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Chemical Structure| 865363-93-5 Chemical Structure| 865363-93-5

Structure of Islatravir
CAS No.: 865363-93-5

Chemical Structure| 865363-93-5

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MK-8591 exhibits potent activity against HIV.

Synonyms: Mk-8591; EFdA; 4′-ethynyl-2-fluoro-2′-Deoxyadenosine

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Product Details of Islatravir

CAS No. :865363-93-5
Formula : C12H12FN5O3
M.W : 293.25
SMILES Code : O[C@@H]1[C@](CO)(C#C)O[C@@H](N2C=NC3=C(N)N=C(F)N=C23)C1
Synonyms :
Mk-8591; EFdA; 4′-ethynyl-2-fluoro-2′-Deoxyadenosine
MDL No. :MFCD28502143
InChI Key :IKKXOSBHLYMWAE-QRPMWFLTSA-N
Pubchem ID :6483431

Safety of Islatravir

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H302-H315-H319-H335
Precautionary Statements:P261-P280-P301+P312-P302+P352-P305+P351+P338

Isoform Comparison

Biological Activity

In Vitro:

Cell Line
Concentration Treated Time Description References
MT-4 cells 42 nM 5 days Evaluate the inhibitory activity of EFdA against HIV-1 EFdAR, results showed EFdA remains active against multidrug-resistant HIV-1 variants Cell Chem Biol. 2018 Oct 18;25(10):1268-1278. e3
MT-4 cells 3 nM 5 days Evaluate the inhibitory activity of EFdA against HIV-167-75, results showed EFdA remains active against drug-resistant HIV-1 variants Cell Chem Biol. 2018 Oct 18;25(10):1268-1278. e3
MT-4 cells 0.3 nM 5 days Evaluate the inhibitory activity of EFdA against HIV-1WT, results showed EFdA has potent antiviral activity Cell Chem Biol. 2018 Oct 18;25(10):1268-1278. e3
A431 5 ng/ml to 50 μg/ml 24 hours To evaluate the cytotoxicity of EFdA and drug-loaded films on A431 cells, results showed that the 50% cytotoxic concentration (CC50) of both EFdA and drug-loaded films was higher than 50 μg/ml. Int J Pharm. 2014 Jan 30;461(1-2):203-13
HEC-1A 5 ng/ml to 50 μg/ml 24 hours To evaluate the cytotoxicity of EFdA and drug-loaded films on HEC-1A cells, results showed that the 50% cytotoxic concentration (CC50) of both EFdA and drug-loaded films was higher than 50 μg/ml. Int J Pharm. 2014 Jan 30;461(1-2):203-13
CaSki 5 ng/ml to 50 μg/ml 24 hours To evaluate the cytotoxicity of EFdA and drug-loaded films on CaSki cells, results showed that the 50% cytotoxic concentration (CC50) of both EFdA and drug-loaded films was higher than 50 μg/ml. Int J Pharm. 2014 Jan 30;461(1-2):203-13
Peripheral blood mononuclear cells 50 pM Evaluate the inhibitory effect of EFdA on HIV-1 NL4-3 Curr Opin HIV AIDS. 2018 Jul;13(4):294-299
MT4 cells 73 pM Evaluate the inhibitory effect of EFdA on HIV-1 IIIb Curr Opin HIV AIDS. 2018 Jul;13(4):294-299
MT4-GFP cells 0.50–12.81 nM 48 and 72 hours To evaluate the combinatorial antiviral activity of ISL and LEN, results showed additive inhibition of HIV-1 replication with no evidence of antagonism. Antimicrob Agents Chemother. 2024 Jul 9;68(7):e0033424
monkey peripheral blood mononuclear cells 2, 5, 15 µM 2 hours To evaluate the uptake and phosphorylation efficiency of Islatravir in monkey PBMCs. Results showed that Islatravir uptake in monkey PBMCs was less efficient than in human PBMCs. Antimicrob Agents Chemother. 2025 Feb 13;69(2):e0103024
human peripheral blood mononuclear cells 2, 5, 15 µM 2 hours To evaluate the uptake and phosphorylation efficiency of Islatravir in PBMCs. Results showed that Islatravir uptake in human PBMCs was more efficient than in monkey PBMCs, with high phosphorylation to ISL-TP. Antimicrob Agents Chemother. 2025 Feb 13;69(2):e0103024
PBMCs 0.23 nM to 5.70 nM 24 hours To evaluate the antiviral activity of ISL in PBMCs, results showed A114S/M184V variants did not replicate in PBMCs. Antimicrob Agents Chemother. 2022 Jun 21;66(6):e0013322
MT4-GFP cells 0.79 nM to 68.68 nM 48 to 72 hours To evaluate the antiviral activity of ISL against HIV-1 variants, results showed M184I and M184V were the only single-codon substitutions that reduced susceptibility >2-fold compared to WT. Antimicrob Agents Chemother. 2022 Jun 21;66(6):e0013322
MT4-GFP cells 0.79 nM 4 days Evaluate the antiviral activity and resistance barrier of the DOR/ISL combination Antimicrob Agents Chemother. 2022 May 17;66(5):e0222321
Sf9 membrane vesicles (containing BSEP, MRP2, MRP3, or MRP4) up to 100 µM 5 minutes Evaluate inhibition of hepatic efflux transporters BSEP, MRP2, MRP3, and MRP4 by islatravir, no inhibition observed Viruses. 2021 Aug 7;13(8):1566
recombinant cell lines (HEK293-OATP1B1, HEK293-OATP1B3, CHO-K1-OCT1) up to 300 µM 30 minutes Evaluate inhibition of hepatic uptake transporters OATP1B1, OATP1B3, and OCT1 by islatravir, no inhibition observed Viruses. 2021 Aug 7;13(8):1566
human hepatocytes 0.1–20 µM 48 hours Evaluate induction of CYP3A4, CYP2B6, or CYP1A2 by islatravir, no induction observed Viruses. 2021 Aug 7;13(8):1566
human liver microsomes 10 and 50 µM 30 minutes Evaluate time-dependent inhibition of CYP isoforms by islatravir, no inhibition observed Viruses. 2021 Aug 7;13(8):1566
human liver microsomes 0.05 to 100 µM (CYP3A4 tested to 200 µM) 10-30 minutes Evaluate reversible inhibition of CYP isoforms (1A2, 2B6, 2C8, 2C9, 2C19, 2D6, 3A4) by islatravir, no inhibition observed Viruses. 2021 Aug 7;13(8):1566
PGP1 overexpressing MDCKII cells 0.005–200 μM 48 hours To assess PGP1 inhibition by EFdA. Results showed that EFdA is not a substrate of PGP1. Eur J Pharmacol. 2014 Jun 5;732:86-95
MDCKII cells 25, 100, or 400 μM 2 hours To evaluate the bidirectional transport characteristics of EFdA across MDCKII cell monolayers. Results indicated that EFdA primarily permeates via the paracellular route. Eur J Pharmacol. 2014 Jun 5;732:86-95
Caco-2 cells 25, 100, or 400 μM 2 hours To evaluate the bidirectional transport characteristics of EFdA across Caco-2 cell monolayers. Results showed that the cumulative transported amounts of EFdA were much higher in the basolateral-to-apical direction than in the apical-to-basolateral direction, suggesting the involvement of active transport mechanisms. Eur J Pharmacol. 2014 Jun 5;732:86-95

In Vivo:

Species
Animal Model
Administration Dosage Frequency Description References
Mouse, rat, rabbit, monkey Intravenous 1 mg/kg Single dose, sampling time 0-24 hours (mouse, rat, monkey) and 0-48 hours (rabbit) Evaluate renal clearance of islatravir in nonclinical species, results showed renal excretion contributed 61%, 17%, 31%, and 51% of total plasma clearance in mouse, rat, rabbit, and monkey models, respectively Viruses. 2021 Aug 7;13(8):1566
NSG-BLT mice HIV infection model Oral gavage 10 mg/kg/day Once daily for 4 weeks EFdA treatment significantly suppressed HIV viremia, and viral rebound was observed after drug cessation Viruses. 2019 Mar 13;11(3):256
Rhesus macaques SIVmac 251 infection model Oral 30 mg/kg Once weekly for 7 days Evaluate the inhibitory effect of EFdA on SIVmac 251 Curr Opin HIV AIDS. 2018 Jul;13(4):294-299
Rats Male rats Oral 5 mg/kg Single dose To evaluate the absorption, metabolism, and excretion of Islatravir in rats. Results showed that Islatravir was primarily excreted in urine, with metabolite M4 as the major metabolite. Antimicrob Agents Chemother. 2025 Feb 13;69(2):e0103024

Protocol

Bio Calculators
Preparing Stock Solutions 1mg 5mg 10mg

1 mM

5 mM

10 mM

3.41mL

0.68mL

0.34mL

17.05mL

3.41mL

1.71mL

34.10mL

6.82mL

3.41mL

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