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  • Inhibitors & Agonists
    10
    TargetMol | Inhibitors_Agonists
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Gabexate mesylate
FOY
T037256974-61-9
Gabexate mesylate (FOY) is a serine proteinase inhibitor used therapeutically in the treatment of pancreatitis, disseminated intravascular coagulation (DIC), and as a regional anticoagulant for hemodialysis. The drug inhibits the hydrolytic effects of thrombin, plasmin, and kallikrein, but not of chymotrypsin and aprotinin.
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Metacetamol
3-Acetamidophenol
T0914621-42-1
Metacetamol (3-Acetamidophenol) is a derivative of acetaminophen, a non-toxic regional isomer of acetaminophen. It is an over-the-counter analgesic and antipyretic and is also used as an organic synthesis intermediate.
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Neridronate
T1379479778-41-9
Neridronate is an aminodiphosphate that is commonly used in diseases associated with disorders of bone metabolism and complex regional pain syndromes (CRPS) such as osteogenesis imperfecta (OI) and Paget's disease of bone (PDB).
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7-10 days
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Mepivacaine hydrochloride
Mepivacaine HCl
T09461722-62-9
Mepivacaine hydrochloride (Mepivacaine HCl) is the hydrochloride salt form of mepivacaine, an amide derivative with local anesthetic properties.
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Dopexamine hydrochloride
FPL60278AR
T1131886484-91-5
Dopexamine hydrochloride (FPL60278AR) is a β2-adrenergic receptor agonist. Dopexamine can attenuate the inflammatory response and protect against organ injury in the absence of significant effects on hemodynamics or regional microvascular flow.
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Fostedil
KB-944,KB944,A 53986,KB 944,A-53986,BRN 3626546
T2735175889-62-2
Fostedil is a calcium channel antagonist. KB-944 increased regional segment function in normal and ischemic regions and maintained distal coronary artery perfusion pressure, coronary flow and transmural regional myocardial blood flow during partial corona
    6-8 weeks
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    Adrenomedullin (22-52) (human) (trifluoroacetate salt)
    T35858
    Adrenomedullin (22-52) is a C-terminal fragment of adrenomedullin (1-52) . In vitro, adrenomedullin (22-52) reduces basal corticosterone production in a mixture of rat adrenocortical and adrenomedulllary cells. It also reverses increases in ACTH-stimulated corticosterone production induced by adrenomedullin (1-52). Adrenomedulin (22-52) (0.5 and 5 μg/kg/min) has no effect on basal regional cerebral blood flow but reverses increases in regional cerebral blood flow induced by rat adrenomedullin in rats. Unlike adrenomedullin (1-52), adrenomedullin (22-52) has no effect on mesenteric arterial perfusion pressure in cats.
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    Antitumor agent-74
    T62509
    Antitumor agent-74 is a quinazoline derivative and an antitumour agent. antitumor agent-74 in combination with the regional tautomer Antitumor agent-75 (compound 14 da) (mriBIQ 13da 14da) exhibits enhanced tumour inhibition. In particular, mriBIQ 13da 14da inhibits DNA synthesis, arrests the cell cycle in S phase and induces mitochondrial apoptosis.
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    10-14 weeks
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    Spinosin
    Flavoayamenin
    T6S222772063-39-9
    1. Spinosin (Flavoayamenin) ameliorated memory impairment induced through AβO, the serotonergic neurotransmitter system, and these effects were regulated, in part, through neuroprotective activity via the anti-inflammatory effects of Spinosin. 2. Spinosin exerts anxiolytic-like effects, and its mechanism of action appears to be modulated by GABAA and 5-HT1A receptors. 3. There was a wide brain regional tissue distribution of Spinosin. The concentrations of Spinosin in corpus striatum and hippocampus were higher than that in other areas.
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    Proadrenomedullin (45-92), human
    TP1488166798-69-2
    Proadrenomedullin (45-92), human, a mid-regional fragment of proadrenomedullin (MR-proADM), consists of amino acids 45–92 of pre-proADM.
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