Hemigossypolone

Details

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Internal ID 31a7fc2d-de4d-4e14-a6aa-8c909467d60c
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Sesquiterpenoids
IUPAC Name 2,3-dihydroxy-6-methyl-5,8-dioxo-4-propan-2-ylnaphthalene-1-carbaldehyde
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C15H14O5/c1-6(2)10-12-11(8(5-16)14(19)15(10)20)9(17)4-7(3)13(12)18/h4-6,19-20H,1-3H3
InChI Key CERPPXZGSNEVMI-UHFFFAOYSA-N
Popularity 10 references in papers

Physical and Chemical Properties

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Molecular Formula C15H14O5
Molecular Weight 274.27 g/mol
Exact Mass 274.08412354 g/mol
Topological Polar Surface Area (TPSA) 91.70 Ų
XlogP 2.30
Atomic LogP (AlogP) 2.36
H-Bond Acceptor 5
H-Bond Donor 2
Rotatable Bonds 2

Synonyms

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35688-47-2
NSC650936
Para-Hemigossypolone
2,3-dihydroxy-6-methyl-5,8-dioxo-4-propan-2-ylnaphthalene-1-carbaldehyde
CHEMBL1988313
DTXSID10189193
CHEBI:174602
NSC-650936
NCI60_017780
8-formyl-6,7-dihydroxy-5-isopropyl-3-methylnaphthoquinone
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of Hemigossypolone

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9937 99.37%
Caco-2 - 0.6519 65.19%
Blood Brain Barrier - 0.6250 62.50%
Human oral bioavailability + 0.6286 62.86%
Subcellular localzation Mitochondria 0.8063 80.63%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.6931 69.31%
OATP1B3 inhibitior + 0.8757 87.57%
MATE1 inhibitior - 0.7600 76.00%
OCT2 inhibitior - 0.9750 97.50%
BSEP inhibitior - 0.8404 84.04%
P-glycoprotein inhibitior - 0.9307 93.07%
P-glycoprotein substrate - 0.9212 92.12%
CYP3A4 substrate - 0.5755 57.55%
CYP2C9 substrate - 0.7962 79.62%
CYP2D6 substrate - 0.8684 86.84%
CYP3A4 inhibition - 0.7703 77.03%
CYP2C9 inhibition + 0.8469 84.69%
CYP2C19 inhibition - 0.5310 53.10%
CYP2D6 inhibition - 0.7675 76.75%
CYP1A2 inhibition + 0.8986 89.86%
CYP2C8 inhibition - 0.9355 93.55%
CYP inhibitory promiscuity + 0.5936 59.36%
UGT catelyzed + 0.8000 80.00%
Carcinogenicity (binary) - 0.9454 94.54%
Carcinogenicity (trinary) Non-required 0.5567 55.67%
Eye corrosion - 0.9879 98.79%
Eye irritation + 0.6186 61.86%
Skin irritation - 0.5795 57.95%
Skin corrosion - 0.8774 87.74%
Ames mutagenesis - 0.6600 66.00%
Human Ether-a-go-go-Related Gene inhibition - 0.8042 80.42%
Micronuclear + 0.7200 72.00%
Hepatotoxicity + 0.7033 70.33%
skin sensitisation + 0.5679 56.79%
Respiratory toxicity + 0.5444 54.44%
Reproductive toxicity + 0.7222 72.22%
Mitochondrial toxicity + 0.6125 61.25%
Nephrotoxicity + 0.7639 76.39%
Acute Oral Toxicity (c) III 0.6292 62.92%
Estrogen receptor binding + 0.6412 64.12%
Androgen receptor binding + 0.5751 57.51%
Thyroid receptor binding - 0.6934 69.34%
Glucocorticoid receptor binding + 0.6073 60.73%
Aromatase binding - 0.7250 72.50%
PPAR gamma - 0.7039 70.39%
Honey bee toxicity - 0.8887 88.87%
Biodegradation - 0.7750 77.50%
Crustacea aquatic toxicity - 0.7500 75.00%
Fish aquatic toxicity + 0.9960 99.60%

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 98.10% 95.56%
CHEMBL2581 P07339 Cathepsin D 95.36% 98.95%
CHEMBL1163101 O75460 Serine/threonine-protein kinase/endoribonuclease IRE1 94.87% 98.11%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 88.88% 90.71%
CHEMBL3401 O75469 Pregnane X receptor 88.69% 94.73%
CHEMBL1937 Q92769 Histone deacetylase 2 87.14% 94.75%
CHEMBL1806 P11388 DNA topoisomerase II alpha 86.36% 89.00%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 86.22% 94.45%
CHEMBL3359 P21462 Formyl peptide receptor 1 85.74% 93.56%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 83.85% 99.23%
CHEMBL5697 Q9GZT9 Egl nine homolog 1 82.77% 93.40%

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.
Gossypium hirsutum

Cross-Links

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PubChem 182249
LOTUS LTS0064933
wikiData Q83061172