Il negozio non funziona correttamente quando i cookie sono disabilitati.
I JavaScript sembrano essere disabilitati nel tuo browser. Per una migliore esperienza sul nostro sito, assicurati di attivare i javascript nel tuo browser.
· · COA & SDS Disponibile per ogni prodotto · Spedizione lo stesso giorno su articoli in magazzino SQ 22,536 - ≥95% , CAS No.17318-31-9
Synonyms
KBio2_005618 | MFCD00210216 | NSC53339 | NSC-53339 | P10102 | CHEBI:90232 | KBioGR_000482 | SR-01000075521-1 | CCG-205266 | SQ 22536 | FT-0688572 | HMS2235P22 | HMS3676B05 | BRD-A56987319-001-05-3 | HMS3266A19 | S-153 | BSPBio_001142 | IDI1_002166 | SCHEM
Shipped In
Ice chest + Ice pads
🧪
Why this grade ≥95% for sensitive chromatographic and analytical workflows requiring minimal baseline interference.
🌡
Storage & shipping Store at -20°C Ships Ice chest + Ice pads Check lot-specific COA for exact specifications.
📋
Quality documents SDS, COA, datasheet, and spec sheet available for download. Lot-specific COA accessible via lot number lookup.
📚
Literature proof Cited in 0 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.
Specifications Sinonimi
KBio2_005618 | MFCD00210216 | NSC53339 | NSC-53339 | P10102 | CHEBI:90232 | KBioGR_000482 | SR-01000075521-1 | CCG-205266 | SQ 22536 | FT-0688572 | HMS2235P22 | HMS3676B05 | BRD-A56987319-001-05-3 | HMS3266A19 | S-153 | BSPBio_001142 | IDI1_002166 | SCHEM
Meccanismi biochimici e fisiologici
Inhibitor of adenylyl cyclase (IC50= 1.4μM). Inhibits PGE1-stimulated increases in cAMP levels in intact human platelets. Cell permeable.
Condizioni di conservazione di stoccaggio
Store at -20°C
Spedito in
Ice chest + Ice pads
Questo prodotto richiede spedizione a catena fredda. I servizi di terra e altri servizi economici non sono disponibili.
Nomi e identificatori Pubchem Sid 504750862 Pubchem Sid Url https://pubchem.ncbi.nlm.nih.gov/substance/504750862 Sorrisi canonici C1CC(OC1)N2C=NC3=C(N=CN=C32)N IUPAC Name 9-(oxolan-2-yl)purin-6-amine InChIKey UKHMZCMKHPHFOT-UHFFFAOYSA-N INCHI 1S/C9H11N5O/c10-8-7-9(12-4-11-8)14(5-13-7)6-2-1-3-15-6/h4-6H,1-3H2,(H2,10,11,12) Isomeri SMILES C1CC(OC1)N2C=NC3=C(N=CN=C32)N WGK Germania 3 PubChem CID 5270 Peso molecolare 205.22
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 Kingdom Organic compounds Superclass Organoheterocyclic compounds Classe Imidazopyrimidines Subclass Purines and purine derivatives Intermediate Tree Nodes Not available Direct Parent 6-aminopurines Alternative Parents Aminopyrimidines and derivatives N-substituted imidazoles Imidolactams Tetrahydrofurans Heteroaromatic compounds Oxacyclic compounds Azacyclic compounds Primary amines Organopnictogen compounds Organooxygen compounds Hydrocarbon derivatives Molecular Framework Aromatic heteropolycyclic compounds Substituents 6-aminopurine - Aminopyrimidine - N-substituted imidazole - Pyrimidine - Imidolactam - Azole - Imidazole - Tetrahydrofuran - Heteroaromatic compound - Azacycle - Oxacycle - Hydrocarbon derivative - Primary amine - Organooxygen compound - Organonitrogen compound - Organopnictogen compound - Amine - Organic nitrogen compound - Organic oxygen compound - Aromatic heteropolycyclic compound Descrizione This compound belongs to the class of organic compounds known as 6-aminopurines. These are purines that carry an amino group at position 6. Purine is a bicyclic aromatic compound made up of a pyrimidine ring fused to an imidazole ring. External Descriptors Not available 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.
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 Solubilità Solvent:DMSO, Max Conc. mg/mL: 10.26, Max Conc. mM: 50 Sensibilità Heat sensitive Punto di fusione (°C) 165 °C Peso molecolare 205.220 g/mol XLogP3 0.400 Hydrogen Bond Donor Count 1 Hydrogen Bond Acceptor Count 5 Rotatable Bond Count 1 Exact Mass 205.096 Da Monoisotopic Mass 205.096 Da Topological Polar Surface Area 78.900 Ų Heavy Atom Count 15 Formal Charge 0 Complexity 239.000 Isotope Atom Count 0 Defined Atom Stereocenter Count 0 Undefined Atom Stereocenter Count 1 Defined Bond Stereocenter Count 0 Undefined Bond Stereocenter Count 0 The total count of all stereochemical bonds 0 Covalently-Bonded Unit Count 1
Domande frequenti e articoli Calcolatori di soluzioni Molarity Calculator Determine the necessary mass, volume, or concentration for preparing a solution.
Dilution Calculator Determine the dilution needed to prepare a stock solution.
Reconstitution Calculator Recensioni
We use cookies to ensure the website functions properly and, where permitted, to improve your experience. You can manage your preferences at any time in Settings. Learn more in our
Cookie Policy. Impostazioni Accetto tutto Decline
Shall we send you a message when we have discounts available?
Remind me later Permetti
Thank you! Please check your email inbox to confirm.
Oops! Notifications are disabled.
Products are supplied to verified businesses, institutions, and qualified professionals for research and development use only. Not for use in humans, animals, diagnosis, or therapy.
Copyright © 2023–present Aladdin Scientific Corp. All rights reserved.
L2403114