Clonixin
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Clonixin
structure -
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CAS No:
17737-65-4
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Formula:
C13H11ClN2O2
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Chemical Name:
Clonixin
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Synonyms:
3-Pyridinecarboxylic acid,2-[(3-chloro-2-methylphenyl)amino]-;Nicotinic acid,2-(3-chloro-o-toluidino)-;2-[(3-Chloro-2-methylphenyl)amino]-3-pyridinecarboxylic acid;2-(3-Chloro-2-methylanilino)nicotinic acid;Clonixin;Chlonixin;2-(2-Methyl-3-chloroanilino)nicotinic acid;2-(2′-Methyl-3′-chloro)-anilinonicotinic acid;Sch 10304;Clonixic acid;Clonixine;2-(3-Chloro-2-methylanilino)-3-pyridinecarboxylic acid;CBA 93626;NSC 335505
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CAS No:
Description
ChEBI: A pyridinemonocarboxylic acid that is nicotinic acid substituted at position 2 by a (2-methyl-3-chlorophenyl)amino group. Used (as its lysine salt) for treatment of renal colic, muscular pain and moderately severe migraine attacks.
Clonixin is a pyridinemonocarboxylic acid that is nicotinic acid substituted at position 2 by a (2-methyl-3-chlorophenyl)amino group. Used (as its lysine salt) for treatment of renal colic, muscular pain and moderately severe migraine attacks. It has a role as a non-steroidal anti-inflammatory drug, a non-narcotic analgesic, an antipyretic, a platelet aggregation inhibitor, a vasodilator agent, an EC 1.14.99.1 (prostaglandin-endoperoxide synthase) inhibitor and a lipoxygenase inhibitor. It is a pyridinemonocarboxylic acid, an aminopyridine and an organochlorine compound. It derives from a nicotinic acid. It is a conjugate acid of a clonixin(1-).|Clonixin is a non-steroidal anti-inflammatory drug.|Anti-inflammatory analgesic.
Characteristics
62.2
3.8
white to beige
1.3230 (rough estimate)
234 °C
410.2±45.0 °C(Predicted)
201.9±28.7 °C
1.5270 (estimate)
DMSO: soluble15mg/mL, clear
room temp
1.83E-07mmHg at 25°C
LD50 in male mice, rats (mg/kg): 415, 335 orally; 198, 148 i.p.; 296, 325 s.c. (Tanaka)
Safety Information
NONH for all modes of transport
3
20/21/22
36/37
QT0960000
Xn
P261, P264, P270, P271, P280, P301+P312, P302+P352, P304+P312, P304+P340, P312, P322, P330, P363, P501
H302
|Warning|H302 (100%): Harmful if swallowed [Warning Acute toxicity, oral]|P261, P264, P270, P271, P280, P301+P312, P302+P352, P304+P312, P304+P340, P312, P322, P330, P363, and P501|Aggregated GHS information provided by 47 companies from 3 notifications to the ECHA C&L Inventory. Each notification may be associated with multiple companies.
Drug Information
Indicated for use in the management of chronic arthritic conditions and certain soft tissue disorders associated with pain and inflammation.
Clonixin is a non-steroidal anti-inflammatory drug (NSAID) similar in structure to [DB00586]. It produces vasodilation and analgesia.
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.)
The mechanism of clonixin does not appear to have been investigated on a molecular level. It is presumed to function similarly to other NSAIDs by inhibiting cycloxygenase enzymes 1 and 2 resulting in a reduction in prostaglandin production.
CBA 93626
Computed Properties
Molecular Weight:262.69
XLogP3:3.8
Hydrogen Bond Donor Count:2
Hydrogen Bond Acceptor Count:4
Rotatable Bond Count:3
Exact Mass:262.0509053
Monoisotopic Mass:262.0509053
Topological Polar Surface Area:62.2
Heavy Atom Count:18
Complexity:301
Covalently-Bonded Unit Count:1
Compound Is Canonicalized:Yes
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