武汉永璨生物科技有限公司
+86-17702719238
sales@sun-shinechem.com
- 首页
- 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
- TGF-beta/Smad
- Ubiquitin
- Vitamin D Related
- PROTAC
- Antibody-drug Conjugate/ADC Related
- Microbiology
- Others
- 分子砌块
- 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
- 中间体
- 技术服务
- 订购信息
- 联系我们
产品名字索引 D
- 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。
- 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)
- DFV-890 (别名: IFM-2427 ) (Catalog# : 25170, Cas# : 2271394-34-2)DFV-890是NLRP3炎性小体的口服小分子抑制剂。
- DS68591889 (Catalog# : 25158, Cas# : 2488609-21-6)DS68591889 (PTDSS1i) 特异性抑制 PTDSS1，而 PTDSS1 可催化丝氨酸掺入 PC。
- 5,7-二氟-3-甲基苯并呋喃-2-甲醛 (Catalog# : 25129, Cas# : 1784086-71-0)
- 6,6-二甲基-4,5,6,7-四氢-1H-吲唑-3-甲酸 (Catalog# : 25102, Cas# : 581083-30-9)
- 2,4-二氯-6-(2,2,2-三氟乙基)噻吩并[2,3-d]嘧啶 (Catalog# : 25098, Cas# : 2055107-43-0)
- Deucrictibant (Catalog# : 25081, Cas# : 2340111-58-0)
- DHPG (Catalog# : 25056, Cas# : 146255-66-5)DHPG, also known as (RS)-3,5-DHPG, is a selective agonist for group I metabotropic gl
- 6-氰基-1,3-二甲基-1H-吲唑 (Catalog# : 25037, Cas# : 1516679-30-3)
- Deutivacaftor (Catalog# : 24096, Cas# : 1413431-07-8)Deutivacaftor, also known as CTP-656 and VX561, is a cystic fibrosis transmembrane co
- 5-氘代-2,4-二溴噻唑 (Catalog# : 24060, Cas# : 960069-34-5)
- Denifanstat (Catalog# : 20596, Cas# : 1399177-37-7)TVB-2640 is an orally bioavailable fatty acid synthase (FASN) inhibitor, with potenti
- 1,1-Dimethylethyl (1S,5S)-1-formyl-3-azabicyclo[3.1.0]hexane-3-carboxylate (Catalog# : 20545, Cas# : 1932352-50-5)
- 1,1-Dimethylethyl (1R,5S)-1-ethynyl-3-azabicyclo[3.1.0]hexane-3-carboxylate (Catalog# : 20544, Cas# : 1932410-93-9)
- (1S,5S)-1-(羟甲基)-3-氮杂双环[3.1.0]己烷-3-羧酸叔丁酯 (Catalog# : 20543, Cas# : 1932534-25-2)
- Danuglipron (Catalog# : 20538, Cas# : 2230198-02-2)Danuglipron, also known as PF-06882961 is a potent, orally bioavailable agonist of th
- 4,5-二碘-2-甲基-1,2,3三氮唑 (Catalog# : 20520, Cas# : 859790-39-9)
- DSN28369 (Catalog# : 20498, Cas# : 2413428-36-9)DSN28369 is a heterobifunctional linker, and useful to make antibody drug conjuate (A
- DSR-6434 (Catalog# : 20497, Cas# : 1059070-10-8)DSR-6434 is a potent TLR7 agonist (EC50 = 7.2 nM). DSR-6434 activates several immune
- DASA-58 (Catalog# : 20489, Cas# : 1203494-49-8)DASa-58, also known as ML-203 and NCGC00185916, is a selective activator of pyruvate
- DC-S100 (Catalog# : 20456, Cas# : 178803-91-3)DC-S100 is a selective histone methyltransferase SET7 inhibitor.
- 4,5-二氯吲哚 (Catalog# : 20442, Cas# : 122509-73-3)
- Deruxtecan (Catalog# : 20437, Cas# : 1599440-13-7)Deruxtecan, a topoisomerase I inhibitor, is an exatecan derivative (DX-8951 derivativ
- 4,6-二氯-1H-吡唑并[3,4-B]吡啶 (Catalog# : 20434, Cas# : 2105905-46-0)
- 2,5-二氨基-2,5-环己二烯-1,4-二酮 (Catalog# : 171654, Cas# : 1521-06-8)
- 2,6-DIFLUORO-4-[2-(PHENYLSULFONYLAMINO)E (Catalog# : G20379, Cas# : 141286-78-4)
- 4,6-dimethylpyrazolo[1,5-a]pyrazine-2-carbaldehyde (Catalog# : 20361, Cas# : 2407725-14-6)
- Diphenylterazine (Catalog# : 20324, Cas# : 344940-63-2)Diphenylterazine is a bioluminescence agent. Diphenylterazine alone yields very littl
- DDD100097 (Catalog# : 20307, Cas# : 1215012-74-0)DDD100097 is an inhibitor of Trypanosoma brucei N-myristoyltransferase (TbNMT) with m
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
- ---- 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
- ---- Potassium Channel
- -- 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
最新产品
- MTX115325 (Catalog# : 186264, Cas# : 2750895-97-5)MTX115325是一种强效、选择性、脑渗透性USP30抑制剂，具有良好的类
- LY-3381916 (Catalog# : 193123, Cas# : 2166616-75-5)LY-3381916是一种强效的、选择性的、脑透性的IDO1活性抑制剂，与缺
- Opakalim (Catalog# : 25193, Cas# : 2376397-93-0)Opakalim（BHV-7000）是Kv7.2/7.3钾通道（KCNQ2/3）的口服小分子激活剂，
- DS68591889 (Catalog# : 25158, Cas# : 2488609-21-6)DS68591889 (PTDSS1i) 特异性抑制 PTDSS1，而 PTDSS1 可催化丝氨酸掺入 PC。
- CAY 10566 (Catalog# : 10403, Cas# : 944808-88-2)CAY 10566是一种强效的选择性SCD-1抑制剂。
- Cadefrecitinib (GLPG-3667) (Catalog# : 20509, Cas# : 2308520-97-8)Cadefrecitinib（GLPG-3667）是一种口服小分子TYK2激酶抑制剂，目前正处
- QBS10072S (Catalog# : 25190, Cas# : 1802735-28-9)QBS10072S 是一种血脑屏障 (BBB) 渗透剂，由细胞毒性化疗结构域 N-双
- 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