2,4-Quinolinediol

AlkaPlorer ID: AK009976

Synonym: 4-Hydroxy-2(1H)-quinolinone, 4-Hydroxycarbostyril, 2,4-Dihydroxyquinoline, 2-Hydroxy-4(1H)-quinolinone, 2,4(1H,3H)-Quinolinedione 

IUPAC Name: 4-hydroxy-1H-quinolin-2-one

Structure

SMILES: OC1=CC(O)=C2C=CC=CC2=N1

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InChI: InChI=1S/C9H7NO2/c11-8-5-9(12)10-7-4-2-1-3-6(7)8/h1-5H,(H2,10,11,12)

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InChIKey: HDHQZCHIXUUSMK-UHFFFAOYSA-N

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Source

Properties Information

Molecule Weight: 161.15999999999997

TPSA: 53.35

MolLogP: 1.6459999999999992

Number of H-Donors: 2

Number of H-Acceptors: 3

RingCount: 2

Activities Information

Organism Target Name Standard Type Standard Value Standard Units doi
Homo sapiens Aldehyde dehydrogenase 1A1 Potency 5011.9 nM None
Homo sapiens Geminin Potency 8199.5 nM None
Homo sapiens Guanine nucleotide-binding protein G(s), subunit alpha Potency 3981.1 nM None
Homo sapiens Histone-lysine N-methyltransferase, H3 lysine-9 specific 3 Potency 79432.8 nM None
Homo sapiens Lysine-specific demethylase 4D-like Potency 39810.7 nM None
Mycobacterium tuberculosis Mycobacterium tuberculosis Inhibition 0.0 % 10.1016/j.bmcl.2006.09.082
Trichophyton benhamiae Trichophyton benhamiae MIC 500000000.0 nM 10.1016/j.bmcl.2006.09.082
None Unchecked Potency 206.0 nM None

Metabolism Information

AKRT ID Reaction Reaction Link ID
AKRT012664 C[33S].O=c1cc(O)c2ccccc2[nH]1>>COc1cc(=O)[nH]c2ccccc12 None
AKRT014742 C[SAH].O=c1cc(O)c2ccccc2[nH]1>>COc1cc(=O)[nH]c2ccccc12 enzymemap_27344
AKRT020702 Nc1ccccc1C(=O)CC(=O)[CoA]>>O=c1cc(O)c2ccccc2[nH]1 RXN-17704
AKRT020771 Nc1ccccc1C(=O)[CoA].O=C(O)CC(=O)[CoA]>>O=c1cc(O)c2ccccc2[nH]1 MNXR176186
AKRT024354 O=c1cc(O)[nH]c2ccccc12>>O=c1cc(O)c2ccccc2[nH]1 RXN-12950
AKRT024355 O=c1cc(O)c2ccccc2[nH]1>>O=c1cc(O)[nH]c2ccccc12 RXN-12950
AKRT024356 O=c1cc(O)c2ccccc2[nH]1>>OC1=CC(O)Nc2ccccc21 MNXR176534
AKRT024802 OC1=CC(O)Nc2ccccc21>>O=c1cc(O)[nH]c2ccccc12 RXN-12951
AKRT024803 OC1=CC(O)Nc2ccccc21>>O=c1cc(O)c2ccccc2[nH]1 RXN-12952