1-Desmethylobtusin

Details

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Internal ID 394ce826-ac52-4c0a-a899-760501ca34c1
Taxonomy Benzenoids > Anthracenes > Anthraquinones > Hydroxyanthraquinones
IUPAC Name 1,2,8-trihydroxy-6,7-dimethoxy-3-methylanthracene-9,10-dione
SMILES (Canonical) CC1=CC2=C(C(=C1O)O)C(=O)C3=C(C(=C(C=C3C2=O)OC)OC)O
SMILES (Isomeric) CC1=CC2=C(C(=C1O)O)C(=O)C3=C(C(=C(C=C3C2=O)OC)OC)O
InChI InChI=1S/C17H14O7/c1-6-4-7-10(15(21)12(6)18)14(20)11-8(13(7)19)5-9(23-2)17(24-3)16(11)22/h4-5,18,21-22H,1-3H3
InChI Key DQLZLEGJAFDFLO-UHFFFAOYSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

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Molecular Formula C17H14O7
Molecular Weight 330.29 g/mol
Exact Mass 330.07395278 g/mol
Topological Polar Surface Area (TPSA) 113.00 Ų
XlogP 2.70
Atomic LogP (AlogP) 1.90
H-Bond Acceptor 7
H-Bond Donor 3
Rotatable Bonds 2

Synonyms

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1,2,8-trihydroxy-6,7-dimethoxy-3-methylanthraquinone

2D Structure

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2D Structure of 1-Desmethylobtusin

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9762 97.62%
Caco-2 + 0.7203 72.03%
Blood Brain Barrier - 0.7750 77.50%
Human oral bioavailability + 0.7714 77.14%
Subcellular localzation Mitochondria 0.7939 79.39%
OATP2B1 inhibitior - 0.7103 71.03%
OATP1B1 inhibitior + 0.9212 92.12%
OATP1B3 inhibitior + 0.8473 84.73%
MATE1 inhibitior - 0.9200 92.00%
OCT2 inhibitior - 1.0000 100.00%
BSEP inhibitior - 0.7631 76.31%
P-glycoprotein inhibitior - 0.8179 81.79%
P-glycoprotein substrate - 0.9410 94.10%
CYP3A4 substrate + 0.5108 51.08%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8089 80.89%
CYP3A4 inhibition - 0.8573 85.73%
CYP2C9 inhibition - 0.9342 93.42%
CYP2C19 inhibition - 0.9320 93.20%
CYP2D6 inhibition - 0.8891 88.91%
CYP1A2 inhibition + 0.8856 88.56%
CYP2C8 inhibition - 0.5869 58.69%
CYP inhibitory promiscuity - 0.8347 83.47%
UGT catelyzed - 0.7000 70.00%
Carcinogenicity (binary) - 0.8895 88.95%
Carcinogenicity (trinary) Non-required 0.5159 51.59%
Eye corrosion - 0.9865 98.65%
Eye irritation + 0.8410 84.10%
Skin irritation - 0.6825 68.25%
Skin corrosion - 0.9384 93.84%
Ames mutagenesis + 0.6700 67.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7837 78.37%
Micronuclear + 0.8000 80.00%
Hepatotoxicity - 0.5820 58.20%
skin sensitisation - 0.8982 89.82%
Respiratory toxicity - 0.6111 61.11%
Reproductive toxicity + 0.5778 57.78%
Mitochondrial toxicity + 0.5500 55.00%
Nephrotoxicity + 0.4516 45.16%
Acute Oral Toxicity (c) II 0.4758 47.58%
Estrogen receptor binding + 0.6814 68.14%
Androgen receptor binding - 0.5966 59.66%
Thyroid receptor binding - 0.5775 57.75%
Glucocorticoid receptor binding + 0.7531 75.31%
Aromatase binding + 0.6109 61.09%
PPAR gamma + 0.5499 54.99%
Honey bee toxicity - 0.9141 91.41%
Biodegradation - 0.7250 72.50%
Crustacea aquatic toxicity - 0.5900 59.00%
Fish aquatic toxicity + 0.9816 98.16%

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
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 95.39% 95.56%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 93.59% 91.11%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 92.00% 94.00%
CHEMBL1806 P11388 DNA topoisomerase II alpha 90.83% 89.00%
CHEMBL2581 P07339 Cathepsin D 89.19% 98.95%
CHEMBL2535 P11166 Glucose transporter 88.73% 98.75%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 85.80% 96.00%
CHEMBL1293249 Q13887 Kruppel-like factor 5 84.65% 86.33%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 82.90% 99.15%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 82.30% 99.23%
CHEMBL1913 P09619 Platelet-derived growth factor receptor beta 81.62% 95.70%
CHEMBL4208 P20618 Proteasome component C5 81.17% 90.00%
CHEMBL2069156 Q14145 Kelch-like ECH-associated protein 1 80.99% 82.38%
CHEMBL3880 P07900 Heat shock protein HSP 90-alpha 80.90% 96.21%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 80.77% 85.14%

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 obtusifolia
Senna tora

Cross-Links

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PubChem 13675113
NPASS NPC2316
LOTUS LTS0004326
wikiData Q104987023