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抑制剂/受体激动剂
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Anti-infection
Apoptosis
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Cas号索引 1
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Cas号索引 1
1346546-69-7 | GSK872
(Catalog# : 17101621)
GSK872是一个受体相互作用蛋白激酶抑制剂(RIP3)。GSK872抑制TNF-α
1539314-06-1 | GSK2881078
(Catalog# : 1791316)
GSK-2881078是一种潜在的对癌症恶病质的治疗选择性雄激素受体调节
1459687-96-7 | GJ-103钠
(Catalog# : 1791116)
GJ103氯化钠是通过自动模拟通读复合物GJ072。
1459687-89-8 | GJ-103 游离酸
(Catalog# : 1791115)
GJ103游离酸是通过自动模拟通读复合物GJ072。化学诱导通读提前终
199657-29-9 | Givinostat HCl
(Catalog# : 17919)
Givinostat或gavinostat,又名ITF2357,是一个强有力的和口服活性的组蛋
1350462-55-3 | 阿那匹韦
(Catalog# : 1783018)
阿那匹韦,也称为MK5172,是一种被批准用于治疗丙型肝炎的药物。
1496581-76-0 | GNE-3511
(Catalog# : 1781006)
GNE-3511是一种具有选择性的双亮氨酸激酶(DLK,MAP3K12)抑制剂,在神经
1336960-13-4 | GSK2193874
(Catalog# : 178914)
GSK2193874被认定为一种选择性的、口服的TRPV4阻断剂。
1622848-92-3 | GSK2982772
(Catalog# : 178911)
GSK2982772是一种ATP竞争性的受体- 1(激酶)抑制剂,IC50值为1 nM。它有
1254036-77-5 | GSK2269557
(Catalog# : 2017883)
GSK2269557,也称为GSK-2269557, 是一种有效且选择性的PI3K抑制剂.。
1282514-88-8 | GDC-0326
(Catalog# : 2017881)
GDC-0326是一种有效且选择性的磷酸肌醇的α-同种型3-激酶抑制剂(PI
1007573-18-3 | GSK-1521498
(Catalog# : 20178215)
GSK-1521498是一种新型阿片受体拮抗剂。它已经被证明可以减弱奖励
1816331-63-1 | GSK321
(Catalog# : 2017821)
GSK321是一种有效的、选择性的IDH1突变抑制剂。GSK321对HT- 1080细胞内
1936428-93-1 | GNE-272
(Catalog# : 20178121)
GNE-272对CBP / EP300的溴域具有很强的选择性(CBP IC50 = 0.02 μM, EP300 IC5
156223-05-1 | GTS-21
(Catalog# : 16123016)
GTS-21, also known as DMBX-A, is a derivative of the natural product anabaseine that
1910124-24-1 | GSK6853 (GSK-6853)
(Catalog# : 16123015)
GSK6853 is a potent (300 pM), soluble, cell active (20 nM), and highly selective inhi
1346547-00-9 | GSK583
(Catalog# : 16123014)
GSK583 is a Highly Potent and Selective Inhibitor of RIP2 Kinase (RIP2K bing IC50=5 n
1010411-21-8 | GSK369796 Dihydrochloride
(Catalog# : 16123013)
GSK369796, also known as N-tert-butylisoquine, is an anti-malaria drug candidate. GSK
1619994-68-1 | GSK2801
(Catalog# : 16123012)
GSK2801 is a A Selective Chemical Probe for BAZ2B/A bromodomains. BAZ2A/B belong to a
1224887-10-8 | GSK-2256098
(Catalog# : 16123011)
GSK2256098, also known as GTPL7939, is a focal adhesion kinase-1 (FAK) inhibitor with
1014691-61-2 | GSK0660
(Catalog# : 16123009)
GSK0660 is a selective PPAR antagonist. GSK0660 differentially regulated 273 transcri
133053-19-7 | Go6983
(Catalog# : 16123008)
GO6983 is a potent protein kinase C (PKC) inhibitor. GO6893 displays cardioprotective
1362154-70-8 | GNE-617
(Catalog# : 16123007)
GNE-617 is a potent nicotinamide phosphoribosyltransferase (NAMPT) inhibitor with IC5
1628260-79-6 | GLPG-1690(ziritaxestat)
(Catalog# : 16123005)
GLPG1690 is a selective autotaxin inhibitor discovered by Galapagos, with potential a
1434048-34-6 | GDC-0853
(Catalog# : 16123004)
GDC-0853 is orally available inhibitor of Bruton's tyrosine kinase (BTK) with potenti
1095173-27-5 | Glasdegib (PF-04449913)
(Catalog# : 16122787)
Glasdegib (PF-04449913) is a potent, and orally bioavailable Smoothened (Smo) inhibit
136194-77-9 | Go6976
(Catalog# : 16122723)
Go6976 is a potent PKC inhibitor with IC50 of 7.9 nM, 2.3 nM, and 6.2 nM for PKC (Rat
1254036-66-2 | GSK2292767
(Catalog# : 16122702)
GSK2292767 is a potent and selective PI3K inhibitor.GSK2292767 is highly selective fo
1474110-21-8 | GSK2981278
(Catalog# : 6111521)
ROR modulator 1 is a retinoid-related orphan receptor gamma (RORy) modulator, extract
1616391-87-7 | GSK-591
(Catalog# : 6111009)
EPZ015866 (GSK591) is a potent selective inhibitor of the arginine methyltransferase
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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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----
Survivin
----
IAP
----
PERK
----
p53
----
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----
E1/E2/E3 Enzyme
-- Autophagy
----
LRRK2
----
CXCR
----
Autophagy
-- Cell Cycle
----
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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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----
Eukaryotic Initiation Factor (eIF)
-- Cytoskeleton
----
HSP
----
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----
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----
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----
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----
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----
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-- DNA Damage
----
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----
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----
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----
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----
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-- Epigenetics
----
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----
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----
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----
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METTL3
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Epigenetic Reader Domain
-- GPCR & G Protein
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Histamine Receptor
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-- Membrane Transporter/Ion Channel
----
BCRP
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HCN Channel
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GlyT1
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-- Metabolism
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PPAR
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Lipoxygenase
----
HMG-CoA Reductase
----
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----
FXR
----
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----
TDO
----
Carbonic Anhydrase
----
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----
IDO
----
Mitochondrial Metabolism
----
MAGL
----
Epoxide Hydrolase
----
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----
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----
RAR/RXR
----
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----
UGT
----
MMP
----
ATP Citrate Lyase
----
Ketohexokinase(KHK)
-- Neuronal Signaling
----
COX
----
Histamine Receptor
----
Dopamine Receptor
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Opioid Receptor
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OX Receptor
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-- NF-κB
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-- Protein Tyrosine Kinase
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-- Proteases
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----
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----
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----
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-- PI3K/Akt/mTOR
----
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----
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----
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----
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----
mTOR
----
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----
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----
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-- Stem Cells & Wnt
----
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----
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----
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----
smo
-- TGF-beta/Smad
----
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----
ROCK
----
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-- Ubiquitin
----
Proteasome
----
p97
----
Deubiquitinase
----
DUB
-- Vitamin D Related
----
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PROTACs
--
Antibody-drug Conjugate/ADC Related
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Newest added products
抑制剂/受体激动剂
中间体
分子砌块
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On Sale
新产品
天然化合物
最新产品
85622-93-1 | Temozolomide
(Catalog# : 25209)
替莫唑胺是一种烷化剂。
2035010-37-6 | ALT-007
(Catalog# : 25157)
ALT-007 是一种口服生物可利用的 SPT 抑制剂,比多球菌素更有效,
2376397-93-0 | Opakalim
(Catalog# : 25193)
Opakalim(BHV-7000)是Kv7.2/7.3钾通道(KCNQ2/3)的口服小分子激活剂,
2102501-84-6 | PF-06835919 ( MDK-1846 )
(Catalog# : 193264)
MDK1846是一种强效的酮己糖激酶(KHK)抑制剂。
2271348-04-8 | MK256
(Catalog# : 25208)
MK256是一种新型CDK8抑制剂,通过下调STAT通路在急性髓系白血病(
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