武汉永璨生物科技有限公司
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- 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
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Name Index S
- 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
- 舒更葡糖钠 (Catalog# : 17011713, Cas# : 343306-79-6)舒更葡糖钠是治疗神经肌肉阻滞的药物。
- 链脲菌素 (Catalog# : 17011712, Cas# : 18883-66-4)链脲菌素是一种从链球菌中分离出来的甲基亚硝基脲类抗肿瘤抗生
- Sotagliflozin (Catalog# : 17011711, Cas# : 1018899-04-1)Sotagliflozin,也称为LX4211,是一种口服活性和双SGLT1 / SGLT2抑制剂，在
- 索利霉素 (Catalog# : 17011710, Cas# : 760981-83-7)索利霉素,也称为CEM-101和OP-1068, 是一种用于治疗社区获得性肺炎(C
- SMER28 (Catalog# : 17011709, Cas# : 307538-42-7)SMER28是一种自噬的小分子调制器，在哺乳动物细胞中独立于雷帕霉
Products Catalog
- ---- 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
- ---- Bradykinin 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
- ---- 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
- ---- Methionine Adenosyltransferase (MAT)
- ---- Lipase
- -- 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
- -- 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
Latest Products
- Dencatistat (STP938) (Catalog# : 25177, Cas# : 2377000-84-3)Dencatistat 是一种口服生物可利用的小分子胞苷三磷酸合酶 1 (CTPS1)
- DS-1001b (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。
- Z57346765 (Catalog# : 25191, Cas# : 1016340-64-9)Z57346765 是一种 PGK1 特异性抑制剂，可降低 PGK1 糖酵解中代谢酶的
- CBR-470-1 (Catalog# : 25192, Cas# : 2416095-06-0)CBR-470-1 是诱导 Nrf2 活性的糖酵解酶 PGK1 的抑制剂。
- Safusidenib (Catalog# : 25149, Cas# : 1898206-17-1)Safusidenib，也称为DS-1001，是一种口服异柠檬酸脱氢酶[NADP]细胞质（
- HC-7366 (Catalog# : 25076, Cas# : 2803470-63-3)HC-7366 is a potent and selective activator of the general control nonderepressible 2
- Flavopiridol ( 夫拉平度 ) (Catalog# : 237071, Cas# : 146426-40-6)Alvocidib is a synthetic dihydroxyflavone that is 5,7-dihydroxyflavone which is subst
- AG-270 (Catalog# : 25176, Cas# : 2201056-66-6)MAT2A 抑制剂 AG-270 是一种口服的蛋氨酸腺苷转移酶 II α (MAT2A) 小分
- AZD-5904 (Catalog# : 181121, Cas# : 618913-30-7)AZD5904是一个有效的口服生物利用率MPO抑制剂。在临床前研究中,AZ
- ALT-007 (Catalog# : 25157, Cas# : 2035010-37-6)ALT-007 是一种口服生物可利用的 SPT 抑制剂，比多球菌素更有效，