cycloartocarpin A

Details

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Internal ID 5c6daf97-14ce-45df-9916-c544b52f286c
Taxonomy Phenylpropanoids and polyketides > Flavonoids > Pyranoflavonoids
IUPAC Name 8,10-dihydroxy-3-methoxy-9-[(E)-3-methylbut-1-enyl]-6-(2-methylprop-1-enyl)-6H-chromeno[4,3-b]chromen-7-one
SMILES (Canonical) CC(C)C=CC1=C(C2=C(C=C1O)OC3=C(C2=O)C(OC4=C3C=CC(=C4)OC)C=C(C)C)O
SMILES (Isomeric) CC(C)/C=C/C1=C(C2=C(C=C1O)OC3=C(C2=O)C(OC4=C3C=CC(=C4)OC)C=C(C)C)O
InChI InChI=1S/C26H26O6/c1-13(2)6-8-16-18(27)12-21-22(24(16)28)25(29)23-20(10-14(3)4)31-19-11-15(30-5)7-9-17(19)26(23)32-21/h6-13,20,27-28H,1-5H3/b8-6+
InChI Key FUOITKFXHPXSCA-SOFGYWHQSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C26H26O6
Molecular Weight 434.50 g/mol
Exact Mass 434.17293854 g/mol
Topological Polar Surface Area (TPSA) 85.20 Ų
XlogP 6.00
Atomic LogP (AlogP) 5.95
H-Bond Acceptor 6
H-Bond Donor 2
Rotatable Bonds 4

Synonyms

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Cycloartocarpin?
CHEMBL463093
CHEBI:187603
LMPK12110936
8,10-dihydroxy-3-methoxy-9-[(E)-3-methylbut-1-enyl]-6-(2-methylprop-1-enyl)-6H-chromeno[4,3-b]chromen-7-one

2D Structure

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2D Structure of cycloartocarpin A

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9789 97.89%
Caco-2 - 0.5807 58.07%
Blood Brain Barrier - 0.6250 62.50%
Human oral bioavailability - 0.5286 52.86%
Subcellular localzation Mitochondria 0.6937 69.37%
OATP2B1 inhibitior - 0.7160 71.60%
OATP1B1 inhibitior + 0.8802 88.02%
OATP1B3 inhibitior + 0.9461 94.61%
MATE1 inhibitior - 0.8400 84.00%
OCT2 inhibitior - 0.9750 97.50%
BSEP inhibitior + 0.8528 85.28%
P-glycoprotein inhibitior + 0.9135 91.35%
P-glycoprotein substrate - 0.5598 55.98%
CYP3A4 substrate + 0.6470 64.70%
CYP2C9 substrate - 0.6012 60.12%
CYP2D6 substrate - 0.8383 83.83%
CYP3A4 inhibition + 0.7344 73.44%
CYP2C9 inhibition + 0.7197 71.97%
CYP2C19 inhibition + 0.9161 91.61%
CYP2D6 inhibition - 0.5865 58.65%
CYP1A2 inhibition + 0.8378 83.78%
CYP2C8 inhibition + 0.5107 51.07%
CYP inhibitory promiscuity + 0.9273 92.73%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.9600 96.00%
Carcinogenicity (trinary) Danger 0.4818 48.18%
Eye corrosion - 0.9867 98.67%
Eye irritation - 0.6643 66.43%
Skin irritation - 0.7291 72.91%
Skin corrosion - 0.9651 96.51%
Ames mutagenesis + 0.5500 55.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5795 57.95%
Micronuclear + 0.7600 76.00%
Hepatotoxicity - 0.6375 63.75%
skin sensitisation - 0.8009 80.09%
Respiratory toxicity + 0.6667 66.67%
Reproductive toxicity + 0.7778 77.78%
Mitochondrial toxicity + 0.6750 67.50%
Nephrotoxicity - 0.7779 77.79%
Acute Oral Toxicity (c) III 0.6548 65.48%
Estrogen receptor binding + 0.9272 92.72%
Androgen receptor binding + 0.8664 86.64%
Thyroid receptor binding + 0.7559 75.59%
Glucocorticoid receptor binding + 0.8826 88.26%
Aromatase binding + 0.7134 71.34%
PPAR gamma + 0.8530 85.30%
Honey bee toxicity - 0.6154 61.54%
Biodegradation - 0.8000 80.00%
Crustacea aquatic toxicity - 0.5300 53.00%
Fish aquatic toxicity + 0.9702 97.02%

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 99.22% 91.11%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 96.71% 95.56%
CHEMBL2581 P07339 Cathepsin D 96.55% 98.95%
CHEMBL1806 P11388 DNA topoisomerase II alpha 95.51% 89.00%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 93.03% 99.15%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 92.37% 94.00%
CHEMBL1951 P21397 Monoamine oxidase A 90.48% 91.49%
CHEMBL3401 O75469 Pregnane X receptor 86.72% 94.73%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 86.35% 96.00%
CHEMBL3830 Q2M2I8 Adaptor-associated kinase 84.67% 83.10%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 84.67% 96.09%
CHEMBL5608 Q16288 NT-3 growth factor receptor 84.36% 95.89%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 83.74% 90.71%
CHEMBL3194 P02766 Transthyretin 83.12% 90.71%
CHEMBL1293249 Q13887 Kruppel-like factor 5 83.05% 86.33%
CHEMBL2335 P42785 Lysosomal Pro-X carboxypeptidase 82.59% 100.00%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 81.52% 94.45%
CHEMBL3060 Q9Y345 Glycine transporter 2 81.32% 99.17%
CHEMBL4303 P08238 Heat shock protein HSP 90-beta 80.19% 96.77%

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.
Artocarpus chama
Artocarpus heterophyllus
Artocarpus integer
Broussonetia papyrifera

Cross-Links

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PubChem 44258302
NPASS NPC474161
ChEMBL CHEMBL463093
LOTUS LTS0107831
wikiData Q105001872