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Vanoxerine

CAS No.
67469-69-6
Chemical Name:
Vanoxerine
Synonyms
Vanoxerine free base;1-(2-(di(4-fluorophenyl)-methoxy)-ethyl)-4-(3-phenylpropyl)piperazine;Piperazine, 1-[2-[bis(4-fluorophenyl)Methoxy]ethyl]-4-(3-phenylpropyl)-
CBNumber:
CB81180039
Molecular Formula:
C28H32F2N2O
Molecular Weight:
450.56
MDL Number:
MFCD00600385
MOL File:
67469-69-6.mol
Last updated:2023-05-21 10:59:17

Vanoxerine Properties

Boiling point 542.7±50.0 °C(Predicted)
Density 1.135±0.06 g/cm3(Predicted)
storage temp. Store at -20°C
solubility Soluble in DMSO
form Powder
pka 7.55±0.10(Predicted)
FDA UNII 90X28IKH43

Vanoxerine price

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
ApexBio Technology B3249 Vanoxerine 67469-69-6 25mg $156 2021-12-16 Buy
CSNpharm CSN12187 Vanoxerine 67469-69-6 50mg $190 2021-12-16 Buy
Crysdot CD31001100 Vanoxerine 98+% 67469-69-6 50mg $450 2021-12-16 Buy
AvaChem 2889B Vanoxerine 67469-69-6 1g $575 2021-12-16 Buy
AvaChem 2889B Vanoxerine 67469-69-6 5g $1950 2021-12-16 Buy
Product number Packaging Price Buy
B3249 25mg $156 Buy
CSN12187 50mg $190 Buy
CD31001100 50mg $450 Buy
2889B 1g $575 Buy
2889B 5g $1950 Buy

Vanoxerine Chemical Properties,Uses,Production

Definition

ChEBI: Vanoxerine is an N-alkylpiperazine that consists of piperazine bearing 2-bis(4-fluorophenyl)methoxy]ethyl and 3-phenylpropyl groups at positions 1 and 4 respectively. Potent, competitive inhibitor of dopamine uptake (Ki = 1 nM for inhibition of striatal dopamine uptake). Has > 100-fold lower affinity for the noradrenalin and 5-HT uptake carriers. Also a potent sigma ligand (IC50 = 48 nM). Centrally active following systemic administration. It has a role as a dopamine uptake inhibitor. It is a N-alkylpiperazine, an organofluorine compound, a tertiary amino compound and an ether. It is a conjugate base of a vanoxerine(2+).

Biological Activity

vanoxerine is an antagonist of dopamine transporter (dat1) with ki value of 16.9nm [1].as an antagonist of dat, vanoxerine is developed for treatment of parkinson's disease and depression but has no effect on these diseases. vanoxerine is also found to have desirable cardiac antiarrhythmic properties. it is a blocker of cardiac herg (hkv11.1) with ic50 value of 0.84nm. it also blocks the ica,l and hnav1.5 channel with ic50 values of 320nm and 830nm, respectively. vanoxerine does not significantly prolong purkinje fiber apd60 and apd90 and has no significant effect on qt or tdr. further, the

References

[1] giros b, el mestikawy s, godinot n, zheng k, han h, yang-feng t, caron mg. cloning, pharmacological characterization, and chromosome assignment of the human dopamine transporter. mol pharmacol. 1992 sep;42(3):383-90.
[2] lacerda ae, kuryshev ya, yan gx, waldo al, brown am. vanoxerine: cellular mechanism of a new antiarrhythmic. j cardiovasc electrophysiol. 2010 mar;21(3):301-10.

Vanoxerine Preparation Products And Raw materials

Raw materials

Preparation Products

Vanoxerine Suppliers

Global( 13)Suppliers
Supplier Tel Email Country ProdList Advantage
TargetMol Chemicals Inc.
+1-781-999-5354 +1-00000000000 marketing@targetmol.com United States 19892 58
Amadis Chemical Company Limited
571-89925085 sales@amadischem.com China 131980 58
Hangzhou Sage Chemical Co., Ltd. +86057186818502 13588463833 info@sagechem.com China 10269 58
TargetMol Chemicals Inc. 021-021-33632979 15002134094 marketing@targetmol.com China 7854 58
LETOPHARM LIMITED +86-21-5821 5861 sales@letopharm.com China 2384 58
SPIRO PHARMA eric_feng1954@126.com China 9254 55
Musechem +1-800-259-7612 info@musechem.com United States 4662 60
Absin Bioscience Inc. 021-38015121 15000105423 chenjw@absin.cn China 24734 58
Shanghai Botuo Biotechnology Co., LTD 16621358918 botuopharma888@163.com China 9215 58
MedBioPharmaceutical Technology Inc 021-69568360 18916172912 order@med-bio.cn China 8141 58
Piperazine, 1-[2-[bis(4-fluorophenyl)Methoxy]ethyl]-4-(3-phenylpropyl)- 1-(2-(di(4-fluorophenyl)-methoxy)-ethyl)-4-(3-phenylpropyl)piperazine Vanoxerine free base 67469-69-6 C28H32F2N2O