(1S,4S)-1-oxodithiolane-4-carboxylic acid

Details

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Internal ID 5cf8371a-12a6-440d-b5f8-db91fed66620
Taxonomy Organoheterocyclic compounds > Dithiolanes > Dithiolanecarboxylic acids > 1,2-dithiolanecarboxylic acids > 1,2-dithiolane-4-carboxylic acids
IUPAC Name (1S,4S)-1-oxodithiolane-4-carboxylic acid
SMILES (Canonical) C1C(CS(=O)S1)C(=O)O
SMILES (Isomeric) C1[C@@H](C[S@@](=O)S1)C(=O)O
InChI InChI=1S/C4H6O3S2/c5-4(6)3-1-8-9(7)2-3/h3H,1-2H2,(H,5,6)/t3-,9-/m0/s1
InChI Key WKCDMZVXQHXDPX-KTCWOMIQSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C4H6O3S2
Molecular Weight 166.20 g/mol
Exact Mass 165.97583640 g/mol
Topological Polar Surface Area (TPSA) 98.90 Ų
XlogP -0.80
Atomic LogP (AlogP) 0.10
H-Bond Acceptor 3
H-Bond Donor 1
Rotatable Bonds 1

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of (1S,4S)-1-oxodithiolane-4-carboxylic acid

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9314 93.14%
Caco-2 - 0.8154 81.54%
Blood Brain Barrier + 0.6250 62.50%
Human oral bioavailability - 0.5286 52.86%
Subcellular localzation Mitochondria 0.6532 65.32%
OATP2B1 inhibitior - 0.8438 84.38%
OATP1B1 inhibitior + 0.9734 97.34%
OATP1B3 inhibitior + 0.9415 94.15%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.8500 85.00%
BSEP inhibitior - 0.9412 94.12%
P-glycoprotein inhibitior - 0.9831 98.31%
P-glycoprotein substrate - 0.9573 95.73%
CYP3A4 substrate - 0.6683 66.83%
CYP2C9 substrate + 0.7907 79.07%
CYP2D6 substrate - 0.8715 87.15%
CYP3A4 inhibition - 0.9495 94.95%
CYP2C9 inhibition - 0.7873 78.73%
CYP2C19 inhibition - 0.7659 76.59%
CYP2D6 inhibition - 0.8991 89.91%
CYP1A2 inhibition - 0.7568 75.68%
CYP2C8 inhibition - 0.9240 92.40%
CYP inhibitory promiscuity - 0.9865 98.65%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.5866 58.66%
Carcinogenicity (trinary) Non-required 0.6598 65.98%
Eye corrosion - 0.8407 84.07%
Eye irritation + 0.8999 89.99%
Skin irritation - 0.6997 69.97%
Skin corrosion - 0.8460 84.60%
Ames mutagenesis - 0.7100 71.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7964 79.64%
Micronuclear + 0.6500 65.00%
Hepatotoxicity + 0.7625 76.25%
skin sensitisation - 0.7508 75.08%
Respiratory toxicity - 0.5556 55.56%
Reproductive toxicity + 0.5444 54.44%
Mitochondrial toxicity - 0.5500 55.00%
Nephrotoxicity - 0.6641 66.41%
Acute Oral Toxicity (c) III 0.5909 59.09%
Estrogen receptor binding - 0.8981 89.81%
Androgen receptor binding - 0.7502 75.02%
Thyroid receptor binding - 0.9118 91.18%
Glucocorticoid receptor binding - 0.8467 84.67%
Aromatase binding - 0.8182 81.82%
PPAR gamma - 0.7817 78.17%
Honey bee toxicity - 0.8346 83.46%
Biodegradation + 0.6500 65.00%
Crustacea aquatic toxicity - 0.5500 55.00%
Fish aquatic toxicity + 0.8731 87.31%

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 90.74% 83.82%
CHEMBL221 P23219 Cyclooxygenase-1 88.24% 90.17%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 85.49% 96.09%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 83.82% 95.50%
CHEMBL3145 P42338 PI3-kinase p110-beta subunit 82.12% 98.75%

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.
Asparagus officinalis

Cross-Links

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PubChem 162801170
LOTUS LTS0097065
wikiData Q105307197