(1S,3S)-2,2,4,4-tetrachloro-1-(dichloromethyl)-5-(dichloromethylidene)cyclopentane-1,3-diol

Details

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Internal ID 9f131b66-c72f-4fb7-8f5f-b8bffefbe106
Taxonomy Organic oxygen compounds > Organooxygen compounds > Alcohols and polyols > Secondary alcohols > Cyclopentanols
IUPAC Name (1S,3S)-2,2,4,4-tetrachloro-1-(dichloromethyl)-5-(dichloromethylidene)cyclopentane-1,3-diol
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C7H4Cl8O2/c8-2(9)1-5(17,4(10)11)7(14,15)3(16)6(1,12)13/h3-4,16-17H/t3-,5-/m0/s1
InChI Key NRIHIELKVOSNAZ-UCORVYFPSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C7H4Cl8O2
Molecular Weight 403.70 g/mol
Exact Mass 403.766051 g/mol
Topological Polar Surface Area (TPSA) 40.50 Ų
XlogP 3.40
Atomic LogP (AlogP) 3.93
H-Bond Acceptor 2
H-Bond Donor 2
Rotatable Bonds 1

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of (1S,3S)-2,2,4,4-tetrachloro-1-(dichloromethyl)-5-(dichloromethylidene)cyclopentane-1,3-diol

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9804 98.04%
Caco-2 - 0.6252 62.52%
Blood Brain Barrier + 0.7500 75.00%
Human oral bioavailability + 0.6286 62.86%
Subcellular localzation Mitochondria 0.5974 59.74%
OATP2B1 inhibitior - 0.8624 86.24%
OATP1B1 inhibitior + 0.9527 95.27%
OATP1B3 inhibitior + 0.9454 94.54%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.8838 88.38%
BSEP inhibitior - 0.8526 85.26%
P-glycoprotein inhibitior - 0.9398 93.98%
P-glycoprotein substrate - 0.9001 90.01%
CYP3A4 substrate - 0.5785 57.85%
CYP2C9 substrate - 0.7907 79.07%
CYP2D6 substrate - 0.7728 77.28%
CYP3A4 inhibition - 0.6085 60.85%
CYP2C9 inhibition - 0.5800 58.00%
CYP2C19 inhibition - 0.5768 57.68%
CYP2D6 inhibition - 0.8726 87.26%
CYP1A2 inhibition - 0.6885 68.85%
CYP2C8 inhibition - 0.9433 94.33%
CYP inhibitory promiscuity + 0.5636 56.36%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.6598 65.98%
Carcinogenicity (trinary) Non-required 0.4655 46.55%
Eye corrosion - 0.8788 87.88%
Eye irritation + 0.7056 70.56%
Skin irritation + 0.5487 54.87%
Skin corrosion - 0.5989 59.89%
Ames mutagenesis + 0.5400 54.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7972 79.72%
Micronuclear - 0.7041 70.41%
Hepatotoxicity + 0.8199 81.99%
skin sensitisation + 0.5885 58.85%
Respiratory toxicity - 0.6000 60.00%
Reproductive toxicity - 0.6111 61.11%
Mitochondrial toxicity - 0.6750 67.50%
Nephrotoxicity + 0.5000 50.00%
Acute Oral Toxicity (c) III 0.8216 82.16%
Estrogen receptor binding + 0.8557 85.57%
Androgen receptor binding - 0.5573 55.73%
Thyroid receptor binding + 0.6331 63.31%
Glucocorticoid receptor binding - 0.5255 52.55%
Aromatase binding - 0.6688 66.88%
PPAR gamma + 0.8613 86.13%
Honey bee toxicity - 0.5259 52.59%
Biodegradation - 0.9500 95.00%
Crustacea aquatic toxicity + 0.6000 60.00%
Fish aquatic toxicity + 0.8101 81.01%

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
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 91.31% 94.45%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 87.39% 91.11%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 84.26% 96.09%
CHEMBL253 P34972 Cannabinoid CB2 receptor 81.37% 97.25%

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 162846191
LOTUS LTS0041595
wikiData Q105184572