
CAS 402942-53-4: Benz[cd]indol-2(1H)-one, 6-chloro-2a-[4-[4-(4-chlorophenyl)-3,6-dihydro-1(2H)-pyridinyl]butyl]-2a,3,4,5-tetrahydro-, hydrochloride (1:1)
Formula:C26H28Cl2N2O·ClH
InChI:InChI=1S/C26H28Cl2N2O.ClH/c27-20-7-5-18(6-8-20)19-11-16-30(17-12-19)15-2-1-13-26-14-3-4-21-22(28)9-10-23(24(21)26)29-25(26)31;/h5-11H,1-4,12-17H2,(H,29,31);1H
InChI key:InChIKey=QAERYGXKDZHTFR-UHFFFAOYSA-N
SMILES:C(CCCN1CCC(=CC1)C2=CC=C(Cl)C=C2)C34C=5C(NC3=O)=CC=C(Cl)C5CCC4.Cl
Synonyms:- Benz[cd]indol-2(1H)-one, 6-chloro-2a-[4-[4-(4-chlorophenyl)-3,6-dihydro-1(2H)-pyridinyl]butyl]-2a,3,4,5-tetrahydro-, monohydrochloride
- Benz[cd]indol-2(1H)-one, 6-chloro-2a-[4-[4-(4-chlorophenyl)-3,6-dihydro-1(2H)-pyridinyl]butyl]-2a,3,4,5-tetrahydro-, hydrochloride (1:1)
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Found 2 products.
Dr 4485 hydrochloride
CAS:Dr 4485 hydrochloride is a synthetic, semi-synthetic drug product that is used as an analytical reference material and in the development of drugs. Dr 4485 hydrochloride is also a metabolite of Dr 4485. The compound has been found to have natural origin from plants, but can also be synthetically made. It is not on the current USP/BP/EP monographs and does not have a CAS number. Dr 4485 hydrochloride has been shown to be metabolized through N-dealkylation, oxidation, and hydroxylation reactions. Dr 4485 hydrochloride may show various impurities that are related to the synthesis process or its metabolism. This compound has been studied for its ability to affect the growth of cancer cells via inhibition of protein synthesis by binding to ribosomes in the cytoplasmic membrane of cancer cells.Formula:C26H29Cl3N2OPurity:Min. 95%Molecular weight:491.9 g/molDR4485 hydrochloride
CAS:5-HT7 antagonistFormula:C26H29Cl3N2OPurity:98%Color and Shape:SolidMolecular weight:491.88