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Drotaverine hydrochloride

Cat. No. M8742

All AbMole products are for research use only, cannot be used for human consumption.

Drotaverine hydrochloride Structure

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Quality Control & Documentation
Biological Activity

Drotaverine (Drotaverin) is an isoquinoline-based PDE4-selective phosphodiesterase (PDE) inhibitor and an L-type voltage-dependent (voltage-operated) calcium channel (L-VDCC or L-VOCC) blocker that exhibits in vivo antispasmodic efficacy without anticholinergic effects.

Chemical Information
Molecular Weight 433.97
Formula C24H31NO4.HCl
CAS Number 985-12-6
Solubility (25°C) Water 90 mg/mL
DMSO 50 mg/mL (ultrasonic and warming)
Storage Powder          -20°C   3 years ;  4°C   2 years
In solvent       -80°C   6 months ;  -20°C   1 month
References

[1] Irena B Ivshina, et al. Drotaverine hydrochloride degradation using cyst-like dormant cells of Rhodococcus ruber

[2] I B Ivshina, et al. Biodegradation of drotaverine hydrochloride by free and immobilized cells of Rhodococcus rhodochrous IEGM 608

[3] Bindiya Gupta, et al. Drotaverine hydrochloride versus hyoscine-N-butylbromide in augmentation of labor

[4] K C Singh, et al. Drotaverine hydrochloride for augmentation of labor

[5] J B Sharma, et al. Drotaverine hydrochloride vs. valethamate bromide in acceleration of labor

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Keywords: Drotaverine hydrochloride supplier, PDE, inhibitors, activators

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