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抑制剂/受体激动剂
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Cas号索引 1
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Cas号索引 1
1270084-92-8 | APX-115 freebase
(Catalog# : 2071628)
1949837-12-0 | ARV-771
(Catalog# : 2071539)
ARV-771 is a small-molecule pan-BET degrader. ARV-771 demonstrates dramatically impro
1446817-84-0 | ABX-1431
(Catalog# : 2071517)
ABX-1431 is a covalent, irreversible MGLL inhibitor. ABX-1431 is currently entering c
1572510-80-5 | AB-423
(Catalog# : 2071503)
AB-423 is a novel inhibitor of hepatitis b virus pregenomic rna encapsidation
1542020-25-6 | 2-aminopyrazolo[1,5-a]pyridine-3-carboxylic acid
(Catalog# : 202323)
114985-63-6 | 1-acetyl-5-nitro-3H-indol-2-one
(Catalog# : 2062319)
1035299-32-3 | 8-Acetyl-5-(benzyloxy)-2H-benzo[b][1,4]oxazin-3(4H)-one
(Catalog# : 2062311)
113305-94-5 | 2-Amino-5-cyanopyrazine
(Catalog# : 2062307)
1452226-14-0 | 5-amino-3,4-dimethylthieno[2,3-c]pyridazine-6-carboxylic acid
(Catalog# : 2062025)
1056901-64-4 | AT13148 intermediate(N1)
(Catalog# : 2062009)
177036-94-1 | Ambrisentan
(Catalog# : 2061308)
Ambrisentan, also known as BSF-208075 and LU-208075, is a drug indicated for use in t
186141-75-3 | A134974
(Catalog# : 204605)
A134974 is a bioactive chemical.
1375557-33-7 | A-1293201
(Catalog# : 204604)
A-1293201 is a potent and selective NAMPT inhibitor.
1219624-62-0 | A-1048400
(Catalog# : 204602)
A-1048400 is a potent and selective N-type and T-type calcium channel blocker.
1821-13-2 | A-1062
(Catalog# : 204601)
A-1062 is a resolvase-binding inhibitor. A1062 inhibits resolvase binding to the res
1103522-45-7 | Aprocitentan
(Catalog# : 112191)
Aprocitentan is an orally active, dual endothelin (ET) receptor antagonist developed
1838651-58-3 | ACT-709478
(Catalog# : 193288)
ACT-709478是一种强效、选择性的T型钙通道阻滞剂,是治疗全身性癫
1893415-00-3 | AZD9567
(Catalog# : 193254)
AZD9567是一种口服分化非甾体选择性糖皮质激素受体调节剂(SGRM)。
133825-81-7 | ATR-101盐酸盐
(Catalog# : 193208)
ATR-101,也被称为PD-132301 (游离)或PD-132301-2 (盐酸盐),正在临床开发
1613710-01-2 | ARN-3236
(Catalog# : 193192)
ARN-3236是一种强效、口服活性和选择性的SIK2抑制剂。在攻击- 3236抑
1373625-34-3 | ARN 077
(Catalog# : 193134)
ARN 077是一种强效选择性N -乙酰乙醇胺酸酰胺酶(NAAA)抑制剂,IC50为
156053-89-3 | Alvimopan
(Catalog# : 19382)
Alvimopan,也称为HSDB-7704和LY246736, 是一种作为一个次要地行动的μ-
1622902-68-4 | Abrocitinib
(Catalog# : 19381)
Abrocitinib(PF-04965842)是Pifzer研发的是一种Janus激酶抑制剂药物,目
1312782-34-5 | AA26-9
(Catalog# : 19372)
AA26-9是一种高效广谱丝氨酸水解酶抑制剂。AA26 -9抑制酶来源于丝
118292-41-4 | AGN-190299
(Catalog# : 19316)
Tazarotene是一种视黄醇类前体药物,通过在动物和人体内的快速脱
1126084-37-4 | ASP9521
(Catalog# : 19312)
ASP9521是日常的,选择性,口服生物利用率17β-羟甾类脱氢酶的抑制
1345614-59-6 | AM095钠
(Catalog# : 191251)
AM095是一个强有力的LPA1受体拮抗剂,因为它抑制GTPγS绑定中国仓鼠
1036404-17-7 | ARRY-797 (ARRY-371797)
(Catalog# : 191112)
ARRY-797(CAS1036404-17-7) is an oral, selective p38 mitogen-activated protein kinase
1557267-42-1 | 艾维替尼
(Catalog# : 19141)
艾维替尼,又称AC0010和Avitinib,是酪氨酸激酶抑制剂,抗肿瘤药物
1041852-85-0 | AZD7507
(Catalog# : 1812294)
AZD7507是一种有效的选择性CSF-1R抑制剂(32 nM 细胞活性), AZD7507被认
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-- Angiogenesis
----
VEGFR
----
JAK
----
EGFR
----
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----
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----
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----
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----
ALK
----
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----
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----
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----
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----
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----
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----
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----
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----
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----
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----
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----
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----
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-- Autophagy
----
LRRK2
----
CXCR
----
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----
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----
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----
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----
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----
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----
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----
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----
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----
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----
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----
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----
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----
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----
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----
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----
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----
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----
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----
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----
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----
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----
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----
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----
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----
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----
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----
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----
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----
MAGL
----
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----
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----
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----
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----
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----
UGT
----
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----
ATP Citrate Lyase
----
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-- Neuronal Signaling
----
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----
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----
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----
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Newest added products
抑制剂/受体激动剂
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新产品
天然化合物
最新产品
2351225-46-0 | NSD1 抑制剂 BT5
(Catalog# : 25207)
BT5可有效抑制NSD1,与细胞中的SET结构域结合,并降低H3K36me2水平。
1049704-18-8 | MA242 TFA
(Catalog# : 25206)
MA242是一种MDM2和NFAT1双重抑制剂,可诱导MDM2自泛素化及降解,并抑
2800223-30-5 | Dabogratinib ( TYRA-300 )
(Catalog# : 24073)
Dabogratinib ( TYRA-300 )是一种口服选择性成纤维细胞生长因子受体3(
N/A | AF710B
(Catalog# : 25205)
AF710B 是一种高效、选择性变构 M1 毒蕈碱和 σ1 受体激动剂。 AF710
2957874-18-7 | MAT2A inhibitor 5
(Catalog# : 25204)
MAT2A抑制剂5具有抑制MAT2A的高效力和对MTAP缺失的癌症细胞系的显著
1235733-73-9 | (Rac)-AF710B
(Catalog# : 24083)
AF-710B 是 σ 和 M1 毒蕈碱受体的激动剂;AF710B 是 AF710 的对映体。
863888-33-9 | Flurpiridaz-nonradiolabeled
(Catalog# : 25203)
Flurpiridaz是一种有前景的新型心脏PET成像示踪剂,是通过用氟-18放
863888-32-8 | Flurpiridaz-Precursor
(Catalog# : 25202)
现货
1800405-30-4 | KL1333
(Catalog# : 25201)
KL1333是一种口服的小有机分子,与NAD(P)H:醌氧化还原酶1(NQO1)
1369489-71-3 | Palupiprant ( E7046 )
(Catalog# : 24055)
E7046 is a potent and selective antagonist of the type 4 prostaglandin E2 (PGE2) rece