Vismione C

Details

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Internal ID 750059ca-7cf8-458c-b7e6-d1dff83e311f
Taxonomy Benzenoids > Anthracenes
IUPAC Name [5,7,10-trihydroxy-2-methyl-6-(3-methylbut-2-enyl)-4-oxo-1,3-dihydroanthracen-2-yl] acetate
SMILES (Canonical) CC(=CCC1=C(C2=C(C3=C(CC(CC3=O)(C)OC(=O)C)C=C2C=C1O)O)O)C
SMILES (Isomeric) CC(=CCC1=C(C2=C(C3=C(CC(CC3=O)(C)OC(=O)C)C=C2C=C1O)O)O)C
InChI InChI=1S/C22H24O6/c1-11(2)5-6-15-16(24)8-13-7-14-9-22(4,28-12(3)23)10-17(25)18(14)21(27)19(13)20(15)26/h5,7-8,24,26-27H,6,9-10H2,1-4H3
InChI Key FLYMKXSUGFPBQY-UHFFFAOYSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

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Molecular Formula C22H24O6
Molecular Weight 384.40 g/mol
Exact Mass 384.15728848 g/mol
Topological Polar Surface Area (TPSA) 104.00 Ų
XlogP 4.50
Atomic LogP (AlogP) 3.92
H-Bond Acceptor 6
H-Bond Donor 3
Rotatable Bonds 3

Synonyms

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CHEMBL486610

2D Structure

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2D Structure of Vismione C

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9896 98.96%
Caco-2 + 0.6057 60.57%
Blood Brain Barrier - 0.6000 60.00%
Human oral bioavailability + 0.5143 51.43%
Subcellular localzation Mitochondria 0.7774 77.74%
OATP2B1 inhibitior - 0.5737 57.37%
OATP1B1 inhibitior + 0.8363 83.63%
OATP1B3 inhibitior - 0.3423 34.23%
MATE1 inhibitior - 0.7400 74.00%
OCT2 inhibitior - 0.9000 90.00%
BSEP inhibitior + 0.7782 77.82%
P-glycoprotein inhibitior - 0.6603 66.03%
P-glycoprotein substrate - 0.6701 67.01%
CYP3A4 substrate + 0.5839 58.39%
CYP2C9 substrate - 0.5906 59.06%
CYP2D6 substrate - 0.8661 86.61%
CYP3A4 inhibition - 0.8215 82.15%
CYP2C9 inhibition - 0.5187 51.87%
CYP2C19 inhibition - 0.5520 55.20%
CYP2D6 inhibition - 0.8860 88.60%
CYP1A2 inhibition + 0.6243 62.43%
CYP2C8 inhibition - 0.6471 64.71%
CYP inhibitory promiscuity - 0.5168 51.68%
UGT catelyzed - 0.5000 50.00%
Carcinogenicity (binary) - 0.9381 93.81%
Carcinogenicity (trinary) Non-required 0.6577 65.77%
Eye corrosion - 0.9942 99.42%
Eye irritation - 0.7549 75.49%
Skin irritation - 0.7382 73.82%
Skin corrosion - 0.9486 94.86%
Ames mutagenesis + 0.5900 59.00%
Human Ether-a-go-go-Related Gene inhibition + 0.7158 71.58%
Micronuclear - 0.6700 67.00%
Hepatotoxicity - 0.5250 52.50%
skin sensitisation - 0.7010 70.10%
Respiratory toxicity + 0.7111 71.11%
Reproductive toxicity + 0.8667 86.67%
Mitochondrial toxicity + 0.7625 76.25%
Nephrotoxicity - 0.6187 61.87%
Acute Oral Toxicity (c) III 0.3929 39.29%
Estrogen receptor binding + 0.8536 85.36%
Androgen receptor binding + 0.5324 53.24%
Thyroid receptor binding + 0.5747 57.47%
Glucocorticoid receptor binding + 0.8491 84.91%
Aromatase binding + 0.6683 66.83%
PPAR gamma + 0.8223 82.23%
Honey bee toxicity - 0.8071 80.71%
Biodegradation - 0.9250 92.50%
Crustacea aquatic toxicity - 0.6600 66.00%
Fish aquatic toxicity + 1.0000 100.00%

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 99.76% 91.11%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 98.53% 94.45%
CHEMBL335 P18031 Protein-tyrosine phosphatase 1B 96.62% 95.17%
CHEMBL2581 P07339 Cathepsin D 96.58% 98.95%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 92.71% 85.14%
CHEMBL1293249 Q13887 Kruppel-like factor 5 92.46% 86.33%
CHEMBL215 P09917 Arachidonate 5-lipoxygenase 91.53% 92.68%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 91.19% 96.09%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 88.42% 96.95%
CHEMBL1951 P21397 Monoamine oxidase A 87.07% 91.49%
CHEMBL2964 P36507 Dual specificity mitogen-activated protein kinase kinase 2 86.58% 80.00%
CHEMBL3401 O75469 Pregnane X receptor 85.13% 94.73%
CHEMBL1293267 Q9HC97 G-protein coupled receptor 35 84.80% 89.34%
CHEMBL4208 P20618 Proteasome component C5 83.81% 90.00%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 83.13% 94.00%
CHEMBL1937 Q92769 Histone deacetylase 2 83.01% 94.75%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 81.28% 99.15%
CHEMBL3060 Q9Y345 Glycine transporter 2 80.46% 99.17%
CHEMBL1907600 Q00535 Cyclin-dependent kinase 5/CDK5 activator 1 80.21% 93.03%

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.
Psorospermum febrifugum
Psorospermum glaberrimum
Psorospermum tenuifolium

Cross-Links

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PubChem 14186716
LOTUS LTS0001287
wikiData Q104397369