SML1010

L-742001 hydrochloride

≥98% (HPLC)

• Synonym(e): (Z)-4-[1-Benzyl-4-[(4-chlorophenyl)methyl]piperidin-4-yl]-2-hydroxy-4-oxobut-2-enoic acid hydrochloride, 4-[4-[(4-Chlorophenyl)methyl]-1-(phenylmethyl)-4-piperidinyl]-2-hydroxy-4-oxo-2-butenoic acid hydrochloride, L-742,001 hydrochloride, L742001 hydrochloride
• Empirische Formel (Hill-System): C₂₃H₂₄ClNO₄ · HCl
• CAS-Nummer: 174605-64-2
• Molekulargewicht: 450.35
• MDL-Nummer: MFCD22587878
• UNSPSC-Code: 51111800
• PubChem Substanz-ID: 329825629
• NACRES: NA.77

Eigenschaften

• Assay: ≥98% (HPLC)
• Form: powder
• Lagerbedingungen: desiccated
• Farbe: white to beige
• Löslichkeit: DMSO: 20 mg/mL, clear
• Lagertemp.: 2-8°C
• SMILES String: O/C(C(O)=O)=C\C(C(CC1)(CC2=CC=C(Cl)C=C2)CCN1CC3=CC=CC=C3)=O.Cl
• InChI: 1S/C23H24ClNO4.ClH/c24-19-8-6-17(7-9-19)15-23(21(27)14-20(26)22(28)29)10-12-25(13-11-23)16-18-4-2-1-3-5-18;/h1-9,14,26H,10-13,15-16H2,(H,28,29);1H/b20-14-;
• InChIKey: LMLNSXCRZNNZBT-VSOKSMTPSA-N

Beschreibung

Biochem./physiol. Wirkung

L-742,001 is an inhibitor of the influenza virus RNA polymerase PA subunit.

L-742,001 is an inhibitor of the influenza virus RNA polymerase PA subunit, implicated in several roles, including endonuclease and protease activities as well as viral RNA/complementary RNA promoter binding. L-742,001 inhibits the influenza endonuclease-dependent polymerase activity with an IC₅₀ of 430 nM.

L-742001 is useful in the treatment of influenza viral infection.[1]

Sicherheitshinweise

• Piktogramme: GHS07,GHS09
• Signalwort: Warning
• H-Sätze: H302,H410
• P-Sätze: P264 - P270 - P273 - P301 + P312 - P391 - P501
• Gefahreneinstufungen: Acute Tox. 4 Oral - Aquatic Acute 1 - Aquatic Chronic 1
• Lagerklassenschlüssel: 11 - Combustible Solids
• WGK: WGK 3
• Flammpunkt (°F): Not applicable
• Flammpunkt (°C): Not applicable