武汉永璨生物科技有限公司
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抑制剂/受体激动剂
Angiogenesis
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TGF-beta/Smad
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Bromides
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联系我们
+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
Antibody-drug Conjugate/ADC Related
Microbiology
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Amino Acids
Anilines
Boronic Acids
Bromides
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Deuterated
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Pyridines
Pyrimidines
Quinolines
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联系我们
公司简介
联系我们
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产品名字索引 T
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产品名字索引 T
Tert-butyl (2R)-2-methylpiperazine-1-carboxylate,hydrochloride
(Catalog# : 81701, Cas# :
1000853-53-1
)
Coming soon!
tert-butyl (2S)-2-methylpiperazine-1-carboxylate,hydrochloride
(Catalog# : 81034, Cas# :
960283-58-3
)
Coming soon!
tert-Butyl (pyrrolidin-3-ylmethyl)carbamate hydrochloride
(Catalog# : 81031, Cas# :
1188263-69-5
)
Coming soon!
tert-butyl 4-(aminomethyl)piperidine-1-carboxylate,hydrochloride
(Catalog# : 81029, Cas# :
359629-16-6
)
Coming soon!
tert-Butyl (piperidin-3-ylmethyl)carbamate hydrochloride
(Catalog# : 81028, Cas# :
1159826-67-1
)
Coming soon!
4-tert-butyl-3-iodobenzoic acid
(Catalog# : 80315, Cas# :
91131-72-5
)
Coming soon!
TG02 ( SB1317 )
(Catalog# : 62502, Cas# :
937270-47-8
)
SB1317 (TG02) is a novel small molecule potent CDK/JAK2/FLT3 inhibitor. SB1317 was so
TCS JNK 5a
(Catalog# : 60202, Cas# :
312917-14-9
)
TCS JNK 5a(JNK Inhibitor IX) is a selective inhibitor of JNK2 and JNK3 (pIC50 values
Torin 1
(Catalog# : 52820, Cas# :
1222998-36-8
)
Torin 1 is a potent inhibitor of mTORC1/2 with IC50 of 2 nM/10 nM; exhibits 1000-fold
Tepotinib (EMD 1214063)
(Catalog# : 52785, Cas# :
1100598-32-0
)
Tepotinib (EMD 1214063) is a potent and selective c-Met inhibit
Terbutaline sulfate
(Catalog# : 52760, Cas# :
23031-32-5
)
Terbutaline sulfate is a 2-adrenergic receptor agonist; a fast-acting bronchodilator
Trelagliptin
(Catalog# : 52725, Cas# :
865759-25-7
)
Trelagliptin(SYR-472) is a long acting dipeptidyl peptidase-4 (DPP-4) inhibitor that
T 705
(Catalog# : 52717, Cas# :
259793-96-9
)
There is no brief introduction to the product
Tedizolid
(Catalog# : 52715, Cas# :
856866-72-3
)
Torezolid (TR-701; tedizolid) is a novel oxazolidinone for gram-positive infections.
Topiroxostat
(Catalog# : 52711, Cas# :
577778-58-6
)
Topiroxostat(FYX-051) is a novel and potent xanthine oxidoreductase (XOR) inhibitor w
TAK-632
(Catalog# : 52562, Cas# :
1228591-30-7
)
TAK-632 is a selective pan-RAF kinase inhibitor with IC50 values of 2.4/1.4 nM for BR
TGR5 Receptor Agonist
(Catalog# : 52557, Cas# :
1197300-24-5
)
TGR5 Receptor Agonist, a potent TGR5(GPCR19) agonist, showed improved potency in the
Tenovin-1
(Catalog# : 52529, Cas# :
380315-80-0
)
Tenovin-1 is a inhibitor of SIRT1 and SIRT2; activator of p21 and p53.
Tenovin-6
(Catalog# : 52528, Cas# :
1011557-82-6
)
Tenovin-6 is the water soluble analog of Tenovin-1 (HY-13423) and acts as a potent SI
Tiplaxtinin
(Catalog# : 52218, Cas# :
393105-53-8
)
Tiplaxtinin(PAI-039) is a selective and orally efficacious inhibitor of plasminogen a
Tirasemtiv
(Catalog# : 52238, Cas# :
1005491-05-3
)
Tirasemtiv(CK 2017357) is a a small-molecule fast-skeletal-troponin activator, which
TPT-260 Dihydrochloride
(Catalog# : 52235, Cas# :
2076-91-7
)
TPT-260 2Hcl (TPU260 2Hcl) is a thiophene thiourea derivative with molecule weight 26
TTP 22
(Catalog# : 52244, Cas# :
329907-28-0
)
TTP 22 is a high affinity, ATP-competitive casein kinase 2 (CK2) inhibitor with IC50/
Torin 2
(Catalog# : 52311, Cas# :
1223001-51-1
)
Torin 2 is a potent and selectivemTORinhibitor withIC50of 0.25 nM; 800-fold greater s
Trametinib (GSK1120212)
(Catalog# : 52109, Cas# :
871700-17-3
)
Trametinib (GSK1120212) is a highly specific and potentMEK1/2inhibitor withIC50of 0.9
TSU-68(SU6668,Orantinib)
(Catalog# : 51916, Cas# :
252916-29-3
)
TSU-68 (SU6668, Orantinib) has greatest potency againstPDGFRautophosphorylation withK
TIC10 ( ONC201 )
(Catalog# : 51802, Cas# :
1616632-77-9
)
ONC201 / TIC10是人类TRAIL基因的新型小分子诱导剂,可改善重组TRAIL的
TGX-221
(Catalog# : 52006, Cas# :
663619-89-4
)
TGX-221 is ap110-specific inhibitor withIC50of 5 nM, 1000-fold more selective for p11
Tasimelteon
(Catalog# : 51601, Cas# :
609799-22-6
)
Tasimelteon (trade name Hetlioz) is a selective agonist for the melatonin receptors M
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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
Linafexor (别名: CS-0159)
(Catalog# : 26A089, Cas# :
2765593-43-7
)
Linafexor(同义词:CS-0159)是法尼醇X受体(FXR)的强效非胆汁酸激
Prifetrastat (Synonyms: PF-07248144)
(Catalog# : 26A088, Cas# :
2569008-99-5
)
Prifetrastat (Synonyms: PF-07248144) 是一款首创、选择性、口服活性的
Camonsertib
(Catalog# : 24052, Cas# :
2417489-10-0
)
Camonsertib,也称为RP 3500,是一种新型、强效和选择性的ATR抑制剂,
MRX-2843
(Catalog# : 26A087, Cas# :
1429882-07-4
)
MRX-2843 是一种口服可用的双受体酪氨酸激酶(RTKs)抑制剂,作用
GDC-0134
(Catalog# : 20432, Cas# :
1637394-01-4
)
GDC-0134是一种MAP3K12(DLK)抑制剂。
BI-847325
(Catalog# : 25046, Cas# :
2128698-24-6
)
BI-847325是一种新型的、可口服的、竞争ATP结合位点的Aurora激酶和M
GDD-261
(Catalog# : 26A084, Cas# :
3137699-54-5
)
GDD-261是一种口服活性的磷酸甘油酸脱氢酶变构抑制剂(IC50=61nM)
Atebimetinib
(Catalog# : 25148, Cas# :
2669009-92-9
)
Atebimetinib(IMM-1-104)是一种口服的小分子MEK1和MEK2激酶变构抑制剂
BH-30643
(Catalog# : 26A047, Cas# :
3062177-59-4
)
BH-30643是一种新型、口服、非共价、大环、突变选择性OMNI-EGFR抑制
ERAS-801 ( JGK-068S )
(Catalog# : 20635, Cas# :
2490431-16-6
)
ERAS-801 ( JGK-068S ) 是一种有效的 EGFR 抑制剂。