Isocudraxanthone K

Details

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Internal ID ef647a3d-bf85-4366-a72f-d4051466cd0c
Taxonomy Organoheterocyclic compounds > Benzopyrans > 1-benzopyrans > Xanthones > Pyranoxanthones
IUPAC Name 5,8,10-trihydroxy-3,3-dimethyl-9-(2-methylbut-3-en-2-yl)pyrano[2,3-c]xanthen-7-one
SMILES (Canonical) CC1(C=CC2=C3C(=CC(=C2O1)O)C(=O)C4=C(O3)C=C(C(=C4O)C(C)(C)C=C)O)C
SMILES (Isomeric) CC1(C=CC2=C3C(=CC(=C2O1)O)C(=O)C4=C(O3)C=C(C(=C4O)C(C)(C)C=C)O)C
InChI InChI=1S/C23H22O6/c1-6-22(2,3)17-13(24)10-15-16(19(17)27)18(26)12-9-14(25)21-11(20(12)28-15)7-8-23(4,5)29-21/h6-10,24-25,27H,1H2,2-5H3
InChI Key DKKSZAXBHZPWMV-UHFFFAOYSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C23H22O6
Molecular Weight 394.40 g/mol
Exact Mass 394.14163842 g/mol
Topological Polar Surface Area (TPSA) 96.20 Ų
XlogP 5.30
Atomic LogP (AlogP) 4.71
H-Bond Acceptor 6
H-Bond Donor 3
Rotatable Bonds 2

Synonyms

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5,8,10-trihydroxy-3,3-dimethyl-9-(2-methylbut-3-en-2-yl)pyrano(2,3-c)xanthen-7-one
5,8,10-trihydroxy-3,3-dimethyl-9-(2-methylbut-3-en-2-yl)pyrano[2,3-c]xanthen-7-one
RefChem:149227
904910-63-0
CHEMBL390040
BDBM50217273

2D Structure

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2D Structure of Isocudraxanthone K

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9591 95.91%
Caco-2 - 0.6109 61.09%
Blood Brain Barrier - 0.6750 67.50%
Human oral bioavailability + 0.6286 62.86%
Subcellular localzation Mitochondria 0.6107 61.07%
OATP2B1 inhibitior - 0.5599 55.99%
OATP1B1 inhibitior + 0.8927 89.27%
OATP1B3 inhibitior + 0.9586 95.86%
MATE1 inhibitior - 0.8000 80.00%
OCT2 inhibitior - 1.0000 100.00%
BSEP inhibitior - 0.4594 45.94%
P-glycoprotein inhibitior + 0.6273 62.73%
P-glycoprotein substrate - 0.6126 61.26%
CYP3A4 substrate + 0.6466 64.66%
CYP2C9 substrate - 0.6166 61.66%
CYP2D6 substrate - 0.8418 84.18%
CYP3A4 inhibition + 0.6446 64.46%
CYP2C9 inhibition - 0.5930 59.30%
CYP2C19 inhibition - 0.5615 56.15%
CYP2D6 inhibition - 0.8284 82.84%
CYP1A2 inhibition + 0.7432 74.32%
CYP2C8 inhibition + 0.5532 55.32%
CYP inhibitory promiscuity + 0.5841 58.41%
UGT catelyzed - 0.6000 60.00%
Carcinogenicity (binary) - 0.9900 99.00%
Carcinogenicity (trinary) Non-required 0.5725 57.25%
Eye corrosion - 0.9874 98.74%
Eye irritation + 0.7048 70.48%
Skin irritation - 0.6804 68.04%
Skin corrosion - 0.8789 87.89%
Ames mutagenesis + 0.5330 53.30%
Human Ether-a-go-go-Related Gene inhibition - 0.4104 41.04%
Micronuclear + 0.6800 68.00%
Hepatotoxicity + 0.5625 56.25%
skin sensitisation - 0.6539 65.39%
Respiratory toxicity + 0.7000 70.00%
Reproductive toxicity + 0.6444 64.44%
Mitochondrial toxicity - 0.5500 55.00%
Nephrotoxicity - 0.8084 80.84%
Acute Oral Toxicity (c) III 0.7041 70.41%
Estrogen receptor binding + 0.8401 84.01%
Androgen receptor binding + 0.6446 64.46%
Thyroid receptor binding + 0.7601 76.01%
Glucocorticoid receptor binding + 0.7885 78.85%
Aromatase binding + 0.7841 78.41%
PPAR gamma + 0.8088 80.88%
Honey bee toxicity - 0.6816 68.16%
Biodegradation - 0.8750 87.50%
Crustacea aquatic toxicity + 0.5400 54.00%
Fish aquatic toxicity + 0.9830 98.30%

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 99.14% 91.11%
CHEMBL1951 P21397 Monoamine oxidase A 98.06% 91.49%
CHEMBL1806 P11388 DNA topoisomerase II alpha 96.52% 89.00%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 94.76% 95.56%
CHEMBL2581 P07339 Cathepsin D 94.57% 98.95%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 92.77% 94.45%
CHEMBL3401 O75469 Pregnane X receptor 90.85% 94.73%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 87.82% 99.23%
CHEMBL4051 P13569 Cystic fibrosis transmembrane conductance regulator 87.57% 95.71%
CHEMBL2335 P42785 Lysosomal Pro-X carboxypeptidase 86.85% 100.00%
CHEMBL2964 P36507 Dual specificity mitogen-activated protein kinase kinase 2 86.64% 80.00%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 85.68% 94.00%
CHEMBL1293267 Q9HC97 G-protein coupled receptor 35 83.34% 89.34%
CHEMBL2553 Q15418 Ribosomal protein S6 kinase alpha 1 83.19% 85.11%
CHEMBL5608 Q16288 NT-3 growth factor receptor 82.24% 95.89%
CHEMBL1293249 Q13887 Kruppel-like factor 5 82.17% 86.33%
CHEMBL3192 Q9BY41 Histone deacetylase 8 81.92% 93.99%
CHEMBL1937 Q92769 Histone deacetylase 2 81.64% 94.75%
CHEMBL2085 P14174 Macrophage migration inhibitory factor 80.11% 80.78%

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.
Maclura tricuspidata

Cross-Links

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PubChem 44426653
NPASS NPC306321
LOTUS LTS0252495
wikiData Q104983423