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Results for "

indazole

" in TargetMol Product Catalog
  • Inhibitors & Agonists
    29
    TargetMol | Inhibitors_Agonists
  • Recombinant Protein
    1
    TargetMol | Recombinant_Protein
Indazole
T2192271-44-3
Indazole is also called benzpyrazole or isoindazone. Its derivatives exhibit a wide range of biological activities. Indazole and its derivatives can be used in the research of cancer, neurological diseases, cardiovascular diseases, and gastrointestinal diseases.
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Indazole-Cl
Indazole Cl
T25534848142-62-1In house
Indazole-Cl is a selective ERß agonist and a selective estrogen receptor modifier (SERM).
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6-8 weeks
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2-Methyl-2H-indazole-3-carboxylic acid
Fr2126534252-44-3
2-Methyl-2H-indazole-3-carboxylic acid can be used as a potentially active molecular skeleton for the design and synthesis of biologically active compounds.
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7-10 days
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TargetMol | Inhibitor Sale
1-(4-Fluorobenzyl)-1H-indazole-3-carboxylic acid
T20314750264-63-6
1-(4-Fluorobenzyl)-1H-indazole-3-carboxylic acid (Compound 31) is a metabolite of AB-FUBINACA. It acts as an MRGPRX4 antagonist with an IC50 greater than 2.5 μM.
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4-Bromo-1H-indazole
TYD-00071186407-74-9
4-Bromo-1H-indazole is a biochemical reagent that can be used as a biomaterial for life science related research and as a sulfonylation reagent for organic synthesis and drug discovery.
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7-10 days
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Indazole-3-carboxylic acid
TYD-001424498-67-3
Indazole-3-carboxylic acid is a biochemical reagent that can be used as a biomaterial for life science related research and as a sulfonylation reagent for organic synthesis and drug discovery.
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7-10 days
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6-Bromo-1H-indazole
TYD-0039479762-54-2
6-Bromo-1H-indazole is a biochemical reagent that can be used as a biomaterial for life science related research and as a sulfonylation reagent for organic synthesis and drug discovery.
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7-10 days
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5-Amino-1H-indazole
TYD-0046819335-11-6
5-Amino-1H-indazole is a biochemical reagent that can be used as a biomaterial for life science related research and as a sulfonylation reagent for organic synthesis and drug discovery.
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7-10 days
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3-Bromo-7-nitroindazole
T1010774209-34-0
3-Bromo-7-nitroindazole is a specific neuronal nitric oxide synthase (nNOS) inhibitor that affects the synthesis of the intercellular messenger NO throughout the brain and body.
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4-6 weeks
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TargetMol | Inhibitor Sale
7-Nitroindazole
T74742942-42-9
7-Nitroindazole is a non-selective inhibitor of NOS isoforms in vitro for neuronal nitric oxide synthase showing a 10-fold selectivity for neuronal NOS.
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1-Methylindazole-3-carboxylic acid
T136950890-83-0
1-Methylindazole-3-carboxylic acid is an excellent solvent with a proper boiling point.
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6-Hydroxyindazole
T6713323244-88-4
6-Hydroxyindazole is a useful organic compound for research related to life sciences. The catalog number is T67133 and the CAS number is 23244-88-4.
    7-10 days
    Inquiry
    Suprafenacine
    N'-[(E)-(4-methylphenyl)methylidene]-4,5,6,7-tetrahydro-1H-indazole-3-carbohydrazide
    T288861477482-50-0In house
    Suprafenacine (N'-[(E)-(4-methylphenyl)methylidene]-4,5,6,7-tetrahydro-1H-indazole-3-carbohydrazide) is a cell-permeable microtubule destabilizer that induces cell cycle arrest and apoptosis in G2 M phase. Suprafenacine binds to microtubules and inhibits aggregation at the colchicine junction. Suprafenacine is selective for cancer cells, including drug-resistant cancer cells.
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    Antiviral agent 38
    T643962247932-38-1In house
    2H-Pyrido[2',1':3,4]pyrazino[1,2-b]indazole-3-carboxylic acid, 6-(1, 1-Dimethylethyl)-6, 7-Dihydro-10 -(3-methoxypropoxy)-2-oxo-, (6R)- has antibacterial and antiviral activity and can be used to study Hepatitis B virus.
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    TargetMol | Inhibitor Sale
    Lonidamine
    AF1890, DICA, Diclondazolic Acid
    T023950264-69-2
    Lonidamine (Diclondazolic Acid) is an indazole carboxylic acid derivative, principally inhibiting aerobic glycolytic activity, by its effect on mitochondrially-bound hexokinase (HK).
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    Benzydamine
    T8807642-72-8
    Benzydamine is a benzyl-indazole having analgesic, antipyretic, and anti-inflammatory effects. Benzydamine is used to reduce post-surgical and post-traumatic pain and edema and to promote healing.
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    Glucagon receptor antagonists-5
    T114162200274-63-9
    Glucagon receptor antagonists-5 is an orally bioavailable indazole-based glucagon receptor antagonist (Ki: 32 nM). It has potential for the treatment of type 2 diabetes mellitus (T2DM).
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    6-8 weeks
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    FKK
    T1932278299-79-3
    FKK [N-(heptyloxycarbonylaminosulfonyl)-2-aminobenzamide] is an indazole derivative and a novel bronchodilator.
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    6-8 weeks
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    AB-FUBINACA 3-fluorobenzyl isomer
    T2014861185282-19-2
    AB-FUBINACA 3-fluorobenzyl isomer is a synthetic cannabinoid and an indazole derivative, exhibiting high affinity for central CB1 receptors (Ki= 0.9 nM) and possessing anticonvulsant activity.
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    10-14 weeks
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    APP-FUBINACA
    T2034711185282-03-4
    APP-FUBINACA is a cannabinoid receptor agonist, classified as a phenylalanine amide-based indazole-3-carboxamide derivative. It exhibits neurostimulatory effects.
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    MK-4827 Racemate
    Niraparib Racemate, 2-(4-piperidin-3-ylphenyl)indazole-7-carboxamide
    T229881038915-75-1
    MK-4827 Racemate (Niraparib Racemate) is a selective PARP1 and PARP2 inhibitor with IC50s of 3.8 nM and 2.1 nM, respectively, over 330-fold selectivity for PARP3, V-PARP and Tank1.
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    CHS-111
    CHS 111
    T27013886755-63-1
    CHS-111 is a benzyl indazole compound that inhibits superoxide anion (O(2)(-)) generation and reduces fMLP-stimulated PLD activity (IC(50) 3.9±1.2μM). It inhibits the interaction of PLD1 with ADP-ribosylation factor (Arf) 6 and Ras homology (Rho) A, and reduces the membrane recruitment of RhoA in fMLP-stimulated cells.
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    6-8 weeks
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    PD 114595
    PD-114595,PD114595
    T2831094636-28-9
    PD 114595 is a Benzothiopyrano-indazole cpd. PD 114595 belongs to a class of DNA complexers, PD 114595 has curative properties against murine solid tumor models.
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    8-10 weeks
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    PD 121373
    PD121373,PD-121373
    T28320113457-06-0
    PD 121373 is a Benzothiopyrano-indazole cpd. The benzothiopyranoindazoles are potent inhibitors of nucleic acid synthesis, reducing both DNA and RNA synthesis to the same extent at similar concentrations.
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    8-10 weeks
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