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Antiviral API
- Arenavirus
- Cytomegalovirus (CMV)
- Dengue virus
- Endogenous Metabolite
- Enterovirus (EV)
- Epstein-Barr virus (EBV)
- Filovirus
- Flavivirus
- HCV Protease
- Hepatitis B Virus (HBV)
- Hepatitis C Virus (HCV)
- Herpes simplex Virus (HSV)
- HIF/HIF Prolyl-Hydroxylase
- HIV Integrase
- HIV Protease
- Human immunodeficiency Virus (HIV)
- Human papillomavirus (HPV)
- Influenza Virus
- Nipah virus
- Orthopoxvirus
- Others
- Rabies virus (RABV)
- Respiratory syncytial Virus (RSV)
- Reverse Transcriptases (RTs)
- SARS-CoV
- Tobacco mosaic virus (TMV)
- Vesicular stomatitis virus (VSV)
- Virus Protease
- West Nile virus
- Antiviral intermediates
Human immunodeficiency Virus (HIV)
CAS No. | Product Name | Inquiry |
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2395777-43-0 |
HIV-1-inhibitor-33HIV-1 inhibitor-33 (compound 5n) is a potent and selective HIV-1 inhibitor with an EC50 of 8.6 nM for HIV-1 and a CC50 of 18 M in MT-4 cells. HIV-1 inhibitor-33 can be used for researching AIDS. |
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2395777-45-2 |
HIV-1-inhibitor-34HIV-1 inhibitor-34 (compound 5q) is a potent and selective HIV-1 inhibitor with an EC50 of 6.4 nM for HIV-1 and a CC50 of 16 M in MT-4 cells. HIV-1 inhibitor-34 can be used for researching AIDS. |
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2396382-78-6 |
HIV-1 capsid inhibitor 1 |
|
24027-80-3 |
2',3'-Dideoxyadenosine 5'-TriphosphateddATP is an inhibitor of reverse transcriptases from retroviruses, such as HIV-1 and visna (Kis = 20 and 37 nM, respectively). ddATP is commonly used to terminate chain extension produced by the Taq polymerase for its competitive effect with dATP in cells. |
|
2408729-03-1 |
HIV-IN-4HIV-IN-4 (Compound 12) is a potent inhibitor of HIV. HIV-IN-4 shows promising anti-HIV activities. |
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2409099-32-5 |
Semzuvolimab |
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2411819-82-2 |
NBD-14270NBD-14270, a pyridine analogue, is a potent HIV-1 entry antagonist with an IC50 of 180 nM against 50 HIV-1 Env-pseudotyped viruses. NBD-14270 binds to HIV-1 gp120 and shows potent antiviral activity. NBD-14270 shows low cytotoxicity (CC50>100M). |
|
2414099-82-2 |
HIV-1-inhibitor-39HIV-1 inhibitor-39 (compound 3c) is a potent HIV-1 inhibitor with an EC50 of >112.88 µM. HIV-1 inhibitor-39 shows anti-RT (HIV-1 reverse transcriptase) activities with an IC50 of 15.75 µM. HIV-1 inhibitor-39 shows cytotoxicity for MT-4 cells with an CC50 of 112.9 µM. |
|
2415504-88-8 |
HIV-1-inhibitor-26HIV-1 inhibitor-26 (compound 9a) is a potent HIV-1 reverse transcriptase (RT) inhibitor with an IC50 value of 1.4 μM. HIV-1 inhibitor-26 has low cytotoxicity with a CC50 of 1486 μM in PBMCs. HIV-1 inhibitor-26 can be used for researching AIDS. |
|
2416971-32-7 |
HIV-1-inhibitor-35HIV-1 inhibitor-35 (compound 74) is a potent HIV-1 inhibitor with EC50s of 80 nM and 70 nM for LTR and CMV in HEK293 cells, respectively. HIV-1 inhibitor-35 has inhibitory activity against liver cancer cell HepG2 with a CC50 of 40 nM. HIV-1 inhibitor-35 can be used as HIV-1 latency reversing agent. |
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2416971-40-7 |
HIV-1 inhibitor-37 |
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2416971-48-5 |
HIV-1-inhibitor-38HIV-1 inhibitor-38 (Compound 91) is a potent HIV-1. HIV-1 inhibitor-38 has the potential for further development as novel latency reversing agents. |
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2417048-11-2 |
GSK878 |
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2417213-75-1 |
Zinlirvimab |
|
2442512-14-1 |
Fipravirimat dihydrochloride |
|
2447-57-6 |
SulfadoxineSulfadoxine is an ultra-long-lasting sulfonamide with an IC50 of 249 μg/ml for P. vivax. Sulfadoxine is an ultra-long-lasting sulfonamide previously used in combination with pyrimethamine to treat or prevent malaria. Due to high levels of resistance, its use is no longer recommended routinely. |
|
2450-53-5 |
Isochlorogenic acid A3,5-Di-O-caffeoylquinic acid isolated from the flowerbud of Lonicera japonica Thunb. It has hepatoprotective and potent anti-hepatitis B activities. |
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2457357-99-0 |
FNC-TPFNC-TP is the intracellular active form of FNC which is a potent nucleoside reverse transcriptase inhibitor (NRTI), with antiviral activity on HIV, HBV and HCV. |
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2459929-46-3 |
HIV-1-inhibitor-42HIV-1 inhibitor-42 (compound 5b) is a potent HIV-1 inhibitor, with an IC50 of 0.06 μM. HIV-1 inhibitor-42 inhibits HIV-1 RT RNA-dependent DNA polymerase and DNA-dependent DNA polymerase, with IC50 values of 0.518 and 0.072 . |
|
2459929-62-3 |
HIV-IN-5HIV-IN-5 is an investigational small molecule with potent inhibitory activity against HIV-1, demonstrating an IC50 of 0.16 μM. It targets key components of the HIV lifecycle, such as reverse transcriptase, integrase, or protease, and effectively inhibits HIV DNA-dependent DNA polymerization with an IC50 of 2.18 μM. By binding to the NNRTI binding pocket (NNIBP) on the reverse transcriptase enzyme, HIV-IN-5 disrupts viral replication, reduces viral load, and slows disease progression, making it a promising candidate for inclusion in antiretroviral therapies for managing and treating HIV/AIDS. |
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