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+86-17702719238
sales@sun-shinechem.com
首页
抑制剂/受体激动剂
Angiogenesis
Anti-infection
Apoptosis
Autophagy
Cell Cycle
Cytoskeleton
DNA Damage
Epigenetics
GPCR & G Protein
Immunology & Inflammation
JAK/STAT
MAPK
Membrane Transporter/Ion Channel
Metabolic Enzyme/Protease
Neuronal Signaling
NF-κB
Protein Tyrosine Kinase
PI3K/Akt/mTOR
Stem Cells & Wnt
TGF-beta/Smad
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Cas号索引 3
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Cas号索引 3
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
323578-37-6 | tert-butyl N-(6-methylpyridin-3-yl)carbamate
(Catalog# : 110202)
Coming soon!
324769-06-4 | tert-butyl 3,3-dimethyl-4-oxopiperidine-1-carboxylate
(Catalog# : 91832)
Coming soon!
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产品分类
信号通路
-- Angiogenesis
----
VEGFR
----
JAK
----
EGFR
----
PDGFR
----
FLT3
----
FGFR
----
Src
----
ALK
----
Syk
----
HIF
-- Anti-infection
----
CMV
----
Filovirus
----
HBV
----
HCV
----
HIV
----
HSV
----
Influenza Virus
----
RSV
----
SARS-CoV
----
Antibacterial
----
Antifungal
----
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
----
APC
----
Wee1
----
DYRK
----
c-Myc
----
Aurora Kinase
----
ROCK inhibitor
----
Eukaryotic Initiation Factor (eIF)
----
NEKs
-- Cytoskeleton
----
HSP
----
Kinesin
----
Integrin
----
Dynamin
----
Wnt
----
β-catenin
----
Gap Junction Protein
-- DNA Damage
----
PARP
----
DNA/RNA Synthesis
----
Sirtuin
----
Topoisomerase
----
DNA-PK
----
Telomerase
----
RAD51
----
HDAC
----
ATM
----
DNA alkylator
----
Mps1
-- Epigenetics
----
PARP
----
JAK
----
Pim
----
PKC
----
PKD
----
Sirtuin
----
Histone Demethylase
----
Histone Acetyltransferase
----
HDAC
----
HIF-PH
----
Aurora Kinase
----
Histone Methyltransferase
----
METTL3
----
Epigenetic Reader Domain
----
Methionine Adenosyltransferase (MAT)
-- GPCR & G Protein
----
Histamine Receptor
----
Dopamine Receptor
----
Opioid Receptor
----
Endothelin Receptor
----
SGLT
----
OX Receptor
----
CaSR
----
CXCR
----
Vasopressin Receptor
----
Glucagon Receptor
----
Prostaglandin Receptor
----
5-HT Receptor
----
Adrenergic Receptor
----
Cannabinoid Receptor
----
Sphingosine 1 Phosphate Receptor
----
PKA
----
Adenosine Receptor
----
GnRH
----
LPL Receptor
----
Ras
----
Cholecystokinin Receptor
----
Melanocortin Receptor
----
RXFP Receptor
----
Bradykinin Receptor
----
GLP Receptor
----
SSTR
-- Immunology & Inflammation
----
PD-1
----
PD-L1
----
COX
----
CCR
----
Histamine Receptor
----
TLR
----
CXCR
----
MALT
----
TDO
----
NOS
----
IDO
----
Thrombopoietin Receptor(TPO)
----
NLR inhibitor
----
Interleukin Related
----
CD73
----
Complement System
----
Aryl Hydrocarbon Receptor
----
Kallikrein
----
IRAK
----
Reactive Oxygen Species(ROS)
----
SOD
-- JAK/STAT
----
JAK
----
STAT
----
Pim
----
EGFR
-- MAPK
----
MEK
----
Raf
----
p38 MAPK
----
ERK
----
MNK
----
Mixed Lineage Kinase
----
JNK
----
MAP4K
-- Membrane Transporter/Ion Channel
----
BCRP
----
CFTR
----
EAAT2
----
GABA Receptor
----
HCN Channel
----
Monoamine Transporter
----
Na+/Ca2+ Exchanger
----
Na+/K+ ATPase
----
nAChR
----
Calcium Channel
----
Chloride Channel
----
CRAC Channel
----
GlyT1
----
iGluR
----
P2X Receptor
----
P-glycoprotein
----
Amino acid transporter
----
Monocarboxylate Transporter
----
Potassium Channel
----
Proton Pump
-- Metabolic Enzyme/Protease
----
PPAR
----
Proteasome
----
P450
----
Caspase
----
HSP
----
HIV Protease
----
PDE
----
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)
----
Hemoglobin
-- Neuronal Signaling
----
COX
----
Histamine Receptor
----
Dopamine Receptor
----
Opioid Receptor
----
GABA Receptor
----
OX Receptor
----
Amyloid-β
----
5-HT Receptor
----
γ-secretase
----
Adrenergic Receptor
----
NMDA Receptor
----
GlyT1
----
Beta-secretase
----
Sigma Receptor
----
mAChR
----
α-Synuclein
----
Tau Protein
----
Cannabinoid Receptor
----
Transthyretin (TTR)
----
Melanocortin Receptor
----
Glucosylceramide Synthase (GCS)
----
CGRP-Receptor
----
TRP-Channel
-- NF-κB
----
NF-κB
----
HDAC
----
IKK
----
Keap1-Nrf2
-- Protein Tyrosine Kinase
----
VEGFR
----
EGFR
----
PDGFR
----
IGF-1R
----
FLT3
----
FGFR
----
c-Kit
----
Src
----
ALK
----
Ephrin receptor
----
BTK
----
Trk receptor
----
c-Met/HGFR
----
Syk (Spleen tyrosine kinase)
----
TAM Receptor
----
ULK1
----
CSF-1R
----
TYK2
----
ROS Kinase
----
Bcr-Abl
----
FAK
----
RET
----
Phosphoglycerate Kinase (PGK)
-- PI3K/Akt/mTOR
----
PI3K
----
Akt
----
GSK-3
----
S6 Kinase
----
AMPK
----
DNA-PK
----
MELK
----
PIKfyve
----
PI4K
----
PTEN
----
mTOR
----
ATM
----
PDK-1
----
ATR
----
Vps34
-- Stem Cells & Wnt
----
GSK-3
----
JAK
----
STAT
----
ROCK
----
TGF-beta/Smad
----
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
----
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
--
Amino Acids
--
Anilines
--
Boronic Acids
--
Bromides
--
Carboxes
--
Catalysts
--
Chiral Compounds
--
Deuterated
--
Fluorides
--
Imidazoles
--
Indoles and Oxindoles
--
Iodos
--
Nitro Compounds
--
Oxazoles
--
Peg Linkers
--
Phenols
--
Piperidines
--
Pyridines
--
Pyrimidines
--
Quinolines
--
Sulfonamides
--
Thiazoles
--
Trifluoroborates
--
Other Azoles
--
Other Heterocycles
--
Other Building Blocks
--
On Sale
新产品
天然化合物
最新产品
2417955-18-9 | Osivelotor (别名: GBT-601; GBT-021601)
(Catalog# : 26A061)
Osivelotor(同义词:GBT-601;GBT-021601)是下一代镰状血红蛋白(HbS)
2389060-50-6 | Linvemastat (别名: FP-020)
(Catalog# : 26A060)
Linvemastat(FP-020)是一种高效、选择性口服MMP-12抑制剂。
3041025-10-6 | BLU-808
(Catalog# : 26A024)
BLU-808是一种针对肥大细胞疾病的野生型c-KIT的强效且具有选择性的
1695564-98-7 | SCO-240
(Catalog# : 26A059)
SCO-240是一种研究性、口服活性和选择性生长抑素受体亚型5(SSTR5
2227154-23-4 | N-Methylamisulpride ( 别名: LB-102 )
(Catalog# : 26A058)
N-甲基咪唑胺(同义词:LB-102)是一种多巴胺D2和D3受体拮抗剂和血
1898207-64-1 | Safusidenib Erbumine
(Catalog# : 25178)
DS-1001 是一种口服的脑渗透性突变 IDH1 选择性抑制剂。
2837993-05-0 | Repinatrabit ( 别称: JNT-517 )
(Catalog# : 26A056)
Repinatrabit(JNT-517)是一种针对Phe转运蛋白SLC6A19的研究性、选择性
1361200-34-1 | Privosegtor ( 别名: OCS-05, ACT-01 )
(Catalog# : 26A055)
Privosegtor(OCS-05,ACT-01)是一种小分子拟肽、BDNF/NT-3生长因子受体
2923356-52-7 | ART-6043
(Catalog# : 26A054)
ART-6043是一种口服的DNA聚合酶θ(POLQ)小分子抑制剂。
2756333-39-6 | Palacaparib ( Synonyms: AZD-9574 )
(Catalog# : 26A053)
Palacioparib(AZD-9574)是一种口服的中枢神经系统渗透剂PARP-1抑制剂