Name: Formycin A - ≥98%(HPLC), from Streptomyces kaniharaensis , CAS No.6742-12-7
SKU: F477621
Availability: InStock

Formycin A - ≥98%(HPLC), from Streptomyces kaniharaensis , CAS No.6742-12-7

CAS: 6742-12-7 Cat. No.: F477621 Formula: C₁₀H₁₃N₅O₄ Peso molecolare: 267.24 Beilstein Registry Number: 624229 Numero EC: 809-733-8

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Formycin A - ≥98%(HPLC), from Streptomyces kaniharaensis CAS No(6742-12-7) by Aladdin Scientific

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Disponibile su ordine

GRADE & PURITY ≥98%(HPLC) from Streptomyces kaniharaensis

Synonyms

Storage

Desiccated,Room temperature

Panoramica Specifications Nomi e identificatori Documentazione Advanced Data Taxonomic Classification Struttura 3D Obiettivi associati (umani) Obiettivi associati (non umani) Meccanismi d'azione Certificati (CoA, COO, BSE/TSE e tabella di analisi) Proprietà chimiche e fisiche Calcolatori di soluzioni Recensioni

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Why this grade

≥98%(HPLC), from Streptomyces kaniharaensis for sensitive chromatographic and analytical workflows requiring minimal baseline interference.

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Storage & shipping

Desiccated,Room temperature Ships 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.

Panoramica

Description

Formycin A is an adenosine analog, and is cytotoxic in nature. It acts as a substrate for the human enzymes human erythrocytic adenosine deaminase and adenosine kinase.Chemical structure: nucleoside

Specifications

Sinonimi

Specifiche e purezza

≥98%(HPLC), from Streptomyces kaniharaensis

Condizioni di conservazione di stoccaggio

Desiccated,Room temperature

Purezza

≥98%(HPLC)

Nomi e identificatori

Sorrisi canonici	C1=NC2=C(NN=C2C(=N1)N)C3C(C(C(O3)CO)O)O
IUPAC Name	(2S,3R,4S,5R)-2-(7-amino-2H-pyrazolo[4,3-d]pyrimidin-3-yl)-5-(hydroxymethyl)oxolane-3,4-diol
InChIKey	KBHMEHLJSZMEMI-KSYZLYKTSA-N
INCHI	1S/C10H13N5O4/c11-10-6-4(12-2-13-10)5(14-15-6)9-8(18)7(17)3(1-16)19-9/h2-3,7-9,16-18H,1H2,(H,14,15)(H2,11,12,13)/t3-,7-,8-,9+/m1/s1
Isomeri SMILES	C1=NC2=C(NN=C2C(=N1)N)[C@H]3[C@@H]([C@@H]([C@H](O3)CO)O)O
Peso molecolare	267.24
Beilstein	624229
Reaxy-Rn	561330
Reaxys-RN_link_address	https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=561330&ln=

Documentazione

📋 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

Taxonomy Tree

Kingdom Organic compounds
- Superclass Organic oxygen compounds
  - Classe Organooxygen compounds
    - Subclass Carbohydrates and carbohydrate conjugates
      - Level5 Glycosyl compounds
        Level6 C-glycosyl compounds

Kingdom	Organic compounds
Superclass	Organic oxygen compounds
Classe	Organooxygen compounds
Subclass	Carbohydrates and carbohydrate conjugates
Intermediate Tree Nodes	Glycosyl compounds
Direct Parent	C-glycosyl compounds
Alternative Parents	Pentoses Pyrazolopyrimidines Aminopyrimidines and derivatives Imidolactams Tetrahydrofurans Pyrazoles Heteroaromatic compounds Secondary alcohols Oxacyclic compounds Dialkyl ethers Azacyclic compounds Primary amines Primary alcohols Organopnictogen compounds Hydrocarbon derivatives
Molecular Framework	Aromatic heteropolycyclic compounds
Substituents	C-glycosyl compound - Pentose monosaccharide - Pyrazolopyrimidine - Aminopyrimidine - Monosaccharide - Imidolactam - Pyrimidine - Azole - Heteroaromatic compound - Pyrazole - Tetrahydrofuran - Secondary alcohol - Dialkyl ether - Ether - Oxacycle - Azacycle - Organoheterocyclic compound - Organic nitrogen compound - Amine - Alcohol - Hydrocarbon derivative - Organonitrogen compound - Primary alcohol - Primary amine - Organopnictogen compound - Aromatic heteropolycyclic compound
Descrizione	This compound belongs to the class of organic compounds known as c-glycosyl compounds. These are glycoside in which a sugar group is bonded through one carbon to another group via a C-glycosidic bond.
External Descriptors	formycin
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

Struttura 3D

Obiettivi associati (umani)

ADA Tclin Adenosine deaminase (129 Activities)

Discover Target: ADA

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

MAOA Tclin Monoamine oxidase A (11911 Activities)

Discover Target: MAOA

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

MAOB Tclin Monoamine oxidase B (8835 Activities)

Discover Target: MAOB

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

CCRF-CEM (65223 Activities)

Solubilità	DMSO: soluble 1mg/mL; H2O: soluble 3mg/mL
Punto di infiammabilità (°F)	Not applicable
Punto di infiammabilità (°C)	Not applicable
Peso molecolare	267.240 g/mol
XLogP3	-2.200
Hydrogen Bond Donor Count	5
Hydrogen Bond Acceptor Count	8
Rotatable Bond Count	2
Exact Mass	267.097 Da
Monoisotopic Mass	267.097 Da
Topological Polar Surface Area	150.000 Å²
Heavy Atom Count	19
Formal Charge	0
Complexity	335.000
Isotope Atom Count	0
Defined Atom Stereocenter Count	4
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