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Cas号索引 1
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Cas号索引 1
1596348-16-1 | KDM5-C49
(Catalog# : 20493)
KDM5-C49 is a potent and selective inhibitor of KDM5 (also known as JARID1). KDM5-C49
1771756-32-1 | KUN56321
(Catalog# : 21246)
KUN56321 is a luminescent agent. The application of KUN56321 comprises: coating the f
1695533-89-1 | KO-947
(Catalog# : 20122101)
KO-947 is a potent and selective ERK inhibitor with slow dissociation kinetics. KO-94
1784282-12-7 | KHS101盐酸盐
(Catalog# : 191281)
KHS101 HCl是一种转化酸性卷曲蛋白3 (TACC3)的抑制剂。它的作用是通
1646795-59-6 | KC01
(Catalog# : 1810294)
KC01是ABHD16A的共价抑制剂。ABHD16A是一种磷脂酰丝氨酸(PS)脂肪酶,
18228-17-6 | KG-501
(Catalog# : 1810226)
KG-501是cAMP反应元件结合蛋白(CREB)抑制剂。
1131456-28-4 | KGP-94
(Catalog# : 3291806)
KGP94 is a reversible, time-dependent and competitive inhibitor of human cathepsin L.
1428729-56-9 | KIN-1148
(Catalog# : 184121)
KIN-1148是一个IRF3激动剂。KIN1148诱导剂量依赖性IRF3核易位和特异性
1799974-70-1 | KI-696
(Catalog# : 1710132)
ki-696代表一个优良的低分子量的工具来研究体内Keap1与Nrf2-Nrf2的相
1261113-96-5 | KAF-156
(Catalog# : 20178211)
KAF-156,也称为GNF-156, 是一种可治疗疟疾的抗疟药。
1188890-41-6 | KN-93 phosphate
(Catalog# : 16123029)
KN-93 is a CaMKII inhibitor. KN-93 suppresses ventricular arrhythmia induced by LQT2
191089-59-5 | K-7174
(Catalog# : 16123028)
K-7174 is a novel orally active, potent proteasome inhibitor. K-7174 exerts anti-myel
182004-65-5 | KB-R7943 mesylate
(Catalog# : 16122826)
KB-R7943 is a potent, selective inhibitor of the reverse mode of the Na+/Ca2+ exchang
142273-20-9 | Kenpaullone
(Catalog# : 16122711)
Kenpaullone is an ATP-competitive inhibitor of cyclin-dependent kinases (CDKs). It al
1309444-75-4 | K145
(Catalog# : 6111523)
K145 is a selective SphK2 inhibitor with an IC50 of 4.300.06 M , while no inhibition
1253452-78-6 | KS176
(Catalog# : 6111510)
KS176 is a potent and selective inhibitor of the breast cancer resistance protein (BC
1956356-56-1 | KYA1797K
(Catalog# : 6111416)
KYA1797K is a highly potent and selective Wnt/-catenin inhibitor with IC50 of 0.75 M
1354037-26-5 | KH-CB19
(Catalog# : 611922)
KH-CB19 is a potent and highly specific inhibitor of the CDC2-like kinase isoforms 1
1000669-72-6 | KW-2449
(Catalog# : 16071012)
KW-2449 is a novel multikinase inhibitor, which suppresses the growth of leukemia cel
1431985-92-0 | K02288
(Catalog# : 52728)
K02288 is a novel small molecule inhibitor of ALK1/2/3/6 with IC50s of 1.8/1.1/34.4/6
1233533-04-4 | kb NB 142-70
(Catalog# : 52568)
kb NB 142-70 is a selective protein kinase D (PKD) inhibitor (IC50 values are 28.3, 5
1118807-13-8 | KY02111
(Catalog# : 52212)
KY02111 is a small molecule which can promote differentiation of hPSCs to cardiomyocy
1350622-33-1 | kb-NB77-78
(Catalog# : 51502)
kb-NB77-78 is an analog of CID797718, which is a by-product of the synthesis of the p
191089-60-8 | K-7174 dihydrochloride
(Catalog# : 52002)
K-7174 dihydrochloride is a novel cell adhesion inhibitor; inhibits the expression of
1260247-42-4 | LLL12
(Catalog# : 25075)
LLL12是一种强效的STAT3抑制剂。LLL12在小鼠异种移植物模型中显示出
1934259-00-3 | Limertinib
(Catalog# : 24093)
Limertinib, also known as ASK120067, is an EGFR inhibitor. ASK120067 displayed potent
190791-29-8 | Lasofoxifene tartrate
(Catalog# : 24054)
Lasofoxifene, also known as CP 336156, is a non-steroidal selective estrogen receptor
180916-16-9 | Lasofoxifene
(Catalog# : 24053)
Lasofoxifene, also known as CP 336156, is a non-steroidal selective estrogen receptor
1820940-17-7 | Lorundrostat
(Catalog# : 20654)
Lorundrostat is an aldosterone synthase inhibitor.
108825-65-6 | Lin281632
(Catalog# : 20551)
Lin28 1632, is a RNA binding protein Lin28 inhibitor. Lin281632 promotes mESC differe
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-- Angiogenesis
----
VEGFR
----
JAK
----
EGFR
----
PDGFR
----
FLT3
----
FGFR
----
Src
----
ALK
----
Syk
----
HIF
-- Anti-infection
----
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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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-- Apoptosis
----
PD-1
----
PD-L1
----
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----
Caspase
----
TNF-alpha
----
Survivin
----
IAP
----
PERK
----
p53
----
Mdm2
----
E1/E2/E3 Enzyme
-- Autophagy
----
LRRK2
----
CXCR
----
Autophagy
-- Cell Cycle
----
CDK
----
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----
PD-L1
----
Chk
----
ROCK
----
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----
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----
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----
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----
c-Myc
----
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----
ROCK inhibitor
----
Eukaryotic Initiation Factor (eIF)
----
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-- 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
----
PARP
----
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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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----
DNA alkylator
----
Mps1
-- Epigenetics
----
PARP
----
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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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----
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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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----
TDO
----
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----
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----
IDO
----
Mitochondrial Metabolism
----
Isocitrate Dehydrogenase (IDH)
----
MAGL
----
Epoxide Hydrolase
----
LXR
----
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----
FPTase
----
RAR/RXR
----
Acetyl-CoA Carboxylase
----
Acyltransferase
----
UGT
----
MMP
----
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----
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----
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----
Lipase
----
Lactate dehydrogenase
----
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----
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----
PANK(pantothenate kinase)
----
Phosphoglycerate Dehydrogenase (PHGDH)
-- Neuronal Signaling
----
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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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-- Protein Tyrosine Kinase
----
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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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----
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----
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----
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----
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----
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----
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----
Vps34
-- Stem Cells & Wnt
----
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----
JAK
----
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----
ROCK
----
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----
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----
γ-secretase
----
β-catenin
----
smo
----
Notch
-- TGF-beta/Smad
----
PKC
----
ROCK
----
TGF-beta/Smad
-- Ubiquitin
----
Proteasome
----
p97
----
Deubiquitinase
----
DUB
-- Vitamin D Related
----
VD/VDR
-- PROTAC
----
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----
PROTACs
--
Antibody-drug Conjugate/ADC Related
--
Microbiology
-- Others
----
PKK
----
Others modulator
----
Estrogen Receptor/ERR
----
ChoKα
----
Newest added products
-- Nuclear Receptor
----
Androgen Receptor(AR)
抑制剂/受体激动剂
中间体
分子砌块
--
Aldehydes
--
Amines
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Amino Acids
--
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--
Boronic Acids
--
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--
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On Sale
新产品
天然化合物
最新产品
3054692-62-2 | ECI830
(Catalog# : 26A031)
ECI830是一种实验性的CDK2抑制剂。
1394076-92-6 | GNE-317
(Catalog# : 52282)
GNE-317 is a potent, brain-penetrantPI3Kinhibitor
3118994-80-9 | DPTX-3186
(Catalog# : 26A010)
DPTX3186 是一种口服的小分子凝聚体调节剂 (c-mod),可抑制 β-catenin
435327-40-5 | Avasopasem manganese (GC-4419; M-40419)
(Catalog# : 25108)
Avasopasem manganese, 也称为GC-4419、M 40419和SC-72325A,是超氧化物歧化酶
1421936-85-7 | Iclepertin (BI-425809)
(Catalog# : 24084)
Iclepertin(BI-425809)是一种口服的GlyT-1小分子抑制剂,用于治疗与
4727-31-5 | Kartogenin ( KGN )
(Catalog# : 52215)
Kartogenin(KGN)是一种合成小分子,通过激活smad-4/5通路刺激软骨细
218791-21-0 | Imisopasem manganese ( M40403; GC4403 )
(Catalog# : 72602)
Imisopasem manganese ( M40403; GC4403 ) 是一种稳定的非肽类 MnSOD 类似物,
2311863-36-0 | Apecotrep (BI 764198)
(Catalog# : 26A048)
Apecotrep(BI 764198)是一种潜在的同类首创、口服、选择性的TRPC6抑
902614-04-4 | Pantothenate kinase-IN-2
(Catalog# : 26A038)
Pantothenate kinase-IN-2是一种泛酸激酶抑制剂,对PanK2的IC50值为92 nM,
3062177-59-4 | BH-30643
(Catalog# : 26A047)
BH-30643是一种新型、口服、非共价、大环、突变选择性OMNI-EGFR抑制