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产品名字索引 S
- 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
- SNX-2112 (Catalog# : 179815, Cas# : 908112-43-6)SNX-2112，又称为PF 04928473，是一种HSP90抑制剂，目前正在进行1期临
- SU-1498 (Catalog# : 17984, Cas# : 168835-82-3)SU-1498是一种选择性的受体酪氨酸激酶抑制剂，血管内皮生长因子
- SF2523 (Catalog# : 17918, Cas# : 1174428-47-7)SF2523是一种高效、选择行的日常pan-PI3K/BRD4抑制剂。具有明显的选
- SAR-20347 (Catalog# : 1781101, Cas# : 1450881-55-6)SAR-20347是一种强力JAK1和酪氨酸激酶2的双抑制剂 (TYK2).
- SB756050 (Catalog# : 20178811, Cas# : 447410-57-3)SB-756050是一种G蛋白结合胆汁酸受体1(GPBAR1)激动剂，可能用于治疗
- SAR-405 (Catalog# : 2017882, Cas# : 1523406-39-4)SAR-405是一种有效且选择性的PIK3C3/Vps34抑制剂，防止自噬和协同MTO
- 雷帕霉素(钠盐) (Catalog# : 20177313, Cas# : 148554-65-8)雷帕霉素是第一个体内open-ring代谢物,不影响mTOR的雷帕霉素抑制Ch
- SU5402 (Catalog# : 174191, Cas# : 215543-92-3)SU5402是一种成纤维细胞生长因子受体（FGFR）特异性酪氨酸激酶抑
- SAR-020106 (Catalog# : 17031004, Cas# : 1184843-57-9)SAR-020106是一种 ATP -竞争性、强效和选择性的CHK1抑制剂，其IC50为1
- SH5-07 (Catalog# : 17031002, Cas# : 1456632-41-9)SH5-07是一种健壮的氧肟抗酸的STAT3抑制剂，它能在体外诱导抗肿瘤
- SUN11602 (Catalog# : 17030603, Cas# : 704869-38-5)SUN11602是一种新型的苯胺类化合物，它模仿了碱性成纤维细胞生长
- Sardomozide HCl (Catalog# : 17030306, Cas# : 138794-73-7)Sardomozide，又名SAM486A或CGP48664，是第二代多胺合成抑制剂，它抑制
- 钠盐沙库必曲 (Catalog# : 17030108, Cas# : 149690-05-1)沙库必曲，也被称为AHU377，是血管紧张素受体神经内肽酶抑制剂被
- SHP099游离 (Catalog# : 17030107, Cas# : 1801747-42-1)<SHP099是强有力的,选择性,具有口服生物利用率,是一种IC50 = 0.07μM的
- 司马西特 (Catalog# : 17022802, Cas# : 425386-60-3)司马西特(LY450139) 是一种针对Aβ42的γ-分泌酶阻断剂, Aβ40和Aβ38的
- 泰地唑胺杂质 A (Catalog# : 17021402, Cas# : 1431699-67-0)泰地唑胺杂质 A是磷酸四唑磷酸酯活跃的一部分，对革兰氏阳性菌
- STO-609 (Catalog# : 17021319, Cas# : 52029-86-4)STO-609是一个特定抑制剂。
- S49076 (Catalog# : 17021309, Cas# : 1265965-22-7)S49076是一种新型的、能有效抑制IC50值低于20 nmol/ L的MET、AXL / MER和
- SRT2183 (Catalog# : 17021306, Cas# : 1001908-89-9)SRT2183是sirtuin子型SIRT1的小分子激活剂，目前由Sirtris制药公司开发
- SW044248 (Catalog# : 17011714, Cas# : 522650-83-5)SW044248是一个强有力的和选择性拓扑异构酶抑制剂。SW044248杀死大
产品分类
- ---- VEGFR
- ---- JAK
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- ---- FGFR
- ---- Src
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- ---- SARS-CoV
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- -- Apoptosis
- ---- PD-1
- ---- PD-L1
- ---- Bcl-2
- ---- Caspase
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- ---- PERK
- ---- p53
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- ---- 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
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- ---- Wnt
- ---- β-catenin
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- -- DNA Damage
- ---- PARP
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- ---- Topoisomerase
- ---- DNA-PK
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- ---- RAD51
- ---- HDAC
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- ---- Mps1
- -- Epigenetics
- ---- PARP
- ---- JAK
- ---- Pim
- ---- PKC
- ---- PKD
- ---- Sirtuin
- ---- Histone Demethylase
- ---- Histone Acetyltransferase
- ---- HDAC
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- ---- 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
- ---- SSTR
- -- Immunology & Inflammation
- ---- PD-1
- ---- PD-L1
- ---- COX
- ---- CCR
- ---- Histamine Receptor
- ---- TLR
- ---- CXCR
- ---- MALT
- ---- TDO
- ---- NOS
- ---- IDO
- ---- Thrombopoietin Receptor(TPO)
- ---- NLR inhibitor
- ---- Interleukin Related
- ---- CD73
- ---- Complement System
- ---- Aryl Hydrocarbon Receptor
- ---- Kallikrein
- ---- IRAK
- ---- Reactive Oxygen Species(ROS)
- ---- SOD
- -- 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
- -- Metabolic Enzyme/Protease
- ---- PPAR
- ---- Proteasome
- ---- P450
- ---- Caspase
- ---- HSP
- ---- HIV Protease
- ---- PDE
- ---- MMP
- ---- Factor Xa
- ---- γ-secretase
- ---- Phospholipase
- ---- DPP4
- ---- FAAH
- ---- CETP
- ---- Lipoxygenase
- ---- HMG-CoA Reductase
- ---- Fatty Acid Synthase
- ---- NADPH-oxidase
- ---- FXR
- ---- NAMPT
- ---- TDO
- ---- Carbonic Anhydrase
- ---- Monoamine Oxidase
- ---- IDO
- ---- Mitochondrial Metabolism
- ---- Isocitrate Dehydrogenase (IDH)
- ---- MAGL
- ---- Epoxide Hydrolase
- ---- LXR
- ---- Myeloperoxidase (MPO)
- ---- FPTase
- ---- RAR/RXR
- ---- Acetyl-CoA Carboxylase
- ---- Acyltransferase
- ---- UGT
- ---- MMP
- ---- ATP Citrate Lyase
- ---- Glutaminase
- ---- Ketohexokinase(KHK)
- ---- Lipase
- ---- Lactate dehydrogenase
- ---- Glyoxalase (GLO)
- ---- E1/E2/E3 Enzyme
- ---- PANK(pantothenate kinase)
- ---- Phosphoglycerate Dehydrogenase (PHGDH)
- ---- Hemoglobin
- -- 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)
- ---- CGRP-Receptor
- ---- TRP-Channel
- -- 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)
- -- 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
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- ---- Estrogen Receptor/ERR
- ---- ChoKα
- ---- Newest added products
- -- Nuclear Receptor
- ---- Androgen Receptor(AR)
- -- Aldehydes
- -- Amines
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- -- Anilines
- -- Boronic Acids
- -- Bromides
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- -- Chiral Compounds
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- -- 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
- Osivelotor (别名: GBT-601; GBT-021601) (Catalog# : 26A061, Cas# : 2417955-18-9)Osivelotor（同义词：GBT-601；GBT-021601）是下一代镰状血红蛋白（HbS）
- Linvemastat (别名: FP-020) (Catalog# : 26A060, Cas# : 2389060-50-6)Linvemastat（FP-020）是一种高效、选择性口服MMP-12抑制剂。
- BLU-808 (Catalog# : 26A024, Cas# : 3041025-10-6)BLU-808是一种针对肥大细胞疾病的野生型c-KIT的强效且具有选择性的
- SCO-240 (Catalog# : 26A059, Cas# : 1695564-98-7)SCO-240是一种研究性、口服活性和选择性生长抑素受体亚型5（SSTR5
- N-Methylamisulpride ( 别名: LB-102 ) (Catalog# : 26A058, Cas# : 2227154-23-4)N-甲基咪唑胺（同义词：LB-102）是一种多巴胺D2和D3受体拮抗剂和血
- Safusidenib Erbumine (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。
- Repinatrabit ( 别称: JNT-517 ) (Catalog# : 26A056, Cas# : 2837993-05-0)Repinatrabit（JNT-517）是一种针对Phe转运蛋白SLC6A19的研究性、选择性
- Privosegtor ( 别名: OCS-05, ACT-01 ) (Catalog# : 26A055, Cas# : 1361200-34-1)Privosegtor（OCS-05，ACT-01）是一种小分子拟肽、BDNF/NT-3生长因子受体
- ART-6043 (Catalog# : 26A054, Cas# : 2923356-52-7)ART-6043是一种口服的DNA聚合酶θ（POLQ）小分子抑制剂。
- Palacaparib ( Synonyms: AZD-9574 ) (Catalog# : 26A053, Cas# : 2756333-39-6)Palacioparib（AZD-9574）是一种口服的中枢神经系统渗透剂PARP-1抑制剂