1,4,7-trihydroxy-5-methoxy-9H-fluoren-9-one

Details

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Internal ID 646df204-4601-4360-b39a-ab8cf391572f
Taxonomy Benzenoids > Fluorenes
IUPAC Name 1,4,7-trihydroxy-5-methoxyfluoren-9-one
SMILES (Canonical) COC1=CC(=CC2=C1C3=C(C=CC(=C3C2=O)O)O)O
SMILES (Isomeric) COC1=CC(=CC2=C1C3=C(C=CC(=C3C2=O)O)O)O
InChI InChI=1S/C14H10O5/c1-19-10-5-6(15)4-7-11(10)12-8(16)2-3-9(17)13(12)14(7)18/h2-5,15-17H,1H3
InChI Key QYZVZXXDXPZMHM-UHFFFAOYSA-N
Popularity 5 references in papers

Physical and Chemical Properties

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Molecular Formula C14H10O5
Molecular Weight 258.23 g/mol
Exact Mass 258.05282342 g/mol
Topological Polar Surface Area (TPSA) 87.00 Ų
XlogP 2.50
Atomic LogP (AlogP) 2.02
H-Bond Acceptor 5
H-Bond Donor 3
Rotatable Bonds 1

Synonyms

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365545-85-3
1,4,7-trihydroxy-5-methoxy-9H-fluoren-9-one
CHEMBL216941
DTXSID40658827

2D Structure

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2D Structure of 1,4,7-trihydroxy-5-methoxy-9H-fluoren-9-one

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9967 99.67%
Caco-2 - 0.8543 85.43%
Blood Brain Barrier - 0.6500 65.00%
Human oral bioavailability - 0.5000 50.00%
Subcellular localzation Mitochondria 0.8369 83.69%
OATP2B1 inhibitior - 0.7135 71.35%
OATP1B1 inhibitior + 0.9591 95.91%
OATP1B3 inhibitior + 0.9822 98.22%
MATE1 inhibitior - 0.9000 90.00%
OCT2 inhibitior - 0.9500 95.00%
BSEP inhibitior - 0.7292 72.92%
P-glycoprotein inhibitior - 0.8932 89.32%
P-glycoprotein substrate - 0.9457 94.57%
CYP3A4 substrate - 0.5552 55.52%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.7800 78.00%
CYP3A4 inhibition - 0.5963 59.63%
CYP2C9 inhibition + 0.7605 76.05%
CYP2C19 inhibition + 0.8229 82.29%
CYP2D6 inhibition - 0.7689 76.89%
CYP1A2 inhibition + 0.9861 98.61%
CYP2C8 inhibition - 0.6322 63.22%
CYP inhibitory promiscuity + 0.6410 64.10%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.7833 78.33%
Carcinogenicity (trinary) Non-required 0.4291 42.91%
Eye corrosion - 0.9807 98.07%
Eye irritation + 0.9612 96.12%
Skin irritation + 0.5055 50.55%
Skin corrosion - 0.9775 97.75%
Ames mutagenesis + 0.6200 62.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7409 74.09%
Micronuclear + 0.8059 80.59%
Hepatotoxicity + 0.5750 57.50%
skin sensitisation - 0.9347 93.47%
Respiratory toxicity - 0.5444 54.44%
Reproductive toxicity + 0.6222 62.22%
Mitochondrial toxicity + 0.5375 53.75%
Nephrotoxicity + 0.8285 82.85%
Acute Oral Toxicity (c) III 0.4647 46.47%
Estrogen receptor binding + 0.8061 80.61%
Androgen receptor binding + 0.6763 67.63%
Thyroid receptor binding + 0.5933 59.33%
Glucocorticoid receptor binding + 0.8657 86.57%
Aromatase binding + 0.5337 53.37%
PPAR gamma + 0.6261 62.61%
Honey bee toxicity - 0.9332 93.32%
Biodegradation - 0.6750 67.50%
Crustacea aquatic toxicity - 0.5649 56.49%
Fish aquatic toxicity + 0.9519 95.19%

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
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 95.36% 91.11%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 95.03% 95.56%
CHEMBL2581 P07339 Cathepsin D 93.23% 98.95%
CHEMBL1951 P21397 Monoamine oxidase A 92.70% 91.49%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 89.90% 96.09%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 88.99% 99.15%
CHEMBL4208 P20618 Proteasome component C5 88.40% 90.00%
CHEMBL1806 P11388 DNA topoisomerase II alpha 88.37% 89.00%
CHEMBL1293249 Q13887 Kruppel-like factor 5 87.43% 86.33%
CHEMBL2535 P11166 Glucose transporter 86.73% 98.75%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 84.51% 94.00%
CHEMBL3194 P02766 Transthyretin 84.12% 90.71%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 82.37% 99.23%
CHEMBL3060 Q9Y345 Glycine transporter 2 80.96% 99.17%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 80.27% 90.71%

Plants that contains it

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Cross-Links

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PubChem 44418788
NPASS NPC216624
ChEMBL CHEMBL216941
LOTUS LTS0094914
wikiData Q82575186