2-Carboxy-3-hydroxy-9,10-dioxoanthracen-1-olate

Details

Top
Internal ID 92d109f1-544d-47a4-b61c-bc9cd669ad8f
Taxonomy Benzenoids > Anthracenes > Anthracenecarboxylic acids and derivatives > Anthracenecarboxylic acids
IUPAC Name 2-carboxy-3-hydroxy-9,10-dioxoanthracen-1-olate
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C15H8O6/c16-9-5-8-10(14(19)11(9)15(20)21)13(18)7-4-2-1-3-6(7)12(8)17/h1-5,16,19H,(H,20,21)/p-1
InChI Key PLDISGVCDWLKQC-UHFFFAOYSA-M
Popularity 0 references in papers

Physical and Chemical Properties

Top
Molecular Formula C15H7O6-
Molecular Weight 283.21 g/mol
Exact Mass 283.02426294 g/mol
Topological Polar Surface Area (TPSA) 115.00 Ų
XlogP 3.40
Atomic LogP (AlogP) 0.94
H-Bond Acceptor 5
H-Bond Donor 2
Rotatable Bonds 1

Synonyms

Top
There are no found synonyms.

2D Structure

Top
2D Structure of 2-Carboxy-3-hydroxy-9,10-dioxoanthracen-1-olate

3D Structure

Top

ADMET Properties (via admetSAR 2)

Top
Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.8941 89.41%
Caco-2 - 0.5444 54.44%
Blood Brain Barrier - 0.8250 82.50%
Human oral bioavailability + 0.7714 77.14%
Subcellular localzation Mitochondria 0.7205 72.05%
OATP2B1 inhibitior - 0.6856 68.56%
OATP1B1 inhibitior + 0.9197 91.97%
OATP1B3 inhibitior - 0.2249 22.49%
MATE1 inhibitior - 0.7600 76.00%
OCT2 inhibitior - 1.0000 100.00%
BSEP inhibitior - 0.8960 89.60%
P-glycoprotein inhibitior - 0.9675 96.75%
P-glycoprotein substrate - 0.9630 96.30%
CYP3A4 substrate - 0.6409 64.09%
CYP2C9 substrate - 0.8192 81.92%
CYP2D6 substrate - 0.8901 89.01%
CYP3A4 inhibition - 0.8820 88.20%
CYP2C9 inhibition + 0.5000 50.00%
CYP2C19 inhibition - 0.8933 89.33%
CYP2D6 inhibition - 0.8933 89.33%
CYP1A2 inhibition - 0.8450 84.50%
CYP2C8 inhibition - 0.8493 84.93%
CYP inhibitory promiscuity - 0.8810 88.10%
UGT catelyzed + 0.9000 90.00%
Carcinogenicity (binary) - 0.8423 84.23%
Carcinogenicity (trinary) Non-required 0.6436 64.36%
Eye corrosion - 0.9945 99.45%
Eye irritation + 0.9452 94.52%
Skin irritation + 0.6950 69.50%
Skin corrosion - 0.9602 96.02%
Ames mutagenesis - 0.5784 57.84%
Human Ether-a-go-go-Related Gene inhibition - 0.8977 89.77%
Micronuclear + 0.8400 84.00%
Hepatotoxicity + 0.6875 68.75%
skin sensitisation - 0.7458 74.58%
Respiratory toxicity + 0.5222 52.22%
Reproductive toxicity - 0.6556 65.56%
Mitochondrial toxicity + 0.7125 71.25%
Nephrotoxicity + 0.6900 69.00%
Acute Oral Toxicity (c) III 0.5984 59.84%
Estrogen receptor binding + 0.6756 67.56%
Androgen receptor binding + 0.6078 60.78%
Thyroid receptor binding - 0.6334 63.34%
Glucocorticoid receptor binding + 0.6520 65.20%
Aromatase binding - 0.5108 51.08%
PPAR gamma + 0.7878 78.78%
Honey bee toxicity - 0.8961 89.61%
Biodegradation - 0.9500 95.00%
Crustacea aquatic toxicity - 0.5800 58.00%
Fish aquatic toxicity + 0.9910 99.10%

Targets

Top

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
CHEMBL2581 P07339 Cathepsin D 96.97% 98.95%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 96.82% 95.56%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 94.62% 91.11%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 89.60% 99.15%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 89.47% 99.23%
CHEMBL1806 P11388 DNA topoisomerase II alpha 86.08% 89.00%
CHEMBL1293249 Q13887 Kruppel-like factor 5 84.36% 86.33%
CHEMBL2535 P11166 Glucose transporter 81.91% 98.75%
CHEMBL3194 P02766 Transthyretin 81.04% 90.71%
CHEMBL2378 P30307 Dual specificity phosphatase Cdc25C 80.37% 96.67%
CHEMBL3359 P21462 Formyl peptide receptor 1 80.03% 93.56%

Plants that contains it

Top
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.
Baileya multiradiata
Gynochthodes umbellata
Ipomoea cairica
Rubia cordifolia

Cross-Links

Top
PubChem 54740334
NPASS NPC42572