Fludarabine CAS NO.21679-14-1

Min.Order Quantity:: 100 Gram

Purity:: 98%

Port:: Qingdao,China

Payment Terms:: L/C,T/T,MoneyGram,Other

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Quick Details

ProName: Fludarabine
CasNo: 21679-14-1
Molecular Formula: C10H12FN5O4
Appearance: White Solid
Application: Irreversible muscarinic agonist .DNA s...
DeliveryTime: Within7-10 days after receipt of your ...
PackAge: As customer request
Port: Qingdao,China
ProductionCapacity: 100 Kilogram/Month
Purity: 98%
Storage: Store in a cool,dry place and keep awa...
Transportation: Common products:Sea/Air/Courier ...
LimitNum: 100 Gram
MW:: 285.23
EINECS:: 244-525-5
Mol File:: 21679-14-1.mol

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lorcaserin(856681-05-5)is an orally administered agent and a selective 5-ht2c receptor agonist for the treatment of obesity. it had been approved for marketing in us by fda on 27 june in 2012. in clinical studies, lorcaserin has demonstrated efficacy in obese and overweight populations by promoting weight loss and improving metabolic parameters, and it is well tolerated.

Details

fludarabine basic information

product name:	fludarabine
synonyms:	2-fluoroadeninearabinoside;9-beta-d-arabinofuranosyl-2-fluoro-9h-purin-6-amin;9-beta-d-arabinofuranosyl-2-fluoro-adenin;f-ara-a;6-amino-9 beta-d-arabinofuranosylfluoropurine;9-bata-d-arabinofuranosyl-2-fluoroadenine;9-beta-d-arabinofuranosyl-2-fluoro-9h-purin-6-amine;9-beta-d-arabinofuranosyl-2-fluoroadenine
cas:	21679-14-1
mf:	c10h12fn5o4
mw:	285.23
einecs:	244-525-5
product categories:	intermediates & fine chemicals;pharmaceuticals;api
mol file:	21679-14-1.mol

fludarabine chemical properties

mp	265-268°c
storage temp.	2-8°c
solubility	dmf: 20 mg/ml, clear, faintly yellow
merck	13,4152
cas database reference	21679-14-1(cas database reference)

safety information

risk statements	23/24/25-36/37/38-39/23/24/25-39
safety statements	26-36/37-45
wgk germany	3
rtecs	au6207000
f	10
hazardous substances data	21679-14-1(hazardous substances data)

fludarabine usage synthesis

chemical properties	white solid
usage	used as an antineoplastic
usage	a stat-1 activation inhibita dna synthesis inhibitor.
biological activity	purine analog that inhibits dna synthesis. exhibits antiproliferative activity (ic 50 = 1.54 μ m in rpmi cells) triggers apoptosis through increasing bax decreasing bid, xiap survivin expression. displays anticancer activity against hematological malignancies in vivo .