Chemodex

Flibanserin

CHF 54.00
In stock
CDX-F0337-M0055 mgCHF 54.00
CDX-F0337-M02525 mgCHF 162.00
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Product Details
Synonyms 1,3-Dihydro-1-[2-[4-[3-(trifluoromethyl)phenyl]-1-piperazinyl]ethyl]-2H-benzimidazol-2-one; BIMT 17; BIMT 17BS
Product Type Chemical
Properties
Formula C20H21F3N4O
MW 390.4
CAS 167933-07-5
Source/Host Chemicals Synthetic
Purity Chemicals ≥98% (HPLC)
Appearance White to beige powder.
Solubility Soluble in DMSO (20mg/ml), DMF (20mg/ml) or ethanol (10mg/ml)
Identity Determined by 1H-NMR.
Declaration Manufactured by Chemodex.
Other Product Data

Click here for Original Manufacturer Product Datasheet
Our product description may differ slightly from the original manufacturers product datasheet.

InChi Key PPRRDFIXUUSXRA-UHFFFAOYSA-N
Smiles O=C1NC2=CC=CC=C2N1CCN3CCN(C4=CC=CC(C(F)(F)F)=C4)CC3
Shipping and Handling
Shipping AMBIENT
Short Term Storage +4°C
Long Term Storage +4°C
Handling Advice Protect from light and moisture.
Use/Stability Stable for at least 2 years after receipt when stored at +4°C.
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Product Specification Sheet
Datasheet Download PDF
Description

Flibanserin is a full agonist of the serotonin 5-HT1A receptor and an antagonist of 5-HT2A (Ki=1nm and 49nM, respectively). It also binds to dopamine D4 receptors with Ki values ranging from 4-24nM, but demonstrates no affinity for the other 5-HT subtypes or other neurotransmitter receptors. Multifunctional serotonergic ligands like flibanserin that can enhance downstream release of dopamine and norepinephrine while concomitantly reducing serotonin release in the brain circuits that mediate symptoms of reduced sexual interest and desire, are being studied clinically for therapeutic potential to improve sexual functioning. Flibanserin was investigated as a novel, non-hormonal treatment for pre-menopausal women with Hypoactive Sexual Desire Disorder (HSDD). Flibanserin was also found to reduce L-DOPA-induced dyskinesia in a model of Parkinson‘s Disease.

Product References

(1) F. Borsini, et al.; Naunyn Schmiedebergs Arch. Pharmacol. 352, 276 (1995) | (2) F. Borsini, et al.; Naunyn Schmiedebergs Arch. Pharmacol. 352, 283 (1995) | (3) F. Borsini, et al.; Psychopharmacology 134, 378 (1997) | (4) A. Scandroglio, et al.; Pharmacol. Res. 43, 179 (2001) | (5) F. Borsini, et al.; CNS Drug Rev. 8, 117 (2002) (Review) | (6) R.W. Invernizzi, et al.; Br. J. Pharmacol. 139, 1281 (2003) | (7) H. Gelez, et al.; J. Sex. Med. 10, 1231 (2013) | (8) S.M. Stahl; CNS Spectr. 20, 1 (2015) (Review) | (9) I. Dhanuka & J.A. Simon; Expert Opin. Pharmacother. 16, 2523 (2015) (Review)

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