武汉永璨生物科技有限公司
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产品名字索引 R
- RBN-2397 (Catalog# : 207101, Cas# : 2381037-82-5)
- (2R,6S)-tert-butyl 4-(4-aminobenzoyl)-2,6-dimethylpiperazine-1-carboxylate (Catalog# : 2062334, Cas# : 2161337-98-8)
- (R)-methyl 2-(tert-butyldimethylsilyloxy)propanoate (Catalog# : 202329, Cas# : 171230-81-2)
- 3-[(2RS)-tetrahydro-2H-pyran-2-yloxy]propanoic acid (Catalog# : 2062017, Cas# : 1221443-23-7)
- [(1R,2S)-2-(3-fluorophenyl)-2-(hydroxymethyl)cyclopropyl]-methyl acetate (Catalog# : 2062004, Cas# : 1369768-29-5)
- Rigosertib (Catalog# : 690120, Cas# : 592542-59-1)Rigosertib(ON-01910) is a multi-kinase inhibitor and a selective anti-cancer agent, w
- Resatorvid (Catalog# : 206102, Cas# : 243984-11-4)Resatorvid, also known as TAK-242, is a cell-permeable inhibitor of TLR4 signaling, b
- RU320521 (Catalog# : 204503, Cas# : 2262452-06-0)RU320521, also known as RU521; RU.521 is a potent and selective inhibitor of cGAS, in
- (2R)-2-乙炔-2-甲基-1-吡咯烷乙酸 1,1-二甲基乙酯 (Catalog# : 580586, Cas# : 2086689-88-3)(2R)-2-乙炔-2-甲基-1-吡咯烷乙酸 1,1-二甲基乙酯 是 Pamiparib合成中一
- Remetinostat (Catalog# : 193111, Cas# : 946150-57-8)Remetinostat，也被称为SHP-141，是一种外用制剂，含有组蛋白脱乙酰
- RG7834 (Catalog# : 19355, Cas# : 2072057-17-9)RG7834,也称为RO7020322,是一种新型口服HBV病毒基因表达抑制剂阻断病
- RWJ-56110 (Catalog# : 19353, Cas# : 252889-88-6)RWJ-56110是一种选择性蛋白酶活化受体-1 (PAR1)拮抗剂。它阻断凝血酶
- RBC8 (Catalog# : 19313, Cas# : 361185-42-4)RBC8是一种RalA和RalB GTPase抑制剂(EC50 ~ 3.5μM)。RBC8抑制小鼠异种移植
- Rogaratinib (Catalog# : 192277, Cas# : 1443530-05-9)Rogaratinib, 也称为BAY-1163877, 是一种异常的成纤维细胞生长因子受体
- Rebimastat (Catalog# : 192254, Cas# : 259188-38-0)Rebimastat，又名BMS275291，是一种具有潜在抗肿瘤活性的巯基第二代
- Retosiban (Catalog# : 192193, Cas# : 820957-38-8)Retosiban，又称GSK-221149-A;是一种口服活性强、选择性强的亚纳米(Ki
- RKI-1313 (Catalog# : 19183, Cas# : 1342276-76-9)RKI-1313是RKI-1447 (GLXC-05200)的阴性对照，是Rho-相关ROCK激酶的有效抑
- RGX-104 free form (Catalog# : 19181, Cas# : 610318-54-2)RGX-104，又称SB 742881，是肝脏X受体激动剂，具有潜在的免疫调节和
- R547 (Catalog# : 1811151, Cas# : 741713-40-6)R547是口服生物有效的二氨基嘧啶环磷酰胺依赖性激酶抑制剂(CDKI)
- Regadenoson (Catalog# : 1810224, Cas# : 313348-27-5)Regadenoson是一种A2A腺苷受体激动剂，是一种冠状血管舒张剂，通常
- RMC-4550 (Catalog# : 186251, Cas# : 2172651-73-7)RMC-4550一种有效且具有选择性的SHP2抑制剂。
- RGX-104盐酸盐 (Catalog# : 186234, Cas# : 610318-03-1)RGX-104是一种具有潜在免疫调节和抗肿瘤活性的肝X受体激动剂。
- Resminostat HCl (Catalog# : 185317, Cas# : 1187075-34-8)Resminostat HCl是一种有效的HDAC1/3/6抑制剂。
- Rovazolac (Catalog# : 185234, Cas# : 1454288-88-0)Rovazolac是一种抗炎药。
- Rolapitant游离 (Catalog# : 185152, Cas# : 5552292-08-7)Rolapitant，也被称为SCH-619734，是一种口服生物可用的，具有中央作
- RO10-5824 (Catalog# : 185141, Cas# : 189744-46-5)RO10-5824是一种D4-选择性局部激动剂。RO10-5824是管理可卡因使用障碍
- 利卡司琼 (Catalog# : 184281, Cas# : 117086-68-7)利卡司琼，也称为Brl 46470，是止吐剂。
- R-IMPP (Catalog# : 18413, Cas# : 2133832-83-2)R-IMPP是PCSK9的转化抑制剂。
- Rimegepant (Catalog# : 18441, Cas# : 1289023-67-1)Rimegepant，也称为BMS-927711，在治疗偏头痛的临床试验中，是一种有
- Ritlecitinib ( PF-06651600 ) (Catalog# : 18435, Cas# : 1792180-81-4)Ritlecitinib ( PF-06651600 )是一种有效的选择性JAK3抑制剂，是一种具有
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