Tropodithietic acid

Details

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Internal ID d0d437cc-27b3-4a53-b388-1801cbd5bfdf
Taxonomy Hydrocarbon derivatives > Tropones
IUPAC Name 3-oxo-8,9-dithiabicyclo[5.2.0]nona-1,4,6-triene-2-carboxylic acid
SMILES (Canonical) C1=CC(=O)C(=C2C(=C1)SS2)C(=O)O
SMILES (Isomeric) C1=CC(=O)C(=C2C(=C1)SS2)C(=O)O
InChI InChI=1S/C8H4O3S2/c9-4-2-1-3-5-7(13-12-5)6(4)8(10)11/h1-3H,(H,10,11)
InChI Key BLFCMITWMARUSM-UHFFFAOYSA-N
Popularity 43 references in papers

Physical and Chemical Properties

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Molecular Formula C8H4O3S2
Molecular Weight 212.20 g/mol
Exact Mass 211.96018633 g/mol
Topological Polar Surface Area (TPSA) 105.00 Ų
XlogP 1.50
Atomic LogP (AlogP) 2.02
H-Bond Acceptor 4
H-Bond Donor 1
Rotatable Bonds 1

Synonyms

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750590-18-2
Tropodithietic acid [TDA]
3-Oxo-8,9-dithiabicyclo[5.2.0]nona-1,4,6-triene-2-carboxylic acid
CHEBI:156455
DTXSID601336703
HY-N6705
NSC781618
AKOS040742784
NSC-781618
BT162750
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of Tropodithietic acid

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9813 98.13%
Caco-2 + 0.7158 71.58%
Blood Brain Barrier - 0.6750 67.50%
Human oral bioavailability + 0.7000 70.00%
Subcellular localzation Mitochondria 0.7181 71.81%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9641 96.41%
OATP1B3 inhibitior + 0.9440 94.40%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.8750 87.50%
BSEP inhibitior - 0.9279 92.79%
P-glycoprotein inhibitior - 0.9796 97.96%
P-glycoprotein substrate - 0.9778 97.78%
CYP3A4 substrate - 0.7290 72.90%
CYP2C9 substrate - 0.6017 60.17%
CYP2D6 substrate - 0.8990 89.90%
CYP3A4 inhibition - 0.8452 84.52%
CYP2C9 inhibition - 0.7359 73.59%
CYP2C19 inhibition - 0.7602 76.02%
CYP2D6 inhibition - 0.8924 89.24%
CYP1A2 inhibition - 0.6636 66.36%
CYP2C8 inhibition - 0.9285 92.85%
CYP inhibitory promiscuity - 0.9813 98.13%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.6902 69.02%
Carcinogenicity (trinary) Non-required 0.6029 60.29%
Eye corrosion - 0.9557 95.57%
Eye irritation + 0.9946 99.46%
Skin irritation - 0.5797 57.97%
Skin corrosion - 0.8771 87.71%
Ames mutagenesis - 0.7400 74.00%
Human Ether-a-go-go-Related Gene inhibition - 0.8606 86.06%
Micronuclear + 0.7500 75.00%
Hepatotoxicity + 0.6250 62.50%
skin sensitisation - 0.7162 71.62%
Respiratory toxicity + 0.6333 63.33%
Reproductive toxicity - 0.5111 51.11%
Mitochondrial toxicity + 0.6875 68.75%
Nephrotoxicity + 0.7069 70.69%
Acute Oral Toxicity (c) III 0.4481 44.81%
Estrogen receptor binding - 0.5110 51.10%
Androgen receptor binding - 0.6127 61.27%
Thyroid receptor binding - 0.7019 70.19%
Glucocorticoid receptor binding - 0.6124 61.24%
Aromatase binding - 0.7587 75.87%
PPAR gamma + 0.5907 59.07%
Honey bee toxicity - 0.9765 97.65%
Biodegradation - 0.5250 52.50%
Crustacea aquatic toxicity - 0.8500 85.00%
Fish aquatic toxicity + 0.9772 97.72%

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
CHEMBL4040 P28482 MAP kinase ERK2 96.55% 83.82%
CHEMBL1293294 P51151 Ras-related protein Rab-9A 95.80% 87.67%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 93.38% 95.56%
CHEMBL1293277 O15118 Niemann-Pick C1 protein 92.01% 81.11%
CHEMBL2581 P07339 Cathepsin D 88.90% 98.95%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 86.54% 99.23%
CHEMBL1293249 Q13887 Kruppel-like factor 5 85.31% 86.33%
CHEMBL2035 P08912 Muscarinic acetylcholine receptor M5 84.64% 94.62%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 82.83% 95.50%
CHEMBL1821 P08173 Muscarinic acetylcholine receptor M4 82.78% 94.08%

Plants that contains it

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Below are displayed all the plants proven (via scientific papers) to contain this compound!
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There are no matching plants.

Cross-Links

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PubChem 44632924
LOTUS LTS0179282
wikiData Q72515630