Clofoctol

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Clofoctol
Clinical data
AHFS/Drugs.com	International Drug Names
Routes of; administration	Rectal (suppository)
ATC code	J01XX03 (WHO) ;
Pharmacokinetic data
Bioavailability	98%
Metabolism	Hepatic glucuronidation
Excretion	Biliary
Identifiers
	IUPAC name 2-[(2,4-dichlorophenyl)methyl]-; 4-(2,4,4-trimethylpentan-2-yl)phenol;
CAS Number	37693-01-9 ;
PubChem CID	2799;
ChemSpider	2697 ;
UNII	704083NI0R;
KEGG	D07244 ;
ChEMBL	ChEMBL1476605;
E number	{{#property:P628}}
ECHA InfoCard	{{#property:P2566}}Lua error in Module:EditAtWikidata at line 36: attempt to index field 'wikibase' (a nil value).
Chemical and physical data
Formula	C21H26Cl2O
Molar mass	365.336 g/mol
3D model (JSmol)	Interactive image;
	SMILES Clc1cc(Cl)ccc1Cc2cc(ccc2O)C(C)(C)CC(C)(C)C;
	InChI InChI=1S/C21H26Cl2O/c1-20(2,3)13-21(4,5)16-7-9-19(24)15(11-16)10-14-6-8-17(22)12-18(14)23/h6-9,11-12,24H,10,13H2,1-5H3 ; Key:HQVZOORKDNCGCK-UHFFFAOYSA-N ;
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Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]

Overview

Clofoctol is a bacteriostatic antibiotic. It is used in the treatment of respiratory tract and ear, nose and throat infections caused by Gram-positive bacteria.^[1] It is marketed in France under the trade name Octoplus and in Italy as Gramplus.

It is only functional against Gram-positive bacteria.^[2]

It penetrates into human lung tissue.^[3]

References

↑ ^1.0 ^1.1 ^1.2 ^1.3 ^1.4 "Gramplus" (in Italian). Studio Medico Torrino. July 25, 2007. Retrieved 2007-08-10.
↑ Combe J, Simonnet F, Yablonsky F, Simonnet G (1980). "[Clofoctol binding by the bacteria (author's transl)]". J Pharmacol (in French). 11 (4): 411–25. PMID 6782374.
↑ Danesi R, Gasperini M, Senesi S, Freer G, Angeletti CA, Del Tacca M (1988). "A pharmacokinetic study of clofoctol in human plasma and lung tissue by using a microbiological assay". Drugs Exp Clin Res. 14 (1): 39–43. PMID 3391105.

Template:Antibiotic-stub Template:Other antibacterials

[Gramplus-1] 1.0 ^1.1 ^1.2 ^1.3 ^1.4 "Gramplus" (in Italian). Studio Medico Torrino. July 25, 2007. Retrieved 2007-08-10.

[pmid6782374-2] Combe J, Simonnet F, Yablonsky F, Simonnet G (1980). "[Clofoctol binding by the bacteria (author's transl)]". J Pharmacol (in French). 11 (4): 411–25. PMID 6782374.

[pmid3391105-3] Danesi R, Gasperini M, Senesi S, Freer G, Angeletti CA, Del Tacca M (1988). "A pharmacokinetic study of clofoctol in human plasma and lung tissue by using a microbiological assay". Drugs Exp Clin Res. 14 (1): 39–43. PMID 3391105.

[1]

[2]

[3]

Clinical data

AHFS/Drugs.com	International Drug Names
Routes of administration	Rectal (suppository)^[1]
ATC code	J01XX03 (WHO)
Pharmacokinetic data
Bioavailability	98%^[1]
Metabolism	Hepatic glucuronidation^[1]
Excretion	Biliary^[1]
Identifiers
IUPAC name 2-[(2,4-dichlorophenyl)methyl]- 4-(2,4,4-trimethylpentan-2-yl)phenol
CAS Number	37693-01-9^Y
PubChem CID	2799
ChemSpider	2697^Y
UNII	704083NI0R
KEGG	D07244^Y
ChEMBL	ChEMBL1476605
E number	{{#property:P628}}
ECHA InfoCard	{{#property:P2566}}Lua error in Module:EditAtWikidata at line 36: attempt to index field 'wikibase' (a nil value).
Chemical and physical data
Formula	C₂₁H₂₆Cl₂O
Molar mass	365.336 g/mol
3D model (JSmol)	Interactive image
SMILES Clc1cc(Cl)ccc1Cc2cc(ccc2O)C(C)(C)CC(C)(C)C
InChI InChI=1S/C21H26Cl2O/c1-20(2,3)13-21(4,5)16-7-9-19(24)15(11-16)10-14-6-8-17(22)12-18(14)23/h6-9,11-12,24H,10,13H2,1-5H3^Y Key:HQVZOORKDNCGCK-UHFFFAOYSA-N^Y
(verify)

Clofoctol

Overview

References

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