Abbottin

Details

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Internal ID 93499552-05f0-4118-a352-165e27fb0fba
Taxonomy Phenylpropanoids and polyketides > Flavonoids > O-methylated flavonoids > 5-O-methylated flavonoids
IUPAC Name 5-methoxy-2-phenyl-8-prop-1-en-2-yl-8,9-dihydro-4H-furo[2,3-h]chromene
SMILES (Canonical) CC(=C)C1CC2=C3C(=C(C=C2O1)OC)CC=C(O3)C4=CC=CC=C4
SMILES (Isomeric) CC(=C)C1CC2=C3C(=C(C=C2O1)OC)CC=C(O3)C4=CC=CC=C4
InChI InChI=1S/C21H20O3/c1-13(2)18-11-16-20(23-18)12-19(22-3)15-9-10-17(24-21(15)16)14-7-5-4-6-8-14/h4-8,10,12,18H,1,9,11H2,2-3H3
InChI Key PNYACUFKSKMATN-UHFFFAOYSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C21H20O3
Molecular Weight 320.40 g/mol
Exact Mass 320.14124450 g/mol
Topological Polar Surface Area (TPSA) 27.70 Ų
XlogP 5.20
Atomic LogP (AlogP) 4.55
H-Bond Acceptor 3
H-Bond Donor 0
Rotatable Bonds 3

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of Abbottin

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 1.0000 100.00%
Caco-2 + 0.8658 86.58%
Blood Brain Barrier + 0.6250 62.50%
Human oral bioavailability - 0.5143 51.43%
Subcellular localzation Mitochondria 0.6746 67.46%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9001 90.01%
OATP1B3 inhibitior + 0.9405 94.05%
MATE1 inhibitior - 0.9000 90.00%
OCT2 inhibitior - 0.8250 82.50%
BSEP inhibitior + 0.8504 85.04%
P-glycoprotein inhibitior + 0.7676 76.76%
P-glycoprotein substrate - 0.7834 78.34%
CYP3A4 substrate + 0.5583 55.83%
CYP2C9 substrate - 0.5827 58.27%
CYP2D6 substrate + 0.4034 40.34%
CYP3A4 inhibition + 0.7478 74.78%
CYP2C9 inhibition + 0.5495 54.95%
CYP2C19 inhibition + 0.8336 83.36%
CYP2D6 inhibition - 0.7837 78.37%
CYP1A2 inhibition + 0.8058 80.58%
CYP2C8 inhibition + 0.6973 69.73%
CYP inhibitory promiscuity + 0.9265 92.65%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.9300 93.00%
Carcinogenicity (trinary) Non-required 0.5987 59.87%
Eye corrosion - 0.9822 98.22%
Eye irritation - 0.8170 81.70%
Skin irritation - 0.7773 77.73%
Skin corrosion - 0.9547 95.47%
Ames mutagenesis - 0.6800 68.00%
Human Ether-a-go-go-Related Gene inhibition + 0.7955 79.55%
Micronuclear - 0.5300 53.00%
Hepatotoxicity - 0.6300 63.00%
skin sensitisation - 0.6821 68.21%
Respiratory toxicity + 0.5222 52.22%
Reproductive toxicity + 0.8000 80.00%
Mitochondrial toxicity - 0.5625 56.25%
Nephrotoxicity + 0.5732 57.32%
Acute Oral Toxicity (c) III 0.5510 55.10%
Estrogen receptor binding + 0.6879 68.79%
Androgen receptor binding + 0.6633 66.33%
Thyroid receptor binding + 0.6246 62.46%
Glucocorticoid receptor binding + 0.7288 72.88%
Aromatase binding + 0.5686 56.86%
PPAR gamma + 0.7351 73.51%
Honey bee toxicity - 0.5852 58.52%
Biodegradation - 0.9000 90.00%
Crustacea aquatic toxicity + 0.7200 72.00%
Fish aquatic toxicity + 0.9868 98.68%

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
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 96.88% 96.09%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 96.41% 91.11%
CHEMBL1293249 Q13887 Kruppel-like factor 5 93.55% 86.33%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 89.40% 95.56%
CHEMBL1966 Q02127 Dihydroorotate dehydrogenase 87.40% 96.09%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 87.35% 95.50%
CHEMBL2581 P07339 Cathepsin D 87.34% 98.95%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 87.07% 85.14%
CHEMBL1951 P21397 Monoamine oxidase A 86.52% 91.49%
CHEMBL3060 Q9Y345 Glycine transporter 2 86.40% 99.17%
CHEMBL5608 Q16288 NT-3 growth factor receptor 85.74% 95.89%
CHEMBL4478 Q00975 Voltage-gated N-type calcium channel alpha-1B subunit 85.45% 97.14%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 82.10% 94.00%
CHEMBL5028 O14672 ADAM10 81.29% 97.50%
CHEMBL2535 P11166 Glucose transporter 80.11% 98.75%
CHEMBL4769 O95749 Geranylgeranyl pyrophosphate synthetase 80.04% 92.08%

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.
Tephrosia crassifolia

Cross-Links

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PubChem 15479309
LOTUS LTS0096905
wikiData Q105212274