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doam

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  • Inhibitors & Agonists
    9
    TargetMol | Inhibitors_Agonists
DOAM
T20336463779-90-8
DOAM is an antagonist of the 5-HT2 receptor.
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Phthalimidoamlodipine
Amlodipine besilate impurity A, (+ -)-Phthalimidoamlodipine, Phthaloylamlodipine
T2126488150-62-3
Phthalimidoamlodipine is an impurity of Amlodipine, a medication used to prevent chest pain and lower blood pressure.
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7-10 days
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KDOAM-25 trihydrochloride (2230731-99-2 free base)
KDOAM-25 trihydrochloride
T11750L
KDOAM-25 trihydrochloride increases global H3K4 methylation at transcriptional start sites and impairs proliferation in multiple myeloma MM1S cells. KDOAM-25 trihydrochloride is a potent and highly selective histone lysine demethylases 5 (KDM5) inhibitor
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10-14 weeks
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KDOAM-25 citrate
T117502448475-08-7
KDOAM-25 citrate is a potent and highly selective histone lysine demethylases 5 (KDM5) inhibitor, with IC50 values of 71 nM, 19 nM, 69 nM, and 69 nM for KDM5A, KDM5B, KDM5C, and KDM5D, respectively. Multiple myeloma MM1S cells treated with KDOAM-25 citrate show increased global H3K4 methylation at transcriptional start sites and impaired proliferation [1].
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10-14 weeks
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KDOAM-25
T117512230731-99-2
KDOAM-25, a potent and highly selective inhibitor of histone lysine demethylases 5 (KDM5) with IC50 values of 71 nM for KDM5A, 19 nM for KDM5B, 69 nM for KDM5C, and 69 nM for KDM5D, enhances global H3K4 methylation at transcriptional start sites and reduces proliferation in multiple myeloma MM1S cells.
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6-8 weeks
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6-Iodoamiloride
T7924660398-23-4
6-Iodoamiloride is a potent inhibitor of acid-sensing ion channel 1 (ASIC1), exhibiting an IC50 value of 88 nM. It also effectively inhibits ASIC3-mediated currents in rat dorsal root ganglion neurons, with an IC50 of 230 nM [1].
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8-10 weeks
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Deiodoamiodarone
Dideiodo Amiodarone
T2530123551-25-9
Deiodoamiodarone is an intermediate of amiodarone. Amiodarone is an α β-adrenergic receptor antagonist and coronary vasodilator.
    7-10 days
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    KDOAM-25 trihydrochloride
    T62166
    KDOAM-25 trihydrochloride is a potent and highly selective inhibitor of histone lysine demethylase 5 (KDM5), targeting KDM5A (IC50: 71 nM), KDM5B (IC50: 19 nM), KDM5C (IC50: 69 nM), and KDM5D (IC50: 69 nM). It enhances overall H3K4 methylation at the transcription start site and hinders the proliferation of multiple myeloma [MM1S cells].
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    10-14 weeks
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    4-Iodoamphetamine hydrochloride
    p-Iodoamphetamine hydrochloride
    T20366621894-58-6
    4-Iodoamphetamine (p-Iodoamphetamine) hydrochloride is a halogenated phenethylamine characterized by the presence of an iodine atom at the para position of the phenyl group. It selectively induces serotonin release and inhibits reuptake in rat brain synaptosomes.
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