Viminol (Dividol) Podwer

Viminol (Dividol) Podwer

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Viminol
Drug
Description
DescriptionViminol is an opioid analgesic developed by a team at the drug company Zambon in the 1960s. Viminol is based on the α-pyrryl-2-aminoethanol structure, unlike any other class of opioids. Viminol has both antitussive and analgesic effects. buy Viminol online
Molar mass: 362.94 g/mol
ChemSpider ID: 59125
ChEMBL Id: 2104940
Other names: Dividol, viminolo, diviminol
Trade name: Dividol
PubChem CID: 65697
People also search for: Tramadol, 3-HO-PCP, Paracetamol,

Description

Description

Buy Viminol Online from Chemicals Pharm Store.

 

Buy Viminol online
Drug
Description
DescriptionViminol is an opioid analgesic developed by a team at the drug company Zambon in the 1960s. Viminol is based on the α-pyrryl-2-aminoethanol structure, unlike any other class of opioids. Viminol has both antitussive and analgesic effects. Wikipedia
Molar mass: 362.94 g/mol
ChemSpider ID: 59125
ChEMBL Id: 2104940
Other names: Dividol, viminolo, diviminol
Trade name: Dividol
PubChem CID: 65697
People also search for: Tramadol, 3-HO-PCP, Paracetamol,

 

Buy Viminol Online/Order Viminol Wholesale /Retail Supplies Usage.

InvivoChem Cat #: V19413
CAS #: 21363-18-8Purity ≥98%

Description: Viminol (marketed under the brandname Dividol) is an opioid analgesic developed by a team at the drug company Zambon in the 1960s. Viminol is based on the α-pyrryl-2-aminoethanol structure, unlike any other class of opioids. References: Shu YJ, Bao RF, Jiang L, Wang Z, Wang XA, Zhang F, Liang HB, Li HF, Ye YY, Xiang SS, Weng H, Wu XS, Li ML, Hu YP, Lu W, Zhang YJ, Zhu J, Dong P, Liu YB. MicroRNA-29c-5p suppresses gallbladder carcinoma progression by directly targeting CPEB4 and inhibiting the MAPK pathway. Cell Death Differ. 2017 Mar;24(3):445-457. doi: 10.1038/cdd.2016.146. Epub 2017 Jan 6. PubMed PMID: 28060377; PubMed Central PMCID: PMC5344207.

 

Molecular Formula: C21H31ClN2O; Molecular Weight: 362.942; Exact Mass: 362.2125; Synonym: Viminol; Z424.; Related CAS#: 21363-18-8; Chemical Name: 1-(o-Chlorobenzyl)-alpha-((di-sec-butylamino)methyl)pyrrole-2-methanol; InChi Key: ZILPIBYANAFGMS-FIKGOQFSSA-N; InChi Code: InChI=1S/C21H31ClN2O/c1-5-16(3)24(17(4)6-2)15-21(25)20-12-9-13-23(20)14-18-10-7-8-11-19(18)22/h7-13,16-17,21,25H,5-6,14-15H2,1-4H3/t16-,17-,21-/m0/s1; SMILES: n1(c(ccc1)[C@@H](O)CN([C@@H](C)CC)[C@@H](C)CC)Cc1ccccc1Cl; References: Shu YJ, Bao RF, Jiang L, Wang Z, Wang XA, Zhang F, Liang HB, Li HF, Ye YY, Xiang SS, Weng H, Wu XS, Li ML, Hu YP, Lu W, Zhang YJ, Zhu J, Dong P, Liu YB. MicroRNA-29c-5p suppresses gallbladder carcinoma progression by directly targeting CPEB4 and inhibiting the MAPK pathway. Cell Death Differ. 2017 Mar;24(3):445-457. doi: 10.1038/cdd.2016.146. Epub 2017 Jan 6. PubMed PMID: 28060377; PubMed Central PMCID: PMC5344207.

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