Thorectandroic acid

Details

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Internal ID 5691438a-a1bc-4aea-a5a5-abea208f3790
Taxonomy Organoheterocyclic compounds > Indoles and derivatives > Pyridoindoles > Beta carbolines
IUPAC Name 2-pyrido[3,4-b]indol-2-ylbenzoic acid
SMILES (Canonical) C1=CC=C(C(=C1)C(=O)O)N2C=CC3=C4C=CC=CC4=NC3=C2
SMILES (Isomeric) C1=CC=C(C(=C1)C(=O)O)N2C=CC3=C4C=CC=CC4=NC3=C2
InChI InChI=1S/C18H12N2O2/c21-18(22)14-6-2-4-8-17(14)20-10-9-13-12-5-1-3-7-15(12)19-16(13)11-20/h1-11H,(H,21,22)
InChI Key ZFQPREUMWUPFMY-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C18H12N2O2
Molecular Weight 288.30 g/mol
Exact Mass 288.089877630 g/mol
Topological Polar Surface Area (TPSA) 55.10 Ų
XlogP 3.10
Atomic LogP (AlogP) 3.83
H-Bond Acceptor 3
H-Bond Donor 1
Rotatable Bonds 2

Synonyms

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NSC725951
NSC-725951

2D Structure

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2D Structure of Thorectandroic acid

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9822 98.22%
Caco-2 + 0.8489 84.89%
Blood Brain Barrier + 0.7500 75.00%
Human oral bioavailability + 0.8571 85.71%
Subcellular localzation Mitochondria 0.8461 84.61%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9359 93.59%
OATP1B3 inhibitior + 0.9391 93.91%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.8386 83.86%
BSEP inhibitior + 0.7610 76.10%
P-glycoprotein inhibitior - 0.8780 87.80%
P-glycoprotein substrate - 0.8987 89.87%
CYP3A4 substrate - 0.5998 59.98%
CYP2C9 substrate - 0.8245 82.45%
CYP2D6 substrate - 0.9182 91.82%
CYP3A4 inhibition - 0.6475 64.75%
CYP2C9 inhibition - 0.6499 64.99%
CYP2C19 inhibition - 0.5172 51.72%
CYP2D6 inhibition - 0.7350 73.50%
CYP1A2 inhibition + 0.6234 62.34%
CYP2C8 inhibition + 0.5000 50.00%
CYP inhibitory promiscuity + 0.5231 52.31%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.9100 91.00%
Carcinogenicity (trinary) Non-required 0.4888 48.88%
Eye corrosion - 0.9898 98.98%
Eye irritation + 0.5386 53.86%
Skin irritation - 0.6324 63.24%
Skin corrosion - 0.9638 96.38%
Ames mutagenesis - 0.5100 51.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7903 79.03%
Micronuclear + 0.8800 88.00%
Hepatotoxicity + 0.7625 76.25%
skin sensitisation - 0.9132 91.32%
Respiratory toxicity + 0.7000 70.00%
Reproductive toxicity + 0.6667 66.67%
Mitochondrial toxicity + 0.7750 77.50%
Nephrotoxicity + 0.5000 50.00%
Acute Oral Toxicity (c) II 0.6063 60.63%
Estrogen receptor binding + 0.9422 94.22%
Androgen receptor binding + 0.6841 68.41%
Thyroid receptor binding + 0.7274 72.74%
Glucocorticoid receptor binding + 0.7595 75.95%
Aromatase binding + 0.9072 90.72%
PPAR gamma + 0.9073 90.73%
Honey bee toxicity - 0.9544 95.44%
Biodegradation - 0.9500 95.00%
Crustacea aquatic toxicity - 0.7700 77.00%
Fish aquatic toxicity + 0.8753 87.53%

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
CHEMBL1293294 P51151 Ras-related protein Rab-9A 94.29% 87.67%
CHEMBL2581 P07339 Cathepsin D 93.01% 98.95%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 92.85% 99.23%
CHEMBL1293277 O15118 Niemann-Pick C1 protein 92.81% 81.11%
CHEMBL1293249 Q13887 Kruppel-like factor 5 91.53% 86.33%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 89.84% 85.14%
CHEMBL2035 P08912 Muscarinic acetylcholine receptor M5 89.41% 94.62%
CHEMBL1868 P17948 Vascular endothelial growth factor receptor 1 88.60% 96.47%
CHEMBL230 P35354 Cyclooxygenase-2 87.80% 89.63%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 87.77% 95.56%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 87.60% 95.50%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 86.17% 96.09%
CHEMBL3807 P17706 T-cell protein-tyrosine phosphatase 85.71% 93.00%
CHEMBL3902 P09211 Glutathione S-transferase Pi 84.11% 93.81%
CHEMBL1899 P46098 Serotonin 3a (5-HT3a) receptor 83.71% 100.00%
CHEMBL1811 P34995 Prostanoid EP1 receptor 83.04% 95.71%
CHEMBL2378 P30307 Dual specificity phosphatase Cdc25C 82.94% 96.67%
CHEMBL5805 Q9NR97 Toll-like receptor 8 81.46% 96.25%

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.
Bouchardatia neurococca

Cross-Links

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PubChem 10108152
LOTUS LTS0009338
wikiData Q105374592