2-Chloromyrcene

Details

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Internal ID a4544532-b37c-465b-8594-4645df2ee056
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Monoterpenoids > Acyclic monoterpenoids
IUPAC Name 2-chloro-7-methyl-3-methylideneocta-1,6-diene
SMILES (Canonical) CC(=CCCC(=C)C(=C)Cl)C
SMILES (Isomeric) CC(=CCCC(=C)C(=C)Cl)C
InChI InChI=1S/C10H15Cl/c1-8(2)6-5-7-9(3)10(4)11/h6H,3-5,7H2,1-2H3
InChI Key FFNJBTUAEWDYEM-UHFFFAOYSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

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Molecular Formula C10H15Cl
Molecular Weight 170.68 g/mol
Exact Mass 170.0862282 g/mol
Topological Polar Surface Area (TPSA) 0.00 Ų
XlogP 4.70
Atomic LogP (AlogP) 4.04
H-Bond Acceptor 0
H-Bond Donor 0
Rotatable Bonds 4

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 2-Chloromyrcene

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9899 98.99%
Caco-2 + 0.8463 84.63%
Blood Brain Barrier + 0.9750 97.50%
Human oral bioavailability + 0.6286 62.86%
Subcellular localzation Nucleus 0.4703 47.03%
OATP2B1 inhibitior - 0.8604 86.04%
OATP1B1 inhibitior + 0.9205 92.05%
OATP1B3 inhibitior + 0.9362 93.62%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.7750 77.50%
BSEP inhibitior - 0.8191 81.91%
P-glycoprotein inhibitior - 0.9786 97.86%
P-glycoprotein substrate - 0.9533 95.33%
CYP3A4 substrate - 0.6153 61.53%
CYP2C9 substrate - 0.8165 81.65%
CYP2D6 substrate - 0.7732 77.32%
CYP3A4 inhibition - 0.9646 96.46%
CYP2C9 inhibition - 0.8572 85.72%
CYP2C19 inhibition - 0.7346 73.46%
CYP2D6 inhibition - 0.9068 90.68%
CYP1A2 inhibition - 0.7100 71.00%
CYP2C8 inhibition - 0.9728 97.28%
CYP inhibitory promiscuity - 0.7298 72.98%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) + 0.5275 52.75%
Carcinogenicity (trinary) Non-required 0.5727 57.27%
Eye corrosion + 0.7011 70.11%
Eye irritation + 0.9339 93.39%
Skin irritation + 0.6974 69.74%
Skin corrosion - 0.6352 63.52%
Ames mutagenesis - 0.6400 64.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5000 50.00%
Micronuclear - 0.9700 97.00%
Hepatotoxicity + 0.6125 61.25%
skin sensitisation + 0.7803 78.03%
Respiratory toxicity - 0.9000 90.00%
Reproductive toxicity - 0.9000 90.00%
Mitochondrial toxicity - 0.8500 85.00%
Nephrotoxicity + 0.7664 76.64%
Acute Oral Toxicity (c) III 0.7911 79.11%
Estrogen receptor binding - 0.9269 92.69%
Androgen receptor binding - 0.9060 90.60%
Thyroid receptor binding - 0.8630 86.30%
Glucocorticoid receptor binding - 0.8000 80.00%
Aromatase binding - 0.8060 80.60%
PPAR gamma - 0.5068 50.68%
Honey bee toxicity - 0.7049 70.49%
Biodegradation + 0.5500 55.00%
Crustacea aquatic toxicity + 0.5500 55.00%
Fish aquatic toxicity + 0.9762 97.62%

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
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 87.11% 91.11%
CHEMBL1293267 Q9HC97 G-protein coupled receptor 35 84.14% 89.34%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 83.83% 96.95%
CHEMBL4769 O95749 Geranylgeranyl pyrophosphate synthetase 82.31% 92.08%
CHEMBL3401 O75469 Pregnane X receptor 81.76% 94.73%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 80.09% 96.09%

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.
There are no matching plants.

Cross-Links

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PubChem 23247410
LOTUS LTS0154001
wikiData Q104994584