Galocitabine - ≥95% , CAS No.124012-42-6

CAS: 124012-42-6 Cat. No.: G1343462 PubChem CID: 65950
Disponible para pedir
CALIDAD & PUREZA ≥95%
Storage
Room temperature
Shipped In
Normal
★
Talla
Alemania (EU)
USA*
Precio
Cantidad
1mg
G1343462-1mg
Fabricado bajo pedido · 8–12 semanas
143,09€
5mg
G1343462-5mg
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310,56€
10mg
G1343462-10mg
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414,69€
25mg
G1343462-25mg
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614,27€
50mg
G1343462-50mg
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817,32€
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Especificaciones

Especificaciones y pureza
≥95%
Condiciones de almacenamiento de almacenamiento
Room temperature
Enviado en
Normal
Tipo de acción
INHIBITOR
Pureza
≥95%
Nombres e identificadores
Sonrisas canónicas
CC1C(C(C(O1)N2C=C(C(=NC2=O)NC(=O)C3=CC(=C(C(=C3)OC)OC)OC)F)O)O
IUPAC Name
N-[1-[(2R,3R,4S,5R)-3,4-dihydroxy-5-methyloxolan-2-yl]-5-fluoro-2-oxopyrimidin-4-yl]-3,4,5-trimethoxybenzamide
InChIKey
TVYPSLDUBVTDIS-FUOMVGGVSA-N
INCHI
1S/C19H22FN3O8/c1-8-13(24)14(25)18(31-8)23-7-10(20)16(22-19(23)27)21-17(26)9-5-11(28-2)15(30-4)12(6-9)29-3/h5-8,13-14,18,24-25H,1-4H3,(H,21,22,26,27)/t8-,13-,14-,18-/m1/s1
Isómeros SMILES
C[C@@H]1[C@H]([C@H]([C@@H](O1)N2C=C(C(=NC2=O)NC(=O)C3=CC(=C(C(=C3)OC)OC)OC)F)O)O
CAS alternativo
124012-42-6
PubChem CID
65950
Términos de entrada MeSH
galocitabine;N-(1-((2R,3R,4S,5R)-3,4-dihydroxy-5-methyloxolan-2-yl)-5-fluoro-2-oxopyrimidin-4-yl)-3,4,5-trimethoxybenzamide

Datos avanzados

Taxonomic Classification

Taxonomy Tree

KingdomOrganic compounds
SuperclassNucleosides, nucleotides, and analogues
Clase5'-deoxyribonucleosides
SubclassNot available
Intermediate Tree Nodes Not available
Direct Parent5'-deoxyribonucleosides
Alternative Parents Glycosylamines  Benzamides  Anisoles  Phenoxy compounds  Benzoyl derivatives  Methoxybenzenes  Alkyl aryl ethers  Pyrimidones  Halopyrimidines  Aryl fluorides  Hydropyrimidines  Imidolactams  Tetrahydrofurans  Heteroaromatic compounds  Secondary alcohols  1,2-diols  Secondary carboxylic acid amides  Oxacyclic compounds  Azacyclic compounds  Hydrocarbon derivatives  Organonitrogen compounds  Organopnictogen compounds  Organofluorides  Organic oxides  
Molecular FrameworkAromatic heteromonocyclic compounds
Substituents 5'-deoxyribonucleoside - Glycosyl compound - N-glycosyl compound - Benzamide - Benzoic acid or derivatives - Anisole - Phenoxy compound - Benzoyl - Phenol ether - Methoxybenzene - Alkyl aryl ether - Halopyrimidine - Pyrimidone - Monocyclic benzene moiety - Aryl halide - Aryl fluoride - Hydropyrimidine - Imidolactam - Pyrimidine - Benzenoid - Heteroaromatic compound - Tetrahydrofuran - 1,2-diol - Secondary alcohol - Secondary carboxylic acid amide - Carboxamide group - Organoheterocyclic compound - Carboxylic acid derivative - Oxacycle - Azacycle - Ether - Organooxygen compound - Organic oxide - Alcohol - Organic oxygen compound - Organic nitrogen compound - Organopnictogen compound - Hydrocarbon derivative - Organohalogen compound - Organofluoride - Organonitrogen compound - Aromatic heteromonocyclic compound
DescripciónThis compound belongs to the class of organic compounds known as 5'-deoxyribonucleosides. These are nucleosides in which the oxygen atom at the 5'position of the ribose moiety has been replaced by another atom. The nucleobases here are limited to purine, pyrimidine, and pyridine derivatives.
External Descriptors Not available
Estructura 3D
Modelo de Estructura Química Interactiva





Certificados (CoA, COO, BSE/TSE y tabla de análisis)
C of A & Other Certificates(BSE/TSE, COO):
Analytical Chart:
Propiedades químicas y físicas
Peso molecular439.400 g/mol
XLogP3-0.100
Hydrogen Bond Donor Count3
Hydrogen Bond Acceptor Count9
Rotatable Bond Count6
Exact Mass439.139 Da
Monoisotopic Mass439.139 Da
Topological Polar Surface Area139.000 Ų
Heavy Atom Count31
Formal Charge0
Complexity748.000
Isotope Atom Count0
Defined Atom Stereocenter Count4
Undefined Atom Stereocenter Count0
Defined Bond Stereocenter Count0
Undefined Bond Stereocenter Count0
The total count of all stereochemical bonds0
Covalently-Bonded Unit Count1
Calculadoras de soluciones
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