1-Chloro-6-(6-prop-1-ynyldithiin-3-yl)hexa-3,5-diyn-2-ol

Details

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Internal ID 257f36bf-49dd-4b35-a078-92a4bd96dad7
Taxonomy Organoheterocyclic compounds > Dithiins
IUPAC Name 1-chloro-6-(6-prop-1-ynyldithiin-3-yl)hexa-3,5-diyn-2-ol
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C13H9ClOS2/c1-2-5-12-8-9-13(17-16-12)7-4-3-6-11(15)10-14/h8-9,11,15H,10H2,1H3
InChI Key LGIIPOBYQDVGNC-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C13H9ClOS2
Molecular Weight 280.80 g/mol
Exact Mass 279.9783349 g/mol
Topological Polar Surface Area (TPSA) 70.80 Ų
XlogP 2.80
Atomic LogP (AlogP) 2.78
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 1-Chloro-6-(6-prop-1-ynyldithiin-3-yl)hexa-3,5-diyn-2-ol

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9887 98.87%
Caco-2 - 0.6802 68.02%
Blood Brain Barrier + 0.9000 90.00%
Human oral bioavailability - 0.5429 54.29%
Subcellular localzation Mitochondria 0.6141 61.41%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9130 91.30%
OATP1B3 inhibitior + 0.9477 94.77%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.9500 95.00%
BSEP inhibitior - 0.9058 90.58%
P-glycoprotein inhibitior - 0.9513 95.13%
P-glycoprotein substrate - 0.8788 87.88%
CYP3A4 substrate - 0.5866 58.66%
CYP2C9 substrate - 0.8057 80.57%
CYP2D6 substrate - 0.8070 80.70%
CYP3A4 inhibition + 0.5000 50.00%
CYP2C9 inhibition - 0.5902 59.02%
CYP2C19 inhibition + 0.5305 53.05%
CYP2D6 inhibition - 0.8418 84.18%
CYP1A2 inhibition + 0.5399 53.99%
CYP2C8 inhibition - 0.7928 79.28%
CYP inhibitory promiscuity + 0.5581 55.81%
UGT catelyzed - 0.5000 50.00%
Carcinogenicity (binary) - 0.5531 55.31%
Carcinogenicity (trinary) Non-required 0.6554 65.54%
Eye corrosion - 0.8650 86.50%
Eye irritation - 0.9231 92.31%
Skin irritation - 0.5705 57.05%
Skin corrosion - 0.5929 59.29%
Ames mutagenesis + 0.5600 56.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4776 47.76%
Micronuclear - 0.6815 68.15%
Hepatotoxicity + 0.7125 71.25%
skin sensitisation - 0.5790 57.90%
Respiratory toxicity + 0.6556 65.56%
Reproductive toxicity - 0.5556 55.56%
Mitochondrial toxicity - 0.6250 62.50%
Nephrotoxicity - 0.5694 56.94%
Acute Oral Toxicity (c) II 0.5106 51.06%
Estrogen receptor binding + 0.6542 65.42%
Androgen receptor binding - 0.6057 60.57%
Thyroid receptor binding + 0.6964 69.64%
Glucocorticoid receptor binding + 0.7974 79.74%
Aromatase binding + 0.7755 77.55%
PPAR gamma + 0.7455 74.55%
Honey bee toxicity - 0.8692 86.92%
Biodegradation - 0.7500 75.00%
Crustacea aquatic toxicity - 0.5900 59.00%
Fish aquatic toxicity - 0.4735 47.35%

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
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 95.84% 96.09%
CHEMBL3401 O75469 Pregnane X receptor 89.50% 94.73%
CHEMBL2581 P07339 Cathepsin D 88.94% 98.95%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 88.29% 91.11%
CHEMBL221 P23219 Cyclooxygenase-1 85.80% 90.17%

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.
Ambrosia chamissonis

Cross-Links

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PubChem 14777882
LOTUS LTS0118328
wikiData Q105151375