abyssinin I

Details

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Internal ID 75d871f3-baf6-4840-952c-f7ca5839abae
Taxonomy Phenylpropanoids and polyketides > Flavonoids > Pyranoflavonoids
IUPAC Name 5,7-dihydroxy-2-(8-methoxy-2,2-dimethylchromen-6-yl)-2,3-dihydrochromen-4-one
SMILES (Canonical) CC1(C=CC2=C(O1)C(=CC(=C2)C3CC(=O)C4=C(C=C(C=C4O3)O)O)OC)C
SMILES (Isomeric) CC1(C=CC2=C(O1)C(=CC(=C2)C3CC(=O)C4=C(C=C(C=C4O3)O)O)OC)C
InChI InChI=1S/C21H20O6/c1-21(2)5-4-11-6-12(7-18(25-3)20(11)27-21)16-10-15(24)19-14(23)8-13(22)9-17(19)26-16/h4-9,16,22-23H,10H2,1-3H3
InChI Key SDUMAACMVUGGAC-UHFFFAOYSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

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Molecular Formula C21H20O6
Molecular Weight 368.40 g/mol
Exact Mass 368.12598835 g/mol
Topological Polar Surface Area (TPSA) 85.20 Ų
XlogP 3.60
Atomic LogP (AlogP) 4.00
H-Bond Acceptor 6
H-Bond Donor 2
Rotatable Bonds 2

Synonyms

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BDBM50212390

2D Structure

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2D Structure of abyssinin I

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9456 94.56%
Caco-2 + 0.5395 53.95%
Blood Brain Barrier - 0.7000 70.00%
Human oral bioavailability - 0.8143 81.43%
Subcellular localzation Mitochondria 0.6946 69.46%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9109 91.09%
OATP1B3 inhibitior + 0.9661 96.61%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.9250 92.50%
BSEP inhibitior + 0.6584 65.84%
P-glycoprotein inhibitior - 0.5315 53.15%
P-glycoprotein substrate - 0.6369 63.69%
CYP3A4 substrate + 0.6588 65.88%
CYP2C9 substrate - 0.7981 79.81%
CYP2D6 substrate - 0.8063 80.63%
CYP3A4 inhibition + 0.7621 76.21%
CYP2C9 inhibition - 0.5398 53.98%
CYP2C19 inhibition + 0.7267 72.67%
CYP2D6 inhibition + 0.5167 51.67%
CYP1A2 inhibition - 0.5559 55.59%
CYP2C8 inhibition + 0.5885 58.85%
CYP inhibitory promiscuity + 0.7174 71.74%
UGT catelyzed + 0.9000 90.00%
Carcinogenicity (binary) - 0.9800 98.00%
Carcinogenicity (trinary) Danger 0.4399 43.99%
Eye corrosion - 0.9886 98.86%
Eye irritation - 0.5222 52.22%
Skin irritation - 0.7893 78.93%
Skin corrosion - 0.9457 94.57%
Ames mutagenesis - 0.5800 58.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5268 52.68%
Micronuclear + 0.6159 61.59%
Hepatotoxicity - 0.5843 58.43%
skin sensitisation - 0.8491 84.91%
Respiratory toxicity + 0.5667 56.67%
Reproductive toxicity + 0.8222 82.22%
Mitochondrial toxicity + 0.5750 57.50%
Nephrotoxicity + 0.7075 70.75%
Acute Oral Toxicity (c) III 0.5842 58.42%
Estrogen receptor binding + 0.8543 85.43%
Androgen receptor binding - 0.4935 49.35%
Thyroid receptor binding + 0.6087 60.87%
Glucocorticoid receptor binding + 0.8023 80.23%
Aromatase binding - 0.6604 66.04%
PPAR gamma + 0.8200 82.00%
Honey bee toxicity - 0.6973 69.73%
Biodegradation - 0.8750 87.50%
Crustacea aquatic toxicity - 0.5600 56.00%
Fish aquatic toxicity + 0.8631 86.31%

Targets

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Proven Targets:

CHEMBL ID UniProt ID Name Min activity Assay type Source
CHEMBL335 P18031 Protein-tyrosine phosphatase 1B 18200 nM
IC50
DOI: 10.6019/CHEMBL1201861

Predicted Targets (via Super-PRED):

CHEMBL ID UniProt ID Name Probability Model accuracy
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 99.36% 91.11%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 99.13% 85.14%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 97.91% 96.09%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 96.46% 94.45%
CHEMBL4040 P28482 MAP kinase ERK2 95.72% 83.82%
CHEMBL4208 P20618 Proteasome component C5 93.29% 90.00%
CHEMBL1806 P11388 DNA topoisomerase II alpha 92.49% 89.00%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 91.36% 99.23%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 90.94% 95.56%
CHEMBL4478 Q00975 Voltage-gated N-type calcium channel alpha-1B subunit 88.30% 97.14%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 87.15% 94.00%
CHEMBL241 Q14432 Phosphodiesterase 3A 86.99% 92.94%
CHEMBL1293249 Q13887 Kruppel-like factor 5 86.66% 86.33%
CHEMBL3137262 O60341 LSD1/CoREST complex 86.19% 97.09%
CHEMBL5608 Q16288 NT-3 growth factor receptor 85.08% 95.89%
CHEMBL2581 P07339 Cathepsin D 84.93% 98.95%
CHEMBL3192 Q9BY41 Histone deacetylase 8 84.63% 93.99%
CHEMBL2535 P11166 Glucose transporter 84.35% 98.75%
CHEMBL2069156 Q14145 Kelch-like ECH-associated protein 1 83.18% 82.38%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 82.31% 92.62%

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.
Erythrina abyssinica
Erythrina abyssinica

Cross-Links

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PubChem 44424650
NPASS NPC473272
ChEMBL CHEMBL389736
LOTUS LTS0068627
wikiData Q105250850