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+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
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GPCR & G Protein
Immunology & Inflammation
JAK/STAT
MAPK
Membrane Transporter/Ion Channel
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NF-κB
Protein Tyrosine Kinase
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Cas号索引 1
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Cas号索引 1
1933460-19-5 | Mitiperstat
(Catalog# : 20457)
Mitiperstat is a myeloperoxidase inhibitor.
129047-38-7 | 4-(4-甲氧苯甲基)-3-甲氧基苯甲醛
(Catalog# : 20398)
1032570-74-3 | 7-methoxy-8-[3-(4-morpholinyl)propoxy]-Imidazo[1,2-c]quinazolin-5-amine
(Catalog# : 20394)
1922153-17-0 | MELK-8a
(Catalog# : L20331)
MELK-8a Dihydrochloride is a novel inhibitor of maternal embryonic leucine zipper kin
1567915-38-1 | MTI-31
(Catalog# : L20329)
MTI-31 is a bioactive chemical.
1338934-59-0 | MKC-8866
(Catalog# : 20325)
MKC-8866, also known as IRE1-IN-8866, is an inhibitor of IRE1 RNase activity. MKC8866
1700637-55-3 | MDK-7553
(Catalog# : 20320)
MDK-7553, also known as CD38 inhibitor 78c and Compound-78c, is a potent CD38 inhibit
1354707-41-7 | Mitochonic Acid 5
(Catalog# : 204122)
Mitochonic Acid 5 is a derivative of the plant hormone indole-3-acetic acid. It has b
1394371-71-1 | MK-8722
(Catalog# : 20293)
MK-8722 is a potent pan-AMPK activator. MK-8722 improves glucose homeostasis but indu
1375066-73-1 | 3-甲基-1,2,4-噻二唑-2(3H)-碳酰肼
(Catalog# : 21256)
1847461-43-1 | Mobocertinib free base
(Catalog# : 20111803)
Mobocertinib, also known as TAK-788 and AP32788, is an investigational TKI with poten
1627138-52-6 | ML380
(Catalog# : 20103003)
ML380 is a highly potent and the first CNS penetrant M5 positive allosteric modulator
14920-87-7 | METHYL 2,6-DICHLOROBENZOATE
(Catalog# : 2071634)
115458-99-6 | Methyl (R)-2-(Benzyloxy)propionate
(Catalog# : 262325)
1312941-07-3 | 3-methoxy-4-(2-morpholinoethoxy)benzoic acid hydrochloride
(Catalog# : 2062018)
1417700-13-0 | ML188
(Catalog# : 2051506)
ML188 is a Potent Noncovalent Small Molecule Inhibitor of the Severe Acute Respirator
1401242-74-7 | ML277
(Catalog# : 2051504)
ML277 is a potent activator of KCNQ1 (Kv7.1) channels with >100-fold selectivity v
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
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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
-- 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
-- NF-κB
----
NF-κB
----
HDAC
----
IKK
-- 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
-- Proteases
----
Proteasome
----
Caspase
----
HIV Protease
----
MMP
----
γ-secretase
----
DPP4
----
Isocitrate Dehydrogenase (IDH)
----
FPTase
----
Acetyl-CoA Carboxylase
----
Glutaminase
----
Methionine Adenosyltransferase (MAT)
-- 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
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分子砌块
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Aldehydes
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--
Amino Acids
--
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Boronic Acids
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--
Chiral Compounds
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Deuterated
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On Sale
新产品
天然化合物
最新产品
2750001-23-9 | AZD0095
(Catalog# : 237072)
AZD0095 is a Selective Inhibitor of Monocarboxylate Transporter 4 (MCT4) for Oncology.
2101538-28-5 | 2-MNG
(Catalog# : 24129)
2-巯基烟酰甘氨酸是一种新型强效黑素生成抑制剂,具有独特的作
2439277-80-0 | MAT2A-IN-9
(Catalog# : 25147)
MAT2A-IN-9(化合物167)是一种2-氧代喹唑啉衍生物,是一种强效的M
1898206-17-1 | Safusidenib
(Catalog# : 25149)
Safusidenib,也称为DS-1001,是一种口服异柠檬酸脱氢酶[NADP]细胞质(
2669009-92-9 | Atebimetinib
(Catalog# : 25148)
阿替美替尼(IMM-1-104)是一种口服的小分子MEK1和MEK2激酶变构抑制
2242751-53-5 | Acoramidis hydrochloride
(Catalog# : 24068)
Acoramidis是一种口服、强效、高选择性小分子转甲状腺素蛋白(TTR
2230263-60-0 | Crelosidenib
(Catalog# : 24101)
Crelosidenib ( [LY3410738)是一种有效的选择性的具有口服活性的突变
2833703-74-3 | LOXO-435
(Catalog# : 25080)
LOXO-435是FGFR3的选择性小分子抑制剂。它对野生型和致癌激活的FGF
2446928-30-7 | Gridegalutamide
(Catalog# : 25138)
Gridegalutamide, also known as BMS-986365 and CC-94676, is a heterobifunctional, firs
1256349-48-0 | Chiauranib
(Catalog# : 25146)
Chiauranib also known as orally available, small molecule inhibitor of select serine-