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K41498

Catalog No. TP2009   CAS 434938-41-7
Synonyms: K 41498

Potent and highly selective CRF2 receptor antagonist (Ki values are 0.66, 0.62 and 425 nM for human CRF2α, CRF2β and CRF1 receptors respectively). Inhibits sauvagine-stimulated cAMP accumulation in hCRF2α- and hCRF2β-expressing cells. In rats in vivo, blocks urocortin-induced hypotension following systemic administration.

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K41498 Chemical Structure
K41498, CAS 434938-41-7
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1 mg 35 days $ 1,390.00
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Biological Description
Chemical Properties
Storage & Solubility Information
Description Potent and highly selective CRF2 receptor antagonist (Ki values are 0.66, 0.62 and 425 nM for human CRF2α, CRF2β and CRF1 receptors respectively). Inhibits sauvagine-stimulated cAMP accumulation in hCRF2α- and hCRF2β-expressing cells. In rats in vivo, blocks urocortin-induced hypotension following systemic administration.
Synonyms K 41498
Molecular Weight 3632.26
Formula C162H276N48O46
CAS No. 434938-41-7

Storage

keep away from moisture

Powder: -20°C for 3 years | In solvent: -80°C for 1 year

Solubility Information

H2O: 5 mg/mL

TargetMolReferences and Literature

1. Ruhmann et al (2002) Design, synthesis and pharmacological characterization of new highly selective CRF2 antagonists: development of 123I-K31440 as a potential SPECT ligand. Peptides 23 453 PMID: 2. Lawrence et al (2002) The highly selective CRF2 receptor antagonist K41498 binds to presynaptic CRF2 receptors in rat brain. Br.J.Pharmacol. 136 896 PMID:

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Keywords

K41498 434938-41-7 K-41498 K 41498 inhibitor inhibit

 

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