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抑制剂/受体激动剂
PI3K/Akt/mTOR
Epigenetics
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Cytoskeletal Signaling
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others
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+86-17702719238
sales@sun-shinechem.com
首页
抑制剂/受体激动剂
PI3K/Akt/mTOR
Epigenetics
Protein Tyrosine Kinase
Angiogenesis
Apoptosis
Autophagy
JAK/STAT
MAPK
Cytoskeletal Signaling
Cell Cycle
TGF-beta/Smad
DNA Damage
Stem Cells & Wnt
Ubiquitin
Neuronal Signaling
NF-κB
GPCR & G Protein
Metabolism
Anti-infection
Proteases
Immunology & Inflammation
Vitamin D Related
Membrane Transporter/Ion Channel
others
PROTAC
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
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On Sale
中间体
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订购信息
联系我们
公司简介
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产品名字索引 B
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产品名字索引 B
BI605906
(Catalog# : 16122867, Cas# :
960293-88-3
)
BI605906 is a IKK inhibitor. BI605906 inhibits TNF-dependent IB degradation and expre
Benzbromarone
(Catalog# : 16122866, Cas# :
3562-84-3
)
Benzbromarone is a uricosuric agent and non-competitive inhibitor of xanthine oxidase
BAY-59-3074
(Catalog# : 16122805, Cas# :
406205-74-1
)
BAY-59-3074 is a novel cannabinoid CB1/CB2 receptor partial agonist with analgesic pr
Batimastat
(Catalog# : 16122804, Cas# :
130370-60-4
)
Batimastat (also known as BB-94) is a synthetic matrix metalloproteinase inhibitor th
BFH772
(Catalog# : 16122778, Cas# :
890128-81-1
)
BFH772 is a novel potent oral VEGFR2 inhibitor, targeting VEGFR2 kinase with IC50 of
BI-78D3
(Catalog# : 16122776, Cas# :
883065-90-5
)
BI-78D3 is a competitive JNK inhibitor with IC50 of 280nM that displays > 100 fold
BDA-366
(Catalog# : 16122769, Cas# :
1909226-00-1
)
BDA-366 is a small-molecule Bcl2-BH4 domain antagonist and binds BH4 with high affini
BI-7273
(Catalog# : 16122742, Cas# :
1883429-21-7
)
BI-7273 is a potent, selective, and cell-permeable BRD9 BD Inhibitor.
BI-9564
(Catalog# : 16122740, Cas# :
1883429-22-8
)
BI-9564 is a selective inhibitor of BRD9 and BRD7 bromodomains with the IC50 of 75 nM
BAW2881 (NVP-BAW2881)
(Catalog# : 16122733, Cas# :
861875-60-7
)
BAW2881 (NVP-BAW2881) is a novel vascular endothelial growth factor (VEGF) receptor t
BMS-983970
(Catalog# : 6111507, Cas# :
1584713-87-0
)
BMS-983970 is an oral pan-Notch inhibitor for the treatment of cancer.
BAY-61-3606
(Catalog# : 6111415, Cas# :
648903-57-5
)
BAY-61-3606 is a potent and selective inhibitor of Syk kinase (Ki = 7.5 nM).
BH3I-1
(Catalog# : 61402, Cas# :
300817-68-9
)
BH3I-1 is an inhibitor of Bcl-xL with IC 50 of 293.95 M. BH3I-1 is a cell permeable B
Bax inhibitor peptide V5
(Catalog# : 61401, Cas# :
579492-81-2
)
Bax inhibitor peptide V5 is a peptide inhibitor of Bax translocation to mitochondria.
BMS-986020
(Catalog# : 61122, Cas# :
1257213-50-5
)
BMS-986020 is a lysophosphatidic acid 1 receptor antagonist. BMS-986020 is in Phase 2
(±)-Bisoprolol hemifumarate
(Catalog# : 6111106, Cas# :
104344-23-2
)
Bisoprolol is a selective type 1 adrenergic receptor blocker.Bisoprolol, on beta 1-ad
BNC105
(Catalog# : 6111023, Cas# :
945771-74-4
)
BNC105 is a tubulin polymerization inhibitor with potent antiproliferative and tumor
6-bromo-[1,2,4]triazolo[1,5-a]pyridine
(Catalog# : 6111002, Cas# :
356560-80-0
)
6-bromo-[1,2,4]triazolo[1,5-a]pyridine
Briciclib
(Catalog# : 611917, Cas# :
865783-99-9
)
Briciclib is a small molecule that suppresses cyclin D1 accumulation in cancer cells.
3-bromo-1-ethyl-1H-pyrrole-2,5-dione
(Catalog# : 1681202, Cas# :
909397-54-2
)
3-bromo-1-ethyl-1H-pyrrole-2,5-dione,CAS#909397-54-2
Bexagliflozin(EGT1442)
(Catalog# : 1673102, Cas# :
1118567-05-7
)
EGT1442, a potent and selective SGLT2 inhibitor, attenuates blood glucose and HbA(1c)
BCX-1777
(Catalog# : 16071105, Cas# :
209799-67-7
)
BCX-1777
BYK204165
(Catalog# : 16071031, Cas# :
1104546-89-5
)
BYK204165 is a potent and selective poly(ADP-ribose) polymerase (PARP)-1 inhibitor (p
BMS-3
(Catalog# : 16071026, Cas# :
1338247-30-5
)
BMS-3 is a LIM kinase 1 (LIMK1) inhibitor. LIMK inhibition with 1 M BMS-3 damaged MTO
BAM 7
(Catalog# : 16071006, Cas# :
331244-89-4
)
BAM 7 is a Bax activator (EC50 = 3.3 M). BCL-2 family proteins are key regulators of
BTZ043
(Catalog# : 16071005, Cas# :
957217-65-1
)
BTZ043 racemate is adecaprenylphosphoryl--D-ribose 2'-epimerase (DprE1)inhibitor acti
Bromosporine
(Catalog# : 16070108, Cas# :
1619994-69-2
)
Bromosporine is a broad spectrum inhibitor for bromodomains and as such will be very
BMS-582949
(Catalog# : 16062903, Cas# :
623152-17-0
)
BMS-582949 is a potent and selective P38 mitogen-activated protein kinase (P38 MAPK)
BAY1217389
(Catalog# : 16060801, Cas# :
1554458-53-5
)
BAY1217389 is an orally bioavailable, selective inhibitor of the serine/threonine kin
6-bromo-2,3,4,4a(S),5,9b(R)-hexahydropyrido[4,3-b]indole
(Catalog# : 633001, Cas# :
1059630-07-7
)
6-bromo-2,3,4,4a(S),5,9b(R)-hexahydropyrido[4,3-b]indole;CAS#1059630-07-7 provide cus
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产品分类
信号通路
-- PI3K/Akt/mTOR
----
PI3K
----
Akt
----
GSK-3
----
S6 Kinase
----
AMPK
----
DNA-PK
----
MELK
----
PIKfyve
----
PI4K
----
PTEN
----
mTOR
----
ATM
----
PDK-1
----
ATR
-- Epigenetics
----
PARP
----
JAK
----
Pim
----
PKC
----
PKD
----
Sirtuin
----
Histone Demethylase
----
Histone Acetyltransferase
----
HDAC
----
HIF-PH
----
Aurora Kinase
----
Histone Methyltransferase
----
METTL3
----
Epigenetic Reader Domain
-- 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
-- Angiogenesis
----
VEGFR
----
JAK
----
EGFR
----
PDGFR
----
FLT3
----
FGFR
----
Bcr-Abl
----
Src
----
ALK
----
Syk
----
FAK
----
BTK
----
HIF
-- Apoptosis
----
PD-1
----
PD-L1
----
Bcl-2
----
Caspase
----
TNF-alpha
----
Survivin
----
IAP
----
PERK
----
p53
----
Mdm2
----
E1/E2/E3 Enzyme
-- Autophagy
----
LRRK2
----
CXCR
----
Autophagy
-- JAK/STAT
----
JAK
----
STAT
----
Pim
----
EGFR
-- MAPK
----
MEK
----
Raf
----
p38 MAPK
----
ERK
----
MNK
----
Mixed Lineage Kinase
----
JNK
----
MAP4K
-- Cytoskeletal Signaling
----
Akt
----
Bcr-Abl
----
PKC
----
FAK
----
HSP
----
Kinesin
----
Integrin
----
Dynamin
----
Wnt
----
β-catenin
-- Cell Cycle
----
CDK
----
PD-1
----
PD-L1
----
Chk
----
ROCK
----
PLK
----
APC
----
Wee1
----
DYRK
----
c-Myc
----
Aurora Kinase
----
ROCK inhibitor
-- TGF-beta/Smad
----
Bcr-Abl
----
PKC
----
ROCK
----
TGF-beta/Smad
-- DNA Damage
----
PARP
----
DNA/RNA Synthesis
----
Sirtuin
----
Topoisomerase
----
DNA-PK
----
Telomerase
----
RAD51
----
HDAC
----
ATM
----
DNA alkylator
----
Mps1
-- Stem Cells & Wnt
----
GSK-3
----
JAK
----
STAT
----
ROCK
----
TGF-beta/Smad
----
Wnt
----
γ-secretase
----
β-catenin
----
smo
-- Ubiquitin
----
Proteasome
----
p97
----
Deubiquitinase
-- 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
----
α-Synuclein
----
Tau Protein
----
Cannabinoid Receptor
----
Transthyretin (TTR)
-- NF-κB
----
NF-κB
----
HDAC
----
IKK
-- 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
----
Sigma Receptor
----
Ras
----
mAChR
----
Cholecystokinin Receptor
----
Melanocortin Receptor
----
RXFP Receptor
-- 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
----
MAGL
----
Epoxide Hydrolase
----
LXR
----
Myeloperoxidase (MPO)
----
RAR/RXR
----
Acyltransferase
----
UGT
----
MMP
----
ATP Citrate Lyase
-- Anti-infection
----
CMV
----
Filovirus
----
HBV
----
HCV
----
HIV
----
HSV
----
Influenza Virus
----
RSV
----
SARS-CoV
----
Antibacterial
----
Antifungal
----
Parasite
-- Proteases
----
Proteasome
----
Caspase
----
HIV Protease
----
MMP
----
γ-secretase
----
DPP4
----
Mitochondrial Metabolism
----
Isocitrate Dehydrogenase (IDH)
----
FPTase
----
Acetyl-CoA Carboxylase
----
Glutaminase
-- 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
-- Vitamin D Related
----
VD/VDR
-- 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
-- others
----
PKK
----
Others modulator
----
Estrogen Receptor/ERR
----
ChoKα
-- PROTAC
----
Molecular Glues
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
STX-478
(Catalog# : 20633, Cas# :
2883540-92-7
)
STX-478 是第二代突变体选择性口服 PI3Ka 小分子变构抑制剂。
Iclepertin (BI-425809)
(Catalog# : 24084, Cas# :
1421936-85-7
)
Iclepertin(BI-425809)是一种口服的GlyT-1小分子抑制剂,用于治疗与
Bomedemstat
(Catalog# : 24001, Cas# :
1990504-34-1
)
Bomedemstat 是一种口服的、不可逆的赖氨酸特异性去甲基酶 1 (LSD1)
PLX-4545
(Catalog# : 24111, Cas# :
2892065-45-9
)
PLX-4545 是一种口服生物可利用的 IKZF2 分子胶降解剂,旨在破坏高
VVD-130037 ( BAY-3605349 )
(Catalog# : 24110, Cas# :
3034880-93-5
)
VVD-130037 (BAY-3605349) 是一种口服小分子 KEAP1 (INrf2) 激活剂。
CBR-5884
(Catalog# : 24109, Cas# :
681159-27-3
)
CBR 5884 是一种磷酸甘油酸脱氢酶 (PHGDH) 抑制剂,能够抑制过度表达
JHU-083
(Catalog# : 24108, Cas# :
1998725-11-3
)
JHU-083 选择性阻断大脑 CD11b+ 细胞中的谷氨酰胺酶活性,并防止慢
LXH-3-71
(Catalog# : 24107, Cas# :
2251753-65-6
)
LXH-3-71是一种新型“分子胶”,可诱导PHGDH和DDB1-CUL4泛素连接酶之
CC-92480 ( Mezigdomide )
(Catalog# : 20510, Cas# :
2259648-80-9
)
CC-92480 是一种有效的新型 CELMoD 化合物,旨在快速最大程度地降解
Adrixetinib ( Q-702 )
(Catalog# : 20617, Cas# :
2394874-66-7
)
Adrixetinib is a tyrosine kinase inhibitor with potential use as an antineoplastic ag