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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Apoptosis
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GPCR & G Protein
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JAK/STAT
MAPK
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Metabolism
Neuronal Signaling
NF-κB
Protein Tyrosine Kinase
Proteases
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Microbiology
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分子砌块
Aldehydes
Amines
Amino Acids
Anilines
Boronic Acids
Bromides
Carboxes
Catalysts
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Deuterated
Fluorides
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Indoles and Oxindoles
Iodos
Nitro Compounds
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Peg Linkers
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Pyridines
Pyrimidines
Quinolines
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Thiazoles
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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
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
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定制合成
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订购信息
联系我们
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产品名字索引 B
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产品名字索引 B
BEC HCl
(Catalog# : 17030110, Cas# :
222638-67-7
)
BEC,也称为S -(2-boronoethyl)-L-cysteine,是一个慢结合和竞争力的精氨酸
BGP-15
(Catalog# : 17109003, Cas# :
66611-37-8
)
BGP-15, 是一种带有PARP抑制活性的烟碱类胺肟衍生物。已经证明BGP-
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.
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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
AD-8007
(Catalog# : 26A018, Cas# :
1497439-74-3
)
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)
ZY-444
(Catalog# : 26A020, Cas# :
1802650-31-2
)
ZY-444是一种通过抑制PC活性发挥抗癌作用的药物。
AD-5584
(Catalog# : 26A019, Cas# :
2306525-79-9
)
AD-5584是一种新型脑渗透性ACSS2抑制剂。
IDB-003
(Catalog# : 26A017, Cas# :
3079716-11-0
)
IDB-003在体内抑制MDA-MB-231肿瘤生长。
Vafidemstat
(Catalog# : 18891, Cas# :
1357362-02-7
)
Vafidemstat又称ORY 2001,是一种赖氨酸特异性组蛋白去甲基化酶(LSD1)
LLL12
(Catalog# : 25075, Cas# :
1260247-42-4
)
LLL12是一种强效的STAT3抑制剂。LLL12在小鼠异种移植物模型中显示出
ECC-5004
(Catalog# : 26A015, Cas# :
2758659-09-3
)
ECC5004是一款每日一次、低剂量、小分子GLP-1受体激动剂。
SILA-123
(Catalog# : 26A014, Cas# :
2911585-37-8
)
SILA-123是一种II型FLT3抑制剂,对FLT3-WT(IC50=2.1 nM)和FLT3-ITD(IC50=1
Encaleret sulfate
(Catalog# : 26A013, Cas# :
1214922-52-7
)
Encaleret是一种正在研究的钙敏感受体的小分子拮抗剂,用于钙稳态
Iadademstat ( ORY-1001 ) hydrochloride
(Catalog# : 26A011, Cas# :
1431303-72-8
)
Iadademstat(ORY-1001)是一种口服活性、高效和选择性的表观遗传酶