(3S,4R,6R)-3,4,6,7-tetrachloro-3,7-dimethyloct-1-ene

Details

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Internal ID 0bb5ba75-50d9-4406-9dfd-ae8a6cd780e1
Taxonomy Organohalogen compounds > Organochlorides
IUPAC Name (3S,4R,6R)-3,4,6,7-tetrachloro-3,7-dimethyloct-1-ene
SMILES (Canonical) CC(C)(C(CC(C(C)(C=C)Cl)Cl)Cl)Cl
SMILES (Isomeric) C[C@](C=C)([C@@H](C[C@H](C(C)(C)Cl)Cl)Cl)Cl
InChI InChI=1S/C10H16Cl4/c1-5-10(4,14)8(12)6-7(11)9(2,3)13/h5,7-8H,1,6H2,2-4H3/t7-,8-,10+/m1/s1
InChI Key KHNLXMPCDVRDFI-MRTMQBJTSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

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Molecular Formula C10H16Cl4
Molecular Weight 278.00 g/mol
Exact Mass 277.997661 g/mol
Topological Polar Surface Area (TPSA) 0.00 Ų
XlogP 4.60
Atomic LogP (AlogP) 4.79
H-Bond Acceptor 0
H-Bond Donor 0
Rotatable Bonds 5

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of (3S,4R,6R)-3,4,6,7-tetrachloro-3,7-dimethyloct-1-ene

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9913 99.13%
Caco-2 - 0.5164 51.64%
Blood Brain Barrier + 0.9750 97.50%
Human oral bioavailability + 0.7000 70.00%
Subcellular localzation Lysosomes 0.5026 50.26%
OATP2B1 inhibitior - 0.8579 85.79%
OATP1B1 inhibitior + 0.9210 92.10%
OATP1B3 inhibitior + 0.9455 94.55%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.8250 82.50%
BSEP inhibitior - 0.8561 85.61%
P-glycoprotein inhibitior - 0.9395 93.95%
P-glycoprotein substrate - 0.9476 94.76%
CYP3A4 substrate - 0.6132 61.32%
CYP2C9 substrate - 0.7933 79.33%
CYP2D6 substrate - 0.7574 75.74%
CYP3A4 inhibition - 0.8606 86.06%
CYP2C9 inhibition - 0.8448 84.48%
CYP2C19 inhibition - 0.7307 73.07%
CYP2D6 inhibition - 0.9215 92.15%
CYP1A2 inhibition - 0.7996 79.96%
CYP2C8 inhibition - 0.9390 93.90%
CYP inhibitory promiscuity - 0.7982 79.82%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) + 0.6558 65.58%
Carcinogenicity (trinary) Non-required 0.6124 61.24%
Eye corrosion + 0.8615 86.15%
Eye irritation - 0.7796 77.96%
Skin irritation + 0.8454 84.54%
Skin corrosion + 0.5363 53.63%
Ames mutagenesis + 0.5700 57.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4112 41.12%
Micronuclear - 0.9700 97.00%
Hepatotoxicity + 0.8875 88.75%
skin sensitisation + 0.8256 82.56%
Respiratory toxicity - 0.6444 64.44%
Reproductive toxicity - 0.9000 90.00%
Mitochondrial toxicity + 0.5428 54.28%
Nephrotoxicity + 0.7017 70.17%
Acute Oral Toxicity (c) III 0.7732 77.32%
Estrogen receptor binding - 0.5859 58.59%
Androgen receptor binding - 0.8129 81.29%
Thyroid receptor binding - 0.6213 62.13%
Glucocorticoid receptor binding - 0.6133 61.33%
Aromatase binding - 0.7307 73.07%
PPAR gamma - 0.5398 53.98%
Honey bee toxicity - 0.4936 49.36%
Biodegradation - 0.8250 82.50%
Crustacea aquatic toxicity - 0.7400 74.00%
Fish aquatic toxicity + 0.9769 97.69%

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
CHEMBL253 P34972 Cannabinoid CB2 receptor 89.50% 97.25%
CHEMBL2581 P07339 Cathepsin D 86.88% 98.95%
CHEMBL1293267 Q9HC97 G-protein coupled receptor 35 85.81% 89.34%
CHEMBL1907 P15144 Aminopeptidase N 84.32% 93.31%
CHEMBL3401 O75469 Pregnane X receptor 80.66% 94.73%
CHEMBL4662 P28074 Proteasome Macropain subunit MB1 80.66% 93.85%

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 162868325
LOTUS LTS0251520
wikiData Q105141244