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  • T76357Neuropeptide Y (18-36) (porcine)；化合物 Neuropeptide Y (18-36) (porcine)Neuropeptide Y (18-36) (porcine

    Neuropeptide Y (18-36) (porcine) acts as a competitive antagonist of the neuropeptide Y (NPY) cardiac receptor, effectively blocking the attachment of I-NPY to cardiac ventricular membranes. Its action is concentration-dependent, exhibiting an IC50 value of 158 nM and a Ki value of 140 nM. This compound is utilized in the study of congestive heart failure [1].

    价 格：￥电议型 号：T76357产 地：中国大陆

  • T76356Neuropeptide Y (2-36) (porcine)；化合物 Neuropeptide Y (2-36) (porcine)Neuropeptide Y (2-36) (porcine)

    Neuropeptide Y (2-36) (porcine) is a pig-sourced peptide closely resembling its rat and human counterparts with 97.14% homology. It acts as an agonist for rat neuropeptide receptors Y5, Y2, and Y1, demonstrating EC50 values of 1.2, 1.6, and 3.4 nM, respectively. This compound is utilized in research on obesity and eating disorders [1].

    价 格：￥电议型 号：T76356产 地：中国大陆

  • T76355Neuropeptide Y (3-36) (porcine)；化合物 Neuropeptide Y (3-36) (porcine)Neuropeptide Y (3-36) (porcine)

    Neuropeptide Y (3-36) (porcine) acts as an agonist for the Y2 subtype of the neuropeptide Y (NPY) receptor, effectively stimulating feeding behavior in rats. This compound exhibits high selectivity for the Y2 receptor compared to the non-selective Y1/Y2 receptor ligand, Neuropeptide Y 1-36 [1] [2] [3].

    价 格：￥电议型 号：T76355产 地：中国大陆

  • T76354LH-RH (4-10)；化合物 LH-RH (4-10)LH-RH (4-10)

    LH-RH (4-10), a heptapeptide, represents one of the primary degradation products of luteinising-hormone releasing hormone (LHRH), occurring through the pathways of the pituitary and hypothalamus. It is produced in macrophages and type II pneumocytes [1].

    价 格：￥电议型 号：T76354产 地：中国大陆

  • T76353LH-RH (7-10)；化合物 LH-RH (7-10)LH-RH (7-10)

    LH-RH (7-10), a tetrapeptide, constitutes a principal degradation product of luteinizing-hormone releasing hormone (LHRH) through the action of the pituitary and hypothalamus. This compound is synthesized in macrophages, as well as type I-like and type II pneumocytes [3].

    价 格：￥电议型 号：T76353产 地：中国大陆

  • T76352Lamprey LH-RH I；化合物 Lamprey LH-RH ILamprey LH-RH I

    Lamprey LH-RH I, a gonadotropin-releasing hormone, effectively increases plasma steroid levels and induces ovulation in lampreys, yet demonstrates no biological activity in other animal models [1].

    价 格：￥电议型 号：T76352产 地：中国大陆

  • T76351[D-Ala6]-LH-RH；化合物 [D-Ala6]-LH-RH[D-Ala6]-LH-RH

    [D-Ala6]-LH-RH, a Luteinizing-hormone-releasing hormone (LHRH) analogue, functions as a gonadotropin-releasing hormone (GnRH) receptor agonist [1].

    价 格：￥电议型 号：T76351产 地：中国大陆

  • T76350[D-Glp1,D-Phe2,D-Trp3,6]-LH-RH；化合物 [D-Glp1,D-Phe2,D-Trp3,6]-LH-RH[D-Glp1,D-Phe2,D-Trp3,6]-LH-RH

    [D-Glp1,D-Phe2,D-Trp3,6]-LH-RH, a luteinizing hormone-releasing hormone (LHRH) analogue, functions as a gonadotropin-releasing hormone (GnRH) receptor antagonist [1].

    价 格：￥电议型 号：T76350产 地：中国大陆

  • T7635Raclopride；雷氯必利Raclopride

    Raclopride is a selective antagonist of dopamine D2/D3 receptor.

    价 格：￥电议型 号：T7635产 地：中国大陆

  • T75635Microcystin-LY；化合物 Microcystin-LYMicrocystin-LY

    Microcystin-LY, a cyclic heptapeptide toxin produced by the cyanobacterium Microcystis aeruginosa [2], functions as a potent activator of the Nrf2 pathway, thereby inducing an oxidative stress response. Its activation effect is most pronounced at a concentration of 3μM [1].

    价 格：￥电议型 号：T75635产 地：中国大陆

  • T7497L1C3a 70-77 acetate；化合物C3a 70-77 acetateC3a 70-77 acetate (63555-63-5 Free base)；C3a 70-77 acetate (63

    C3a 70-77 acetate is the octapeptide acetate corresponding to the COOH terminus of C3a, exhibits the specificity and 1 to 2% biologic activities of C3a.

    价 格：￥电议型 号：T7497L1产 地：中国大陆

  • T7497LC3a 70-77 2TFA(63555-63-5(free base))；化合物C3a 70-77 2TFAComplement 3a (70-77)；Complement 3a (70-77)

    C3a 70-77 2TFA(63555-63-5(free base)) (Complement 3a (70-77)) is an octapeptide corresponding to the COOH terminus of C3a.

    价 格：￥电议型 号：T7497L产 地：中国大陆

  • T74635MS9449；化合物 MS9449MS9449

    MS9449 is a potent PROTAC EGFR degrader, exhibiting dissociation constants (Kd) of 17 nM for EGFR WT and 10 nM for EGFR L858R. It effectively mediates the degradation of mutant EGFRs via both ubiquitin/proteasome system (UPS) and autophagy/lysosome pathways, and robustly suppresses the proliferation of NSCLC cells, indicating its potential utility in anticancer research [1].

    价 格：￥电议型 号：T74635产 地：中国大陆

  • T74632TP0556351；化合物 TP0556351TP0556351

    TP0556351, a potent and selective inhibitor of matrix metalloproteinase-2 (MMP2), exhibits significant efficacy with an IC50 of 0.2 nM and demonstrates the capability to decrease collagen accumulation in a Bleomycin-induced pulmonary fibrosis mouse model. This compound shows promise as a research tool for idiopathic pulmonary fibrosis (IPF) [1].

    价 格：￥电议型 号：T74632产 地：中国大陆

  • T73635γ-Glu-Phe TFA；γ-Glu-Phe TFAγ-Glu-Phe TFA

    γ-Glu-Phe TFA (γ-Glutamylphenylalanine TFA) is synthesized by Bacillus amyloliquefaciens (GBA) and Aspergillus oryzae (GAO). γ-Glu-Phe TFA or the post-enzymatic reaction mixture enhances the umami intensity of commercial soy sauce and model chicken broth [1] .

    价 格：￥电议型 号：T73635产 地：中国大陆

  • T72635AMPD2 inhibitor 2；化合物 AMPD2 inhibitor 2AMPD2 inhibitor 2

    AMPD2 Inhibitor 2 is a potent inhibitor of AMP deaminase 2 (AMPD2), demonstrating inhibitory concentration 50 (IC50) values of 0.1 μM for human AMPD2 (hAMPD2) and 0.28 μM for mouse AMPD2 (mAMPD2). This compound is valuable for research into the physiological roles of AMPD2, especially in mice on a high-fat diet.

    价 格：￥电议型 号：T72635产 地：中国大陆

  • T71635Murayaquinone；化合物 MurayaquinoneMurayaquinone

    Murayaquinone is a hepatitis C virus proteinase inhibitor and small molecule antagonist of the oncogenic Tcf/β-catenin protein complex.

    价 格：￥电议型 号：T71635产 地：中国大陆

  • T71294BMS-763534；化合物 BMS-763534BMS-763534

    BMS-763534 is a potent antagonist of corticotropin-releasing factor/hormone receptor 1 (CRHR-1).

    价 格：￥电议型 号：T71294产 地：中国大陆

  • T70943AM-9635；化合物 AM-9635AM-9635

    AM-9635 is a potent and selective PI3Kδ inhibitor. AM-9635 showes good cellular potency (in vitro pAKT IC50 = 4.2 nM ). AM-96352 inhibits KLH-specific IgG and IgM in a dosedependent manner AM-9635 is well tolerated at all doses and exhibits significantly reduced IgG and IgM specific antibodies . PI3Kα and PI3Kβ are ubiquitously expressed and play a role in cell growth, division, and survival.

    价 格：￥电议型 号：T70943产 地：中国大陆

  • T70635ELND007；化合物 ELND007ELND007

    ELND007 is a Gamma secretase inhibitor.

    价 格：￥电议型 号：T70635产 地：中国大陆

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