PD 168568 dihydrochloride, Tocris Bioscience™

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CAS: 210688-56-5 Molecular Formula: C22H29Cl2N3O Molecular Weight (g/mol): 422.394 InChI Key: RMNWLEGGYCVHFD-UHFFFAOYSA-N Synonym: pd 168568 dihydrochloride,3-2-4-3,4-dimethylphenyl-1-piperazinyl ethyl-2,3-dihydro-1h-isoindol-1-one dihydrochloride,3-2-4-3,4-dimethylphenyl piperazin-1-yl ethyl isoindolin-1-one dihydrochloride,3-2-4-3,4-dimethylphenyl-1-piperazinyl ethyl-2,3-dihydro-1h-isoindol-1-onedihydrochloride,3-2-4-3,4-dimethylphenyl piperazin-1-yl ethyl-2,3-dihydro-1h-isoindol-1-one-hydrogen chloride 1/2 PubChem CID: 56972231 IUPAC Name: 3-[2-[4-(3,4-dimethylphenyl)piperazin-1-yl]ethyl]-2,3-dihydroisoindol-1-one;dihydrochloride SMILES: CC1=C(C=C(C=C1)N2CCN(CC2)CCC3C4=CC=CC=C4C(=O)N3)C.Cl.Cl

Cambridge Isotope Laboratories DOPAMINE:HCL (2-(3,4-DIHYDROXYPHENYL)- ETHYLAMINE:HCL) (2,2-D2, 97-98%), 0.1 G, 27160-01-6

DOPAMINE:HCL (2-(3,4-DIHYDROXYPHENYL)- ETHYLAMINE:HCL) (2,2-D2, 97-98%), 0.1 G, 27160-01-6

Cambridge Isotope Laboratories DOPAMINE:HCL (2-(3,4-DIHYDROXYPHENYL)- ETHYLAMINE:HCL) (1,1,2,2-D4, 97-98%), 0.1 G, 203633-19-6

DOPAMINE:HCL (2-(3,4-DIHYDROXYPHENYL)- ETHYLAMINE:HCL) (1,1,2,2-D4, 97-98%), 0.1 G, 203633-19-6

Cambridge Isotope Laboratories DOPAMINE:HCL (2-(3,4-DIHYDROXYPHENYL)- ETHYLAMINE:HCL) (RING-D3, 98%), 0.1 G, 53587-30-7

DOPAMINE:HCL (2-(3,4-DIHYDROXYPHENYL)- ETHYLAMINE:HCL) (RING-D3, 98%), 0.1 G, 53587-30-7

Cambridge Isotope Laboratories DOPAMINE:HCL (2-(3,4-DIHYDROXYPHENYL)- ETHYLAMINE:HCL) (1-13C, 99%), 0.05 G

DOPAMINE:HCL (2-(3,4-DIHYDROXYPHENYL)- ETHYLAMINE:HCL) (1-13C, 99%), 0.05 G

Cayman Chemical PalmItIc AcId-d31 1g

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A cannabinoid CB1 receptor antagonist (Kis 224 and 10000 nM for CB1 and CB2 respectively) selective for CB1 over a1- and a2- adrenergic D1 and D2 dopamine benzodiazepine histamine H1 GABA 5-HT and muscarinic receptors reverses the inhibition of forskolin-induced cAMP accumulation induced by arachidonoyl ethanolamide (anandamide) reverses inhibition of light-induced phase shifts in hamsters induced by the CB1 agonist CP 55940 when used at a dose of 1 mg/kg

Cayman Chemical LInzolId-d3 1mg

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A pH-dependent fluorescent probe to label dopaminergic cells excitation spectra of 340 and 370 nm at pH 5 and 7.4 respectively which correspond to vesicular and cytoplasmic pH values emission spectrum of 453 nm with a higher intensity at pH 7.4 inhibits DAT (13.6 at a concentration of 10 UM) and the 5-HT receptor subtype 5-HT2c (Ki ~3 UM) does not bind to 37 central nervous system receptors including dopamine and serotonin receptors up to a concentration of 10 UM

Cayman Chemical DL-AspartIcAcId-d3 100mg

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An alkaloid with diverse biological activities partial agonist at dopamine D2 receptors as well as an inverse agonist at the serotonin receptor subtype 5-HT7 and an antagonist at the 5-HT2B and 5-HT2C receptors (EC50s 65 07 150 478 and 131 nM respectively) an antagonist at schistosome Sm 5-HTRL receptors (IC50 240 nM) inhibits 5-HT-induced motility of larval and adult S mansoni at 10 UM activates PPARa PPARB/ and PPARY transcriptional activity prevents RSL3-induced ferroptotic cell death in HK-2 and HEK293T cells at 10 20 and 40 UM reduces serum hyperlipidemia and hepatic steatosis in a mouse model of high-fat diet-induced hyperlipidemia