DERMAPROT

DERMAPROT Uses, Dosage, Side Effects, Food Interaction and all others data.

An aromatic ether that is phenol which is substituted at C-5 by a chloro group and at C-2 by a 2,4-dichlorophenoxy group. It is widely used as a preservative and antimicrobial agent in personal care products such as soaps, skin creams, toothpaste and deodorants as well as in household items such as plastic chopping boards, sports equipment and shoes.

Trade Name DERMAPROT
Generic Triclosan
Triclosan Other Names Triclosán, Triclosan, Triclosanum
Type
Formula C12H7Cl3O2
Weight Average: 289.542
Monoisotopic: 287.951162589
Groups Approved, Investigational
Therapeutic Class
Manufacturer
Available Country
Last Updated: September 19, 2023 at 7:00 am
DERMAPROT
DERMAPROT

Uses

DERMAPROT is an antimicrobial agent in clinical setting for disinfection, and prevention of spread and growth of bacteria, fungus, and mildew.

DERMAPROT is used in a variety of common household products, including soaps, mouthwashes, dish detergents, toothpastes, deodorants, and hand sanitizers. It is also used in health care settings in surgical scrubs and personnel hand washes.

DERMAPROT is also used to associated treatment for these conditions: Acne, Dental Cavity, Dermabrasion, Gingivitis, Oral Infection, Plaque, Dental, Skin Infections, Bacterial, Abrasions, Minor burns, Antibacterial therapy, Antibiotic pre-surgical prophylaxis

How DERMAPROT works

DERMAPROT is a biocidal compound with multiple targets in the cytoplasm and membrane. At lower concentrations, however, triclosan appears bacteriostatic and is seen to target bacteria mainly by inhibiting fatty acid synthesis. DERMAPROT binds to enoyl-acyl carrier protein reductase enzyme (ENR). This complex has increased affinity for NAD+ and forms a ternary complex. This complex is unable to participate in fatty acid synthesis, weakening the cell membrane and causing cell death. Humans do not have an ENR enzyme, and thus are not affected.

Toxicity

Oral LD50, Rat: 3700 mg/kg; Dermal LD50, Rabbit: 9300 mg/kg

Food Interaction

No interactions found.

Elimination Route

A study conducted in 2000 demonstrated that low amounts of triclosan can be absorbed through skin and can enter the bloodstream. [PMID: 10722890] DERMAPROT is rapidly absorbed and distributed in the human body (Sandborgh-Englund et al., 2006). Maximum concentrations are reached within three hours after oral intake. However, the metabolism and excretion of the compound is fast.

Half Life

The terminal plasma half life of triclosan is 21 h (Sandborgh-Englund et al., 2006).

Elimination Route

In one study, after in vivo topical application of a 64.5mM alcoholic solution of [(3)H]triclosan to rat skin, 12% radioactivity was recovered in the faeces, 8% in the carcass 1% in the urine, 30% in the stratum corneum and 26% was rinsed from the skin surface at 24 hours after application. [PMID: 10722890]

Innovators Monograph

You find simplified version here DERMAPROT

http://classyfire.wishartlab.com/tax_nodes/C0000000
http://classyfire.wishartlab.com/tax_nodes/C0002448
http://classyfire.wishartlab.com/tax_nodes/C0002279
http://classyfire.wishartlab.com/tax_nodes/C0004155
http://classyfire.wishartlab.com/tax_nodes/C0004155
http://classyfire.wishartlab.com/tax_nodes/C0002463
http://classyfire.wishartlab.com/tax_nodes/C0004742
http://classyfire.wishartlab.com/tax_nodes/C0002341
http://classyfire.wishartlab.com/tax_nodes/C0002770
http://classyfire.wishartlab.com/tax_nodes/C0002564
http://classyfire.wishartlab.com/tax_nodes/C0004647
http://classyfire.wishartlab.com/tax_nodes/C0004646
http://classyfire.wishartlab.com/tax_nodes/C0001030
http://classyfire.wishartlab.com/tax_nodes/C0001516
http://classyfire.wishartlab.com/tax_nodes/C0004150
https://www.ebi.ac.uk/chebi/searchId.do?chebiId=CHEBI:164200
http://metacyc.org/META/new-image?type=COMPOUND&object=CPD0-1227
http://www.hmdb.ca/metabolites/HMDB0061385
http://www.genome.jp/dbget-bin/www_bget?drug:D06226
http://www.genome.jp/dbget-bin/www_bget?cpd:C12059
https://pubchem.ncbi.nlm.nih.gov/summary/summary.cgi?cid=5564
https://pubchem.ncbi.nlm.nih.gov/summary/summary.cgi?sid=99445075
https://www.chemspider.com/Chemical-Structure.5363.html
http://www.bindingdb.org/bind/chemsearch/marvin/MolStructure.jsp?monomerid=8726
https://mor.nlm.nih.gov/RxNav/search?searchBy=RXCUI&searchTerm=10795
https://www.ebi.ac.uk/chebi/searchId.do?chebiId=164200
https://www.ebi.ac.uk/chembldb/index.php/compound/inspect/CHEMBL849
https://zinc.docking.org/substances/ZINC000000002216
https://www.ebi.ac.uk/pdbe-srv/pdbechem/chemicalCompound/show/TCL
https://en.wikipedia.org/wiki/Triclosan
*** Taking medicines without doctor's advice can cause long-term problems.
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