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抑制剂/受体激动剂
Angiogenesis
Anti-infection
Apoptosis
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Metabolism
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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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Chiral Compounds
Deuterated
Fluorides
Imidazoles
Indoles and Oxindoles
Iodos
Nitro Compounds
Oxazoles
Peg Linkers
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Piperidines
Pyridines
Pyrimidines
Quinolines
Sulfonamides
Thiazoles
Trifluoroborates
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产品名字索引 B
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产品名字索引 B
Butylphthalide
(Catalog# : 16122908, Cas# :
6066-49-5
)
Butylphthalide, also known as 3-n-butylphthalide or NBP, is an antioxidant and one of
Buthionine Sulphoximine
(Catalog# : 16122907, Cas# :
5072-26-4
)
Buthionine Sulphoximine, also known as NSC-326231, is a gamma-glutamylcysteine synthe
布瓦西坦
(Catalog# : 16122906, Cas# :
357336-20-0
)
Brivaracetam, also known as UCB 34714, is a chemical analog of levetiracetam, is a ra
Brigatinib (AP-26113)
(Catalog# : 16122905, Cas# :
1197953-54-0
)
Brigatinib, also known as AP-26113, is an orally active, potent and selective Dual AL
Brevianamide F
(Catalog# : 16122904, Cas# :
38136-70-8
)
Brevianamide F , also known as cyclo-(L-Trp-L-Pro), belongs to a class of naturally o
Bohemine
(Catalog# : 16122903, Cas# :
189232-42-6
)
Bohemine is a potent and selective, cell-permeable, cyclin-dependent kinase (CDK) inh
BMS-687453
(Catalog# : 16122902, Cas# :
1000998-59-3
)
BMS-687453 is a potent and selective peroxisome proliferator activated receptor (PPAR
BML-210
(Catalog# : 16122901, Cas# :
537034-17-6
)
BML-210, also known as CAY10433, is HDAC inhibitor. BML-210 induces growth inhibition
BIIB021
(Catalog# : 16122868, Cas# :
848695-25-0
)
BIIB021, also known as CNF2024, is an orally active, purine-scaffold, small-molecule
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)
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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-