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抑制剂/受体激动剂
Angiogenesis
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Aldehydes
Amines
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Boronic Acids
Bromides
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Deuterated
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Indoles and Oxindoles
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Peg Linkers
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联系我们
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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
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
Others
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Aldehydes
Amines
Amino Acids
Anilines
Boronic Acids
Bromides
Carboxes
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Deuterated
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Peg Linkers
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Piperidines
Pyridines
Pyrimidines
Quinolines
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产品名字索引 B
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产品名字索引 B
BMS-986104
(Catalog# : 193285, Cas# :
1622180-31-7
)
BMS-986104是一种强效的选择性S1P1受体调节剂,具有配体偏倚信号转
BAY-1316957
(Catalog# : 193263, Cas# :
1613264-40-6
)
BAY-1316957是一种高效、选择性、口服的人前列腺素E2受体亚型4 (hEP
BMS-986158
(Catalog# : 193255, Cas# :
1800340-40-2
)
BMS-986158是一种有效的选择性BET抑制剂。BMS-986158与BET蛋白BRD中的乙
BMS-986163
(Catalog# : 193207, Cas# :
1801151-09-6
)
BMS-986163是GluN2B的负变构调节剂,在重度抑郁症中具有潜在的应用
BAY-293
(Catalog# : 193121, Cas# :
2244904-70-7
)
BAY-293是一种有效的SOS1抑制剂,通过破坏IC50为21 nM的RAS-SOS1的相互
BMS-816336
(Catalog# : 19351, Cas# :
1009583-20-3
)
BMS-816336是一种口服活性、有效和选择性的11β-HSD1抑制剂。BMS- 8163
Belvarafenib
(Catalog# : 19341, Cas# :
1446113-23-0
)
Belvarafenib,又名GDC-5573、HM95573、RG6185,是RAF家族激酶的选择性抑制
Burixafor HBr
(Catalog# : 192221, Cas# :
1191450-19-7
)
Burixafor,又名TG-0054,是CXC趋化因子受体4 (CXCR4)的口服生物利用抑
BMS-986142
(Catalog# : 191284, Cas# :
1643368-58-4
)
BMS-986142是一种高效、选择性、可逆的BTK抑制剂。
Blu667
(Catalog# : 191282, Cas# :
2097132-94-8
)
BLU-667是一种有效的选择性 RET 抑制剂, IC50 为0.4 nM,对突变体 RET
BAY1238097
(Catalog# : 191257, Cas# :
1564268-08-1
)
BAY1238097是一种有效的选择性BET抑制剂。BAY1238097与BET蛋白BRD上乙酰
BMS-189453
(Catalog# : 191253, Cas# :
166977-43-1
)
BMS-189453也被称为BMS453,是一个强有力的和选择性RARβ受体激动剂和
BI-671800
(Catalog# : 191213, Cas# :
1093108-50-9
)
BI-671800是一种治疗哮喘患者的CRTH2拮抗剂。BI 671800与症状控制单纯
BI-3812
(Catalog# : 19124, Cas# :
2166387-64-8
)
BI-3812是BCL6 BTB/POZ区域与多个共抑制因子相互作用的有效抑制剂。
BAY 678
(Catalog# : 1812286, Cas# :
675103-36-3
)
BAY 678是一种有效且具有选择性的人类中性粒细胞弹性蛋白酶(HNE)抑
BN-82002
(Catalog# : 1812261, Cas# :
396073-89-5
)
BN-82002又称CDC25磷酸酶抑制剂I,是一种具有抗肿瘤特性的细胞渗透
BMS-509744
(Catalog# : 1811291, Cas# :
439575-02-7
)
BMS-509744是一种有效的白介素-2诱导T细胞激酶(ITK)抑制剂(IC50 = 19 nM
BMS-688521
(Catalog# : 1811281, Cas# :
893397-44-9
)
BMS-688521是白细胞功能相关抗原-1 (LFA-1)的小分子拮抗剂。它为LFA-1
BMS-986195
(Catalog# : 1811264, Cas# :
1912445-55-6
)
BMS-986195是一种有效,共价,Bruton’s酪氨酸激酶的不可逆抑制剂(B
BAY-299
(Catalog# : 1811262, Cas# :
2080306-23-4
)
BAY-299是一种有效且具有选择性的BRD1和TAF1抑制剂(IC50的值分别为
BMS-986165
(Catalog# : 1810163, Cas# :
1609392-27-9
)
BMS-986165是具有选择性、强效、变构抑制剂的酪氨酸激酶2 (Tyk2)。
Bictegravir
(Catalog# : 187181, Cas# :
1611493-60-7
)
Bictegravir,也称为GS - 9883,是一个强有力的,无助推的每日一次HIV- 1整
Basimglurant
(Catalog# : 187121, Cas# :
1034442-21-1
)
Basimglurant,又称RO 4917523和RG-7090,是一种新型的mGlu5阴性变构调制
3BDO
(Catalog# : 186232, Cas# :
890405-51-3
)
3BDO,一种丁基内酯衍生物,可以靶向FKBP1A,激活mTOR信号通路。它
BMS-986205
(Catalog# : 185314, Cas# :
1923833-60-6
)
BMS-986205是一种抗癌药物。
Birinapant
(Catalog# : 185182, Cas# :
1260251-31-7
)
Birinapant,也被称为TL32711,是一种合成的小分子,具有潜在的抗肿
Bryostatin 1
(Catalog# : 18573, Cas# :
83314-01-6
)
苔藓虫素1是一种有效的蛋白激酶C调制器,从苔藓虫体内分离出来
BMS-813160
(Catalog# : 1842812, Cas# :
1286279-29-5
)
BMS-813160是一种有效的选择性CCR2/CCR5拮抗剂,具有潜在的免疫调节
BRD7116
(Catalog# : 184282, Cas# :
329059-55-4
)
BRD7116是白血病干细胞(LSC)活性的有效选择性抑制剂(EC50 = 200 nM)。
盐酸巴多昔芬
(Catalog# : 18496, Cas# :
198480-56-7
)
Bazedoxifene,又名WAY-140424,是第三代选择性雌激素受体调节剂(SERM)
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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)
-- 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
-- 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
-- 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)
-- 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
-- NF-κB
----
NF-κB
----
HDAC
----
IKK
-- 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
-- Proteases
----
Proteasome
----
Caspase
----
HIV Protease
----
MMP
----
γ-secretase
----
DPP4
----
Isocitrate Dehydrogenase (IDH)
----
FPTase
----
Acetyl-CoA Carboxylase
----
Glutaminase
----
Methionine Adenosyltransferase (MAT)
-- 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
-- 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
AZD0095
(Catalog# : 237072, Cas# :
2750001-23-9
)
AZD0095 is a Selective Inhibitor of Monocarboxylate Transporter 4 (MCT4) for Oncology.
2-MNG
(Catalog# : 24129, Cas# :
2101538-28-5
)
2-巯基烟酰甘氨酸是一种新型强效黑素生成抑制剂,具有独特的作
MAT2A-IN-9
(Catalog# : 25147, Cas# :
2439277-80-0
)
MAT2A-IN-9(化合物167)是一种2-氧代喹唑啉衍生物,是一种强效的M
Safusidenib
(Catalog# : 25149, Cas# :
1898206-17-1
)
Safusidenib,也称为DS-1001,是一种口服异柠檬酸脱氢酶[NADP]细胞质(
Atebimetinib
(Catalog# : 25148, Cas# :
2669009-92-9
)
阿替美替尼(IMM-1-104)是一种口服的小分子MEK1和MEK2激酶变构抑制
Acoramidis hydrochloride
(Catalog# : 24068, Cas# :
2242751-53-5
)
Acoramidis是一种口服、强效、高选择性小分子转甲状腺素蛋白(TTR
Crelosidenib
(Catalog# : 24101, Cas# :
2230263-60-0
)
Crelosidenib ( [LY3410738)是一种有效的选择性的具有口服活性的突变
LOXO-435
(Catalog# : 25080, Cas# :
2833703-74-3
)
LOXO-435是FGFR3的选择性小分子抑制剂。它对野生型和致癌激活的FGF
Gridegalutamide
(Catalog# : 25138, Cas# :
2446928-30-7
)
Gridegalutamide, also known as BMS-986365 and CC-94676, is a heterobifunctional, firs
Chiauranib
(Catalog# : 25146, Cas# :
1256349-48-0
)
Chiauranib also known as orally available, small molecule inhibitor of select serine-