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SML2864

Sigma-Aldrich

Loviride

≥98% (HPLC)

Synonym(s):

α-[(2-Acetyl-5-methylphenyl)amino]-2,6-dichloro-benzeneacetamide, (±)-2-(6-Acetyl-m-toluidino)-2-(2,6-dichlorophenyl)acetamide, R 89439

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About This Item

Empirical Formula (Hill Notation):
C17H16Cl2N2O2
CAS Number:
147362-57-0
Molecular Weight:
351.23
MDL number:
MFCD00867484
UNSPSC Code:
51111800
NACRES:
NA.77

Quality Level

100

assay

≥98% (HPLC)

form

powder

color

white to beige

solubility

DMSO: 2 mg/mL, clear

storage temp.

2-8°C

InChI

1S/C17H16Cl2N2O2/c1-9-6-7-11(10(2)22)14(8-9)21-16(17(20)23)15-12(18)4-3-5-13(15)19/h3-8,16,21H,1-2H3,(H2,20,23)

InChI key

CJPLEFFCVDQQFZ-UHFFFAOYSA-N

Biochem/physiol Actions

Loviride is an orally available, potent and selective inhibitor of reverse transcriptase HIV-1 that inhibits HIV replication in cells. Also, loviride inhibits replication of HIV-2 and SIV in cells.

Storage Class

11 - Combustible Solids

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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R Pauwels et al.
Proceedings of the National Academy of Sciences of the United States of America, 90(5), 1711-1715 (1993-03-01)
In vitro evaluation of a large chemical library of pharmacologically acceptable prototype compounds in a high-capacity, cellular-based screening system has led to the discovery of another family of human immunodeficiency virus type 1 (HIV-1) inhibitors. Through optimization of a lead
Philippe Berben et al.
International journal of pharmaceutics, 537(1-2), 22-29 (2017-12-16)
In view of the increasing interest of pharmaceutical companies for cell- and tissue-free models to implement permeation into formulation testing, this study explored the capability of an artificial membrane insert system (AMI-system) as predictive tool to evaluate the performance of
M Witvrouw et al.
AIDS (London, England), 13(12), 1477-1483 (1999-08-28)
After the initial discovery of 1-(2-hydroxyethoxymethyl)-6-(phenylthio)thymine (HEPT) and tetrahydroimidazo[4,5,1-jk][1,4]benzodiazepin-2(1H)-one and thione (TIBO) derivatives, several other non-nucleoside reverse transcriptase (RT) inhibitors (NNRTI), including nevirapine (BI-RG-587), pyridinone derivatives (L-696,229 and L-697,661), delavirdine (U-90152), alpha-anilinophenylacetamides (alpha-APA) and various other classes of NNRTI have

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