BMY 7378

Catalog No. A11208

BMY 7378 is a 5-HT1A partial agonist and high affinity α1D adrenoceptor antagonist.

Technical details

Catalog Num	A11208
M. Wt	458.42
Formula	C22H31N3O3.2HCl
Purity	>98%
Storage	at -20 °C 3 years (powder form); at -20 °C 6 months (Solution base)
CAS No.	21102-95-4
Synonyms	BMY7378, BMY-7378
SMILES	COC1=CC=CC=C1N2CCN(CC2)CCN3C(=O)CC4(CCCC4)CC3=O.Cl.Cl

Biological Activity

BMY 7378 is a 5-HT1A partial agonist and high affinity α1D adrenoceptor antagonist.

Targets

Target	Value
5-HT1A	pIC50: 8.3
α1D-adrenoceptor	pki: 8.2
DopamineD2receptor	pIC50: 7.4
α2C-adrenoceptor	pki: 6.54
5-HT1C	pIC50: 6.4
5-HT1D	pIC50: 5.9
H1receptor	pIC50: 5.7
5-HT2	pIC50: 5.5
H2receptor	pIC50: 5.3
α2-adrenoceptor	pIC50: 5.1
β1-adrenoceptor	pIC50: 5.1
DopamineD1receptor	pIC50: 5
Nicotinicreceptor	pIC50: 4.9
β2-adrenoceptor	pIC50: <5.0
5-HT3	pIC50: <5.0
H3receptor	pIC50: <5.0
GABAAreceptor	pIC50: <5.0
GABABreceptor	pIC50: <5.0
MuscarinicM1receptor	pIC50: <5.0
MuscarinicM2receptor	pIC50: <5.0
MuscarinicM3receptor	pIC50: <5.0
NMDAreceptor	pIC50: <5.0
AT1receptor	pIC50: <5.0
AT2receptor	pIC50: <5.0
EndothelinReceptor	pIC50: <5.0
AdenosineA1receptor	pIC50: <5.0
AdenosineA2receptor	pIC50: <5.0

Solubility *

In vitro (25°C)	DMSO	81 mg/mL (176.69 mM)
	Water	81 mg/mL (176.69 mM)
	Ethanol	18 mg/mL (39.26 mM)
In vivo	Saline	14 mg/mL
* <1 mg/ml means slightly soluble or insoluble. * Please note that Adooq tests the solubility of all compounds in-house, and the actual solubility may differ slightly from published values. This is normal and is due to slight batch-to-batch variations.

Preparing Stock Solutions

Concentration / Solvent Volume / Mass	1 mg	5 mg	10 mg
0.1 mM	21.81 mL	109.07 mL	218.14 mL
0.5 mM	4.36 mL	21.81 mL	43.63 mL
1 mM	2.18 mL	10.91 mL	21.81 mL
5 mM	0.44 mL	2.18 mL	4.36 mL

*The above data is based on the productmolecular weight 458.42. Batch specific molecular weights may vary from batch to batch due to solvent of hydration, which will affect the solvent volumes required to prepare stock solutions.