Fig. 1 · Structure

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Ledipasvir hydrochloride

HCV NS5A Inhibitor

Ledipasvir hydrochloride is a potent inhibitor of the hepatitis C virus NS5A, exhibiting EC50 values of 34 pM and 4 pM for genotype 1a and 1b replicons, respectively. In addition to its antiviral activity against HCV, Ledipasvir hydrochloride functions as an inhibitor of SARS-CoV 3CLpro, with an IC50 of 1.62 μM. This compound is valuable for researching hepatitis C therapies and studying coronavirus protease functions in viral replication.

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Specifications

Manufacturer Adooq Bioscience
Actions Inhibitor
CAS Number 2128695-48-5
Applications HCV NS5A Inhibitor
Formula C49H55ClF2N8O6
Molecular Weight 925.46
Synonyms GS-5885 hydrochloride
SMILES
O=C(OC)N[C@H](C(N([C@H](C1=NC=C(C2=CC(C(F)(F)C3=C4C=CC(C5=CC=C6N=C([C@H]7N(C([C@@H](NC(OC)=O)C(C)C)=O)[C@]8([H])CC[C@@]7([H])C8)NC6=C5)=C3)=C4C=C2)N1)C9)CC%109CC%10)=O)C(C)C.Cl

Storage & Solubility

In Vitro Solubility

Reported Solubility

No reported solubility data are available for this product.

Preparing Stock Solutions

Stock preparation is unavailable for this product molecular weight.

Calculated stock concentrations do not establish solvent solubility. Refer to the reported solubility data for experimental guidance.

Storage

Store powder at -20°C, keep desiccated.
In powder form, the chemical is stable for 36 months.
In solution, store at -20°C and use within 1 month to prevent loss of potency. Aliquot to avoid multiple freeze/thaw cycles.

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