Fig. 1 · Structure

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BMY 7378

Cat. No. A11208 CAS 21102-95-4

5-HT1A agonist

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

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Biological Activity

Target & Activity

Target Activity 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

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Specifications

Manufacturer Adooq Bioscience
Actions Partial Agonist
CAS Number 21102-95-4
Applications 5-HT1A agonist
Formula C22H31N3O3.2HCl
Molecular Weight 458.42
SMILES
COC1=CC=CC=C1N2CCN(CC2)CCN3C(=O)CC4(CCCC4)CC3=O.Cl.Cl

Storage & Solubility

In Vitro Solubility

Reported Solubility

SolventReported Solubility
DMSO 81 mg/mL (176.69 mM)
Water 81 mg/mL (176.69 mM)
Ethanol 18 mg/mL (39.26 mM)

Preparing Stock Solutions

Stock preparation is unavailable for this product molecular weight.

Calculated stock concentrations do not establish solvent solubility. Refer to the reported solubility data for experimental guidance.

In Vivo Preparation

Concentration
14 mg/mL
Vehicle
Saline

Storage

Store powder at -20°C, keep desiccated.
In powder form, the chemical is stable for 36 months.
In solution, store at -20°C and use within 1 month to prevent loss of potency. Aliquot to avoid multiple freeze/thaw cycles.

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