2-(2-Hydroxypentyl)-7-methoxy-4-oxochromene-5-carboxylic acid

Details

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Internal ID 9ad9eb92-245b-4708-88f7-5142d2288382
Taxonomy Organoheterocyclic compounds > Benzopyrans > 1-benzopyrans > Chromones
IUPAC Name 2-(2-hydroxypentyl)-7-methoxy-4-oxochromene-5-carboxylic acid
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C16H18O6/c1-3-4-9(17)5-11-7-13(18)15-12(16(19)20)6-10(21-2)8-14(15)22-11/h6-9,17H,3-5H2,1-2H3,(H,19,20)
InChI Key XSFAYPJLJAJJPJ-UHFFFAOYSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

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Molecular Formula C16H18O6
Molecular Weight 306.31 g/mol
Exact Mass 306.11033829 g/mol
Topological Polar Surface Area (TPSA) 93.10 Ų
XlogP 1.90
Atomic LogP (AlogP) 2.20
H-Bond Acceptor 5
H-Bond Donor 2
Rotatable Bonds 6

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 2-(2-Hydroxypentyl)-7-methoxy-4-oxochromene-5-carboxylic acid

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9595 95.95%
Caco-2 + 0.5733 57.33%
Blood Brain Barrier - 0.6500 65.00%
Human oral bioavailability + 0.5714 57.14%
Subcellular localzation Mitochondria 0.6971 69.71%
OATP2B1 inhibitior - 0.8595 85.95%
OATP1B1 inhibitior + 0.8958 89.58%
OATP1B3 inhibitior + 0.8942 89.42%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.9250 92.50%
BSEP inhibitior + 0.5741 57.41%
P-glycoprotein inhibitior - 0.7417 74.17%
P-glycoprotein substrate - 0.7828 78.28%
CYP3A4 substrate - 0.5638 56.38%
CYP2C9 substrate - 0.6150 61.50%
CYP2D6 substrate - 0.8609 86.09%
CYP3A4 inhibition - 0.6390 63.90%
CYP2C9 inhibition - 0.8719 87.19%
CYP2C19 inhibition - 0.7714 77.14%
CYP2D6 inhibition - 0.8760 87.60%
CYP1A2 inhibition - 0.5820 58.20%
CYP2C8 inhibition - 0.8381 83.81%
CYP inhibitory promiscuity - 0.8591 85.91%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.9400 94.00%
Carcinogenicity (trinary) Non-required 0.6746 67.46%
Eye corrosion - 0.9862 98.62%
Eye irritation + 0.6101 61.01%
Skin irritation - 0.8469 84.69%
Skin corrosion - 0.9415 94.15%
Ames mutagenesis - 0.6700 67.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6854 68.54%
Micronuclear - 0.6100 61.00%
Hepatotoxicity - 0.6091 60.91%
skin sensitisation - 0.9260 92.60%
Respiratory toxicity + 0.7333 73.33%
Reproductive toxicity + 0.8333 83.33%
Mitochondrial toxicity + 0.7375 73.75%
Nephrotoxicity - 0.7732 77.32%
Acute Oral Toxicity (c) III 0.6923 69.23%
Estrogen receptor binding + 0.8394 83.94%
Androgen receptor binding + 0.7473 74.73%
Thyroid receptor binding - 0.6028 60.28%
Glucocorticoid receptor binding + 0.8793 87.93%
Aromatase binding + 0.7320 73.20%
PPAR gamma + 0.8352 83.52%
Honey bee toxicity - 0.8951 89.51%
Biodegradation - 0.8000 80.00%
Crustacea aquatic toxicity - 0.7000 70.00%
Fish aquatic toxicity + 0.9493 94.93%

Targets

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Proven Targets:

CHEMBL ID UniProt ID Name Min activity Assay type Source
No proven targets yet!

Predicted Targets (via Super-PRED):

CHEMBL ID UniProt ID Name Probability Model accuracy
CHEMBL2581 P07339 Cathepsin D 95.75% 98.95%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 94.16% 85.14%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 92.84% 91.11%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 92.46% 96.09%
CHEMBL3060 Q9Y345 Glycine transporter 2 92.10% 99.17%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 90.55% 95.50%
CHEMBL1811 P34995 Prostanoid EP1 receptor 90.02% 95.71%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 89.12% 94.45%
CHEMBL1293249 Q13887 Kruppel-like factor 5 88.53% 86.33%
CHEMBL3807 P17706 T-cell protein-tyrosine phosphatase 87.68% 93.00%
CHEMBL1293294 P51151 Ras-related protein Rab-9A 87.52% 87.67%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 87.33% 95.56%
CHEMBL3864 Q06124 Protein-tyrosine phosphatase 2C 86.06% 94.42%
CHEMBL3401 O75469 Pregnane X receptor 85.62% 94.73%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 84.54% 90.71%
CHEMBL340 P08684 Cytochrome P450 3A4 84.09% 91.19%
CHEMBL1293277 O15118 Niemann-Pick C1 protein 82.34% 81.11%
CHEMBL1293267 Q9HC97 G-protein coupled receptor 35 82.07% 89.34%
CHEMBL1907 P15144 Aminopeptidase N 81.12% 93.31%
CHEMBL2535 P11166 Glucose transporter 81.01% 98.75%

Plants that contains it

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Below are displayed all the plants proven (via scientific papers) to contain this compound!
To see more specific details click the taxa you are interested in.
Stratiotes aloides

Cross-Links

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PubChem 44139741
LOTUS LTS0220039
wikiData Q105340998