Structure of Islatravir
CAS No.: 865363-93-5
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The BI-3802 was designed by Boehringer Ingelheim and could be obtained free of charge through the Boehringer Ingelheim open innovation portal opnMe.com, associated with its negative control.
MK-8591 exhibits potent activity against HIV.
Synonyms: Mk-8591; EFdA; 4′-ethynyl-2-fluoro-2′-Deoxyadenosine
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Batch number can be found on the product's label following the word 'Batch'.
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Search for reports by entering the product batch number.
Batch number can be found on the product's label following the word 'Batch'.
Search for reports by entering the product batch number.
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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 |
GHS Pictogram: |
![]() |
Signal Word: | Warning |
Hazard Statements: | H302-H315-H319-H335 |
Precautionary Statements: | P261-P280-P301+P312-P302+P352-P305+P351+P338 |
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 |
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 |
Tags: Islatravir | MK-8591 | MK8591 | MK 8591 | HIV | Reverse Transcriptase | Human immunodeficiency virus | inhibitor | 865363-93-5 |
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H311 | Toxic in contact with skin |
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H319 | Causes serious eye irritation |
H320 | Causes eye irritation |
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H351 | Suspected of causing cancer |
H360 | May damage fertility or the unborn child |
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H361d | Suspected of damaging the unborn child |
H362 | May cause harm to breast-fed children |
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H412 | Harmful to aquatic life with long-lasting effects |
H413 | May cause long-lasting harmful effects to aquatic life |
H420 | Harms public health and the environment by destroying ozone in the upper atmosphere |
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