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抑制剂/受体激动剂
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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
Ubiquitin
Vitamin D Related
PROTAC
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Amines
Amino Acids
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Cas号索引 2
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Cas号索引 2
224177-60-0 | Siramesine hydrochloride
(Catalog# : 52549)
Siramesine(Lu 28-179) Hcl is a selective sigma-2 receptor agonist, which has been sho
218156-96-8 | SRPIN340
(Catalog# : 52210)
SRPIN340 is a serine/arginine-rich protein kinase (SRPK)-specific inhibitor with an I
204005-46-9 | Semaxanib (SU5416)
(Catalog# : 51803)
Semaxanib (SU5416) is a potent and selectiveVEGFR(Flk-1/KDR) inhibitor withIC50of 1.2
2283422-04-6 | Tebapivat
(Catalog# : 25137)
Tebapivat is a pyruvate kinase activator.
229005-80-5 | TAK-779
(Catalog# : 25049)
TAK-779 is a C-C chemokine receptor type 5 (CCR5) receptor antagonist potentially for
2319722-53-5 | TM5441sodium
(Catalog# : 24149)
TM-5441, also known as EBP 883 and BMS-790052, is a potent plasminogen activator inhi
2032123-28-5 | TCRS-417
(Catalog# : 24141)
TCRS-417 (T417) is a small molecule compound capable of docking to the interface betw
2559759-04-3 | tambiciclib dimaleate
(Catalog# : 24071)
2653254-31-8 | TYA-018
(Catalog# : 20667)
TYA-018 is an orally active, potent and highly selective HDAC6 inhibitor.
209746-59-8 | T-1095
(Catalog# : 24004)
T-1095 is a potent and selective inhibitor of Na+-glucose cotransporters (SGLTs).
2760481-53-4 | TNG908 抑制剂
(Catalog# : 20646)
TNG908 是一种临床阶段的 MTA 协同 PRMT5 抑制剂,通过利用合成致死
2883540-92-7 | Tersolisib ( STX-478 )
(Catalog# : 20633)
Tersolisib ( STX-478 ) 是第二代突变体选择性口服 PI3Ka 小分子变构抑制
2567459-64-5 | Tilpisertib Fosmecarbil
(Catalog# : 20598)
Tilpisertib fosmecarbil is a potent serine/threonine kinase inhibitor.
2218754-19-7 | TZ3O
(Catalog# : 20557)
TZ3O (compound TZ30) is an anticholinergic agent with neuroprotective effects.
2230490-29-4 | Tinengotinib ( TT-00420)
(Catalog# : 20553)
Tinengotinib ( TT-00420) 是一种新型多激酶抑制剂,在生化检测中强烈
2044686-42-0 | TP1287
(Catalog# : 236271)
Alvocidib Prodrug TP-1287 is an orally bioavailable, highly soluble phosphate prodrug
224441-73-0 | 5-叔丁基-2-(氯甲基)恶唑
(Catalog# : 20392)
2377858-38-1 | 1,7,9-Triazaspiro[4.5]dec-1-ene-6,10-dione, 2,4-bis(4-chlorophenyl)-8-thioxo-
(Catalog# : G20373)
2062661-53-2 | TOVINONTRINE ( IMR-687 )
(Catalog# : 218701)
TOVINONTRINE (IMR-687) 是一种高选择性和有效的磷酸二酯酶 9 (PDE9) 小分
2139287-33-3 | THAL-SNS-032
(Catalog# : 2091903)
THAL-SNS-032 is a selective CDK9 degrader. THAL-SNS-032 consists of a CDK-binding SNS
262433-01-2 | tert-butyl N-(4-bromo-2-methoxyphenyl)carbamate
(Catalog# : 2062310)
2244678-29-1 | TH257
(Catalog# : 2061311)
TH257 is a Potent and selective allosteric LIMK 1/2 inhibitor.
2250288-69-6 | TD-106
(Catalog# : 193184)
TD-106是一种可用于靶向蛋白降解的小脑(CRBN)调制器。TD-106诱导BRD4
2196203-96-8 | TH34
(Catalog# : 192273)
TH34是一种有效的HDAC6/8/10抑制剂。TH34在人类高级别神经母细胞瘤细
203564-54-9 | Tebanicline盐酸盐
(Catalog# : 181231)
Tebanicline盐酸盐,也被称为ABT-594和Ebanicline,是雅培公司开发的一
29767-20-2 | 替尼泊甙
(Catalog# : 17011723)
替尼泊甙是一种具有抗肿瘤活性的足叶草毒素的半合成衍生物。
293754-55-9 | T-0901317
(Catalog# : 16122840)
T-0901317, also known as T-1317; TO-091317; TO 901317, is a liver X receptor (LXR) ag
238750-77-1 | Tosedostat
(Catalog# : 123003)
Tosedostat is a proprietary orally bioavailable inhibitor of the M1 family of aminope
24150-24-1 | Terameprocol
(Catalog# : 122915)
Terameprocol is a synthetic tetra-methylated derivative of nordihydroguaiaretic acid
262352-17-0 | Torcetrapib
(Catalog# : 121433)
Torcetrapib is a CETP inhibitor with IC50 of 37 nM, elevates HDL-C and reduces nonHDL
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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