Cytosine - Moligand™, 10mM in DMSO , CAS No.71-30-7

CAS: 71-30-7 Cat. No.: C425633 Fórmula: C₄H₅N₃O Peso molecular: 111.1 Beilstein Registry Number: 2637 Número CE: 200-749-5

GRADE & PURITY Moligand™, 10mM in DMSO

Synonyms

AC-2489 | Lamivudine impurity c rs | LAMIVUDINE IMPURITY E (EP IMPURITY) | EC 200-749-5 | LAMIVUDINE IMPURITY C (USP IMPURITY) | 2-Pyrimidinol, 1,4-dihydro-4-imino-, (Z)- (9CI) | UNII-8J337D1HZY | 2(1H)-Pyrimidinone, 3,4-dihydro-4-imino-, (Z)- (9CI) | 4-a

Storage

Store at -80°C

Shipped In

Dry ice packs + Cold packs

Visão geral

application：

Cytosine has been used:

for the preparation of nucleobase solutions

as a standard for high-performance liquid chromatography (HPLC)

for the estimation of global methylation rate

for nucleoside 5′-triphosphate (NTP) synthesis

purification

Specifications

Sinónimos

AC-2489 | Lamivudine impurity c rs | LAMIVUDINE IMPURITY E (EP IMPURITY) | EC 200-749-5 | LAMIVUDINE IMPURITY C (USP IMPURITY) | 2-Pyrimidinol, 1,4-dihydro-4-imino-, (Z)- (9CI) | UNII-8J337D1HZY | 2(1H)-Pyrimidinone, 3,4-dihydro-4-imino-, (Z)- (9CI) | 4-a

Especificações e pureza

Moligand™, 10mM in DMSO

Mecanismos bioquímicos e fisiológicos

Nucleoside. Pyrimidine derivative. One of the four main bases found in DNA and RNA, along with adenine, guanine, and thymine (uracil in RNA). Cytosine reagent is used in a wide variety of research applications, as an enzyme substrate or precursor of effec

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.

Grau

Moligand™

Nomes e identificadores

• Pubchem Sid: 528774978
• Sorrisos canónicos: C1=C(NC(=O)N=C1)N
• IUPAC Name: 6-amino-1H-pyrimidin-2-one
• InChIKey: OPTASPLRGRRNAP-UHFFFAOYSA-N
• INCHI: 1S/C4H5N3O/c5-3-1-2-6-4(8)7-3/h1-2H,(H3,5,6,7,8)
• SMILES isoméricas: C1=C(NC(=O)N=C1)N
• WGK Alemanha: 1
• RTECS: UW7350150
• Peso molecular: 111.1
• Beilstein: 2637
• Reaxy-Rn: 606406
• Reaxys-RN_link_address: https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=606406&ln=

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Organoheterocyclic compounds
    • Classe Diazines
      • Subclass Pyrimidines and pyrimidine derivatives

• Kingdom: Organic compounds
• Superclass: Organoheterocyclic compounds
• Classe: Diazines
• Subclass: Pyrimidines and pyrimidine derivatives
• Intermediate Tree Nodes: Not available
• Direct Parent: Pyrimidones
• Alternative Parents: Aminopyrimidines and derivatives Hydropyrimidines Heteroaromatic compounds Azacyclic compounds Primary amines Organopnictogen compounds Organooxygen compounds Organic oxides Hydrocarbon derivatives
• Molecular Framework: Aromatic heteromonocyclic compounds
• Substituents: Pyrimidone - Aminopyrimidine - Hydropyrimidine - Heteroaromatic compound - Azacycle - Organic nitrogen compound - Organic oxygen compound - Organopnictogen compound - Organic oxide - Hydrocarbon derivative - Primary amine - Organooxygen compound - Organonitrogen compound - Amine - Aromatic heteromonocyclic compound
• Descrição: This compound belongs to the class of organic compounds known as pyrimidones. These are compounds that contain a pyrimidine ring, which bears a ketone. Pyrimidine is a 6-membered ring consisting of four carbon atoms and two nitrogen centers at the 1- and 3- ring positions.
• External Descriptors: a pyrimidine-related compound - a pyrimidine base

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

Alvos associados (humanos)

DCK Tchem Deoxycytidine kinase (530 Activities)

Discover Target: DCK

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

GMNN Tbio Geminin (128009 Activities)

Discover Target: GMNN

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

Alvos associados (não humanos)

L1210 (27553 Activities)

Explore this target

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

Mecanismos de ação

Propriedades químicas e físicas

• Ponto de fusão (°C): 300°C
• Peso molecular: 111.100 g/mol
• XLogP3: -1.700
• Hydrogen Bond Donor Count: 2
• Hydrogen Bond Acceptor Count: 2
• Rotatable Bond Count: 0
• Exact Mass: 111.043 Da
• Monoisotopic Mass: 111.043 Da
• Topological Polar Surface Area: 67.500 Ų
• Heavy Atom Count: 8
• Formal Charge: 0
• Complexity: 170.000
• Isotope Atom Count: 0
• Defined Atom Stereocenter Count: 0
• 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