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Results for "

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" in TargetMol Product Catalog.
  • Inhibitors & Agonists
    1465
    TargetMol | All_Pathways
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    15
    TargetMol | Compound_Libraries
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    58
    TargetMol | Peptide_Products
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    TargetMol | Inhibitory_Antibodies
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    TargetMol | All_Dye_Reagents
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    TargetMol | PROTAC
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    TargetMol | Recombinant_Protein
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    TargetMol | Isotope_Products
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    133
    TargetMol | Antibody_Products
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    TargetMol | Disease_Modeling_Products
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    123
    TargetMol | Cell_Research_Reagents
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    58
    TargetMol | Standard_Products
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    TargetMol | All_Pathways
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    15
    TargetMol | All_Pathways
  • AG-270
    T90502201056-66-6In house
    AG-270 is an allosteric and orally active inhibitor of MAT2A.
    • $112
    In Stock
    Size
    QTY
  • JNJ-5207852
    T7413398473-34-2
    JNJ-5207852 is a novel, non-imidazole histamine H3 receptor antagonist, with high affinity at the rat (pKi=8.9) and human (pKi=9.24) H3 receptor.
    • $30
    In Stock
    Size
    QTY
    TargetMol | Inhibitor Sale
  • JNJ-5207852 dihydrochloride
    T88221782228-76-5
    JNJ-5207852 dihydrochloride is a novel, non-imidazole histamine H3 receptor antagonist, with high affinity at the rat (pKi=8.9) and human (pKi=9.24) H3 receptor.
    • $30
    In Stock
    Size
    QTY
    TargetMol | Inhibitor Sale
  • BMS-1001 hydrochloride
    T105652113650-04-5
    BMS-1001 hydrochloride is an orally active inhibitor of human PD-1/PD-L1 immune checkpoint with low-toxicity in cells.BMS-1001 alleviates the inhibitory effect of the soluble PD-L1 on the T-cell receptor-mediated activation of T-lymphocytes. BMS-1001 is capable of alleviating the PD-1/PD-L1 immune checkpoint-mediated exhaustion of Jurkat T-lymphocytes.
    • $51
    In Stock
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  • (R)-Terazosin
    T12643109351-34-0
    (R)-Terazosin is an active R-enantiomer of Terazosin and a potent antagonist of α1-adrenoceptor [(α1a, α1b, and α1d-adrenoceptor] with Ki values of 6.51 nM, 1.01 nM, and 1.97 nM, respectively).
    • $39
    In Stock
    Size
    QTY
  • UC-514321
    T13950299420-83-0
    UC-514321 directly targets STAT3/5 and represses TET1 expression. UC-514321 has the potential to treat acute myeloid leukemia (AML) both in vitro and in vivo, with low toxicity.
    • $68
    In Stock
    Size
    QTY
  • ZL0580
    T139742377151-10-3
    ZL0580 induces HIV suppression by inhibiting Tat transactivation and transcription elongation as well as by inducing repressive chromatin structure at the HIV promoter.
    • $34
    In Stock
    Size
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    TargetMol | Citations Cited
  • CDKI-73
    T149191421693-22-2
    CDKI-73 is a potent CDK9 inhibitor (Ki: 4 nM). It shows selective toxicity to CLL cells(LD50=80 nM) versus normal B cell and normal CD34+ cell(LD50>20 uM).The inhibition of CDK9 induces apoptosis and potentiates the effect of cisplatin.
    • $146
    In Stock
    Size
    QTY
  • Andarine
    S-4, GTx-007
    T2108401900-40-1
    Andarine (GTx-007) (S-4) is an active partial agonist and an investigational selective androgen receptor modulator (SARM).
    • $40
    In Stock
    Size
    QTY
  • COTI-2
    COTI2, COTI 2
    T43251039455-84-9
    COTI-2, an orally available thiosemicarbazone, is an activator of mutant forms of the p53 protein with potential antineoplastic activity.
    • $38
    In Stock
    Size
    QTY
    TargetMol | Citations Cited
  • Pseudoprotodioscin
    T5S0246102115-79-7
    1. Pseudoprotodioscin has moderate cytotoxicity.
    • $35
    In Stock
    Size
    QTY
  • Clevudine
    L-FMAU, Levovir
    T6446163252-36-6
    Clevudine (Levovir) is a synthetic pyrimidine analogue with activity against hepatitis B virus (HBV). Intracellularly, clevudine is phosphorylated to its active metabolites, clevudine monophosphate and triphosphate. The triphosphate metabolite competes with thymidine for incorporation into viral DNA, thereby causing DNA chain termination and inhibiting the function of HBV DNA polymerase (reverse transcriptase). Clevudine has a long half-life and shows significant reduction of covalently closed circular DNA (cccDNA), therefore the patient is less likely to have a relapse after treatment is discontinued.
    • $37
    In Stock
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  • DCLK1-IN-1
    T84182222635-15-4
    DCLK1-IN-1 is a selective, in vivo compatible chemical probe of the kinase domain of doublecortin-like kinase 1 (DCLK1) and a highly selective DCLK1/2 inhibitor with IC50 values ​​of 9.5/57.2 nM (DCLK1) and 31/103 nM (DCLK2) by binding and kinase assays, respectively. It has low toxicity and is used to study DCLK1 biology and determine its role in cancer.
    • $98
    In Stock
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  • URB937
    T86461357160-72-5
    URB937 is an inhibitor of FAAH and increases anandamide levels(IC50 : 26.8 nM).
    • $42
    In Stock
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  • ACH-000143
    T91932225836-30-4
    ACH-000143 have been identified as a novel agonist of the melatonin receptors MT1 and MT2.
    • $48
    In Stock
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    QTY
  • TP0586532
    T93182427584-96-9
    TP0586532 is effective against carbapenem-resistant Klebsiella pneumoniae and does not pose a cardiovascular risk.
      Inquiry
    • MRTX9768
      T95752629314-68-5
      MRTX-9768 is a synthetic lethal-based inhibitor designed to bind the PRMT5-MTA complex and selectively target MTAP/CDKN2A-deleted tumors.
      • $203
      In Stock
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      TargetMol | Citations Cited
    • Agarose,Low melting point
      TN76219012-36-6
      Agarose (Low melting point) is a type of agarose, a polysaccharide derived from seaweed, commonly used in molecular biology and biochemistry for isolating and purifying DNA and RNA fragments. This low melting point agarose is suitable for recovering large DNA fragments and enzymatic reactions in gels, as well as for applications in pulsed field gel electrophoresis and capillary electrophoresis for genetic material analysis.
      • Inquiry Price
      Inquiry
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    • Oxidized low density lipoprotein (Human)
      Human ox-LDL
      T200276
      Oxidized low density lipoprotein (Human) (Human ox-LDL) is the oxidized form of human low-density lipoprotein (LDL), used to study lipid transport and atherosclerosis. Human ox-LDL stimulates endothelial cell activation and adhesion molecule production, inhibits eNOS activity and NO generation, and activates NLRP3 inflammasomes in macrophages.
      • Inquiry Price
      1-2 weeks
      Size
      QTY
    • Poly(guluronate) (low endotoxin)
      TCL-00394
      Poly(guluronate), low endotoxin, represents the segment of the Alginate molecule responsible for its gelling properties, featuring ionic cross-linking.
      • Inquiry Price
      Inquiry
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    • Ovalbumin (low endotoxin)
      9006-59-1
      TRP-00183
      Ovalbumin (low endotoxin) is a major egg white protein, processed to contain low endotoxin levels, used as a model antigen in immunological research to study allergic reactions or vaccines, and can also be used to construct asthma models.
      • $236
      In Stock
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    • Low density lipoprotein (human)
      Low density lipoprotein (human), Human LDL
      TRP-00198
      Low-density lipoprotein (human) is one of the five main lipoproteins responsible for transporting cholesterol to various tissues such as the adrenal glands, gonads, muscle, and adipose tissue.
      • Inquiry Price
      Inquiry
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      QTY
    • Oxidized low density lipoprotein (mouse)
      Oxidized low density lipoprotein (mouse), Mouse ox-LDL
      TRP-00230
      Oxidized low density lipoprotein (mouse) is a modified form of low-density lipoprotein (LDL). It induces atherosclerosis (AS) by promoting endothelial dysfunction and accelerating the growth and migration of vascular smooth muscle cells (VSMCs).
      • Inquiry Price
      Inquiry
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    • Chitosan (≥90% deacetylated, Low viscosity,<200mPa.s)
      Poly(D-glucosamine) (≥90% deacetylated, Low viscosity,<200mPa.s), Deacetylated chitin (≥90% deacetylated, Low viscosity,<200mPa.s)
      TSW-01158
      Chitosan (Deacetylated chitin) is a biochemical reagent that serves as a biomaterial or organic compound, useful in life science research.
      • Inquiry Price
      Inquiry
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