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产品目录

编号化学名称Cas号纯度化学结构
20103002Senaparib1401682-78-7≧98.0%
Senaparib (IMP4297) is a novel agent targeting PARP (poly-ADP ribose polymerase) with
2091901SAR1316751433953-83-398% Min.
SAR131675 is a potent and selective VEGFR-3 inhibitor. It inhibited VEGFR-3 tyrosine
2091205(1S,5R)-1-(3-fluorophenyl)-3-oxabicyclo[3.1.0]hexan-2-one528587-70-498% Min.
2071609 SJB2-04363388-44-398% Min.
SJB2-043 is an inhibitor of USP1 target ID1 degradation in leukemic cells.
2071521Spastazoline2351882-11-498% Min.
Spastazoline is a novel inhibitor for aaa+ (atpases associated with diverse cellular
2071510SB 22500218298-32-498% Min.
2071501SCH-23390 maleate87134-87-098% Min.
SCH-23390 hydrochloride is a potent dopamine receptor antagonist (Ki values are 0.2 n
202331((1S,2R)-1-(3-fluorophenyl)cyclopropane-1,2-diyl)dimethanol1369767-20-3≧96.0%
我们可以提供公斤级定制合成。((1S,2R)-1-(3-fluorophenyl)cyclopropane-1,2
2062002(S)-4-(((1-Propyl-1H-imidazol-5-yl)methyl)sulfinyl)aniline497223-38-896% Min.
2051514SJ000291942425613-09-898% Min.
SJ000291942 is a bone morphogenic protein (BMP) signaling activator.
2051502Selinexor HClUnknown (HCl)98% Min.
Selinexor, also known as KPT-330, is an orally bioavailable, potent and selective XPO
2051501Selinexor free base1393477-72-9 (free base)98% Min.
Selinexor, also known as KPT-330, is an orally bioavailable, potent and selective XPO
2041504Simurosertib1330782-76-798% Min.
Simurosertib, also known as TAK-931, is an orally bioavailable inhibitor of cell divi
204609SGC2085 free base1821908-48-8 (free base)98% Min.
SGC2085 is a Potent and Selective Coactivator Associated Arginine Methyltransferase 1
204501Segetalin B164991-89-398% Min.
Segetalin B is natural product isolated from Seeds of Vaccaria Segetalis. Segetalin B
112592S26131296280-56-398% Min.
S26131 is a bioactive chemical.
111896SI-1131392816-46-498% Min.
SI113 is a specific inhibitor of the Sgk1 kinase activity, counteracting cancer cell
196301IPI145中间体1350643-72-996% Min.
52001Selisistat ( EX-527 )49843-98-3≧98.0%
Selisistat 是第一个确定的有效且可渗透细胞的 SIRT1 特异性抑制剂,
193261ST-193 489416-12-8>98%
ST-193是一种有效的广谱沙粒病毒抑制剂。抑制Guanarito、Junin、Lassa
193209SPL-707 2195361-33-0>98%
SPL-707是第一种选择性口服活性SPPL2a抑制剂。密切相关的酶γ-secret
193122SHP3942055757-40-7>98%
SHP394是一种有效的口服SHP2抑制剂(IC50 = 23nm),具有高亲脂性、增强
193113SGC-GAK-1 2226517-76-4>98%
SGC-GAK-1是一种针对atp结合位点的高效选择性GAK激酶探查。
19314SU 5214186611-04-1>98%
SU 5214是酪氨酸激酶信号转导的调制器。
192278Silvestrol697235-38-4>98%
Silvestrol,一种黄酮类化合物家族的成员,在体外和体内,从属的
192276Selpercatinib2152628-33-4>98%
Selpercatinib是一种具有抗肿瘤作用的酪氨酸激酶抑制剂。
192215SM16614749-78-9>98%
SM16是一种新型类型I的TGF-β信号传导抑制剂。
192151SB-674042483313-22-0>98%
SB-674042是一种有效的选择性OX1R拮抗剂。SB-674042与OX1R高亲和力结合
192147Seclidemstat1423715-37-0>98%
Seclidemstat是一种抗肿瘤药物候选药物。
192146Setafrastat1399715-48-0>98%
Setafrastat是一种转胺酶抑制剂和血管内皮生长因子(VEGF)促进剂。