SARS-CoV

CAS No.	Product Name	Inquiry
129-46-4	Suramin Sodium The sodium salt of Suramin which is a P2 purinergic antagonist and has been also found to have the effect in blocking the G protein binds to GPCRs so that it was studied the activity against sorts of cancer cell lines.
1311271-71-2	SARS-CoV-2-IN-44
1312711-71-9	(25S)-Antcin B
131707-25-0	Umifenovir Arbidol is an antiviral agent using for the treatment of influenza infection in Russia and China. It inhibits membrane fusion and prevents contact between the virus and target host cells. Fusion between the viral capsid and the cell membrane of the target cell is inhibited and this prevents viral entry to the target cell. Although some Russian studies have shown it to be effective, it is not approved for use in Western countries.
1323633-98-2	Fluphenazine-d8 Dihydrochloride Flufenazin-[d8] is the labelled analogue of Flufenazin, which is an antipsychotic medication.
132796-52-2	Emodin-[d4] Emodin-[d4] is the labelled analogue of Emodin, which is an anthraquinone found naturally in the roots and barks of numerous plants. It exerts antiproliferative effects in cancer cells that are regulated by different signaling pathways. It has anti-cancer, anti-depressant and anti-microbial effects.
1345406-09-8	BPR3P0128
134863-91-5	10-Hydroxyaloin A
1350462-55-3	MK-5172 hydrate In biochemical assays, MK-5172 was effective against a panel of major genotypes and variants engineered with common resistant mutations observed in clinical studies with other NS3/4a protease inhibitors. In the replicon assay, MK-5172 demonstrated subnanomolar to low-nanomolar EC50s against genotypes 1a, 1b, and 2a. In rats, MK-5172 showed a plasma clearance of 28 ml/min/kg and plasma half-life of 1.4 hr. When dosed p.o. at 5 mg/kg, the plasma exposure of MK-5172 was good with an AUC of 0.7 uM.hr. The liver exposure of the compound was quite good (23 uM at 4 hr), and MK-5172 remained in liver 24 hr after a single p.o. 5 mg/kg dose. At 24 hr, the liver concentration of MK-5172 was 0.2 uM, which was over 25-fold higher than the IC50 in the replicon assay with 50% NHS. When dosed to dogs, MK-5172 showed low clearance of 5 ml/min/kg and a 3 hr half-life after i.v. 2 mg/kg dosing and had good plasma exposure (AUC=0.4 uM.hr) after a p.o. 1 mg/kg dose.
1352920-57-0	Gallinamide A (TFA)
1355050-21-3	GS-443902 trisodium GS-443902 trisodium is a potent inhibitor of viral RNA-dependent RNA-polymerases (RdRp), with IC50s of 1.1 µM, 5 µM for RSV RdRp and HCV RdRp, respectively.
1356355-11-7	Saquinavir-[d9] A deuterated squinavir. Saquinavir binds to the active site of the viral protease and prevents cleavage of viral polyproteins, preventing maturation of the virus. Saquinavir inhibits both HIV-1 and HIV-2 proteases.
1365970-03-1	glecaprevir Glecaprevir is a suppressive agent of hepatitis C virus (HCV). Glecaprevir is also a SARS-CoV 3CLpro inhibitor with an IC50 of 4.09 μM.
137433-23-9	(R)-Hydroxychloroquine (R)-Hydroxychloroquine is the enantiomer of Hydroxychloroquine which is a medication used for the treatment of certain malaria. Hydroxychloroquine is efficiently inhibits SARS-CoV-2 infection in vitro.
137433-24-0	(S)-Hydroxychloroquine Hydroxychloroquine is a synthetic antimalarial drug, which can also inhibit Toll-like receptor 7/9 (TLR7/9) signaling.
1375105-96-6	FASN-IN-4 FAS-IN-1, a diazaspiro derivative, has been found to be a fatty acid synthase inhibitor that probably have potential biological usage in anticancer study.
1379746-42-5	Astodrimer
1398046-21-3	Proxalutamide Proxalutamide is a non-steroidal androgen receptor (AR) antagonist with potential anti-tumor activity for the treatment of prostate cancer and breast cancer.
1417700-13-0	ML188 ML188 is a non-covalent SARS-CoV 3CLpro inhibitor with IC50 of 1.5 μM.
1418733-36-4	Hydroxyethylamine Hydroxyethylamine (Compd VII) is a SARS-CoV-2 3CLpro inhibitor with an IC50 of ~10 μM in the spread assay.

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