SML0225

LY255582

≥98% (HPLC)

• Synonim(y): (3R,4R)-3,4-Dimethyl-1-[(3S)-3-hydroxy-3-cyclohexyl-propyl]-4-(3-hydroxyphenyl)piperidine, (aS,3R,4R)-a-Cyclohexyl-4-(3-hydroxyphenyl)-3,4-dimethyl-1-piperidinepropanol, LY-255582
• Wzór empiryczny (zapis Hilla): C₂₂H₃₅NO₂
• Numer CAS: 119193-09-8
• Masa cząsteczkowa: 345.52
• Numer MDL: MFCD00878181
• Kod UNSPSC: 12352200
• Identyfikator substancji w PubChem: 329825244
• NACRES: NA.77

Właściwości

• Próba: ≥98% (HPLC)
• Postać: powder
• warunki przechowywania: desiccated
• kolor: white to beige
• rozpuszczalność: DMSO: ≥15 mg/mL
• inicjator: Eli Lilly
• temp. przechowywania: 2-8°C
• ciąg SMILES: C[C@H]1CN(CC[C@H](O)C2CCCCC2)CC[C@@]1(C)c3cccc(O)c3
• InChI: 1S/C22H35NO2/c1-17-16-23(13-11-21(25)18-7-4-3-5-8-18)14-12-22(17,2)19-9-6-10-20(24)15-19/h6,9-10,15,17-18,21,24-25H,3-5,7-8,11-14,16H2,1-2H3/t17-,21-,22+/m0/s1
• Klucz InChI: LVVHEFJXPXAUDD-BULFRSBZSA-N

Opis

Zastosowanie

LY255582 may be used in opioid receptor-mediated cell signaling studies.

Działania biochem./fizjol.

LY255582 inhibits the diet-associated increases in mesolimbic dopamine levels and reduces the consumption of highly-palatable food intake.

LY255582 is a centrally active opioid receptor antagonist (defined as an inverse agonist in 2011 JPET paper) that inhibited weight gain in obese Zucker rats over 30 days. It is more that 5-fold selective for mu opioid receptor compared to kappa opioid receptors and 13-fold selective over delta opioid receptors.

Cechy i korzyści

This compound is featured on the Opioid Receptors page of the Handbook of Receptor Classification and Signal Transduction. To browse other handbook pages, click here.

This compound was developed by Eli Lilly. To browse the list of other pharma-developed compounds and Approved Drugs/Drug Candidates, click here.

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Informacja o środkach bezpieczeństwa

• Kod klasy składowania: 11 - Combustible Solids
• Klasa zagrożenia wodnego (WGK): WGK 3
• Temperatura zapłonu (°F): Not applicable
• Temperatura zapłonu (°C): Not applicable