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产品目录

编号化学名称Cas号纯度化学结构
17982BAY-5981906919-67-298.0%
BAY-598是一种强效的针对SMYD2中肽-竞争的化学探测器。BAY-598拥有一
17981BAY-598 R-异构体1906920-28-298.0%
BAY-598 R-异构体是BAY589 R-异构体。bay-598 R-异构体可以作为一个参照
17916布索芬新171655-91-798.0%
布索芬新是一种充分的单胺再摄取阻滞剂,已被开发用于治疗帕金
1783013B021290541-46-698.0%
B02,也叫RAD51 - in - 02,是一种RAD51抑制剂。B02能增强MM细胞的DOX敏
1781003BLU-2851703793-34-398.0% 
BLU-285是一种有效、具有选择性的抑制剂。
1781002BAY-18953441876467-74-198.0% 
BAY-1895344是一种有效的、具有选择性的ATM抑制剂。
178813BIBR1532321674-73-198.0% 
BIBR1132对端粒酶的抑制具有很强的选择性,导致肿瘤细胞延迟生长
2017877BMS-9324811263871-36-898.0% 
BMS-932481调节Aβ肽在血浆和脑脊液的健康志愿者。
20178216B-1613214066-78-198.0% 
(2S,4S)-4-(氨基甲基)吡咯烷-1,2-二羧酸 1-叔丁酯 2-甲酯;(2S,4S)-1-tert
2017822Balamapimod863029-99-698.0% 
<span style="color:#34495E;font-family:" font-Balamapimod, 也称为MKI-822,是一种
17030606BP-1-1021334493-07-098% 
BP-1-102是一种有效的口服生物和选择性抑制剂。
17030604BAY-8761799753-84-698% 
BAY-876是一种有效的、选择性的谷氨酸抑制剂。BAY- 876在体外具有良
17030312BRD-75521137359-47-798% 
BRD-7552是一种PDX1转录诱导因子。它主要在人类胰岛和导管细胞中调
17030305BDA-3661821496-27-898% 
BDA - 366是BCL - BH4拮抗剂。BDA - 366抑制人骨髓瘤的生长。BDA - 366诱导
17030116Bimiralisib1225037-39-798% 
Bimiralisib,也被称为PQR309,是一种口服生物可用的磷脂- 3 -激酶抑
17030110BEC HCl222638-67-798% 
BEC,也称为S -(2-boronoethyl)-L-cysteine,是一个慢结合和竞争力的精氨酸
17109003BGP-1566611-37-898% 
BGP-15, 是一种带有PARP抑制活性的烟碱类胺肟衍生物。已经证明BGP-
16122908Butylphthalide6066-49-598% 
Butylphthalide, also known as 3-n-butylphthalide or NBP, is an antioxidant and one of
16122907Buthionine Sulphoximine5072-26-498%
Buthionine Sulphoximine, also known as NSC-326231, is a gamma-glutamylcysteine synthe
16122906布瓦西坦357336-20-098% 
Brivaracetam, also known as UCB 34714, is a chemical analog of levetiracetam, is a ra
16122905Brigatinib (AP-26113)1197953-54-098% 
Brigatinib, also known as AP-26113, is an orally active, potent and selective Dual AL
16122904Brevianamide F38136-70-898% 
Brevianamide F , also known as cyclo-(L-Trp-L-Pro), belongs to a class of naturally o
16122903Bohemine189232-42-698% 
Bohemine is a potent and selective, cell-permeable, cyclin-dependent kinase (CDK) inh
16122902BMS-6874531000998-59-398% 
BMS-687453 is a potent and selective peroxisome proliferator activated receptor (PPAR
16122901BML-210537034-17-698% 
BML-210, also known as CAY10433, is HDAC inhibitor. BML-210 induces growth inhibition
16122868BIIB021848695-25-098% 
BIIB021, also known as CNF2024, is an orally active, purine-scaffold, small-molecule
16122867BI605906960293-88-398% 
BI605906 is a IKK inhibitor. BI605906 inhibits TNF-dependent IB degradation and expre
16122866Benzbromarone3562-84-398% 
Benzbromarone is a uricosuric agent and non-competitive inhibitor of xanthine oxidase
16122805BAY-59-3074406205-74-198% 
BAY-59-3074 is a novel cannabinoid CB1/CB2 receptor partial agonist with analgesic pr
16122804Batimastat130370-60-498% 
Batimastat (also known as BB-94) is a synthetic matrix metalloproteinase inhibitor th