(Z)-4-Chloro-2,3-dimethyl-1,3-hexadiene

Details

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Internal ID 22ddd335-9aab-45a9-b4ca-19b8f7c6d4e4
Taxonomy Organohalogen compounds > Vinyl halides > Vinyl chlorides
IUPAC Name (3Z)-4-chloro-2,3-dimethylhexa-1,3-diene
SMILES (Canonical) CCC(=C(C)C(=C)C)Cl
SMILES (Isomeric) CC/C(=C(\C)/C(=C)C)/Cl
InChI InChI=1S/C8H13Cl/c1-5-8(9)7(4)6(2)3/h2,5H2,1,3-4H3/b8-7-
InChI Key RIDCARBEKJXPKS-FPLPWBNLSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C8H13Cl
Molecular Weight 144.64 g/mol
Exact Mass 144.0705781 g/mol
Topological Polar Surface Area (TPSA) 0.00 Ų
XlogP 4.20
Atomic LogP (AlogP) 3.49
H-Bond Acceptor 0
H-Bond Donor 0
Rotatable Bonds 2

Synonyms

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RIDCARBEKJXPKS-FPLPWBNLSA-N
(3Z)-4-Chloro-2,3-dimethyl-1,3-hexadiene #

2D Structure

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2D Structure of (Z)-4-Chloro-2,3-dimethyl-1,3-hexadiene

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9942 99.42%
Caco-2 + 0.7956 79.56%
Blood Brain Barrier + 0.9750 97.50%
Human oral bioavailability + 0.7143 71.43%
Subcellular localzation Lysosomes 0.5503 55.03%
OATP2B1 inhibitior - 0.8626 86.26%
OATP1B1 inhibitior + 0.9493 94.93%
OATP1B3 inhibitior + 0.9415 94.15%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.8250 82.50%
BSEP inhibitior - 0.8926 89.26%
P-glycoprotein inhibitior - 0.9717 97.17%
P-glycoprotein substrate - 0.9197 91.97%
CYP3A4 substrate - 0.6493 64.93%
CYP2C9 substrate - 0.8165 81.65%
CYP2D6 substrate - 0.7732 77.32%
CYP3A4 inhibition - 0.9234 92.34%
CYP2C9 inhibition - 0.8132 81.32%
CYP2C19 inhibition - 0.6770 67.70%
CYP2D6 inhibition - 0.8928 89.28%
CYP1A2 inhibition - 0.7083 70.83%
CYP2C8 inhibition - 0.9195 91.95%
CYP inhibitory promiscuity - 0.6396 63.96%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) + 0.6456 64.56%
Carcinogenicity (trinary) Non-required 0.5692 56.92%
Eye corrosion + 0.6793 67.93%
Eye irritation + 0.9682 96.82%
Skin irritation + 0.7427 74.27%
Skin corrosion - 0.5000 50.00%
Ames mutagenesis - 0.6577 65.77%
Human Ether-a-go-go-Related Gene inhibition - 0.7096 70.96%
Micronuclear - 0.9400 94.00%
Hepatotoxicity + 0.7625 76.25%
skin sensitisation + 0.7963 79.63%
Respiratory toxicity - 0.8889 88.89%
Reproductive toxicity - 0.8111 81.11%
Mitochondrial toxicity - 0.5875 58.75%
Nephrotoxicity + 0.6697 66.97%
Acute Oral Toxicity (c) III 0.5951 59.51%
Estrogen receptor binding - 0.8879 88.79%
Androgen receptor binding - 0.6720 67.20%
Thyroid receptor binding - 0.7558 75.58%
Glucocorticoid receptor binding - 0.8511 85.11%
Aromatase binding - 0.7393 73.93%
PPAR gamma - 0.7542 75.42%
Honey bee toxicity - 0.7951 79.51%
Biodegradation - 0.6250 62.50%
Crustacea aquatic toxicity - 0.6000 60.00%
Fish aquatic toxicity + 0.9874 98.74%

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 90.24% 96.09%
CHEMBL4040 P28482 MAP kinase ERK2 90.11% 83.82%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 86.78% 96.95%
CHEMBL253 P34972 Cannabinoid CB2 receptor 85.44% 97.25%
CHEMBL4657 Q6V1X1 Dipeptidyl peptidase VIII 84.31% 97.21%

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.
Mentha arvensis
Mentha canadensis

Cross-Links

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PubChem 5372743
NPASS NPC148182