Dihydrolanosterol - Moligand™, ≥95% , CAS No.79-62-9

CAS: 79-62-9 Cat. No.: D350029 Formula: C₃₀H₅₂O Peso molecolare: 428.73

QUALITÀ & PUREZZA Moligand™, ≥95%

Synonyms

Lanost-8-en-3-ol #|5alpha-Lanost-8-en-3 beta-ol|Dihydrolanosterol|24-dihydrolanosterol|Lanost-8-en-3beta-ol|3beta-Hydroxylanost-8-ene|24,25-Dihydrolanosterol|Lanost-8-en-3-ol, (3.beta.)-|Lanost-8-en-3-ol|(3S,10S,13R,14R,17R)-4,4,10,13,14-pentamethyl-17-[(2R)-6-methylheptan-2-yl]-2,3,5,6,7,11,12,15,16,17-decahydro-1H-cyclopenta[a]phenanthren-3-ol|Lanostenol|4,4,14a-trimethyl-5a-cholesta-8-en-3b-ol|(3beta)-Lanost-8-en-3-ol|4,4,14alpha-trimethyl-5alpha-cholesta-8-en-3beta-ol|(3S,5R,10S,13R,14R,17R)-4,4,10,13,14-pentamethyl-17-((R)-6-methylheptan-2-yl)-2,3,4,5,6,7,10,11,12,13,14,15,16,17-tetradecahydro-1H-cyclopenta[a]phenanthren-3-ol|5.ALPHA.-LANOST-8-EN-3.BETA.-OL|Dihydrolanosterin|(3S,5R,10S,13R,14R,17R)-4,4,10,13,14-pentamethyl-17-[(2R)-6-methylheptan-2-yl]-2,3,5,6,7,11,12,15,16,17-decahydro-1H-cyclopenta[a]phenanthren-3-ol|DIHYDROLANOSTEROL [INCI]|Lanost-8-en-3.beta.-ol|Lanostenol;Dihydrolanosterin|5alpha-Lanost-8-en-3beta-ol

Storage

Store at 2-8°C,Protected from light

Shipped In

Wet ice

Panoramica

Dihydrolanosterol is a subtrate of CYP51 and a cholesterol biosynthesis inhibitor.

Specifiche

Sinonimi

Lanost-8-en-3-ol # | 5alpha-Lanost-8-en-3 beta-ol | Dihydrolanosterol | 24-dihydrolanosterol | Lanost-8-en-3beta-ol | 3beta-Hydroxylanost-8-ene | 24,25-Dihydrolanosterol | Lanost-8-en-3-ol, (3.beta.)- | Lanost-8-en-3-ol | (3S,10S,13R,14R,17R)-4,4,10,13,14-pentamethyl-17-[(2R)-6-methylheptan-2-yl]-2,3,5,6,7,11,12,15,16,17-decahydro-1H-cycl Mostra altro

Specifiche e purezza

Moligand™, ≥95%

Condizioni di conservazione di stoccaggio

Store at 2-8°C,Protected from light

Spedito in

Wet ice

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

Grado

Moligand™

Purezza

≥95%

Nomi e identificatori

Pubchem Sid

504758733

Pubchem Sid Url

https://pubchem.ncbi.nlm.nih.gov/substance/504758733

Sorrisi canonici

CC(C)CCCC(C)C1CCC2(C1(CCC3=C2CCC4C3(CCC(C4(C)C)O)C)C)C

IUPAC Name

(3S,5R,10S,13R,14R,17R)-4,4,10,13,14-pentamethyl-17-[(2R)-6-methylheptan-2-yl]-2,3,5,6,7,11,12,15,16,17-decahydro-1H-cyclopenta[a]phenanthren-3-ol

InChIKey

MBZYKEVPFYHDOH-BQNIITSRSA-N

INCHI

1S/C30H52O/c1-20(2)10-9-11-21(3)22-14-18-30(8)24-12-13-25-27(4,5)26(31)16-17-28(25,6)23(24)15-19-29(22,30)7/h20-22,25-26,31H,9-19H2,1-8H3/t21-,22-,25+,26+,28-,29-,30+/m1/s1

Isomeri SMILES

C[C@H](CCCC(C)C)[C@H]1CC[C@@]2([C@@]1(CCC3=C2CC[C@@H]4[C@@]3(CC[C@@H](C4(C)C)O)C)C)C

Peso molecolare

428.73

Reaxy-Rn

45962208

Reaxys-RN_link_address

https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=45962208&ln=

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Lipids and lipid-like molecules
    • Classe Prenol lipids
      • Subclass Triterpenoids

• Kingdom: Organic compounds
• Superclass: Lipids and lipid-like molecules
• Classe: Prenol lipids
• Subclass: Triterpenoids
• Intermediate Tree Nodes: Not available
• Direct Parent: Triterpenoids
• Alternative Parents: 3-beta-hydroxysteroids 14-alpha-methylsteroids Secondary alcohols Cyclic alcohols and derivatives Hydrocarbon derivatives
• Molecular Framework: Aliphatic homopolycyclic compounds
• Substituents: Triterpenoid - 14-alpha-methylsteroid - 3-beta-hydroxysteroid - Hydroxysteroid - 3-hydroxysteroid - 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 triterpenoids. These are terpene molecules containing six isoprene units.
• External Descriptors: Cholesterol and 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 (umani)

HMGCR Tclin HMG-CoA reductase (2475 Activities)

Discover Target: HMGCR

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

Obiettivi associati (non umani)

Srebf1 Sterol regulatory element-binding protein 1 (3 Activities)

Discover Target: Srebf1

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

Meccanismi d'azione

Proprietà chimiche e fisiche

• Solubilità: Soluble in chloroform (slightly), and ethyl acetate (slightly, heated).
• Punto di ebollizione (°C): 454.33° C (Predicted)
• Punto di fusione (°C): 190.97° C
• Peso molecolare: 428.700 g/mol
• XLogP3: 9.400
• Hydrogen Bond Donor Count: 1
• Hydrogen Bond Acceptor Count: 1
• Rotatable Bond Count: 5
• Exact Mass: 428.402 Da
• Monoisotopic Mass: 428.402 Da
• Topological Polar Surface Area: 20.200 Ų
• Heavy Atom Count: 31
• Formal Charge: 0
• Complexity: 716.000
• Isotope Atom Count: 0
• Defined Atom Stereocenter Count: 7
• 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