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Cas号索引 6
- 68755-37-3 | 6-(Trifluoromethyl)-1-indanone (Catalog# : 83104)Coming soon!
- 68755-42-0 | 4-(Trifluoromethyl)-1-indanone (Catalog# : 83103)Coming soon!
- 663619-89-4 | TGX-221 (Catalog# : 52006)TGX-221 is ap110-specific inhibitor withIC50of 5 nM, 1000-fold more selective for p11
- 609799-22-6 | Tasimelteon (Catalog# : 51601)Tasimelteon (trade name Hetlioz) is a selective agonist for the melatonin receptors M
- 644981-35-1 | Val-Cit-PAB-MMAE (Catalog# : 20112601)Val-Cit-PAB-MMAE is a MMAE derivative with a cleavable linker, which is useful to mak
- 646502-53-6 | VcMMAE (Catalog# : 18582)VcMMAE是一种MMAE衍生物，它与valine-citrulline (Vc)链接器。VcMMAE可用于
- 60643-86-9 | 氨己烯酸 (Catalog# : 17011903)氨己烯酸, 是一种抗癫痫药物,抑制γ-aminobutyric酸的分解(GABA)充当
- 618385-01-6 | Vorapaxar(free base) (Catalog# : 16070916)Vorapaxar, also known as SCH 530348, is a thrombin receptor (protease-activated recep
- 67469-69-6 | Vanoxerine (Catalog# : 61001)Vanoxerine (GBR12909) is a potent and selective DRI (Dopamine reuptake inhibitor).
- 6501-72-0 | VGX-1027 (Catalog# : 52316)VGX-1027(GIT27) is an isoxazole compound that exhibits various immunomodulatory prope
- 639089-54-6 | VX-680(Tozasertib,MK-0457) (Catalog# : 52005)VX-680 (Tozasertib, MK-0457) is a pan-Aurora inhibitor, mostly against Aurora A wit
- 632-85-9 | 汉黄芩素 (Catalog# : 17031003)汉黄芩素是一种天然的生物活性黄酮，在植物中发现，据报道它对
- 634911-81-2 | Z-VAD(OH)-FMK (Catalog# : 16062110)Z-VAD(OH)-FMK
- 690206-97-4 | ZM 306416 (Catalog# : 122923)ZM-306416 is a VEGFR inhibitor that inhibits Flk-1 (KDR) (IC50=100 nM) and Flt (IC50
产品分类
- ---- 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
- -- 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
- 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-