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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
Metabolism
Neuronal Signaling
NF-κB
Protein Tyrosine Kinase
Proteases
PI3K/Akt/mTOR
Stem Cells & Wnt
TGF-beta/Smad
Ubiquitin
Vitamin D Related
PROTAC
Antibody-drug Conjugate/ADC Related
Microbiology
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分子砌块
Aldehydes
Amines
Amino Acids
Anilines
Boronic Acids
Bromides
Carboxes
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Chiral Compounds
Deuterated
Fluorides
Imidazoles
Indoles and Oxindoles
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Peg Linkers
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Pyridines
Pyrimidines
Quinolines
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On Sale
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Cas号索引 2
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Cas号索引 2
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
206873-63-4 | Tariquidar
(Catalog# : 111911)
Tariquidar is a P-glycoprotein inhibitor undergoing research as an adjuvant against m
21919-05-1 | Tretazicar (CB1954)
(Catalog# : 100906)
Tretazicar is a dinitrobenzamide prodrug that is converted in the presence of the enz
202207-79-2 | tert-butyl N-[2-(methylamino)ethyl]carbamate,hydrochloride
(Catalog# : 81912)
Coming soon!
202207-78-1 | tert-butyl N-(2-aminoethyl)-N-methylcarbamate,hydrochloride
(Catalog# : 81909)
Coming soon!
205434-75-9 | tert-butyl 2-(hydroxymethyl)piperazine-1-carboxylate
(Catalog# : 81826)
Coming soon!
206273-87-2 | tert-butyl 4-(benzylamino)piperidine-1-carboxylate
(Catalog# : 81727)
Coming soon!
23031-32-5 | Terbutaline sulfate
(Catalog# : 52760)
Terbutaline sulfate is a 2-adrenergic receptor agonist; a fast-acting bronchodilator
259793-96-9 | T 705
(Catalog# : 52717)
There is no brief introduction to the product
2076-91-7 | TPT-260 Dihydrochloride
(Catalog# : 52235)
TPT-260 2Hcl (TPU260 2Hcl) is a thiophene thiourea derivative with molecule weight 26
252916-29-3 | TSU-68(SU6668,Orantinib)
(Catalog# : 51916)
TSU-68 (SU6668, Orantinib) has greatest potency againstPDGFRautophosphorylation withK
2226789-82-6 | UNC5293
(Catalog# : 24094)
UNC5293 is a MERTK -selective and potent inhibitor ( Ki=190 pM).
2414349-93-0 | UJN49930 ( UGT8-IN-1 )
(Catalog# : 20677)
UJN49930 ( UGT8-IN-1 ) 是 UDP-半乳糖神经酰胺半乳糖基转移酶 (UGT8) 的抑
2455519-86-3 | Usnoflast
(Catalog# : 20629)
Usnoflast is a non-steroidal anti-inflammatory (NSAID).
2244989-34-0 | UCB9608
(Catalog# : 2071516)
UCB9608 is a Potent, Orally Bioavailable PI4KIIIβ Inhibitor. UCB9608 showed the impr
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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
-- 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
-- Immunology & Inflammation
----
PD-1
----
PD-L1
----
COX
----
CCR
----
Histamine Receptor
----
TLR
----
CXCR
----
MALT
----
TDO
----
NOS
----
NADPH-oxidase
----
IDO
----
Thrombopoietin Receptor(TPO)
----
NLR inhibitor
----
Interleukin Related
----
CD73
----
Complement System
----
Aryl Hydrocarbon Receptor
----
Kallikrein
----
IRAK
-- 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
----
Potassium Channel
-- Metabolism
----
PPAR
----
P450
----
HSP
----
PDE
----
Factor Xa
----
Phospholipase
----
FAAH
----
CETP
----
Lipoxygenase
----
HMG-CoA Reductase
----
Fatty Acid Synthase
----
FXR
----
NAMPT
----
TDO
----
Carbonic Anhydrase
----
Monoamine Oxidase
----
IDO
----
Mitochondrial Metabolism
----
MAGL
----
Epoxide Hydrolase
----
LXR
----
Myeloperoxidase (MPO)
----
RAR/RXR
----
Acyltransferase
----
UGT
----
MMP
----
ATP Citrate Lyase
----
Ketohexokinase(KHK)
----
Lactate dehydrogenase
----
Glyoxalase (GLO)
-- 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)
-- 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)
-- Proteases
----
Proteasome
----
Caspase
----
HIV Protease
----
MMP
----
γ-secretase
----
DPP4
----
Isocitrate Dehydrogenase (IDH)
----
FPTase
----
Acetyl-CoA Carboxylase
----
Glutaminase
----
Methionine Adenosyltransferase (MAT)
----
Lipase
-- PI3K/Akt/mTOR
----
PI3K
----
Akt
----
GSK-3
----
S6 Kinase
----
AMPK
----
DNA-PK
----
MELK
----
PIKfyve
----
PI4K
----
PTEN
----
mTOR
----
ATM
----
PDK-1
----
ATR
-- Stem Cells & Wnt
----
GSK-3
----
JAK
----
STAT
----
ROCK
----
TGF-beta/Smad
----
Wnt
----
γ-secretase
----
β-catenin
----
smo
-- 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
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
1802632-22-9 | CT1812 ( Zervimesine )
(Catalog# : 193283)
CT-1812是一种同类首创的、可口服的sigma-2/PGRMC1拮抗剂(αβ寡聚体
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
2243882-74-6 | Zedoresertib
(Catalog# : 26A023)
Zedoresertib(Debio 0123)是一种脑渗透剂,高选择性WEE1激酶抑制剂。
3033961-38-2 | BEN-28010
(Catalog# : 26A022)
BEN-28010是一种自由脑渗透剂,强效且具有选择性的CHK1抑制剂。
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)
2565656-70-2 | Muvalaplin
(Catalog# : 20528)
Muvalaplin是一种小分子,通过干扰载脂蛋白(a)与载脂蛋白B100的结合
2925330-18-1 | MAT2A-IN-22
(Catalog# : 26A021)
MAT2A-IN-22 (Compound 29-1) 是一种可透过血脑屏障的和口服有效的 MAT2A
1497439-74-3 | AD-8007
(Catalog# : 26A018)
AD-8007是一种选择性且可穿透血脑屏障的乙酰辅酶A合成酶2(ACSS2)
1802650-31-2 | ZY-444
(Catalog# : 26A020)
ZY-444是一种通过抑制PC活性发挥抗癌作用的药物。
2306525-79-9 | AD-5584
(Catalog# : 26A019)
AD-5584是一种新型脑渗透性ACSS2抑制剂。