99%min Tofacitinib Citrate 540737-29-9 CAS NO.540737-29-9

Min.Order Quantity:: 10 Gram

Purity:: 99%min

Port:: ShangHai

Payment Terms:: T/T,MoneyGram

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Keywords

99%min Tofacitinib Citrate
Tofacitinib Citrate Manufacturer
For Hypoglycemic Agents

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ProName: 99%min Tofacitinib Citrate 540737-29-9
CasNo: 540737-29-9
Molecular Formula: C16H20N6O.C6H8O7
Appearance: White Powder
Application: For Pharmaceutical Raw Materials
DeliveryTime: 2-4 days after confirmed your payments
PackAge: 100g/ bag, 2 kg/ bag, 25kg/ carton or ...
Port: ShangHai
ProductionCapacity: 1000 Metric Ton/Month
Purity: 99%min
Storage: Dry and cool place
Transportation: By DHL, TNT, FedEx, HKEMS, UPS, Etc
LimitNum: 10 Gram

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hubei xinrunde chemical co., ltd is a renowned pharmaceutical manufacturer. we can offer high quality products at competitive price in quick delivery with 100% custom pass guaranteed. never stop striving to offer our best service is our philosophy. we have flexible and untraceable payment terms. as a leading manufacture, our products have been exported to germany, norway, poland, finland, spain, uk, france, russia, usa, brazil, mexico, australia, japan, korea, thailand, indonesia, uruguay and many other countries.

1. quality.every batch of steroid powders have tobetested by our qc(quality control) before they are allowed to sell.

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Details

tofacitinib citrate basic information

description in vitro in vivo references

product name:	tofacitinib citrate
synonyms:	1-piperidinepropanenitrile, 4-methyl-3-(methyl-7h-pyrrolo[2,3-d]pyrimidin-4-ylamino)-beta-oxo-, (3r,4r)-, 2-hydroxy-1,2,3-propanetricarboxylate (1:1);1-piperidinepropanenitrile, 4-methyl-3-(methyl-7h-pyrrolo[2,3-d]pyrimidin-4-ylamino)-β-oxo-, (3r,4r)-, 2-hydroxy-1,2,3-propanetricarboxylate (1:1);tofacitinib citrate (cp-690550);tofacitinib citrate;tasocitinib citrate;tasocitinib citric acid s...;xeljanz;cp-690550 (tofacitinib citrate)
cas:	540737-29-9
mf:	c16h20n6o.c6h8o7
mw:	504.497
einecs:	1592732-453-0
product categories:	inhibitor;inhibitors;jak;stat
mol file:	540737-29-9.mol

tofacitinib citrate chemical properties

storage temp.	room temp
solubility	dmso: soluble5mg/ml (clear solution; warmed)
color	white to beige

tofacitinib citrate usage and synthesis

description	tofacitinib citrate is a king of drugs developed by the us pharmaceutical company pfizer for treating rheumatoid arthritis, trade name xeljanz, for the treatment of methotrexate inadequate response or intolerance to severe active rheumatoid arthritis (ra) in adult patients. this product is a janus kinase inhibitor, administered twice daily. november 6, 2012, the us food and drug administration (fda) and pfizer jointly announced tofacitinib citrate is approved for the treatment of methotrexate inadequate response or intolerance to severe active rheumatoid joints arthritis (ra) in adult patients. xeljanz can be used as monotherapy or in combination with methotrexate or other non-biological disease-modifying antirheumatic drugs (the dmard) in combination. this medicine should not be in combination with biological dmard or strong immunosuppressants (such as cyclosporine and azathioprine). xeljanz is approved by the daily dose of 2 times, each time 5mg. seven clinical trials evaluated the safety and efficacy of tofacitinib citrate in moderate to severe active ra in adult patients. in all tests, compared with patients receiving placebo, patients receiving xeljanz treatment showed significant improvement in clinical response and physical function. in clinical trials, the most common adverse events were upper respiratory tract infection, headache, diarrhea, nasal congestion, sore throat, and nasopharyngitis. using xeljanz was associated with an increased risk of serious infections, including opportunistic infections, tuberculosis, cancer and lymphoma. xeljanz product label attaches boxed warning on these security risks. xeljanz treatment is also associated with reducing blood cell counts and increasing cholesterol and liver enzyme values. in order to study xeljanz long-term impact on heart disease, cancer and severe infections, fda requires for a post-marketing study, which will evaluate two doses of xeljanz (tofacitinib citrate) therapy, and accept a integration of another group of patients approved by the treatment as a control.
in vitro	cp-690550 is a specific, orally inhibitor of jak3, it is 20-to 100-fold less potent for jak2 and jak1 with ic50 of 20 nm and 112 nm, respectively. cp-690550 doesn't have potent activity against 30 other kinases (all median ic50 > 3000 nm). cp-690,550 inhibits il-2–induced proliferation with 30-fold greater potency than its effects on gm-csf–induced proliferation. cp-690550 effectively inhibits a murine mixed lymphocyte reaction (mlr) (ic50 = 91 nm). cp-690550 potently inhibits il-4 induced upregulation of cd23 (ic50=57 nm) and class ii major histocompatibility complex (mhcii) expression (ic50=71 nm) on murine b cells. a recent research indicates low dose of cp-690550 accelerates the onset of experimental autoimmune encephalomyelitis by potentiating th17 differentiation.
in vivo	in a murine model of heterotopic heart transplantation (dba2 donor heart into c57/bl6 host), cp-690550 results in a dose-dependent increase in survival of transplanted hearts.the ec50 (drug concentration in blood at which 50% of mice will maintain their graft for >28 days) to be ～60 ng/ml.cp-690550 prevents rejection of allogeneic kidneys in nonhuman primate (nhps, macaca fascicularis) (mst of 62 and 83 days for the 50 to 100 ng/ml groups and 200 to 400 ng/ml groups, respectively). mice chronically dosed with cp-690550 (1.5-15 mg/kg/day) demonstrate dose and time-dependent alterations in lymphocyte subsets when examined by flow cytometry. the most dramatic change observed is a 96% reduction in splenic nk1.1+tcrb-cell numbers following 21 days of treatment. delayed-type hypersensitivity (dth) responses in sensitized mice are reduced in a dose-dependent manner following treatment with cp-690550 (1.87–30 mg/kg, s.c.).

definition	chebi: a citrate salt obtained by combining equimolar amounts of tofacitinib and citric acid. used to treat moderately to severely active rheumatoid arthritis.