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  • T76332Biotinyl-Glucagon (1-29), human, bovine, porcine；化合物 Biotinyl-Glucagon (1-29), human, bovine, porcin

    Biotinyl-Glucagon (1-29), encompassing human, bovine, and porcine versions, is a biotinylated form of glucagon. This peptide hormone, synthesized by the pancreas´s α-cells, elevates glucose and fatty acid levels in the bloodstream [1] [2].

    价 格：￥电议型 号：T76332产 地：中国大陆

  • T7598Calcium N5-methyltetrahydrofolate；N5-甲基四氢叶酸钙NSC173328；5-甲基四氢叶酸钙|||N5-甲基四氢叶酸钙|||NSC173328

    Calcium N5-methyltetrahydrofolate (NSC-173328) is the calcium salt of levomefolic acid, which has been proposed for treatment of cardiovascular disease and advanced cancers such as breast and colorectal cancers

    价 格：￥电议型 号：T7598产 地：中国大陆

  • T753327-Hydroxy-4-methyl-2(1H)-quinolone；化合物 7-Hydroxy-4-methyl-2(1H)-quinolone7-Hydroxy-4-methyl-2(1H)-qu

    7-Hydroxy-4-methyl-2(1H)-quinolone (compound 2b), a fluorescent hydroxylated derivative, serves as a probe for detecting hydroxyl radicals associated with DNA damage [1]. For preservation, it should be protected from light.

    价 格：￥电议型 号：T75332产 地：中国大陆

  • T74332Rifasutenizol；化合物 RifasutenizolRifasutenizol

    Rifasutenizol (TNP-2198) is an orally bioavailable, dual-targeted antibacterial agent with potent effectiveness against both microaerophilic and anaerobic bacterial pathogens [1].

    价 格：￥电议型 号：T74332产 地：中国大陆

  • T73332BI-685509；化合物 BI-685509BI-685509

    BI-685509 is a potent and orally active sGC activator. BI-685509 restores cyclic guanosine monophosphate (cGMP) and improves functionality of nitric oxide (NO) pathways. BI-685509 can be used in research of chronic kidney disease (CKD) and diabetic kidney disease (DKD) [1] .

    价 格：￥电议型 号：T73332产 地：中国大陆

  • T73329MMV676584；化合物 MMV676584MMV676584

    MMV676584 has anti-tuberculosis avtivity. MMV676584 is a novel drug candidate for eumycetoma [1] .

    价 格：￥电议型 号：T73329产 地：中国大陆

  • T73328LP 218；化合物 P 218P 218

    P 218 is a novel DHFR inhibitor with antimalarial activity and antifolate effects and can be used to study Buruli ulcer.

    价 格：￥电议型 号：T73328L产 地：中国大陆

  • T73328DHFR-IN-5；化合物 DHFR-IN-5DHFR-IN-5

    DHFR-IN-5, an orally active and potent inhibitor of dihydrofolate reductase (DHFR), exhibits a K_i value of 0.54 nM against the quadruple mutant Plasmodium falciparum DHFR, demonstrating anti-malarial activity.

    价 格：￥电议型 号：T73328产 地：中国大陆

  • T73327Merigolix；化合物 MerigolixMerigolix

    Merigolix is a potent gonadotrophin releasing hormone (GnRH) antagonist [1] .

    价 格：￥电议型 号：T73327产 地：中国大陆

  • T73326CB2R-IN-3；化合物 CB2R-IN-3CB2R-IN-3

    CB2R-IN-3 is a selective antagonist of cannabinoid type 2 receptor (CB2R) . CB2R-IN-3 has high affinity for human CB2R and specific selectivity for CB1R. CB2R-IN-3 can be combined with CB65 , the activator of CB2R. CB2R-IN-3 effectively up-regulates the expression of anti-inflammatory cytokines and down-regulates the expression of pro-inflammatory cytokines [1] .

    价 格：￥电议型 号：T73326产 地：中国大陆

  • T73325MenA-IN-1；化合物 MenA-IN-1MenA-IN-1

    MenA IN-1, a potent inhibitor of 1,4-dihydroxy-2-naphthoate isoprenyltransferase (MenA) from Mycobacterium tuberculosis (MTB), exhibits an IC50 value of 13 ?M and a GIC50 value of 8 ?M, suggesting its potential utility in halting the ongoing proliferation of tuberculosis.

    价 格：￥电议型 号：T73325产 地：中国大陆

  • T73324PARL-IN-1；化合物 PARL-IN-1PARL-IN-1

    PARL-IN-1, a potent PARL inhibitor, exhibits an IC50 value of 28 nM. It effectively inhibits PARL, consequently robustly activating the PINK1/Parkin pathway and promoting PINK1/Parkin-dependent mitophagy.

    价 格：￥电议型 号：T73324产 地：中国大陆

  • T73323RdRP-IN-5；化合物 RdRP-IN-5RdRP-IN-5

    RdRP-IN-5 (compound 20), a potent inhibitor of the influenza virus RNA-dependent RNA polymerase (RdRP), has potential application in influenza research [1].

    价 格：￥电议型 号：T73323产 地：中国大陆

  • T73322TBK1-IN-1；TBK1 抑制剂 1TBK1-IN-1

    TBK1-IN-1 is a specific and potent TANK-binding kinase 1 (TBK1) inhibitor (IC50: 22.4 nM) with anticancer activity.TBK1-IN-1 inhibits the expression of TBK1 downstream target genes, cxcl10 and ifnβ.

    价 格：￥电议型 号：T73322产 地：中国大陆

  • T73321CLK1-IN-2；化合物 CLK1-IN-2CLK1-IN-2

    CLK1-IN-2, a metabolically stable Clk1 inhibitor, exhibits selective activity for Clk1 with an IC50 value of 1.7 nM. It is applicable in researching tumor, Duchenne´s muscular dystrophy, and viral infections including HIV-1 and influenza.

    价 格：￥电议型 号：T73321产 地：中国大陆

  • T7332(E)-2-Decenoic acid；反式-2-癸烯酸trans-2-Decenoic acid；trans-2-Decenoic acid|||反式-2-癸烯酸

    (E)-2-Decenoic acid (trans-2-Decenoic acid) is an unsaturated fatty acid found in royal jelly produced from the hypopharyngeal and mandibular gland secretions of honeybees.

    价 格：￥电议型 号：T7332产 地：中国大陆

  • T73225OTS193320；化合物 OTS193320OTS193320

    OTS193320, an imidazopyridine compound, acts as an inhibitor of SUV39H2 methyltransferase activity. It effectively reduces global histone H3 lysine 9 tri-methylation levels in breast cancer cells, promoting apoptotic cell death. When combined with Doxorubicin (DOX; HY-15142A), OTS193320 enhances the reduction of γ-H2AX levels and decreases cancer cell viability more significantly than when either agent is used alone.

    价 格：￥电议型 号：T73225产 地：中国大陆

  • T72507Palbociclib orotate；化合物 Palbociclib orotatePD 0332991 orotate；PD 0332991 orotate

    Palbociclib (PD 0332991) orotate, an orally active selective inhibitor of CDK4 and CDK6, exhibits IC50 values of 11 and 16 nM, respectively. This compound demonstrates potent anti-proliferative effects and induces cell cycle arrest in cancer cells, applicable in research concerning HR-positive, HER2-negative breast cancer, and hepatocellular carcinoma [1] [3] [4].

    价 格：￥电议型 号：T72507产 地：中国大陆

  • T72247Ladostigil hydrochloride；化合物 Ladostigil hydrochlorideTV-3326 hydrochloride；TV-3326 hydrochloride

    Ladostigil hydrochloride (TV-3326), an orally active compound, acts as a dual inhibitor targeting both cholinesterase and brain-selective monoamine oxidase (MAO), demonstrating inhibition constants (IC50s) of 31.8 μM for acetylcholinesterase (AChE) and 37.1 μM for MAO-B. This compound exhibits neuroprotective, antioxidant, and anti-inflammatory properties, making it useful for research into depression and Alzheimer´s disease.

    价 格：￥电议型 号：T72247产 地：中国大陆

  • T71332NRC-2694 hydrochloride；化合物 NRC-2694 hydrochlorideNRC-2694 hydrochloride

    NRC-2694 hydrochloride is an epidermal growth factor receptor (EGFR) antagonist potentially for the treatment of solid tumors.

    价 格：￥电议型 号：T71332产 地：中国大陆

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