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· · COA & SDS Disponível para todos os produtos · Envio no mesmo dia em itens em estoque Bevirimat - 10mM in DMSO , CAS No.174022-42-5
Disponível para encomenda
GRADE & PURITY 10mM in DMSO
Synonyms
Bevirimat|174022-42-5|PA-457|Bevirimat [INN]|YK FH312|MPC-4326|3-O-(3',3'-Dimethylsuccinyl)betulinic acid|UNII-S125DW66N8|YK-FH312|S125DW66N8|PA 457|BVM|O-(3,3-Dimethylsuccinyl)betulinic acid|CHEMBL404519|CHEBI:65484|3-O-(3',3'-dimethylsuccinyl) betulinic
Shipped In
Dry ice packs + Cold packs
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Why this grade 10mM in DMSO for sensitive chromatographic and analytical workflows requiring minimal baseline interference.
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Storage & shipping Store at -80°C Ships Dry ice packs + Cold packs Check lot-specific COA for exact specifications.
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Quality documents SDS, COA, datasheet, and spec sheet available for download. Lot-specific COA accessible via lot number lookup.
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Literature proof Cited in 0 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.
Specifications Sinónimos
Bevirimat | 174022-42-5 | PA-457 | Bevirimat [INN] | YK FH312 | MPC-4326 | 3-O-(3',3'-Dimethylsuccinyl)betulinic acid | UNII-S125DW66N8 | YK-FH312 | S125DW66N8 | PA 457 | BVM | O-(3,3-Dimethylsuccinyl)betulinic acid | CHEMBL404519 | CHEBI:65484 | 3-O-(3',3'-dimethylsuccinyl) betulinic
Especificações e pureza
10mM in DMSO
Mecanismos bioquímicos e fisiológicos
Bevirimat is the first in class HIV maturation inhibitor. It acts by inhibiting the processing of the Gag capsid (CA)/spacer peptide 1 (SP1), which causes accumulation of CA/SP1 (p25) precursor proteins and blocks maturation of the viral core particle.
It
Condições de armazenamento de armazenamento
Store at -80°C
Enviado em
Dry ice packs + Cold packs
Este produto requer transporte de cadeia fria. Serviços terrestres e outros serviços econômicos não estão disponíveis.
Nomes e identificadores Pubchem Sid 528763571 Sorrisos canónicos CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)OC(=O)CC(C)(C)C(=O)O)C)C(=O)O IUPAC Name (1R,3aS,5aR,5bR,7aR,9S,11aR,11bR,13aR,13bR)-9-(3-carboxy-3-methylbutanoyl)oxy-5a,5b,8,8,11a-pentamethyl-1-prop-1-en-2-yl-1,2,3,4,5,6,7,7a,9,10,11,11b,12,13,13a,13b-hexadecahydrocyclopenta[a]chrysene-3a-carboxylic acid InChIKey YJEJKUQEXFSVCJ-WRFMNRASSA-N INCHI 1S/C36H56O6/c1-21(2)22-12-17-36(30(40)41)19-18-34(8)23(28(22)36)10-11-25-33(7)15-14-26(42-27(37)20-31(3,4)29(38)39)32(5,6)24(33)13-16-35(25,34)9/h22-26,28H,1,10-20H2,2-9H3,(H,38,39)(H,40,41)/t22-,23+,24-,25+,26-,28+,33-,34+,35+,36-/m0/s1 SMILES isoméricas CC(=C)[C@@H]1CC[C@]2([C@H]1[C@H]3CC[C@@H]4[C@]5(CC[C@@H](C([C@@H]5CC[C@]4([C@@]3(CC2)C)C)(C)C)OC(=O)CC(C)(C)C(=O)O)C)C(=O)O Peso molecular 584.83 Reaxy-Rn 29374001 Reaxys-RN_link_address https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=29374001&ln=
Documentation 📋 Safety Data Sheet (SDS) Comprehensive hazard, handling, storage, and regulatory compliance document.
Download SDS → ✅ Certificate of Analysis (COA) Lot-specific quality data. Enter your lot number to retrieve the exact COA.
Look up COA → 📊 Datasheet Quick-reference summary of product specifications and applications.
View datasheet → 🔬 Specification Sheet Full quality attributes and acceptance criteria for this grade.
View spec sheet →
Advanced Data Taxonomic Classification Kingdom Organic compounds Superclass Lipids and lipid-like molecules Classe Prenol lipids Subclass Triterpenoids Intermediate Tree Nodes Not available Direct Parent Triterpenoids Alternative Parents 18-hydroxysteroids Oxosteroids Tricarboxylic acids and derivatives Fatty acid esters Carboxylic acid esters Carboxylic acids Organic oxides Hydrocarbon derivatives Carbonyl compounds Molecular Framework Aliphatic homopolycyclic compounds Substituents Triterpenoid - 18-hydroxysteroid - 18-oxosteroid - Hydroxysteroid - Oxosteroid - Steroid - Tricarboxylic acid or derivatives - Fatty acid ester - Fatty acyl - Carboxylic acid ester - Carboxylic acid - Carboxylic acid derivative - Hydrocarbon derivative - Organooxygen compound - Organic oxide - Organic oxygen compound - Carbonyl group - Aliphatic homopolycyclic compound Descrição This compound belongs to the class of organic compounds known as triterpenoids. These are terpene molecules containing six isoprene units. External Descriptors dicarboxylic acid monoester - monocarboxylic acid - pentacyclic triterpenoid 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.
Estrutura 3D Alvos associados (humanos) Alvos associados (não humanos) Mecanismos de ação Certificados（CoA,COO,BSE/TSE e Mapa de Análise) Propriedades químicas e físicas Peso molecular 584.800 g/mol XLogP3 9.100 Hydrogen Bond Donor Count 2 Hydrogen Bond Acceptor Count 6 Rotatable Bond Count 7 Exact Mass 584.408 Da Monoisotopic Mass 584.408 Da Topological Polar Surface Area 101.000 Ų Heavy Atom Count 42 Formal Charge 0 Complexity 1170.000 Isotope Atom Count 0 Defined Atom Stereocenter Count 10 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
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