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+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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Aldehydes
Amines
Amino Acids
Anilines
Boronic Acids
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Cas号索引 1
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Cas号索引 1
1201935-85-4 | 3-甲氧基-1-甲基-4-硝基-1H-吡唑
(Catalog# : 523192)
Sun-shine Chemical provides 3-methoxy-1-methyl-4-nitro-1H-pyrazole(CAS 1201935-85-4)
1260075-17-9 | Mitapivat
(Catalog# : 192191)
Mitapivat,又称PKM2激活剂1020,是一种治疗丙酮酸激酶缺乏症的PKM2激
1219737-12-8 | MK-3903
(Catalog# : 192183)
MK-3903是一种有效的选择性AMPK激活剂(EC50 = 8 nM)。
1049704-18-8 | MA242 TFA
(Catalog# : 191256)
MA242是MDM2和NFAT1在胰腺癌治疗中的双重抑制剂。无论p53状态如何,
1799631-75-6 | MIK665
(Catalog# : 191252)
MIK665,又称s64315,诱导骨髓白血病细胞分化蛋白(mcl1;Bcl2-L-3),具有
183721-13-3 | MRS1177
(Catalog# : 1812296)
MRS1177是一种生物活性化学物。
1642288-47-8 | Mavacamten
(Catalog# : 181255)
Mavacamten,又称SAR-439152和MYK-461,是一种潜在的治疗肥厚性心肌病的
147116-67-4 | 马罗皮坦
(Catalog# : 1811261)
马罗皮坦,又称CJ11972,是一种神经激肽(NK1)受体拮抗剂。
183721-15-5 | MRS1220
(Catalog# : 1810228)
MRS1220是人A3腺苷受体的一种有效且高度选择性的拮抗剂。
1445251-22-8 | ME0328
(Catalog# : 1810174)
ME0328是一种PARP-3的抑制剂(IC50 = 0.89 μM)。
1908414-82-3 | MDK-4823
(Catalog# : 18962)
MDK-4823,又称LMPTP抑制剂1;是低分子量酪氨酸磷酸酶(LMPTP)的有效抑
1644342-14-2 | ML-792
(Catalog# : 18941)
ML-792是一种有效的选择性SAE抑制剂,在细胞检测中具有纳米极的效
1883510-31-3 | ML327
(Catalog# : 187162)
ML327是MYC的阻滞剂。ML327介导了E-cadherin的转录去抑制和对上皮-间充
1421373-62-7 | MDK3627
(Catalog# : 187161)
MDK3627,也被称为突变EGFR抑制剂,是一种选择性和强效突变的EGFR抑
1303607-07-9 | MI-773
(Catalog# : 185251)
MI-773是一种新型的口服MDM2拮抗剂。
1417997-93-3 | MDK-7933
(Catalog# : 184161)
MDK-7933,也称为HDAC8-IN-1,是一种HDAC8 抑制剂,在癌症细胞器的IC50
1448189-80-7 | MDK7526盐酸盐
(Catalog# : 184104)
MDK7526, 也称为VHL Ligand 1,Protein degrader 1是一种有效的、选择性的蛋
1190379-70-4 | MRT68921
(Catalog# : 184103)
MRT68921是ULK1和ULK2的抑制剂(IC50 分别为= 2.9和1.1 nM)。
1870916-87-2 | Mc-Val-Ala-PAB
(Catalog# : 184219)
Mc-Val-Ala-PAB 是一种用于靶向药物传递的药物-药物结合剂(ADC)的有用
111797-22-9 | MDK7229
(Catalog# : 184211)
MDK7229, also known as MD2-IN-1 is a MD2 (Myeloid differentiation protein 2) inhibito
1215310-75-0 | 4-methylsulfonyl-2-(trifluoromethyl)benzaldehyde
(Catalog# : 1712293)
4-methylsulfonyl-2-(trifluoromethyl)benzaldehyde isa building blocks.
1187990-87-9 | MK-8617
(Catalog# : 1710163)
MK-8617是一种缺氧诱导因子(HIF脯氨酰羟化酶1−3 PHD1−3),具有强效
1883423-59-3 | MSC2530818
(Catalog# : 1710135)
MSC2530818是一种强效、选择性,口服生物利用度与抑制剂的IC50 = 2.
132819-92-2 | MDK19922
(Catalog# : 1791512)
MDK19922,也称为NOD-IN-1或化合物4,是一种有效的核苷酸结合寡聚化
137975-06-5 | 游离莫扎伐普坦
(Catalog# : 179154)
莫扎伐普坦,又名OPC 31260,是由大冢销售的血管加压素受体拮抗剂
1016535-83-3 | MDK35833
(Catalog# : 179114)
MDK35833又称为Oct3/4-inducer-1,是一种有效率的Oct3/4诱导者。MDK35833可
1991986-30-1 | ML364
(Catalog# : 179833)
ML364是具有潜在抗癌活性的小分子抑制剂的去泛素化酶USP2。
1422269-30-4 | ML-18
(Catalog# : 179810)
ML-18是蛙皮素受体亚型3(BRS-3)拮抗剂(IC50 = 4.8μm)。ML-18抑制肺
1207253-08-4 | MK-1064
(Catalog# : 16123054)
MK-1064是一种有效的、选择性和口服的Orexin OX2受体拮抗剂,用于治
1857417-13-0 | MI-503
(Catalog# : 178908)
MI-503是一种具有IC50为14.7 nM的有效和选择性的menin - mll抑制剂。在
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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
--
Antibody-drug Conjugate/ADC Related
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
2375779-31-8 | GP130 modulator-1
(Catalog# : 25062)
GP130 modulator-1 (compound A33) 是一种GP130信号通路调节剂。GP130 modulato
877459-36-4 | TGN 073
(Catalog# : 25061)
TGN 073 is a facilitator of aquaporin-4 (AQP4), an astroglial water channel. The rats
2257492-95-6 | OPN expression inhibitor 1
(Catalog# : 25060)
OPN expression inhibitor 1 (Compound 11) is an osteopontin (OPN) expression inhibitor
3036109-10-8 | SDU-071
(Catalog# : 25059)
SDU-071 is a potent and orally active inhibitor of BRD4-p53 inhibitor. SDU-071 suppre
2644662-83-7 | BBC0403
(Catalog# : 25058)
BBC0403 is a selective BRD2 inhibitor. BBC0403 inhibits the progression of osteoarthr
694488-83-0 | MFI8
(Catalog# : 25057)
MFI8 is a Mitochondrial Fusion Inhibitor
146255-66-5 | DHPG
(Catalog# : 25056)
DHPG, also known as (RS)-3,5-DHPG, is a selective agonist for group I metabotropic gl
2413020-56-9 | BAY-593 free base
(Catalog# : 25055)
BAY-593 is an orally active inhibitor of geranylgeranyltransferase-I (GGTase-I) that
188425-85-6 | Boscalid
(Catalog# : 25054)
Boscalid is a broad spectrum fungicide used in agriculture to protect crops from fung
690681-65-3 | SABA1
(Catalog# : 25053)
SABA1 is an antibacterial agent against Pseudomonas aeruginosa and Escherichia coli.