Proflavine

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Proflavine
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Names
IUPAC name
acridine-3,6-diamine
Identifiers
92-62-6 YesY
ChEBI CHEBI:8452 YesY
ChEMBL ChEMBL55400 YesY
ChemSpider 6832 YesY
DrugBank DB01123 YesY
Jmol 3D model Interactive image
KEGG C11181 YesY
PubChem 7099
UNII CY3RNB3K4T YesY
  • InChI=1S/C13H11N3/c14-10-3-1-8-5-9-2-4-11(15)7-13(9)16-12(8)6-10/h1-7H,14-15H2 YesY
    Key: WDVSHHCDHLJJJR-UHFFFAOYSA-N YesY
  • InChI=1/C13H11N3/c14-10-3-1-8-5-9-2-4-11(15)7-13(9)16-12(8)6-10/h1-7H,14-15H2
    Key: WDVSHHCDHLJJJR-UHFFFAOYAC
  • n1c3c(cc2c1cc(N)cc2)ccc(c3)N
Properties
C13H11N3
Molar mass 209.25 g·mol−1
Vapor pressure {{{value}}}
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
YesY verify (what is YesYN ?)
Infobox references

Proflavine (pron. pro-fla¢vin), also called proflavin and diaminoacridine and bate na bina, is an acriflavine derivative, a disinfectant bacteriostatic against many gram-positive bacteria. It has been used in the form of the dihydrochloride and hemisulfate salts as a topical antiseptic, and was formerly used as a urinary antiseptic.

Proflavine is also known to have a mutagenic effect on DNA by intercalating between nucleic acid base pairs. It differs from most other mutagenic components by causing basepair-deletions or basepair-insertions and not substitutions.

Proflavine absorbs strongly in the blue region at 445 nm (in water at pH 7) with molar extinction coefficient of c. 40,000[1]

References

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