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Indoles and Oxindoles
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联系我们
+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
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Amines
Amino Acids
Anilines
Boronic Acids
Bromides
Carboxes
Catalysts
Chiral Compounds
Deuterated
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Iodos
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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
BAY41-4109消旋体
(Catalog# : 1791117, Cas# :
298708-79-9
)
Bay41-4109消旋体是对Bay41-4109和S-异构体Bay41-4109 R-异构体的混合物。
BAR-501
(Catalog# : 179821, Cas# :
1632118-69-4
)
BAR-501是一种选择性GPBAR1激动剂,没有任何的FXR激动剂活性。BAR-50
Batefenterol(free base)
(Catalog# : 179820, Cas# :
743461-65-6
)
Batefenterol,也称为 GSK961081和TD-5959,是一种毒蕈碱拮抗剂和β2-受体
BI-847325
(Catalog# : 83101, Cas# :
1207293-36-4
)
BI-847325是一种口服、具有选择性的日常生物MEK/Aurora激酶抑制剂,
BAY-598
(Catalog# : 17982, Cas# :
1906919-67-2
)
BAY-598是一种强效的针对SMYD2中肽-竞争的化学探测器。BAY-598拥有一
BAY-598 R-异构体
(Catalog# : 17981, Cas# :
1906920-28-2
)
BAY-598 R-异构体是BAY589 R-异构体。bay-598 R-异构体可以作为一个参照
布索芬新
(Catalog# : 17916, Cas# :
171655-91-7
)
布索芬新是一种充分的单胺再摄取阻滞剂,已被开发用于治疗帕金
B02
(Catalog# : 1783013, Cas# :
1290541-46-6
)
B02,也叫RAD51 - in - 02,是一种RAD51抑制剂。B02能增强MM细胞的DOX敏
BLU-285
(Catalog# : 1781003, Cas# :
1703793-34-3
)
BLU-285是一种有效、具有选择性的抑制剂。
BAY-1895344
(Catalog# : 1781002, Cas# :
1876467-74-1
)
BAY-1895344是一种有效的、具有选择性的ATM抑制剂。
BIBR1532
(Catalog# : 178813, Cas# :
321674-73-1
)
BIBR1132对端粒酶的抑制具有很强的选择性,导致肿瘤细胞延迟生长
BMS-932481
(Catalog# : 2017877, Cas# :
1263871-36-8
)
BMS-932481调节Aβ肽在血浆和脑脊液的健康志愿者。
B-1613
(Catalog# : 20178216, Cas# :
214066-78-1
)
(2S,4S)-4-(氨基甲基)吡咯烷-1,2-二羧酸 1-叔丁酯 2-甲酯;(2S,4S)-1-tert
Balamapimod
(Catalog# : 2017822, Cas# :
863029-99-6
)
<span style="color:#34495E;font-family:" font-Balamapimod, 也称为MKI-822,是一种
BP-1-102
(Catalog# : 17030606, Cas# :
1334493-07-0
)
BP-1-102是一种有效的口服生物和选择性抑制剂。
BAY-876
(Catalog# : 17030604, Cas# :
1799753-84-6
)
BAY-876是一种有效的、选择性的谷氨酸抑制剂。BAY- 876在体外具有良
BRD-7552
(Catalog# : 17030312, Cas# :
1137359-47-7
)
BRD-7552是一种PDX1转录诱导因子。它主要在人类胰岛和导管细胞中调
BDA-366
(Catalog# : 17030305, Cas# :
1821496-27-8
)
BDA - 366是BCL - BH4拮抗剂。BDA - 366抑制人骨髓瘤的生长。BDA - 366诱导
Bimiralisib
(Catalog# : 17030116, Cas# :
1225037-39-7
)
Bimiralisib,也被称为PQR309,是一种口服生物可用的磷脂- 3 -激酶抑
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
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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