武汉永璨生物科技有限公司
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抑制剂/受体激动剂
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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
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Microbiology
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Amino Acids
Anilines
Boronic Acids
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Carboxes
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Deuterated
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Pyrimidines
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产品名字索引 G
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产品名字索引 G
GLO1 inhibitor-Compound 60
(Catalog# : 26A012, Cas# :
2314467-61-1
)
GLO1抑制剂-化合物60是一种新型强效的甘油醛-3-磷酸脱氢酶1(GLO1)
Gridegalutamide ( 别名: BMS-986365 )
(Catalog# : 25138, Cas# :
2446928-30-7
)
Gridegalutamide,也称为 BMS-986365 和 CC-94676,是一种口服生物可利用的
Givinostat HCl hydrate
(Catalog# : 25118, Cas# :
732302-99-7
)
Givinostat hydrochloride is a novel histone deacetylase inhibitor with potential anti
Glecirasib
(Catalog# : 25105, Cas# :
2658538-04-4
)
GSK-2330672
(Catalog# : 25082, Cas# :
1345982-69-5
)
GSK-2330672, also known as linerixibat, is highly potent, nonabsorbable apical sodium
GP130 modulator-1
(Catalog# : 25062, Cas# :
2375779-31-8
)
GP130 modulator-1 (compound A33) 是一种GP130信号通路调节剂。GP130 modulato
GSK1059865
(Catalog# : 24131, Cas# :
1191044-58-2
)
GSK1059865 is a potent orexin 1 receptor antagonist.
G-5758
(Catalog# : 24076, Cas# :
2413455-99-7
)
GW-280264 ( GW-280264X )
(Catalog# : 24031, Cas# :
866924-39-2
)
GW-280264 ( GW-280264X ) 是混合 ADAM10/TACE (ADAM17) 金属蛋白酶抑制剂。
Golidocitinib ( AZD-4205 )
(Catalog# : 24028, Cas# :
2091134-68-6
)
Golidocitinib (AZD-4205) 是一种口服 JAK1 选择性激酶抑制剂。
Glecirasib
(Catalog# : 20672, Cas# :
2657613-87-9
)
Ganaxolone
(Catalog# : 20630, Cas# :
38398-32-2
)
Ganaxolone, also known as CCD 1042 and C1042, is a CNS-selective GABAA modulator that
GNE-7883
(Catalog# : 20589, Cas# :
2648450-42-2
)
GNE-7883 is a pan-TEAD inhibitor.
苯丁酸甘油酯
(Catalog# : 230401, Cas# :
611168-24-2
)
Glycerol phenylbutyrate 是 sigma-2 (σ2) 受体的一个配体,其 pKi 值
GSK 525762A
(Catalog# : 171459, Cas# :
1260907-17-2
)
GSK5182
(Catalog# : 20375, Cas# :
877387-37-6 (free base)
)
GSK5182 is a specific inverse agonist for estrogen-related receptor γ.
GF-109203X
(Catalog# : L20356, Cas# :
133052-90-1
)
GF-109203X is a potent and highly selective PCK inhibitor, which inhibits PKC isozyme
GDC-046
(Catalog# : L20342, Cas# :
1258292-64-6
)
GDC-046 is a potent, selective, and orally bioavailable TYK2 inhibitor for TYK2, JAK1
GDC-0214
(Catalog# : c20341, Cas# :
1831144-46-7
)
iJak-381 is a highly potent, selective, and inhalable Janus kinase-1 (JAK-1) inhibito
GYY4137
(Catalog# : L20339, Cas# :
106740-09-4
)
GYY4137 is a novel water-soluble and slow releasing H2S donor. Hydrogen sulfide (H2S)
GDC-0077
(Catalog# : L20335, Cas# :
2060571-02-8
)
Inavolisib, also known as GDC-0077, is a potent and selective PI3K inhibitor. GDC-007
Gloxazone
(Catalog# : 20304, Cas# :
2507-91-7
)
Gloxazone is an effective but toxic anaplasmacide.
Glymidine sodium
(Catalog# : 20295, Cas# :
3459-20-9
)
Glymidine sodium is a sulfonamide hypoglycemic agent which stimulates insulin secreti
Golgicide A
(Catalog# : 20292, Cas# :
1139889-93-2
)
Golgicide A is a Potent, selective and reversible inhibitor of GBF1 ArfGEF. Golgicide
GDC-0077
(Catalog# : 20283)
GDC-0077 is a potent and selective PI3K inhibitor. GDC-0077 blocks an enzyme involved
GS 0573 ( PMEDAP )
(Catalog# : 20275, Cas# :
113852-41-8
)
GS 0573 is an antiviral compound that has been studied for potential treatment of Fel
Giredestrant tartrate
(Catalog# : 20263, Cas# :
2407529-33-1
)
Giredestrant tartrate (GDC-9545 tartrate), a non-steroidal ER ligand, is an orally ac
Giredestrant
(Catalog# : 21248, Cas# :
1953133-47-5
)
Giredestrant, also known as GDC-9545 and RG6171, is a SERD. GDC-9545 is an orally ava
GNF-PF-3777
(Catalog# : 21226, Cas# :
77603-42-0
)
GNF-PF-3777 is a derivative of tryptanthrin.
GSK484 HCl
(Catalog# : 20111801, Cas# :
1652591-81-5
)
GSK484 is a potent PAD-4 inhibitor (Protein-arginine deiminase type-4). GSK484 potent
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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
----
Methionine Adenosyltransferase (MAT)
-- 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
----
Reactive-Oxygen-Species-ROS
-- 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)
----
Lactate dehydrogenase
----
Glyoxalase (GLO)
----
E1/E2/E3 Enzyme
----
PANK(pantothenate kinase)
-- 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
----
Lipase
-- PI3K/Akt/mTOR
----
PI3K
----
Akt
----
GSK-3
----
S6 Kinase
----
AMPK
----
DNA-PK
----
MELK
----
PIKfyve
----
PI4K
----
PTEN
----
mTOR
----
ATM
----
PDK-1
----
ATR
----
Vps34
-- Stem Cells & Wnt
----
GSK-3
----
JAK
----
STAT
----
ROCK
----
TGF-beta/Smad
----
Wnt
----
γ-secretase
----
β-catenin
----
smo
----
Notch
-- 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
Mitoquinol mesylate (MitoQ)
(Catalog# : 26A042, Cas# :
845959-55-9
)
Mitoquinol mesylate (MitoQ) 是一种线粒体靶向抗氧化剂,具体而言,它
SPG-601 ( VSN-16R )
(Catalog# : 24042, Cas# :
1246960-09-7
)
SPG-601(原名VSN-16R)是一种口服给药、同类首创的小分子药物,是
LY3039478 ( Crenigacestat )
(Catalog# : 17021601, Cas# :
1421438-81-4
)
LY3039478 ( Crenigacestat ) 是一种选择性 NOTCH1 抑制剂,通过阻断 VEGFA/
PF-9366
(Catalog# : 184107, Cas# :
72882-78-1
)
PF-9366是一种新型的人蛋氨酸腺苷转移酶2A (Mat2A),肝外同种型。
MAT2A-IN-22
(Catalog# : 26A021, Cas# :
2925330-18-1
)
MAT2A-IN-22 (Compound 29-1) 是一种可透过血脑屏障的和口服有效的 MAT2A
Pantothenate kinase-IN-3
(Catalog# : 26A041)
泛酸激酶-IN-3(亦称化合物21,https://doi.org/10.1021/acs.jmedchem.5c03452)
Claziprotamidum ( Claziprotamide ; BBP-671 )
(Catalog# : 26A040, Cas# :
2361124-03-8
)
Claziprotamidum(Claziprotamide;BBP-671)是一种强效、口服有效且能透过
PZ-3022
(Catalog# : 26A039, Cas# :
2170608-85-0
)
PZ-3022是一种别构型的PanK激活剂,能够抵消C3-CoA的抑制作用。
PZ-2891
(Catalog# : 193282, Cas# :
2170608-82-7
)
PZ-2891是一种强效的、选择性的、口服活性泛酸激酶(PANK)调制剂,
Pantothenate kinase-IN-2
(Catalog# : 26A038, Cas# :
902614-04-4
)
Pantothenate kinase-IN-2是一种泛酸激酶抑制剂,对PanK2的IC50值为92 nM,