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sales@sun-shinechem.com
首页
抑制剂/受体激动剂
Angiogenesis
Anti-infection
Apoptosis
Autophagy
Cell Cycle
Cytoskeleton
DNA Damage
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Cas号索引 3
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Cas号索引 3
307538-42-7 | SMER28
(Catalog# : 17011709)
SMER28是一种自噬的小分子调制器,在哺乳动物细胞中独立于雷帕霉
312636-16-1 | SKI II
(Catalog# : 6111526)
SKI-II is a synthetic inhibitor of sphingosine kinase (SK) activity with IC50 of 78 M
305834-79-1 | SC79
(Catalog# : 161009025)
Akt Activator II, SC79, CAS 305834-79-1, is a cell-permeable compound that interacts
380899-24-1 | SB-649868
(Catalog# : 011815)
Coming soon!
379231-04-6 | Saracatinib
(Catalog# : 122913)
Saracatinib is an orally available 5-, 7-substituted anilinoquinazoline with anti-inv
356559-20-1 | SB 525334
(Catalog# : 102205)
SB 525334 is a potent and selective inhibitor of TGF_beta_ receptor I (ALK5) with IC5
321429-48-5 | (1S)-1-(3-fluorophenyl)ethanamine,hydrochloride
(Catalog# : 90726)
Coming soon!
325145-35-5 | (S)-1-Boc-2-Ethylpiperazine
(Catalog# : 81901)
Coming soon!
314741-40-7 | (S)-1-Boc-3-(Hydroxymethyl)piperazine
(Catalog# : 81825)
Coming soon!
330161-87-0 | SU6656
(Catalog# : 52754)
SU 6656 is a selective inhibitor of Src kinases, Including Src, Yes, Lyn, and Fyn (IC
377090-84-1 | SU9516
(Catalog# : 52579)
SU-9516 is a selective CDK2 inhibtor with IC50 of 22 nM; less potent for CDK1/CDK4(IC
301836-41-9 | SB431542
(Catalog# : 52312)
SB431542 is a potent and selective inhibitor ofALK5withIC50of 94 nM, 100-fold more se
345627-80-7 | SNS-032 ( BMS-387032 )
(Catalog# : 52105)
SNS-032 has firstly been described as a selective inhibitor ofCDK2withIC50of 48 nM an
3117940-39-0 | TRI-611
(Catalog# : 26A033)
TRI-611是一种口服ALK分子胶降解剂。
3107291-07-3 | 4-((2-(甲氨基)-6-(2,2,2-三氟乙基)噻吩并[2,3-d]嘧啶-4-基)氨基)哌啶-1-甲酸叔丁酯
(Catalog# : 26B007)
3024657-88-0 | 6,11-二氧代-6,11-二氢-5H-苯并[b]咔唑-2-甲酸叔丁酯
(Catalog# : 24002)
Tert-butyl 6,11-dioxo-6,11-dihydro-5H-benzo[b]carbazole-2-carboxylate, CAS 3024657-88
359629-19-9 | tert-Butyl 4-(1-oxoisoindolin-2-yl-methyl)piperidine-1-carboxylate
(Catalog# : 2062034)
313520-94-4 | TH-263
(Catalog# : 2061303)
TH-263 is an inactive analog control for the type III allosteric LIM-kinase (LIMK) in
31274-51-8 | 2,4,6-三[(1,1-联苯)-4-基]-1,3-5-三嗪
(Catalog# : S-204158)
309915-12-6 | 他匹莫德盐酸盐
(Catalog# : 181252)
他匹莫德,又称SCIO-469,是一种口服生物可利用的小分子p38丝裂原
303162-79-0 | TAK-715
(Catalog# : 187202)
TAK-715是一种有效的p38 MAPK抑制剂。它表现出有效的抑制活性,对主
305860-41-7 | tert-butyl ((1H-benzo[d][1,2,3]triazol-1-yl)methyl)carbamate
(Catalog# : 183214)
tert-butyl (1H-benzo[d][1,2,3]triazol-1-yl)methylcarbamate is a drug intermediate.
328898-40-4 | 泰地罗新
(Catalog# : 17011904)
泰地罗新 (TIP) 是一种新型十六环的巨环,用于治疗牛和猪呼吸系
372523-75-6 | TCS-OX2-29
(Catalog# : 61117)
TCS-OX2-29 is a potent and selective OX2 receptor antagonist with IC50 of 40 nM. Disp
327036-89-5 | TDZD-8
(Catalog# : 161009029)
TDZD-8 protects the brain against I/R injury by inhibiting GSK-3beta activity. TDZD-8
35943-35-2 | Triciribine
(Catalog# : 161009022)
Triciribine inhibits the phosphorylation, activation, and signalling of Akt-1, -2, an
387867-13-2 | Tandutinib
(Catalog# : 123015)
Tandutinib is a potent FLT3 antagonist with IC50 of 0.22 M, also inhibits PDGFR and c
385367-47-5 | Tarafenacin
(Catalog# : 122215)
Tarafenacin(SVT-40776) is a highly selective M3 muscarinic receptor antagonist (Ki= 0
332012-40-5 | Telatinib
(Catalog# : 121432)
Telatinib is a potent inhibitor of VEGFR2/3, c-Kit and PDGFR with IC50 of 6 nM/4 nM,
300801-52-9 | TG003
(Catalog# : 110226)
TG003 is a novel benzothiazole compound that demonstrates potent inhibition of Clk1/S
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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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----
Antibacterial
----
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----
Parasite
-- Apoptosis
----
PD-1
----
PD-L1
----
Bcl-2
----
Caspase
----
TNF-alpha
----
Survivin
----
IAP
----
PERK
----
p53
----
Mdm2
----
E1/E2/E3 Enzyme
-- Autophagy
----
LRRK2
----
CXCR
----
Autophagy
-- Cell Cycle
----
CDK
----
PD-1
----
PD-L1
----
Chk
----
ROCK
----
PLK
----
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----
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----
DYRK
----
c-Myc
----
Aurora Kinase
----
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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----
Gap Junction Protein
-- DNA Damage
----
PARP
----
DNA/RNA Synthesis
----
Sirtuin
----
Topoisomerase
----
DNA-PK
----
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----
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----
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----
ATM
----
DNA alkylator
----
Mps1
-- Epigenetics
----
PARP
----
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----
Pim
----
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----
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----
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----
Histone Demethylase
----
Histone Acetyltransferase
----
HDAC
----
HIF-PH
----
Aurora Kinase
----
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----
METTL3
----
Epigenetic Reader Domain
----
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-- GPCR & G Protein
----
Histamine Receptor
----
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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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-- Immunology & Inflammation
----
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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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-- JAK/STAT
----
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----
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----
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----
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-- MAPK
----
MEK
----
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----
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----
ERK
----
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----
Mixed Lineage Kinase
----
JNK
----
MAP4K
-- Membrane Transporter/Ion Channel
----
BCRP
----
CFTR
----
EAAT2
----
GABA Receptor
----
HCN Channel
----
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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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-- Metabolic Enzyme/Protease
----
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----
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----
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----
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----
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----
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----
MMP
----
Factor Xa
----
γ-secretase
----
Phospholipase
----
DPP4
----
FAAH
----
CETP
----
Lipoxygenase
----
HMG-CoA Reductase
----
Fatty Acid Synthase
----
NADPH-oxidase
----
FXR
----
NAMPT
----
TDO
----
Carbonic Anhydrase
----
Monoamine Oxidase
----
IDO
----
Mitochondrial Metabolism
----
Isocitrate Dehydrogenase (IDH)
----
MAGL
----
Epoxide Hydrolase
----
LXR
----
Myeloperoxidase (MPO)
----
FPTase
----
RAR/RXR
----
Acetyl-CoA Carboxylase
----
Acyltransferase
----
UGT
----
MMP
----
ATP Citrate Lyase
----
Glutaminase
----
Ketohexokinase(KHK)
----
Lipase
----
Lactate dehydrogenase
----
Glyoxalase (GLO)
----
E1/E2/E3 Enzyme
----
PANK(pantothenate kinase)
----
Phosphoglycerate Dehydrogenase (PHGDH)
-- Neuronal Signaling
----
COX
----
Histamine Receptor
----
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----
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----
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----
OX Receptor
----
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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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-- NF-κB
----
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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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----
RET
----
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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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----
PTEN
----
mTOR
----
ATM
----
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----
ATR
----
Vps34
-- Stem Cells & Wnt
----
GSK-3
----
JAK
----
STAT
----
ROCK
----
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----
Wnt
----
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
----
Molecular Glues
----
PROTACs
--
Antibody-drug Conjugate/ADC Related
--
Microbiology
-- Others
----
PKK
----
Others modulator
----
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----
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
--
Amino Acids
--
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--
Boronic Acids
--
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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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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