Maraviroc – CAS 376348-65-1

€500 – €3500

Maraviroc is provided by Santiago Lab. 

Purity (LC-MS)

99 %

Package contents

Maraviroc

This compound is for research use only. We do not sell to patients.
SizeAvailabilityPriceQuantity
100 mg

In stock

 €500
1 g

In stock

 €3500

Characterization

CAS: 376348-65-1

IUPAC Name: Cyclohexanecarboxamide, 4, 4-difluoro-N– [(1S) -3-[(3-exo)-3-[3-methyl-5-(1-methylethyl)-4H-1,2,4-triazol-4-yl]-8-azabicyclo[3.2.1]oct-8-yl]-1-phenylpropyl]-

Other names: 4,4-Difluoro-N-[(1S)-3-[(3-exo)-3-[3-methyl-5-(1-methylethyl)-4H-1,2,4-triazol-4-yl]-8-azabicyclo[3.2.1]oct-8-yl]-1-phenylpropyl]cyclohexanecarboxamide, UK 427857, Selzentry, Celsentri

Molecular weight: 513.67  g/mol

Molecular formula: C29H41F2N5O

Description

Maraviroc is an antagonist of the C-C motif chemokine receptor CCR5, which is involved in the cell penetration process by HIV. As a CCR5 receptor antagonist, Maraviroc has a therapeutic application as an antiviral drug for the treatment of HIV infection. Maraviroc is sold under the brand names of Celsentry (EU) or Selzentry (US).

Chemicals are distributed worldwide

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Payment

  • We are sending the invoice the same day as the shipment
  • We are able to modify the invoice for the academic institution, so the order can be paid from grants
References

1. Eneroth, A.; Klasson, B.; Nilsson, M.; Pinho, P.; Samuelsson, B.; Sund, C. Preparation of antiviral nucleotides and their use as HCV polymerase inhibitors. 2012-13693729, US 20130143835, 20121204., 2013.
2. Klasson, B.; Eneroth, A.; Nilsson, M.; Pinho, P.; Samuelsson, B.; Sund, C. Preparation of antiviral nucleotides as HCV polymerase inhibitors. 2012-IB56994, WO 2013084165, 20121205., 2013.
3. Kalayanov, G.; Pinho, P.; Westerlind, H.; Wiktelius, D.; Waehling, H. Preparation of nucleotides as hepatitis C virus polymerase inhibitors. 2014-IB65370, WO 2015056213, 20141016., 2015.
4. Kalayanov, G.; Torssell, S.; Waehling, H. Hepatitis C virus polymerase inhibitors. 2014 SE51005, WO 2015034420, 20140902., 2015.
5. Bethel, R.; Eneroth, A.; Klasson, B.; Oeberg, F. Preparation of dioxolane analogues of uridine for the treatment of cancer. 2015-EP69370, WO 2016030335, 20150824., 2016.