Campesterol - ≥65% , CAS No.474-62-4

CAS: 474-62-4 Cat. No.: C137607 Formula: C₂₈H₄₈O Peso molecolare: 400.68 Beilstein Registry Number: 3216975 Numero EC: 207-484-4

QUALITÀ & PUREZZA ≥65%

Synonyms

(24R)-Methylcholest-5-en-3.beta.-ol | (24S)-beta-Methyl cholesterol | CAMPESTEROL [MI] | cholest 5-en-3-ol, 24-methyl | Ergost-5-en-3beta-ol, (24R)- | 24a-Methyl-5-cholesten-3b-ol | 24-Methylcholest-5-en-3beta-ol | 5L5O665639 | AC-34100 | 24-methyl-5-Chol

Storage

Store at -20°C

Shipped In

Ice chest + Ice pads

Panoramica

Campesterol was used as standard in GC and HPLC analysis of oil samples from plants.

Specifiche

Sinonimi

(24R)-Methylcholest-5-en-3.beta.-ol | (24S)-beta-Methyl cholesterol | CAMPESTEROL [MI] | cholest 5-en-3-ol, 24-methyl | Ergost-5-en-3beta-ol, (24R)- | 24a-Methyl-5-cholesten-3b-ol | 24-Methylcholest-5-en-3beta-ol | 5L5O665639 | AC-34100 | 24-methyl-5-Chol

Specifiche e purezza

≥65%

Meccanismi biochimici e fisiologici

Campesterol is a phytosterol, primarily found in nuts, fruits, legumes and seeds. Campesterol is poorly absorbed in humans and competitively inhibits the absorption of cholesterol. Campesterol decreases the transcription of genes involved in cholesterol m

Condizioni di conservazione di stoccaggio

Store at -20°C

Spedito in

Ice chest + Ice pads

Questo prodotto richiede spedizione a catena fredda. I servizi di terra e altri servizi economici non sono disponibili.

Purezza

≥65%

Product Line

C137607-5mg

Nomi e identificatori

Pubchem Sid

528775518

Pubchem Sid Url

https://pubchem.ncbi.nlm.nih.gov/substance/528775518

Sorrisi canonici

CC(C)C(C)CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C

IUPAC Name

(3S,8S,9S,10R,13R,14S,17R)-17-[(2R,5R)-5,6-dimethylheptan-2-yl]-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol

InChIKey

SGNBVLSWZMBQTH-PODYLUTMSA-N

INCHI

1S/C28H48O/c1-18(2)19(3)7-8-20(4)24-11-12-25-23-10-9-21-17-22(29)13-15-27(21,5)26(23)14-16-28(24,25)6/h9,18-20,22-26,29H,7-8,10-17H2,1-6H3/t19-,20-,22+,23+,24-,25+,26+,27+,28-/m1/s1

Isomeri SMILES

C[C@H](CC[C@@H](C)C(C)C)[C@H]1CC[C@@H]2[C@@]1(CC[C@H]3[C@H]2CC=C4[C@@]3(CC[C@@H](C4)O)C)C

WGK Germania

3

Peso molecolare

400.68

Beilstein

3216975

Reaxy-Rn

2061433

Reaxys-RN_link_address

https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=2061433&ln=

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Lipids and lipid-like molecules
    • Classe Steroids and steroid derivatives
      • Subclass Ergostane steroids

• Kingdom: Organic compounds
• Superclass: Lipids and lipid-like molecules
• Classe: Steroids and steroid derivatives
• Subclass: Ergostane steroids
• Intermediate Tree Nodes: Not available
• Direct Parent: Ergosterols and derivatives
• Alternative Parents: 3-beta-hydroxysteroids 3-beta-hydroxy delta-5-steroids Delta-5-steroids Secondary alcohols Cyclic alcohols and derivatives Hydrocarbon derivatives
• Molecular Framework: Aliphatic homopolycyclic compounds
• Substituents: Ergosterol-skeleton - 3-beta-hydroxysteroid - 3-beta-hydroxy-delta-5-steroid - Hydroxysteroid - 3-hydroxysteroid - 3-hydroxy-delta-5-steroid - Delta-5-steroid - Cyclic alcohol - Secondary alcohol - Organic oxygen compound - Hydrocarbon derivative - Organooxygen compound - Alcohol - Aliphatic homopolycyclic compound
• Descrizione: This compound belongs to the class of organic compounds known as ergosterols and derivatives. These are steroids containing ergosta-5,7,22-trien-3beta-ol or a derivative thereof, which is based on the 3beta-hydroxylated ergostane skeleton.
• External Descriptors: Ergosterols and C24-methyl derivatives

Data sources

1. Djoumbou Feunang Y, Eisner R, Knox C, Chepelev L, Hastings J, Owen G, Fahy E, Steinbeck C, Subramanian S, Bolton E, Greiner R, and Wishart DS. ClassyFire: Automated Chemical Classification With A Comprehensive, Computable Taxonomy. Journal of Cheminformatics, 2016, 8:61.

DOI: 10.1186/s13321-016-0174-y

Obiettivi associati (non umani)

Staphylococcus aureus (210822 Activities)

Explore this target

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

Meccanismi d'azione

Proprietà chimiche e fisiche

• Solubilità: ≤0.25mg/ml in ethanol;1mg/ml in dimethyl formamide
• Peso molecolare: 400.700 g/mol
• XLogP3: 8.800
• Hydrogen Bond Donor Count: 1
• Hydrogen Bond Acceptor Count: 1
• Rotatable Bond Count: 5
• Exact Mass: 400.371 Da
• Monoisotopic Mass: 400.371 Da
• Topological Polar Surface Area: 20.200 Ų
• Heavy Atom Count: 29
• Formal Charge: 0
• Complexity: 620.000
• Isotope Atom Count: 0
• Defined Atom Stereocenter Count: 9
• Undefined Atom Stereocenter Count: 0
• Defined Bond Stereocenter Count: 0
• Undefined Bond Stereocenter Count: 0
• The total count of all stereochemical bonds: 0
• Covalently-Bonded Unit Count: 1