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Sumatriptan (CAS No.: 103628-46-2)

Manus Aktteva Biopharma LLP, a global supplier of Sumatriptan, 103628-46-2 offers for your requirements of RND / Development quantities or commercials, based on status of the product. We can also offer its intermediates with supportive technical package required for evaluation.

CAS number:

103628-46-2

Chemical Name:

1-[3-(2-Dimethylaminoethyl)-1H-indol-5-yl]-N-methyl-methanesulfonamide, Sumatriptan (CAS No.: 103628-46-2)

Pharmacopeia:

USP, EP, BP

Certificate:

GMP, cGMP, EUGMP, WHO GMP, ISO Certified, USFDA, Cofepris Mexico, Korea FDA

Application:

For R&D Purpose

Properties
Related Intermediates

Synonym

1-[3-(2-Dimethylaminoethyl)-1H-indol-5-yl]-N-methyl-methanesulfonamide, Sumatriptan (CAS No.: 103628-46-2)

Molecular Formula

C14H21N3O2S

Molecular Weight

295.40

Specifications

Available on request

Packing

Export worthy packing

Material Safety Data Sheet

Available on request

Comments

Sumatriptan Base : Anti Migraine : Sumatriptan is metabolised primarily by monoamine oxidase A into an indole acetic acid analogue, part of which is further conjugated with glucuronic acid.

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Description:

Sumatriptan, CAS NO 103628-46-2, is a synthetic drug belonging to the triptan class, used for the treatment of migraine headaches. Sumatriptan is used to treat migraines. It helps to relieve headaches, pain and other symptoms of migraines, including sensitivity to light/sound, nausea, and vomiting. Sumatriptan succinate constricts bloodvessels and is used to treat migraine attacks. During migraine attacks certain bloodvessels in the brain become enlarged and this causes pain. Manus Aktteva Biopharma LLP, a global supplier of Oxyclozanide offers for your requirements with supportive technical package equired for evaluation.

Documentation / Approvals :

USDMF	EDMF	CEP / COS	TDP	DMF - CTD	ICH

Products protected by valid patents are not offered for sale in countries where the sale of such products constitutes a patent infringement and its liability is at buyer's risk.
Products currently covered by valid US Patents are offered for R&D use in accordance with 35 USC 271 +A13(1)
Products falling in to controlled substance category / list of schedule drugs shall be exported directly from the manufacturer principals only against receipt of original import permission issued by concerned authorities of the importing country.
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