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Tiflucarbine
Tiflucarbine
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Tiflucarbine
Tiflucarbine
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Tiflucarbine

Tiflucarbine
Identifiers
  • 9-Ethyl-4-fluoro-1-methyl-7,8,9,10-tetrahydro-6H-pyrido[4,3-b]thieno[3,2-e]indole
CAS Number
PubChem CID
ChemSpider
UNII
ChEMBL
CompTox Dashboard (EPA)
Chemical and physical data
FormulaC16H17FN2S
Molar mass288.38 g·mol−1
3D model (JSmol)
  • CCN1CCC2=C(C1)C3=C4C(=CSC4=C(C=C3N2)F)C
  • InChI=1S/C16H17FN2S/c1-3-19-5-4-12-10(7-19)15-13(18-12)6-11(17)16-14(15)9(2)8-20-16/h6,8,18H,3-5,7H2,1-2H3
  • Key:BNKIWXODDDABSJ-UHFFFAOYSA-N

Tiflucarbine (BAY-P 4495) is an experimental drug which acts as an agonist of the 5-HT1 and 5-HT2 serotonin receptor families, and also acts as a calmodulin inhibitor. It has antidepressant effects in animal studies.[1][2][3][4] It is similar in structure to but distinct from β-carbolines.

References

[edit]
  1. ^ Maj J, Rogóz Z, Sowińska H, Zalewski Z (1987). "Some central effects of tiflucarbine, a new potential antidepressant drug". Polish Journal of Pharmacology and Pharmacy. 39 (1): 63–74. PMID 2823240.
  2. ^ Glennon RA, De Vry J, Spencer DG, Glaser T (December 1990). "Stimulus properties of tiflucarbine: a novel antidepressant agent". Pharmacology, Biochemistry, and Behavior. 37 (4): 769–771. doi:10.1016/0091-3057(90)90561-u. PMID 2151199.
  3. ^ Schmidt BH, Glaser T, Seidel PR, Traber J (December 1990). "Evidence for a specific recognition site for tiflucarbine on calmodulin". European Journal of Pharmacology. 189 (6): 411–418. doi:10.1016/0922-4106(90)90039-z. PMID 1963605.
  4. ^ Hegemann L, Fruchtmann R, Bonnekoh B, Schmidt BH, Traber J, Mahrle G, et al. (1991). "Effects of tiflucarbine as a dual protein kinase C/calmodulin antagonist on proliferation of human keratinocytes and release of reactive oxygen species from human leukocytes". Archives of Dermatological Research. 283 (7): 456–460. doi:10.1007/BF00371782. PMID 1801655.
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