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About This Item
Empirical Formula (Hill Notation):
C12H9NO3
CAS Number:
Molecular Weight:
215.20
MDL number:
UNSPSC Code:
12161501
PubChem Substance ID:
description
Light sensitive
Assay
≥90% (at 254 nm, HPLC)
form
powder
solubility
DMSO: soluble
fluorescence
λem 411 nm (+/- 4nm)
SMILES string
CCOc1ccc2C=C(C#N)C(=O)Oc2c1
InChI
1S/C12H9NO3/c1-2-15-10-4-3-8-5-9(7-13)12(14)16-11(8)6-10/h3-6H,2H2,1H3
InChI key
YAFGHMIAFYQSCF-UHFFFAOYSA-N
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Biochem/physiol Actions
Fluorescent probe useful in microsomal dealkylase studies.
Fluorescent probe useful in microsomal dealkylase studies. Typical drug-drug interactions resulting from enzyme inhibition.
Signal Word
Warning
Hazard Statements
Precautionary Statements
Hazard Classifications
Acute Tox. 4 Dermal - Acute Tox. 4 Inhalation - Acute Tox. 4 Oral - Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
Target Organs
Respiratory system
Storage Class Code
11 - Combustible Solids
WGK
WGK 3
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
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Drug resistance by Plasmodium falciparum remains a challenge in malaria chemotherapy. This paper will focus on physicochemical and drug metabolism characterization of a series of 4-aminoquinoline-3-hydroxypyridin-4-one hybrid shown to have antimalarial activity against chloroquine-resistant P. falciparum. The aim is to
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