Basic information Safety Supplier Related
ChemicalBook >  Product Catalog >  Biochemical Engineering >  Inhibitors >  Neuronal Signaling >  5-HT Receptor modulators >  BMY 7378 DIHYDROCHLORIDE

BMY 7378 DIHYDROCHLORIDE

Basic information Safety Supplier Related

BMY 7378 DIHYDROCHLORIDE Basic information

Product Name:
BMY 7378 DIHYDROCHLORIDE
Synonyms:
  • BMY 7378 2hydrochloride
  • BMY 7378 DIHYDROCHLORIDE;BMY 7378
  • 8-(2-(4-(2-Methoxyphenyl)
  • -8-azaspiro[4.5]decane-7,9-dione dihydrochloride
  • BMY7378 HCl
  • 1-cyclopentanediacetimide,n-(2-(4-(o-methoxyphenyl)-1-piperazinyl)ethyl)-d
  • n-(2-(4-(o-methoxyphenyl)-1-piperazinyl)ethyl)-1,1-cyclopentanediacetimided
  • BMY 7378 DIHYDROCHLORIDE >98% PARTIAL 5- HT1A SEROTO
CAS:
21102-95-4
MF:
C22H32ClN3O3
MW:
421.97
Product Categories:
  • Serotonin receptor
  • Inhibitors
Mol File:
21102-95-4.mol
More
Less

BMY 7378 DIHYDROCHLORIDE Chemical Properties

storage temp. 
Inert atmosphere,Room Temperature
solubility 
H2O: soluble
form 
solid
color 
white
Water Solubility 
Soluble to 100 mM in water
More
Less

Safety Information

WGK Germany 
3
RTECS 
GY3996000

MSDS

More
Less

BMY 7378 DIHYDROCHLORIDE Usage And Synthesis

Uses

BMY 7378 dihydrochloride is a SR-1A agonist and a selective α1D-AR antagonist.

Biological Activity

5-HT 1A partial agonist and high affinity α 1D adrenoceptor antagonist (K i values are 2, 800 and 600 nM at cloned rat α 1D , rat α 1A and hamster α 1B receptors respectively). Also available as part of the α 1 -Adrenoceptor Tocriset™ .

Biochem/physiol Actions

BMY 7378 dihydrochloride is a partial 5-HT1A serotonin receptor agonist and selective α1D-adrenoceptor antagonist.

storage

Room temperature

References

1. yocca fd, hyslop dk, smith dw et al. bmy 7378, a buspirone analog with high affinity, selectivity and low intrinsic activity at the 5-ht1a receptor in rat and guinea pig hippocampal membranes. eur j pharmacol. 1987 jun 4;137(2-3):293-4.2. zemlan fp, zieleniewski-murphy a, maureen murphy r et al bmy 7378: partial agonist at spinal cord 5-ht(1a) receptors. neurochem int. 1990;16(4):515-22.3. goetz as, king hk, ward sd et al. bmy 7378 is a selective antagonist of the d subtype of alpha 1-adrenoceptors. eur j pharmacol. 1995 jan 16;272(2-3):r5-6.4. cleary l, murad k, bexis s et al. the alpha (1d)-adrenoceptor antagonist bmy 7378 is also an alpha (2c)-adrenoceptor antagonist. auton autacoid pharmacol. 2005 oct;25(4):135-41.5. sharp t, backus li, hjorth s et al. further investigation of the in vivo pharmacological properties of the putative 5-ht1a antagonist, bmy 7378. eur j pharmacol. 1990 feb 13;176(3):331-40.

BMY 7378 DIHYDROCHLORIDESupplier

3B Pharmachem (Wuhan) International Co.,Ltd.
Tel
821-50328103-801 18930552037
Email
3bsc@sina.com
Nanjing Chemlin Chemical Co., Ltd
Tel
025-83697070
Email
info@chemlin.com.cn
Chengdu NoVi Biotechnology Co., Ltd.
Tel
028-81458053
Email
novibiotech@163.com sales@novi-biotech.com
NCE Biomedical Co.,Ltd.
Tel
4000-027-021 |24 +86-13986109188 | +86-15623472865 | +81-08033611988
Shanghai Aladdin Bio-Chem Technology Co.,LTD
Tel
400-400-6206333 18521732826
Email
market@aladdin-e.com