REV5901
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REV5901
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CAS No:
101910-24-1
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Formula:
C22H25NO2
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Chemical Name:
REV5901
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Synonyms:
ALPHA-PENTYL-3-(2-QUINOLINYLMETHOXY)-BENZENEMETHANOL;ALPHA-PENTYL-3-[2-QUINOLINYLMETHOXY]BENZYL ALCOHOL;REV 5901;α-pentyl-3-[2-quinolinylmethoxy]benzyl alcohol;2-[3-(1-Hydroxyhexyl)phenoxymethyl]quinoline;3-[(Quinolin-2-yl)methoxy]-α-pentylbenzenemethanol;PF-5901;RG-5901
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CAS No:
Safety Information
3
36/37/38
26-36
Xi
|Warning|H315 (100%): Causes skin irritation [Warning Skin corrosion/irritation]|P261, P264, P271, P280, P302+P352, P304+P340, P305+P351+P338, P312, P321, P332+P313, P337+P313, P362, P403+P233, P405, and P501|Aggregated GHS information provided by 38 companies from 1 notifications to the ECHA C&L Inventory. Each notification may be associated with multiple companies.
Drug Information
Anti-inflammatory agents that are non-steroidal in nature. In addition to anti-inflammatory actions, they have analgesic, antipyretic, and platelet-inhibitory actions.They act by blocking the synthesis of prostaglandins by inhibiting cyclooxygenase, which converts arachidonic acid to cyclic endoperoxides, precursors of prostaglandins. Inhibition of prostaglandin synthesis accounts for their analgesic, antipyretic, and platelet-inhibitory actions; other mechanisms may contribute to their anti-inflammatory effects. (See all compounds classified as Anti-Inflammatory Agents, Non-Steroidal.)|Drugs or agents which antagonize or impair any mechanism leading to blood platelet aggregation, whether during the phases of activation and shape change or following the dense-granule release reaction and stimulation of the prostaglandin-thromboxane system. (See all compounds classified as Platelet Aggregation Inhibitors.)|Naturally occurring or synthetic substances that inhibit or retard oxidation reactions. They counteract the damaging effects of oxidation in animal tissues. (See all compounds classified as Antioxidants.)|Compounds that bind to and inhibit that enzymatic activity of LIPOXYGENASES. Included under this category are inhibitors that are specific for lipoxygenase subtypes and act to reduce the production of LEUKOTRIENES. (See all compounds classified as Lipoxygenase Inhibitors.)
alpha-pentyl-3-(2-quinolinylmethoxy)benzenemethanol
REV5901 Use and Manufacturing
REV 5901 is an antagonist of cysteinyl-leukotriene receptors with a Ki value of 0.7 μM for guinea pig lung membranes. It is also an inhibitor of rat neutrophil 5-LO with an IC50 value of 0.12 μM.
Computed Properties
Molecular Weight:335.4
XLogP3:5.2
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:8
Exact Mass:335.188529040
Monoisotopic Mass:335.188529040
Topological Polar Surface Area:42.4
Heavy Atom Count:25
Complexity:375
Undefined Atom Stereocenter Count:1
Covalently-Bonded Unit Count:1
Compound Is Canonicalized:Yes