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  • T80336DFTamP1；化合物 DFTamP1DFTamP1

    DFTamP1 is an antimicrobial peptide that exhibits activity against Staphylococcus aureus USA300, with a minimum inhibitory concentration (MIC) of 3.1 μM [1].

    价 格：￥电议型 号：T80336产 地：中国大陆

  • T80214cRGDfK-thioacetyl ester；化合物 cRGDfK-thioacetyl estercRGDfK-thioacetyl ester

    cRGDfK-thioacetyl ester, a bioactive polypeptide, exhibits selective affinity for integrins and can modify near-infrared (NIR) fluorescent probes for targeted cancer imaging [1] [2].

    价 格：￥电议型 号：T80214产 地：中国大陆

  • T80130SDF-1α (human)；化合物 SDF-1α (human)SDF-1α (human)

    SDF-1α (human) serves as a chemotactic agent for mononuclear cells through its interaction with the CXCR4 receptor, facilitating critical biological processes such as stem cell homing, retention, survival, and proliferation, in addition to cardiomyocyte repair, angiogenesis, and ventricular remodeling post-myocardial infarction. It holds significant utility in cardiovascular disease research [1] [2].

    价 格：￥电议型 号：T80130产 地：中国大陆

  • T78433DfTat；化合物 DfTatDfTat

    DfTat, a fluorescently-labeled TAT peptide dimer, effectively facilitates the intracellular delivery of small molecules, peptides, and proteins into live cells with notable efficiency. When tagged with rhodamine, DfTat serves as a traceable marker for simplified detection [1].

    价 格：￥电议型 号：T78433产 地：中国大陆

  • T78399FD-1080 free acid；化合物 FD-1080 free acidFD-1080 free acid

    FD-1080 free acid, an NIR-II region fluorophore (Ex=1064 nm, Em=1080 nm), facilitates in vivo imaging [1].

    价 格：￥电议型 号：T78399产 地：中国大陆

  • T76282Friulimicin D；化合物 Friulimicin DFriulimicin D

    Friulimicin D, a lipopeptide antibiotic similar to Friulimicin B, is derived from the actinomycete Actinoplanes friuliensis [1].

    价 格：￥电议型 号：T76282产 地：中国大陆

  • T75627Ganoderic acid Df；化合物 Ganoderic acid DfGanoderic acid Df

    Ganoderic acid Df, a lanostane-type triterpenoid isolated from the fruiting body of Ganoderma lucidum, potently inhibits aldose reductase with an IC 50 of 22.8 ± 0.6 μM [1].

    价 格：￥电议型 号：T75627产 地：中国大陆

  • T73966Febuxostat sec-butoxy acid；化合物 Febuxostat sec-butoxy acidFebuxostat sec-butoxy acid

    Febuxostat sec-butoxy acid is an impurity of Febuxostat. Febuxostat is selective xanthine oxidase inhibitor with a K i of 0.6 nM [1] .

    价 格：￥电议型 号：T73966产 地：中国大陆

  • T73650Forigerimod；化合物 ForigerimodForigerimod

    Forigerimod (IPP-201101), a potent CD4 T-cell modulator, is a 21-amino-acid fragment of the U1 small nuclear ribonucleoprotein 70 kDa, phosphorylated at Ser140, known for its ability to inhibit autophagy effectively. It has applications in researching autoimmune disorders, including systemic lupus erythematosus (SLE) [1] [2] [3] [4].

    价 格：￥电议型 号：T73650产 地：中国大陆

  • T71986Fmoc-4-aminobutanoic acid；化合物 Fmoc-4-aminobutanoic acidFmoc-4-aminobutanoic acid

    Fmoc-4-aminobutanoic acid can be used as a PROTAC linker in the synthesis of PROTACs and other conjugation applications. Fmoc-4-aminobutanoic acid is an alkane chian with terminal Fmoc-protected amine and carboxylic acid groups. The Fmoc group can be deprotected under basic condition to obtain the free amine which can be used for further conjugations. The terminal carboxylic acid can react with primary amine groups in the presence of activators (e.g. EDC, or HATU) to form a stable amide bond.

    价 格：￥电议型 号：T71986产 地：中国大陆

  • T71976Fmoc-5-aminopentanoic acid；化合物 Fmoc-5-aminopentanoic acidFmoc-5-aminopentanoic acid

    Fmoc-5-aminopentanoic acid is an alkane chian with terminal Fmoc-protected amine and carboxylic acid groups. The compound can be used as a PROTAC linker in the synthesis of PROTACs. The Fmoc group can be deprotected under basic condition to obtain the free amine which can be used for further conjugations. The terminal carboxylic acid can react with primary amine groups in the presence of activators (e.g. EDC, or HATU) to form a stable amide bond.

    价 格：￥电议型 号：T71976产 地：中国大陆

  • T71970Fmoc-7-amino-heptanoic acid；化合物 Fmoc-7-amino-heptanoic acidFmoc-7-amino-heptanoic acid

    Fmoc-7-amino-heptanoic acid is an alkane chian with terminal Fmoc-protected amine and carboxylic acid groups. The compound can be used as a PROTAC linker in the synthesis of PROTACs. The Fmoc group can be deprotected under basic condition to obtain the free amine which can be used for further conjugations. The terminal carboxylic acid can react with primary amine groups in the presence of activators (e.g. EDC, or HATU) to form a stable amide bond.

    价 格：￥电议型 号：T71970产 地：中国大陆

  • T71967Fmoc-12-aminododecanoic acid；化合物 Fmoc-12-aminododecanoic acidFmoc-12-aminododecanoic acid

    Fmoc-12-aminododecanoic acid is an alkane chian with terminal Fmoc-protected amine and carboxylic acid groups. The compound can be used as a PROTAC linker in the synthesis of PROTACs. The Fmoc group can be deprotected under basic condition to obtain the free amine which can be used for further conjugations. The terminal carboxylic acid can react with primary amine groups in the presence of activators (e.g. EDC, or HATU) to form a stable amide bond.

    价 格：￥电议型 号：T71967产 地：中国大陆

  • T71731Fmoc-11-aminoundecanoic acid；化合物 Fmoc-11-aminoundecanoic acidFmoc-11-aminoundecanoic acid

    Fmoc-11-aminoundecanoic acid can be used as a PROTAC linker in the synthesis of PROTACs and other conjugation applicaitons. Fmoc-11-aminoundecanoic acid is an alkane chian with terminal Fmoc-protected amine and carboxylic acid groups. The Fmoc group can be deprotected under basic condition to obtain the free amine which can be used for further conjugations. The terminal carboxylic acid can react with primary amine groups in the presence of activators (e.g. EDC, or HATU) to form a stable amide bo

    价 格：￥电议型 号：T71731产 地：中国大陆

  • T71485Famotidine propionic acid；化合物 Famotidine propionic acidFamotidine propionic acid

    Famotidine propionic acid is a histamine H2-receptor antagonist that inhibits stomach acid production. It is commonly used in the treatment of peptic ulcer disease and gastroesophageal reflux disease.

    价 格：￥电议型 号：T71485产 地：中国大陆

  • T70632DFL23448；化合物 DFL23448DFL23448

    DFL23448 is a TRPM8-selective ion channel antagonist, modifying bladder function and reduces bladder overactivity in awake rats.

    价 格：￥电议型 号：T70632产 地：中国大陆

  • T69887Fmoc-9-aminononanoic acid；化合物 Fmoc-9-aminononanoic acidFmoc-9-aminononanoic acid

    Fmoc-9-aminononanoic acid is an alkane chian with terminal Fmoc-protected amine and carboxylic acid groups. The compound can be used as a PROTAC linker in the synthesis of PROTACs and and other conjugation applications. The Fmoc group can be deprotected under basic condition to obtain the free amine which can be used for further conjugations. The terminal carboxylic acid can react with primary amine groups in the presence of activators (e.g. EDC, or HATU) to form a stable amide bond.

    价 格：￥电议型 号：T69887产 地：中国大陆

  • T68602AZ-DF 265；化合物 AZ-DF 265AZ-DF 265

    AZ-DF 265 is a hypoglycaemic drug which stimulates insulin release. AZ-DF-265 inhibits ATP-sensitive potassium channels and displaces [3H]-glibenclamide from the sulphonylurea receptor.

    价 格：￥电议型 号：T68602产 地：中国大陆

  • T68579Fluvoxamine acid；化合物 Fluvoxamine acidFluvoxamine acid

    Fluvoxamine acid is a medication which functions as a selective serotonin reuptake inhibitor (SSRI) and σ1 receptor agonist. Fluvoxamine is used primarily for the treatment of obsessive-compulsive disorder (OCD), and is also used to treat major depressive disorder (MDD), and anxiety disorders such as panic disorder and post-traumatic stress disorder (PTSD).

    价 格：￥电议型 号：T68579产 地：中国大陆

  • T6812LCyclo(-RGDfK) TFA；化合物Cyclo(-RGDfK) TFACyclo(-RGDfK) TFA

    Cyclo(-RGDfK) is a selective αvβ3 integrin inhibitor(IC50 : 0.94 nM).

    价 格：￥电议型 号：T6812L产 地：中国大陆

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