武汉永璨生物科技有限公司
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Bromides
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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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产品名字索引 A
Asapiprant
(Catalog# : 2051515, Cas# :
932372-01-5
)
Asapiprant 是一个强效且有选择性的 DP1 受体拮抗剂,其 Ki 值为 0.44
AKOS B018304
(Catalog# : 2051513, Cas# :
6308-22-1
)
AKOS B018304 is a potent inhibitor of chikungunya virus with low micro molar activity.
AC-90179 HCl
(Catalog# : 23178, Cas# :
359878-19-6
)
AC-90179 is a high selective 5-hydroxytryptamine2A receptor inverse agonist. It is an
6-氨基异喹啉
(Catalog# : S-203043, Cas# :
23687-26-5
)
A134974
(Catalog# : 204605, Cas# :
186141-75-3
)
A134974 is a bioactive chemical.
A-1293201
(Catalog# : 204604, Cas# :
1375557-33-7
)
A-1293201 is a potent and selective NAMPT inhibitor.
A-119637
(Catalog# : 204603, Cas# :
255713-47-4
)
A-119637 is a novel, selective and potent alpha1D antagonist.
A-1048400
(Catalog# : 204602, Cas# :
1219624-62-0
)
A-1048400 is a potent and selective N-type and T-type calcium channel blocker.
A-1062
(Catalog# : 204601, Cas# :
1821-13-2
)
A-1062 is a resolvase-binding inhibitor. A1062 inhibits resolvase binding to the res
AMG-510
(Catalog# : 112193, Cas# :
2296729-00-3
)
AMG-510 is a potent KRAS G12C covalent inhibitor. AMG-510 selectively targets the KRA
AMG-510 racemate
(Catalog# : 112194, Cas# :
2252403-56-6
)
AMG-510 is a potent KRAS G12C covalent inhibitor. AMG-510 selectively targets the KRA
Aprocitentan
(Catalog# : 112191, Cas# :
1103522-45-7
)
Aprocitentan is an orally active, dual endothelin (ET) receptor antagonist developed
Aramchol
(Catalog# : 6111903, Cas# :
246529-22-6
)
From:https://galmedpharma.com/about-aramchol/Aramchol(arachidyl amido cholanoic aci
阿拉酸式苯
(Catalog# : 513191, Cas# :
35272-27-6
)
benzo[d][1,2,3]thiadiazole-7-carboxylic acid,Acibenzolar acid,CGA 210 007
AR-C155858
(Catalog# : 193291, Cas# :
496791-37-8
)
AR-C155858是一种强效的单羧酸转运蛋白MCT1和MCT2的抑制剂,它与细胞
ACT-709478
(Catalog# : 193288, Cas# :
1838651-58-3
)
ACT-709478是一种强效、选择性的T型钙通道阻滞剂,是治疗全身性癫
A1874
(Catalog# : 193287, Cas# :
2064292-12-0
)
A1874是一种以核桃仁为基础的,BRD4降解的丙交酯,诱导BRD4在细胞
AZD9567
(Catalog# : 193254, Cas# :
1893415-00-3
)
AZD9567是一种口服分化非甾体选择性糖皮质激素受体调节剂(SGRM)。
AZ1495
(Catalog# : 193222, Cas# :
2196204-23-4
)
AZ1495是一种有效且具有选择性的IRAK4抑制剂。
ATR-101盐酸盐
(Catalog# : 193208, Cas# :
133825-81-7
)
ATR-101,也被称为PD-132301 (游离)或PD-132301-2 (盐酸盐),正在临床开发
ARN-3236
(Catalog# : 193192, Cas# :
1613710-01-2
)
ARN-3236是一种强效、口服活性和选择性的SIK2抑制剂。在攻击- 3236抑
ARN 077
(Catalog# : 193134, Cas# :
1373625-34-3
)
ARN 077是一种强效选择性N -乙酰乙醇胺酸酰胺酶(NAAA)抑制剂,IC50为
阿格列扎
(Catalog# : 193125, Cas# :
475479-34-6
)
阿格列扎, 也称为RG-1439或RO-0728804,是一个过氧物酶体增生激活受
Alvimopan
(Catalog# : 19382, Cas# :
156053-89-3
)
Alvimopan,也称为HSDB-7704和LY246736, 是一种作为一个次要地行动的μ-
Abrocitinib
(Catalog# : 19381, Cas# :
1622902-68-4
)
Abrocitinib(PF-04965842)是Pifzer研发的是一种Janus激酶抑制剂药物,目
AA26-9
(Catalog# : 19372, Cas# :
1312782-34-5
)
AA26-9是一种高效广谱丝氨酸水解酶抑制剂。AA26 -9抑制酶来源于丝
AZD-0284
(Catalog# : 19365, Cas# :
2101291-07-8
)
AZD-0284是一种强有力的、有选择性的反兴奋剂,可以潜在治疗核受
AZ304
(Catalog# : 19363, Cas# :
942507-42-8
)
AZ304是一种ATP-竞争性双BRAF激酶抑制剂,对野生型BRAF、V600E突变型
AZ876
(Catalog# : 19356, Cas# :
898800-26-5
)
AZ876,又称AZ-876,是一种肝脏X受体激动剂。AZ876可预防病理性心肌
AGN-190299
(Catalog# : 19316, Cas# :
118292-41-4
)
Tazarotene是一种视黄醇类前体药物,通过在动物和人体内的快速脱
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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
----
Bradykinin 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
----
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
-- 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
Dencatistat (STP938)
(Catalog# : 25177, Cas# :
2377000-84-3
)
Dencatistat 是一种口服生物可利用的小分子胞苷三磷酸合酶 1 (CTPS1)
DS-1001b
(Catalog# : 25178, Cas# :
1898207-64-1
)
DS-1001 是一种口服的脑渗透性突变 IDH1 选择性抑制剂。
Z57346765
(Catalog# : 25191, Cas# :
1016340-64-9
)
Z57346765 是一种 PGK1 特异性抑制剂,可降低 PGK1 糖酵解中代谢酶的
CBR-470-1
(Catalog# : 25192, Cas# :
2416095-06-0
)
CBR-470-1 是诱导 Nrf2 活性的糖酵解酶 PGK1 的抑制剂。
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(
HC-7366
(Catalog# : 25076, Cas# :
2803470-63-3
)
HC-7366 is a potent and selective activator of the general control nonderepressible 2
Flavopiridol ( 夫拉平度 )
(Catalog# : 237071, Cas# :
146426-40-6
)
Alvocidib is a synthetic dihydroxyflavone that is 5,7-dihydroxyflavone which is subst
AG-270
(Catalog# : 25176, Cas# :
2201056-66-6
)
MAT2A 抑制剂 AG-270 是一种口服的蛋氨酸腺苷转移酶 II α (MAT2A) 小分
AZD-5904
(Catalog# : 181121, Cas# :
618913-30-7
)
AZD5904是一个有效的口服生物利用率MPO抑制剂。在临床前研究中,AZ
ALT-007
(Catalog# : 25157, Cas# :
2035010-37-6
)
ALT-007 是一种口服生物可利用的 SPT 抑制剂,比多球菌素更有效,