Isoviocristin

Details

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Internal ID cc9f0b79-b472-44e3-b855-db6674f7d223
Taxonomy Benzenoids > Anthracenes > Anthraquinones
IUPAC Name 5,10-dihydroxy-7-methoxy-2-methylanthracene-1,4-dione
SMILES (Canonical) CC1=CC(=O)C2=C(C3=C(C=C(C=C3C=C2C1=O)OC)O)O
SMILES (Isomeric) CC1=CC(=O)C2=C(C3=C(C=C(C=C3C=C2C1=O)OC)O)O
InChI InChI=1S/C16H12O5/c1-7-3-11(17)14-10(15(7)19)5-8-4-9(21-2)6-12(18)13(8)16(14)20/h3-6,18,20H,1-2H3
InChI Key UGNZSMZSJYOGNX-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C16H12O5
Molecular Weight 284.26 g/mol
Exact Mass 284.06847348 g/mol
Topological Polar Surface Area (TPSA) 83.80 Ų
XlogP 2.90
Atomic LogP (AlogP) 2.58
H-Bond Acceptor 5
H-Bond Donor 2
Rotatable Bonds 1

Synonyms

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Isoviocristin-
5MAN5VZZ4Q
UNII-5MAN5VZZ4Q
74815-58-0
1,4-Anthracenedione, 5,10-dihydroxy-7-methoxy-2-methyl-
5,10-Dihydroxy-7-methoxy-2-methyl-anthracene-1,4-dione
5,10-DIHYDROXY-7-METHOXY-2-METHYLANTHRACENE-1,4-DIONE
5,10-Dihydroxy-7-methoxy-2-methyl-1,4-anthracenedione
SCHEMBL29663815
CHEBI:208096
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of Isoviocristin

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9913 99.13%
Caco-2 + 0.7443 74.43%
Blood Brain Barrier - 0.6879 68.79%
Human oral bioavailability - 0.5143 51.43%
Subcellular localzation Mitochondria 0.7560 75.60%
OATP2B1 inhibitior - 0.7147 71.47%
OATP1B1 inhibitior + 0.8750 87.50%
OATP1B3 inhibitior + 0.9507 95.07%
MATE1 inhibitior - 0.9000 90.00%
OCT2 inhibitior - 0.9838 98.38%
BSEP inhibitior - 0.8471 84.71%
P-glycoprotein inhibitior - 0.8521 85.21%
P-glycoprotein substrate - 0.9107 91.07%
CYP3A4 substrate + 0.5268 52.68%
CYP2C9 substrate - 0.8007 80.07%
CYP2D6 substrate - 0.8458 84.58%
CYP3A4 inhibition + 0.5292 52.92%
CYP2C9 inhibition + 0.8536 85.36%
CYP2C19 inhibition + 0.7491 74.91%
CYP2D6 inhibition - 0.6967 69.67%
CYP1A2 inhibition + 0.9312 93.12%
CYP2C8 inhibition - 0.6157 61.57%
CYP inhibitory promiscuity + 0.8782 87.82%
UGT catelyzed + 0.8000 80.00%
Carcinogenicity (binary) - 0.8519 85.19%
Carcinogenicity (trinary) Non-required 0.5989 59.89%
Eye corrosion - 0.9927 99.27%
Eye irritation + 0.7989 79.89%
Skin irritation - 0.6621 66.21%
Skin corrosion - 0.9351 93.51%
Ames mutagenesis + 0.5200 52.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7227 72.27%
Micronuclear + 0.8500 85.00%
Hepatotoxicity + 0.5750 57.50%
skin sensitisation - 0.7502 75.02%
Respiratory toxicity + 0.5444 54.44%
Reproductive toxicity + 0.7111 71.11%
Mitochondrial toxicity + 0.6625 66.25%
Nephrotoxicity + 0.5449 54.49%
Acute Oral Toxicity (c) II 0.4659 46.59%
Estrogen receptor binding + 0.8040 80.40%
Androgen receptor binding + 0.6172 61.72%
Thyroid receptor binding + 0.5420 54.20%
Glucocorticoid receptor binding + 0.8533 85.33%
Aromatase binding - 0.5093 50.93%
PPAR gamma + 0.6217 62.17%
Honey bee toxicity - 0.8915 89.15%
Biodegradation - 0.8500 85.00%
Crustacea aquatic toxicity - 0.5700 57.00%
Fish aquatic toxicity + 0.9942 99.42%

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
CHEMBL215 P09917 Arachidonate 5-lipoxygenase 97.87% 92.68%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 96.01% 99.15%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 95.27% 95.56%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 94.53% 91.11%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 93.06% 94.00%
CHEMBL2581 P07339 Cathepsin D 92.92% 98.95%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 90.55% 85.14%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 89.26% 99.23%
CHEMBL1937 Q92769 Histone deacetylase 2 88.36% 94.75%
CHEMBL2378 P30307 Dual specificity phosphatase Cdc25C 87.36% 96.67%
CHEMBL4208 P20618 Proteasome component C5 86.57% 90.00%
CHEMBL1806 P11388 DNA topoisomerase II alpha 86.21% 89.00%
CHEMBL1293249 Q13887 Kruppel-like factor 5 85.19% 86.33%
CHEMBL3192 Q9BY41 Histone deacetylase 8 84.02% 93.99%
CHEMBL3864 Q06124 Protein-tyrosine phosphatase 2C 83.50% 94.42%
CHEMBL1929 P47989 Xanthine dehydrogenase 82.99% 96.12%
CHEMBL2056 P21728 Dopamine D1 receptor 80.12% 91.00%

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.
Senna multiglandulosa

Cross-Links

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PubChem 85990998
LOTUS LTS0209041
wikiData Q77517092