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  • TJS2216Aurantiamide acetateAurantiamide acetate,Inhibitor,cathepsin L,Piper aurantiacum,adjuvant-arthritic,

    Aurantiamide acetate was isolated from the fermentation broth of Aspergillus penicilloides for the first time. Aurantiamide acetate is a selective and orally active cathepsin inhibitor. Aurantiamide acetate has anti-inflammatory activities and can be used for the study of inflammatory diseases[1][2].

    价 格：￥电议型 号：TJS2216产 地：中国大陆

  • T5148Atosiban acetate (90779-69-4 free base)RWJ22164；RW22164；Atosiban acetate；醋酸阿托西班

    Atosiban is an inhibitor of the hormones oxytocin and vasopressin. It is used as an intravenous medication as a labour repressant (tocolytic) to halt premature labor. Atosiban inhibits the oxytocin-mediated release of inositol trisphosphate from the myome

    价 格：￥电议型 号：T5148产 地：中国大陆

  • T2445FG-2216FG 2216；YM-311；FG2216

    FG-2216 is a potent HIF-prolyl hydroxylase inhibitor for the PDH2 enzyme (IC50: 3.9 uM); orally bioavailable and induced reversible and significant Epo induction in vivo.

    价 格：￥电议型 号：T2445产 地：中国大陆

  • T2221610-Undecen-1-ol

    10-Undecen-1-ol is converted from ricinoleic acid. 10-Undecen-1-ol can be used as a comonomer for the introduction of functional groups[1][2].

    价 格：￥电议型 号：T22216产 地：中国大陆

  • T2216EntacaponeOR-611；恩他卡朋

    Entacapone is a selective and reversible inhibitor of catechol-O-methyltransferase (COMT).

    价 格：￥电议型 号：T2216产 地：中国大陆

  • T13665DT2216

    DT2216 inhibits various Bcl-XL-dependent leukemias and cancer cells, but is significantly less toxic to platelets.DT2216 is a selective B-cell lymphoma, extremely large (BCL-XL), proteolytic targeting chimera (PROTAC).DT2216 targets bcl-XL to the Von Hipp

    价 格：￥电议型 号：T13665产 地：中国大陆

  • T12216NF-56-EJ40

    NF-56-EJ40 is an effective and highly selective antagonist of human SUCNR1 with an IC50 of 25 nM and a Ki of 33 nM.

    价 格：￥电议型 号：T12216产 地：中国大陆

  • T12216NF-56-EJ40NF-56-EJ40

    NF-56-EJ40 is a high-affinity and highly selective antagonist of human SUCNR1 (GPR91) (IC50 of 25 nM).

    价 格：￥电议型 号：T12216产 地：美洲

  • T2216EntacaponeEntacapone,OR-611,

    Entacapone is a selective and reversible inhibitor of catechol-O-methyltransferase (COMT).

    价 格：￥电议型 号：T2216产 地：美洲

  • T2445FG-2216FG-2216,FG2216,FG 2216

    FG-2216 is a potent HIF-prolyl hydroxylase inhibitor for the PDH2 enzyme (IC50: 3.9 uM); orally bioavailable and induced reversible and significant Epo induction in vivo.

    价 格：￥电议型 号：T2445产 地：美洲

  • T4996AtosibanAtosiban,RWJ22164,RW22164

    Atosiban is an inhibitor of the hormones oxytocin and vasopressin. It is used as an intravenous medication as a labour repressant (tocolytic) to halt premature labor. Atosiban inhibits the oxytocin-mediated release of inositol trisphosphate from the myome

    价 格：￥电议型 号：T4996产 地：美洲

  • T5148Atosiban acetateAtosiban acetate,RW22164,RWJ22164

    Atosiban is an inhibitor of the hormones oxytocin and vasopressin. It is used as an intravenous medication as a labour repressant (tocolytic) to halt premature labor. Atosiban inhibits the oxytocin-mediated release of inositol trisphosphate from the myome

    价 格：￥电议型 号：T5148产 地：美洲

  • T8808LLYN-1604 dihydrochloride；化合物LYN-1604 2HClLYN-1604 2HCl（2216753-86-3 free base)；LYN-1604 2HCl（2216753

    LYN-1604 is a novel ULK1 activator.It inducing cell death involved in ATF3, RAD21, and caspase3, accompanied by autophagy and apoptosis.

    价 格：￥电议型 号：T8808L产 地：中国大陆

  • T83893SLB1122168；化合物 SLB1122168SLB1122168

    SLB1122168, an inhibitor targeting the sphingosine-1-phosphate (S1P) transporter Spns2 (with an IC50 of 94 nM for the mouse transporter), selectively reduces circulating lymphocyte counts without altering plasma S1P concentrations in mice at a dosage of 10 mg/kg.

    价 格：￥电议型 号：T83893产 地：中国大陆

  • T82216Helospectin II；化合物 Helospectin IIHelospectin II

    Helospectin II, a member of the vasoactive intestinal peptide (VIP) family, exhibits vasodilatory and antihypertensive properties that reduce blood pressure. This neuropeptide was initially isolated from the venom of the salivary glands of the Heloderma suspectum lizard [1] [2].

    价 格：￥电议型 号：T82216产 地：中国大陆

  • T78998FITC-labeled ODN 2216 sodium；化合物 FITC-labeled ODN 2216 sodiumFITC-labeled ODN 2216 sodium

    FITC-labeled ODN 2216 (sodium), a specific agonist for human toll-like receptor 9 (TLR9), facilitates the assessment of CpG ODN cellular uptake and localization through confocal laser-scanning microscopy (excitation 495 nm, emission 520 nm) or flow cytometry.

    价 格：￥电议型 号：T78998产 地：中国大陆

  • T78997Biotin-labeled ODN 2216 sodium；化合物 Biotin-labeled ODN 2216 sodiumBiotin-labeled ODN 2216 sodium

    Biotin-labeled ODN 2216 (sodium) serves as a specific agonist for human TLR9 (toll-like receptor 9), facilitating the assessment of CpG ODN cellular uptake and localization through a biotin detection system coupled with light microscopy.

    价 格：￥电议型 号：T78997产 地：中国大陆

  • T78160SLB1122168 formic；化合物 SLB1122168 formicSLB1122168 formic

    SLB1122168 is a potent inhibitor of Spns2-mediated sphingosine-1-phosphate (S1P) release, exhibiting an IC50 value of 94 nM [1].

    价 格：￥电议型 号：T78160产 地：中国大陆

  • T72216DPM-1001 trihydrochloride；化合物 DPM-1001 trihydrochlorideDPM-1001 trihydrochloride

    DPM-1001 trihydrochloride, an analog of the specific protein-tyrosine phosphatase (PTP1B) inhibitor MSI-1436, is a potent, specific, non-competitive, orally active inhibitor of PTP1B with an IC50 of 100 nM, exhibiting anti-diabetic properties.

    价 格：￥电议型 号：T72216产 地：中国大陆

  • T68154TC-2216；化合物TC-2216TC-2216

    TC-2216 is a partial agonist at the neural nicotinic acetylcholine receptor and is used to treat anxiety and depression.

    价 格：￥电议型 号：T68154产 地：中国大陆

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