Chlorprothixene

CAS: 113-59-7

Ref. 3D-FC37587

Produktinformation

• Name: Chlorprothixene
• Synonyme: (3E)-3-(2-chloro-9H-thioxanthen-9-ylidene)-N,N-dimethylpropan-1-aminium chloride, (3Z)-3-(2-Chloro-9H-thioxanthen-9-ylidene)-N,N-dimethyl-1-propanamine, (3Z)-3-(2-chloro-9H-thioxanthen-9-ylidene)-N,N-dimethylpropan-1-amine, (Z)-3-(2-Chloro-9H-thioxanthen-9-ylidene)-N,N-dimethyl-1-propanamine, 1-Propanamine, 3-(2-chloro-9H-thioxanthen-9-ylidene)-N,N-dimethyl-, (3Z)-, 1-Propanamine, 3-(2-chloro-9H-thioxanthen-9-ylidene)-N,N-dimethyl-, (Z)-, 2-Chloro-3-(Dibenzo(B,E)Thiin-10-Ylidene)Propyldimethylamine, 9H-Thioxanthene, 1-propanamine deriv., CPT, CPX, Chlorprothixen, Chlorprotixen, Chlorprotixene, Chlothixen, Chorprothixene, Clorprotixeno, Cloxan, Iaractan, Mk 184, N 714, Paxyl, Rentovet, Ro 4-0403, Ro 4-04033, Tactaran, Taractan, Tarasan, Tardan, Thioxanthene-Δ9,γ-propylamine, 2-chloro-N,N-dimethyl-, (Z)-, Thioxanthene-Δ^9,γ-propylamine, 2-chloro-N,N-dimethyl-, (Z)-, Traquilan, Trictal, Truxal, Truxaletten, Truxil, Vetacalm, cis-Chlorprothixene, α-Chlorprothixene

Beschreibung

Chlorprothixene is a derivative of fluorescein and has been used in the treatment of bone cancer. The reaction mechanism of chlorprothixene is not well understood, but it is believed to be due to its ability to bind with 5-HT2 receptors. Chlorprothixene also has anti-inflammatory properties, which may be due to the inhibition of nitrogen atoms in immune cells. This drug has low potency and can cause drug interactions with other drugs that are metabolized by enzymes in the liver such as cytochrome P450 enzymes. It also has a trifluoroacetic acid substituent, which can cause significant pharmacokinetic changes when given intravenously.

• Marke: Biosynth

Chemische Eigenschaften

• Molekulargewicht: 315.86 g/mol
• Formel: C₁₈H₁₈ClNS
• Reinheit: Min. 95%
• Farbe/Form: Powder
• InChl: InChI=1S/C18H18ClNS/c1-20(2)11-5-7-14-15-6-3-4-8-17(15)21-18-10-9-13(19)12-16(14)18/h3-4,6-10,12H,5,11H2,1-2H3/b14-7-
• InChI Key: InChIKey=WSPOMRSOLSGNFJ-AUWJEWJLSA-N
• SMILES: CN(C)CC/C=C1/c2ccccc2Sc2ccc(Cl)cc21