[CAS NO. 1338225-97-0]  Doravirine

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PRODUCTS SPECIFICATIONS [1338225-97-0]

Catelog
HY-16767
Brand
MCE
CAS
1338225-97-0

DESCRIPTION [1338225-97-0]

Overview

MDLMFCD22417167
Molecular Weight425.75
Molecular FormulaC17H11ClF3N5O3
SMILESN#CC1=CC(OC2=C(C(F)(F)F)C=CN(CC(N3C)=NNC3=O)C2=O)=CC(Cl)=C1

For research use only. We do not sell to patients.


Summary

Doravirine (MK-1439) is a highly specific HIV-1 nonnucleoside reverse transcriptase inhibitor with IC 50 s of 4.5 nM, 5.5 nM and 6.1 nM against the wild type and K103N and Y181C reverse transcriptase mutants, respectively [1] .


IC50 & Target

IC50: 4.5 nM (wild type reverse transcriptase ); 5.5 nM ( K103N reverse transcriptase ); 6.1 nM ( Y181C reverse transcriptase ) [1]


In Vitro

Selectivity and cytotoxicity studies confirmed that Doravirine is a highly specific nonnucleoside reverse transcriptase inhibitors with minimum off-target activities. In the presence of 50% normal human serum (NHS), Doravirine shows excellent potency in suppressing the replication of WT virus, with a 95% effective concentration ( EC 95 ) of 20 nM, as well as K103N, Y181C, and K103N/Y181C mutant viruses with EC 95 95 of 43, 27, and 55 nM, respectively. Doravirine exhibits similar antiviral activities against 10 different HIV-1 subtype viruses (a total of 93 viruses) [1] .

MCE has not independently confirmed the accuracy of these methods. They are for reference only.


In Vivo

Administration of 50 mg Doravirine with a high-fat meal is associated with slight elevations in AUC time zero to infinity and C24 h with no change in C max [2] .

MCE has not independently confirmed the accuracy of these methods. They are for reference only.


Clinical Trial

NCT Number Sponsor Condition Start Date Phase
NCT02275780 Merck Sharp & Dohme LLC
HIV-1
December 1, 2014 Phase 3
NCT04097925 Fundación FLS de Lucha Contra el Sida, las Enfermedades Infecciosas y la Promoción de la Salud y la Ciencia|Institut d´Investigació Biomèdica de Bellvitge|Hospital Universitari de Bellvitge
HIV-1-infection
February 18, 2020 Phase 2
NCT02089659 Merck Sharp & Dohme LLC
HIV-1 Infection
March 26, 2014 Phase 1

Appearance

Solid


Shipping

Room temperature in continental US; may vary elsewhere.


Storage

Powder -20°C 3 years
4°C 2 years
In solvent -80°C 6 months
-20°C 1 month

Solvent & Solubility

In Vitro:

DMSO : 100 mg/mL ( 234.88 mM ; Need ultrasonic)

Preparing
Stock Solutions
Concentration Solvent Mass 1 mg 5 mg 10 mg
1 mM 2.3488 mL 11.7440 mL 23.4880 mL
5 mM 0.4698 mL 2.3488 mL 4.6976 mL
10 mM 0.2349 mL 1.1744 mL 2.3488 mL
* Please refer to the solubility information to select the appropriate solvent.
In Vivo:
  • 1.

    Add each solvent one by one: 10% DMSO >> 40% PEG300 >> 5% Tween-80 >> 45% saline

    Solubility: 2.5 mg/mL (5.87 mM); Suspended solution; Need ultrasonic

  • 2.

    Add each solvent one by one: 10% DMSO >> 90% corn oil

    Solubility: ≥ 2.5 mg/mL (5.87 mM); Clear solution

* All of the co-solvents are available by MCE.


Synonyms

Benzonitrile, 3-chloro-5-[[1-[(4,5-dihydro-4-methyl-5-oxo-1H-1,2,4-triazol-3-yl)methyl]-1,2-dihydro-2-oxo-4-(trifluoromethyl)-3-pyridinyl]oxy]-
3-Chloro-5-[[1-[(4,5-dihydro-4-methyl-5-oxo-1H-1,2,4-triazol-3-yl)methyl]-1,2-dihydro-2-oxo-4-(trifluoromethyl)-3-pyridinyl]oxy]benzonitrile
MK 1439
Doravirine
3-Chloro-5-[1-[(4-methyl-5-oxo-1H-1,2,4-triazol-3-yl)methyl]-2-oxo-4-(trifluoromethyl)pyridin-3-yl]oxybenzonitrile
Pifeltro