(2Z,6E)-3-chloromethyl-1-chloroocta-2,6-dien-8-al

Details

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Internal ID 76e32ace-f4d2-49c8-ac3a-3b6a55a88cfd
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Monoterpenoids > Acyclic monoterpenoids
IUPAC Name (2E,6Z)-8-chloro-6-(chloromethyl)-2-methylocta-2,6-dienal
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C10H14Cl2O/c1-9(8-13)3-2-4-10(7-12)5-6-11/h3,5,8H,2,4,6-7H2,1H3/b9-3+,10-5-
InChI Key JQUUTSBSWFKCKS-AWTZEJBTSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C10H14Cl2O
Molecular Weight 221.12 g/mol
Exact Mass 220.0421705 g/mol
Topological Polar Surface Area (TPSA) 17.10 Ų
XlogP 2.80
Atomic LogP (AlogP) 3.32
H-Bond Acceptor 1
H-Bond Donor 0
Rotatable Bonds 6

Synonyms

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RefChem:69054
CHEBI:224968
(2E,6Z)-8-chloro-6-(chloromethyl)-2-methylocta-2,6-dienal

2D Structure

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2D Structure of (2Z,6E)-3-chloromethyl-1-chloroocta-2,6-dien-8-al

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9909 99.09%
Caco-2 + 0.7544 75.44%
Blood Brain Barrier + 0.9750 97.50%
Human oral bioavailability + 0.5571 55.71%
Subcellular localzation Mitochondria 0.4216 42.16%
OATP2B1 inhibitior - 0.8589 85.89%
OATP1B1 inhibitior + 0.9059 90.59%
OATP1B3 inhibitior + 0.9373 93.73%
MATE1 inhibitior - 0.9000 90.00%
OCT2 inhibitior - 0.7500 75.00%
BSEP inhibitior - 0.7484 74.84%
P-glycoprotein inhibitior - 0.9858 98.58%
P-glycoprotein substrate - 0.8555 85.55%
CYP3A4 substrate - 0.5339 53.39%
CYP2C9 substrate - 0.5928 59.28%
CYP2D6 substrate - 0.8372 83.72%
CYP3A4 inhibition - 0.9739 97.39%
CYP2C9 inhibition - 0.9072 90.72%
CYP2C19 inhibition - 0.8482 84.82%
CYP2D6 inhibition - 0.9329 93.29%
CYP1A2 inhibition - 0.6260 62.60%
CYP2C8 inhibition - 0.9625 96.25%
CYP inhibitory promiscuity - 0.8016 80.16%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.5256 52.56%
Carcinogenicity (trinary) Danger 0.4415 44.15%
Eye corrosion + 0.9472 94.72%
Eye irritation - 0.7723 77.23%
Skin irritation + 0.7471 74.71%
Skin corrosion + 0.7646 76.46%
Ames mutagenesis + 0.6600 66.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4675 46.75%
Micronuclear - 0.9800 98.00%
Hepatotoxicity + 0.6125 61.25%
skin sensitisation + 0.8136 81.36%
Respiratory toxicity - 0.7556 75.56%
Reproductive toxicity - 0.8333 83.33%
Mitochondrial toxicity - 0.9125 91.25%
Nephrotoxicity + 0.7637 76.37%
Acute Oral Toxicity (c) III 0.6645 66.45%
Estrogen receptor binding - 0.8770 87.70%
Androgen receptor binding - 0.9323 93.23%
Thyroid receptor binding - 0.7653 76.53%
Glucocorticoid receptor binding - 0.5602 56.02%
Aromatase binding - 0.8101 81.01%
PPAR gamma + 0.5709 57.09%
Honey bee toxicity - 0.8201 82.01%
Biodegradation - 0.5750 57.50%
Crustacea aquatic toxicity - 0.5200 52.00%
Fish aquatic toxicity + 0.9535 95.35%

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
CHEMBL1293267 Q9HC97 G-protein coupled receptor 35 89.25% 89.34%
CHEMBL3492 P49721 Proteasome Macropain subunit 87.00% 90.24%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 86.40% 96.09%
CHEMBL3401 O75469 Pregnane X receptor 84.16% 94.73%
CHEMBL2664 P23526 Adenosylhomocysteinase 83.79% 86.67%
CHEMBL2581 P07339 Cathepsin D 83.61% 98.95%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 81.48% 91.11%
CHEMBL3060 Q9Y345 Glycine transporter 2 80.50% 99.17%

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 14865331
LOTUS LTS0173654
wikiData Q77509745