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产品名字索引 S
- Seletalisib (Catalog# : 1810221, Cas# : 1362850-20-1)Seletalisib，也被称为UCB-5857，是一种有效的选择性PI3激酶抑制剂，
- Simenepag (Catalog# : 1810172, Cas# : 910562-15-1)Simenepag，又名AGN-210676，是一种用于治疗青光眼和高眼压的小分子
- SB-273005 (Catalog# : 186221, Cas# : 205678-31-5)SB-273005是一种整合素αvβ3的抑制剂。
- STF-083010 (Catalog# : 185151, Cas# : 307543-71-1)STF-083010,也称为IRE1抑制剂I, 是IRE1/XBP1通路的抑制剂。
- SAR407899游离 (Catalog# : 185115, Cas# : 923359-38-0)SAR407899是一种有效且具有选择性的、前景的抗高血压活性Rho激酶抑
- SB-334867游离 (Catalog# : 185114, Cas# : 792173-99-0)SB-334867是一种阿立新拮抗剂。
- SC-560 (Catalog# : 185113, Cas# : 188817-13-2)SC-560是一种有效的具有口服活性和选择性的COX-1抑制剂。
- Seladelpar (Catalog# : 185112, Cas# : 851528-79-5)Seladelpar，也被称为MBX-8025和RWJ-800025，是一种选择性的过氧化物酶
- SEL120-34A盐酸盐 (Catalog# : 18574, Cas# : 1609452-30-3)SEL120-34A是一种高效、选择性的CDK8抑制剂，活跃于AML细胞中，具有
- SR-4370 (Catalog# : 1842814, Cas# : 1816294-67-3)SR-4370是一种HDAC抑制剂。
- SGC2085盐酸盐 (Catalog# : 184287, Cas# : 1821908-49-9)SGC2085是一种强效的选择性共激活剂，它可以使精氨酸甲基转移酶
- S38093盐酸盐 (Catalog# : 184176, Cas# : 1222097-72-4)S38093是组胺H3受体的反向激动剂。
- STO-609醋酸盐 (Catalog# : 184123, Cas# : 1173022-21-3)STO-609是一种细胞渗透性抑制剂，钙/钙调蛋白依赖性激酶激酶(CaMK
- Super-TDU (Catalog# : 18495, Cas# : 1599441-71-0)Super-TDU是靶向YAP-TEADs interaction的抑制性多肽。
- SSD114 HCl (Catalog# : 18427, Cas# : N/A)SSD114是一种GABAB阳性变构调制器。SSD114增强gaba刺激[35S]GTP S与本地
- (S)-(4-(3-(tert-butoxycarbonyl)-1-(isoquinolin-6-ylamino)-1-oxopropan-2-yl)phenyl)methyl 2,4-dimethylbenzoate (Catalog# : 183219, Cas# : 1253955-19-9)(S)-(4-(3-(tert-butoxycarbonyl)-1-(isoquinolin-6-ylamino)-1-oxopropan-2-yl)phenyl)met
- (S)-3-(tert-butoxycarbonyl)-2-(4-((2,4-dimethylbenzoyloxy)methyl)phenyl)propanoic acid (Catalog# : 183218, Cas# : 2097334-20-6)(S)-3-(tert-butoxycarbonyl)-2-(4-((2,4-dimethylbenzoyloxy)methyl)phenyl)propanoic aci
- (S)-2-羟基丁酸正丁酯 (Catalog# : 1712291, Cas# : 132513-51-0)(S)-2-羟基丁酸正丁酯是一种分子砌块。
- SCR7 pyrazine (Catalog# : 1712261, Cas# : 14892-97-8)SCR7吡嗪是DNA连接酶IV的小分子抑制剂,防止非同源端连接通过干扰
- S38093 (Catalog# : 17101615, Cas# : 862896-30-8)S 38093 是一种大脑渗透的 H3 receptor 拮抗剂，对大鼠，小鼠和人的
- SAR-7334盐酸 (Catalog# : 17101610, Cas# : 1333207-63-8)SAR-7334是一种新颖的、高效的、生物可利用的TRPC6通道，打开了新
- SEN-826 (Catalog# : 1710168, Cas# : 1160833-51-1)SEN-826是一种潜在抗癌剂。
- SRT3025 HCl (Catalog# : 17101310, Cas# : 2070015-26-6)SRT3025是一种可口服的小分子激活SIRT1酶。
- Senexin A (Catalog# : 1710136, Cas# : 1366002-50-7)Senexin A是一种强效的选择性与抑制剂（IC50 = 280 nm）。Senexin A结合
- S63845 (Catalog# : 171071, Cas# : 1799633-27-4)s63845是专门结合MCL1的BH3结合槽高亲和力的小分子。s63845有效杀死
- Salermide (Catalog# : 1791511, Cas# : 1105698-15-4)salermide是一个强大的肿瘤特异性凋亡的影响长寿基因蛋白质抑制剂
- SD-06 (Catalog# : 1791320, Cas# : 271576-80-8)SD-06是治疗关节炎的MAPK p38α抑制剂。
- Sulfatinib (Catalog# : 179135, Cas# : 1308672-74-3)Sulfatinib是一种口服的血管内皮生长因子受体（VEGFR）1, 2，3，和成
- S107 HCl (Catalog# : 1791111, Cas# : 927871-76-9)S107是类型1 利阿诺定受体（RYR1）稳定剂；结合 RyR1提高calstabin-1亲
- 司美利特盐酸盐 (Catalog# : 179830, Cas# : 101526-62-9)司美利特，也称为CK-1752，是III类抗心律失常药。它是一种选择性
产品分类
- ---- 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
- -- 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
最新产品
- MGD-28 (Catalog# : 25073, Cas# : 2991818-13-2)MGD-28 is a potent molecular glue degrader that demonstrates significant in vitro eff
- TG101209 analog 1 (Catalog# : 25072)TG101209 analog 1 (Compound 8h) is an inhibitor of BUB1B with an IC50 of 10.36 μ M.
- AT-007 (Catalog# : 25071, Cas# : 2170729-29-8)AT-007 is an orally active central nervous system (CNS) penetrant Aldose Reductase in
- TAK-653 (Catalog# : 25070, Cas# : 1358751-06-0)TAK-653 is a novel AMPA receptor potentiator, strictly potentiating a glutamate-induc
- Emavusertib (Catalog# : 25069, Cas# : 1801344-14-8)Emavusertib, also known as CA-4948 is a potent IRAK4/FLT3 inhibitor with anti-tumor a
- Roginolisib (Catalog# : 25068, Cas# : 1305267-37-1)Roginolisib, also known as MSC2360844 and IOA-244, is a potent, orally active and sel
- NT219 (Catalog# : 25067, Cas# : 1198078-60-2)NT219 is a novel inhibitor of the insulin/igf signaling cascade (iis), mediating a lo
- SPB linker (Catalog# : 25066, Cas# : 858128-57-1)SPB is a agent-linker conjugate for ADC with potent anti-inflammatory activity by usi
- JTE-151 (Catalog# : 20594, Cas# : 1404380-58-0)JTE-151 是一种 RORγ 抑制剂，可通过抑制与 Th17 细胞活化相关的 ROR
- Ecopipam ( SCH 39166 ) (Catalog# : 25065, Cas# : 112108-01-7)Ecopipam (SCH 39166) 是一种有效的、选择性、具有口服活性的多巴胺