2,5-Dihydroxy-4-methoxy-9H-fluoren-9-one

Details

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Internal ID c781b2cf-f234-4b76-b4e6-1bff5278fc8c
Taxonomy Benzenoids > Fluorenes
IUPAC Name 2,5-dihydroxy-4-methoxyfluoren-9-one
SMILES (Canonical) COC1=CC(=CC2=C1C3=C(C2=O)C=CC=C3O)O
SMILES (Isomeric) COC1=CC(=CC2=C1C3=C(C2=O)C=CC=C3O)O
InChI InChI=1S/C14H10O4/c1-18-11-6-7(15)5-9-13(11)12-8(14(9)17)3-2-4-10(12)16/h2-6,15-16H,1H3
InChI Key BNLICISMBGNGFN-UHFFFAOYSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

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Molecular Formula C14H10O4
Molecular Weight 242.23 g/mol
Exact Mass 242.05790880 g/mol
Topological Polar Surface Area (TPSA) 66.80 Ų
XlogP 2.30
Atomic LogP (AlogP) 2.32
H-Bond Acceptor 4
H-Bond Donor 2
Rotatable Bonds 1

Synonyms

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2,5-Dihydroxy-4-methoxy-9H-fluoren-9-one
SCHEMBL7792240
BNLICISMBGNGFN-UHFFFAOYSA-N
97915-33-8

2D Structure

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2D Structure of 2,5-Dihydroxy-4-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 - 0.7657 76.57%
Blood Brain Barrier - 0.6500 65.00%
Human oral bioavailability + 0.6286 62.86%
Subcellular localzation Mitochondria 0.8369 83.69%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9428 94.28%
OATP1B3 inhibitior + 0.9822 98.22%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.9500 95.00%
BSEP inhibitior - 0.6345 63.45%
P-glycoprotein inhibitior - 0.8712 87.12%
P-glycoprotein substrate - 0.8462 84.62%
CYP3A4 substrate + 0.5233 52.33%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate + 0.3460 34.60%
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 + 0.4578 45.78%
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 + 0.9530 95.30%
Skin irritation + 0.5055 50.55%
Skin corrosion - 0.9775 97.75%
Ames mutagenesis + 0.6400 64.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7598 75.98%
Micronuclear + 0.8059 80.59%
Hepatotoxicity + 0.6157 61.57%
skin sensitisation - 0.9347 93.47%
Respiratory toxicity - 0.6333 63.33%
Reproductive toxicity + 0.6222 62.22%
Mitochondrial toxicity + 0.5375 53.75%
Nephrotoxicity + 0.8713 87.13%
Acute Oral Toxicity (c) III 0.4647 46.47%
Estrogen receptor binding + 0.8238 82.38%
Androgen receptor binding + 0.6310 63.10%
Thyroid receptor binding + 0.5344 53.44%
Glucocorticoid receptor binding + 0.7456 74.56%
Aromatase binding + 0.5193 51.93%
PPAR gamma + 0.5404 54.04%
Honey bee toxicity - 0.9290 92.90%
Biodegradation - 0.8000 80.00%
Crustacea aquatic toxicity - 0.5549 55.49%
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
CHEMBL2581 P07339 Cathepsin D 97.80% 98.95%
CHEMBL1951 P21397 Monoamine oxidase A 97.26% 91.49%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 96.86% 95.56%
CHEMBL2535 P11166 Glucose transporter 92.92% 98.75%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 92.34% 91.11%
CHEMBL1293249 Q13887 Kruppel-like factor 5 91.59% 86.33%
CHEMBL1806 P11388 DNA topoisomerase II alpha 89.52% 89.00%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 89.18% 96.09%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 88.22% 99.23%
CHEMBL1937 Q92769 Histone deacetylase 2 86.93% 94.75%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 86.89% 94.00%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 86.16% 99.15%
CHEMBL1907 P15144 Aminopeptidase N 85.01% 93.31%
CHEMBL4208 P20618 Proteasome component C5 83.08% 90.00%
CHEMBL2146302 O94925 Glutaminase kidney isoform, mitochondrial 82.25% 100.00%
CHEMBL5608 Q16288 NT-3 growth factor receptor 81.75% 95.89%
CHEMBL3060 Q9Y345 Glycine transporter 2 81.67% 99.17%
CHEMBL2378 P30307 Dual specificity phosphatase Cdc25C 80.82% 96.67%

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.
Dendrobium chrysotoxum
Dendrobium densiflorum
Dendrobium plicatile

Cross-Links

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PubChem 10879298
NPASS NPC279479
LOTUS LTS0215778
wikiData Q104938874