028665.115   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0    8659.9688664.345   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0    8659.9688662.805   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0    8661.3028662.035   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0    8665.2928667.444   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0    8663.9598666.674   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0    8663.9638665.118   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0    8662.6298664.348   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0    8662.6298662.808   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0    8663.9638662.038   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0    8665.2978662.808   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0    8665.2978664.348   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0    8666.6268666.674   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0    8666.6268665.134   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0    8668.0918664.658   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0    8668.9968665.904   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0    8668.0918667.150   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0    8668.0918668.690   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0    8669.4278669.460   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0    8666.7598669.460   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0    8670.7598668.690   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0    8672.0958669.460   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0    8672.0958671.000   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0    8673.4318668.690   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0    8673.4318671.770   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0    8670.7598671.770   0.000  0.00  0.00           C+0
HETATM   33  C   UNK     0    8674.7638669.460   0.000  0.00  0.00           C+0
HETATM   34  H   UNK     0    8669.4278667.920   0.000  0.00  0.00           H+0
CONECT    1   19                                                            
CONECT    2   14                                                            
CONECT    3    9                                                            
CONECT    4   13                                                            
CONECT    5   20                                                            
CONECT    6   15                                                            
CONECT    7    8   14                                                       
CONECT    8    7    9                                                       
CONECT    9    8   10    3                                                  
CONECT   10    9   15                                                       
CONECT   11   12   19                                                       
CONECT   12   11   13                                                       
CONECT   13   14   18   12    4                                             
CONECT   14   13   15    7    2                                             
CONECT   15   14   16   10    6                                             
CONECT   16   15   17                                                       
CONECT   17   16   18                                                       
CONECT   18   13   17   20                                                  
CONECT   19   20   23   11    1                                             
CONECT   20   19   21    5   18                                             
CONECT   21   20   22                                                       
CONECT   22   21   23                                                       
CONECT   23   24   34   19   22                                             
CONECT   24   23   25   26                                                  
CONECT   25   24   27                                                       
CONECT   26   24                                                            
CONECT   27   25   28                                                       
CONECT   28   27   29   30                                                  
CONECT   29   28   31   32                                                  
CONECT   30   28   33                                                       
CONECT   31   29                                                            
CONECT   32   29                                                            
CONECT   33   30                                                            
CONECT   34   23                                                            
MASTER        0    0    0    0    0    0    0    0   34    0   74    0
END

View in JSmol

Synonyms

Value	Source
7-Dehydroavenasterol	KEGG
Δ7-Avenasterol	Generator
(24Z)-24-Ethyl-5alpha-cholesta-7,24(28)-dien-3beta-ol	HMDB
(24Z)-5alpha-Stigmasta-7,24(28)-dien-3beta-ol	HMDB
(Z)-5alpha-Stigmasta-7,24(28)-dien-3beta-ol	HMDB
24Z-Ethylidenelathosterol	HMDB
3beta-Hydroxy-5alpha-stigmasta-7,24(28)Z-diene	HMDB
5alpha-Stigmasta-7,24(28)-dien-3-ol	HMDB
5alpha-Stigmasta-7,24(28)-dien-3beta-ol	HMDB
5alpha-Stigmasta-7,Z-24(28)-diene-3.beta-ol	HMDB
Avenasterol	HMDB
Z-24-Ethylidene-5alpha-cholest-7-en-3beta-ol	HMDB
(24Z)-24-Ethyl-5α-cholesta-7,24(28)-dien-3β-ol	HMDB
(24Z)-5α-Stigmasta-7,24(28)-dien-3β-ol	HMDB
(3beta,5alpha,24Z)-Stigmasta-7,24(28)-dien-3-ol	HMDB
(3β,5α,24Z)-Stigmasta-7,24(28)-dien-3-ol	HMDB
(Z)-5α-Stigmasta-7,24(28)-dien-3β-ol	HMDB
3β-Hydroxy-5α-stigmasta-7,24(28)Z-diene	HMDB
5alpha-Stigmasta-7,Z-24(28)-diene-3beta-ol	HMDB
5α-Stigmasta-7,24(28)-dien-3-ol	HMDB
5α-Stigmasta-7,Z-24(28)-diene-3β-ol	HMDB
Z-24-Ethylidene-5α-cholest-7-en-3β-ol	HMDB
delta7-Avenasterol	HMDB

Chemical Formula

C₂₉H₄₈O

Average Mass

412.7020 Da

Monoisotopic Mass

412.37052 Da

IUPAC Name

(1R,2S,5S,7S,11R,14R,15R)-2,15-dimethyl-14-[(2R,5Z)-5-(propan-2-yl)hept-5-en-2-yl]tetracyclo[8.7.0.0^{2,7}.0^{11,15}]heptadec-9-en-5-ol

Traditional Name

(1R,2S,5S,7S,11R,14R,15R)-14-[(2R,5Z)-5-isopropylhept-5-en-2-yl]-2,15-dimethyltetracyclo[8.7.0.0^{2,7}.0^{11,15}]heptadec-9-en-5-ol

CAS Registry Number

23290-26-8

SMILES

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

InChI Identifier

InChI=1S/C29H48O/c1-7-21(19(2)3)9-8-20(4)25-12-13-26-24-11-10-22-18-23(30)14-16-28(22,5)27(24)15-17-29(25,26)6/h7,11,19-20,22-23,25-27,30H,8-10,12-18H2,1-6H3/b21-7-/t20-,22+,23+,25-,26+,27+,28+,29-/m1/s1

InChI Key

MCWVPSBQQXUCTB-OQTIOYDCSA-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
Amaranthus hybridus	LOTUS Database	35616633
Arabidopsis thaliana	Plant	KNApSAcK
Avena sativa	LOTUS Database	35616633
Axinella cannabina	LOTUS Database	35616633
Baccharoides anthelmintica	LOTUS Database	35616633
Bryonia dioica	LOTUS Database	35616633
Campanula medium	LOTUS Database	35616633
Canavalia ensiformis	LOTUS Database	35616633
Cannabis sativa	CannabisDB	Not Available
Carthamus tinctorius	LOTUS Database	35616633
Coffea canephora	Plant	KNApSAcK
Coffea charrieriana	Plant	KNApSAcK
Coffea congensis	Plant	KNApSAcK
Coffea eugenioides	Plant	KNApSAcK
Coffea hetero calyx	Plant	KNApSAcK
Coffea humblotiana	Plant	KNApSAcK
Coffea humilis	Plant	KNApSAcK
Coffea kapakata	Plant	KNApSAcK
Coffea liberica var.dewevrei	Plant	KNApSAcK
Coffea liberica var.liberica	Plant	KNApSAcK
Coffea pseudozanguebariae	Plant	KNApSAcK
Coffea racemosa	Plant	KNApSAcK
Coffea salvatrix	Plant	KNApSAcK
Coffea sessiliflora	Plant	KNApSAcK
Coffea stenophylla	Plant	KNApSAcK
Cucurbita maxima	LOTUS Database	35616633
Eryngium foetidum	LOTUS Database	35616633
Ethulia conyzoides	LOTUS Database	35616633
Helianthus annuus	LOTUS Database	35616633
Kalanchoe marmorata	LOTUS Database	35616633
Lagenaria siceraria	LOTUS Database	35616633
Mangifera indica	LOTUS Database	35616633
Medicago monspeliaca	LOTUS Database	35616633
Nicotiana benthamiana	Plant	KNApSAcK
Nicotiana tabacum	LOTUS Database	35616633
Nigella sativa	LOTUS Database	35616633
Olea capensis	LOTUS Database	35616633
Panax quinquefolius	LOTUS Database	35616633
Pyracantha coccinea	LOTUS Database	35616633
Sesamum indicum	LOTUS Database	35616633
Solanum argentinum	LOTUS Database	35616633
Solanum sisymbriifolium	LOTUS Database	35616633
Vanilla x tahitensis	LOTUS Database	35616633
Zea mays	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as stigmastanes and derivatives. These are sterol lipids with a structure based on the stigmastane skeleton, which consists of a cholestane moiety bearing an ethyl group at the carbon atom C24.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Steroids and steroid derivatives

Sub Class

Stigmastanes and derivatives

Direct Parent

Stigmastanes and derivatives

Alternative Parents

Substituents

Triterpenoid
Stigmastane-skeleton
3-beta-hydroxysteroid
Hydroxysteroid
3-hydroxysteroid
3-hydroxy-delta-7-steroid
Delta-7-steroid
Cyclic alcohol
Secondary alcohol
Organic oxygen compound
Hydrocarbon derivative
Organooxygen compound
Alcohol
Aliphatic homopolycyclic compound

Molecular Framework

Aliphatic homopolycyclic compounds

External Descriptors

Stigmasterols and C24-ethyl derivatives (LMST01040154 )

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	7.62	ALOGPS
logP	7.44	ChemAxon
logS	-6.6	ALOGPS
pKa (Strongest Acidic)	18.36	ChemAxon
pKa (Strongest Basic)	-1.3	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	5	ChemAxon
Refractivity	130.62 m³·mol⁻¹	ChemAxon
Polarizability	53.66 Å³	ChemAxon
Number of Rings	4	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

HMDB0006851

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FoodDB ID

KNApSAcK ID

Chemspider ID

KEGG Compound ID

BioCyc ID

BiGG ID

Not Available

Wikipedia Link

Avenasterol

METLIN ID

Not Available

PubChem Compound

12795736

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Turner CE, Elsohly MA, Boeren EG: Constituents of Cannabis sativa L. XVII. A review of the natural constituents. J Nat Prod. 1980 Mar-Apr;43(2):169-234. doi: 10.1021/np50008a001. [PubMed:6991645 ]
Jesch ED, Carr TP: Food Ingredients That Inhibit Cholesterol Absorption. Prev Nutr Food Sci. 2017 Jun;22(2):67-80. doi: 10.3746/pnf.2017.22.2.67. Epub 2017 Jun 30. [PubMed:28702423 ]
Ramprasath VR, Awad AB: Role of Phytosterols in Cancer Prevention and Treatment. J AOAC Int. 2015 May-Jun;98(3):735-738. doi: 10.5740/jaoacint.SGERamprasath. [PubMed:26086253 ]

Showing NP-Card for 5alpha-Stigmasta-7,24(28)-dien-3beta-ol (NP0044238)

MOL for NP0044238 (5alpha-Stigmasta-7,24(28)-dien-3beta-ol)

3D MOL for NP0044238 (5alpha-Stigmasta-7,24(28)-dien-3beta-ol)

3D SDF for NP0044238 (5alpha-Stigmasta-7,24(28)-dien-3beta-ol)

3D-SDF for NP0044238 (5alpha-Stigmasta-7,24(28)-dien-3beta-ol)

PDB for NP0044238 (5alpha-Stigmasta-7,24(28)-dien-3beta-ol)

3D PDB for NP0044238 (5alpha-Stigmasta-7,24(28)-dien-3beta-ol)

SMILES for NP0044238 (5alpha-Stigmasta-7,24(28)-dien-3beta-ol)

INCHI for NP0044238 (5alpha-Stigmasta-7,24(28)-dien-3beta-ol)

Structure for NP0044238 (5alpha-Stigmasta-7,24(28)-dien-3beta-ol)

3D Structure for NP0044238 (5alpha-Stigmasta-7,24(28)-dien-3beta-ol)