伐尼克兰（盐酸）

Varenicline Hcl(CP 526555;Champix) is a nicotinic receptor partial agonist; it stimulates nicotine receptors more weakly than nicotine itself does.

上海嵘崴达实业有限公司，专业经营生命科学领域的科研试剂、仪器和实验室消耗品，
致力于向国内生命科学研究人员提供一流的产品和服务。

主要经营的试剂品牌：
Roche试剂，部分常用现货，周三定货，2-3周到货。
GE试剂，耗材，部分常用现货，周二，周五定货，3周左右到货。
R&D试剂，周三定货，2-3周到货。
SIGMA试剂，周一，五定货，3周左右到货。
Millipore试剂，每周三定货，2-3周到货。
Invitrogen试剂，部分现货，周三定货，2-3周到货。
ABCAM试剂，周三定货，2-3周到货。
eBioscience试剂，部分常用现货，周三定货，2-3周到货。
STANT CRUZ试剂，周三定货，2-3周到货。
Biolegend试剂，周三定货，2-3周到货。
Peprotech试剂，部分常用现货，周三定货，2-3周到货。
USB试剂，常备现货，周五定货，4周到货。
Amresco试剂，常备现货，3-4周到货。
罗氏原料，请来电来邮咨询。
Thermo试剂，pierce, Hyclone部分常用现货。

主要经营的耗材品牌：
1. BIOHIT，单道移液半支消毒长期促销，350/支。
2. BD Fa2. BD Falcon耗材，常用常备现货。

HY-10020	Varenicline (Hydrochloride)伐尼克兰（盐酸）	Varenicline Hcl(CP 526555;Champix) is a nicotinic receptor partial agonist; it stimulates nicotine receptors more weakly than nicotine itself does.		230615-23-3	CP 526555 hydrochloride; Champix hydrochloride; Chantix hydrochloride
HY-14768	T 705	T 705(Favipiravir) is a RNA-directed RNA polymerase NS5B inhibitor.		259793-96-9	Favipiravir;T-705;T705
HY-10396	Emricasan	Emricasan (IDN-6556, PF-03491390) is a potent irreversible pan-caspase inhibitor.		254750-02-2	IDN 6556;PF 03491390;PF03491390;PF-03491390;IDN-6556
HY-14398	Celecoxib塞来昔布	Celecoxib(Celebra; Celebrex; SC 58635) is a highly selective COX-2 inhibitor and primarily inhibits this isoform of cyclooxygenase (and thus causes inhibition of prostaglandin production).		169590-42-5	Celebra; Celebrex; SC 58635
HY-11038	PU-H71	PU-H71是Hsp90抑制剂，IC50为50 nM。	873436-91-0	PU-H 71; PU H71
HY-50098	PF-2545920	PF-2545920 a highly selective and potent PDE10A inhibitor with an IC50 of 0.37 nM.		898562-94-2	PF 2545920; PF2545920
HY-13272	Dacomitinib	Dacomitinib(PF299804) is a potent, orally available, irreversible tyrosine kinase HER 1 (EGFR), HER2 and HER4 inhibitor with IC50 of 6, 45.7 and 73.7 nM for EGFR, ERBB2 and ERBB4, respectively.		1110813-31-4	PF-00299804; PF-299804; PF 299804; PF 00299804
HY-13265	AR-42	AR-42 is a novel HDAC inhibitor with an IC50 of 0.61 μM for acute lymphoblastic leukemia (697) cell lines.		935881-37-1	HDAC-42; OSU-HDAC42;AR42;AR 42
HY-10403	PH-797804	PH-797804 is an ATP-competitive, readily reversible inhibitor of the α isoform of human p38 MAP kinase, exhibiting a Ki = 5.8 nM.		586379-66-0	PH797804;PH 797804
HY-10681	PKI-587	PKI-587 is a highly potent dual PI3K/mTOR kinase inhibitor with IC50 of 0.4 nM and <0.1 μM for PI3K-α and mTOR, respectively.		1197160-78-3	PF-05212384; PKI587; PKI 587