3,7-Dimethylocta-1,3,7-triene

Details

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Internal ID c8c8e0c6-cf7f-415a-ab83-04a61a391097
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Monoterpenoids > Acyclic monoterpenoids
IUPAC Name (3E)-3,7-dimethylocta-1,3,7-triene
SMILES (Canonical) CC(=C)CCC=C(C)C=C
SMILES (Isomeric) CC(=C)CC/C=C(\C)/C=C
InChI InChI=1S/C10H16/c1-5-10(4)8-6-7-9(2)3/h5,8H,1-2,6-7H2,3-4H3/b10-8+
InChI Key XJPBRODHZKDRCB-CSKARUKUSA-N
Popularity 25 references in papers

Physical and Chemical Properties

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Molecular Formula C10H16
Molecular Weight 136.23 g/mol
Exact Mass 136.125200510 g/mol
Topological Polar Surface Area (TPSA) 0.00 Ų
XlogP 4.30
Atomic LogP (AlogP) 3.48
H-Bond Acceptor 0
H-Bond Donor 0
Rotatable Bonds 4

Synonyms

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3,7-Dimethylocta-1,3,7-triene
502-99-8
1,3,7-Octatriene, 3,7-dimethyl-
trans-alpha-Ocimene
8DBO41SLJL
alpha-trans-Ocimene
(E)-alpha-ocimene
alpha-Ocimene, (E)-
Ocimene trans-alpha-form
alpha-Ocimene, (3E)-
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of 3,7-Dimethylocta-1,3,7-triene

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9853 98.53%
Caco-2 + 0.9039 90.39%
Blood Brain Barrier + 1.0000 100.00%
Human oral bioavailability - 0.5571 55.71%
Subcellular localzation Nucleus 0.5689 56.89%
OATP2B1 inhibitior - 0.8611 86.11%
OATP1B1 inhibitior + 0.9164 91.64%
OATP1B3 inhibitior + 0.9289 92.89%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.7750 77.50%
BSEP inhibitior - 0.8938 89.38%
P-glycoprotein inhibitior - 0.9848 98.48%
P-glycoprotein substrate - 0.9601 96.01%
CYP3A4 substrate - 0.6296 62.96%
CYP2C9 substrate - 0.8209 82.09%
CYP2D6 substrate - 0.7550 75.50%
CYP3A4 inhibition - 0.9690 96.90%
CYP2C9 inhibition - 0.9398 93.98%
CYP2C19 inhibition - 0.9036 90.36%
CYP2D6 inhibition - 0.9301 93.01%
CYP1A2 inhibition - 0.7329 73.29%
CYP2C8 inhibition - 0.9635 96.35%
CYP inhibitory promiscuity - 0.7412 74.12%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.5200 52.00%
Carcinogenicity (trinary) Warning 0.4578 45.78%
Eye corrosion + 0.8327 83.27%
Eye irritation + 0.9823 98.23%
Skin irritation + 0.8475 84.75%
Skin corrosion - 0.9399 93.99%
Ames mutagenesis - 0.7300 73.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6848 68.48%
Micronuclear - 1.0000 100.00%
Hepatotoxicity - 0.5375 53.75%
skin sensitisation + 0.9462 94.62%
Respiratory toxicity - 0.8667 86.67%
Reproductive toxicity - 0.9111 91.11%
Mitochondrial toxicity - 0.8875 88.75%
Nephrotoxicity + 0.5941 59.41%
Acute Oral Toxicity (c) III 0.8134 81.34%
Estrogen receptor binding - 0.9470 94.70%
Androgen receptor binding - 0.9205 92.05%
Thyroid receptor binding - 0.8870 88.70%
Glucocorticoid receptor binding - 0.8044 80.44%
Aromatase binding - 0.8268 82.68%
PPAR gamma - 0.7711 77.11%
Honey bee toxicity - 0.8378 83.78%
Biodegradation + 0.9000 90.00%
Crustacea aquatic toxicity - 0.7000 70.00%
Fish aquatic toxicity + 0.9677 96.77%

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
CHEMBL2581 P07339 Cathepsin D 85.28% 98.95%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 85.12% 96.09%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 83.73% 91.11%
CHEMBL203 P00533 Epidermal growth factor receptor erbB1 80.51% 97.34%
CHEMBL3401 O75469 Pregnane X receptor 80.21% 94.73%

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.
Citrus × aurantium
Machilus thunbergii
Zanthoxylum schinifolium

Cross-Links

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PubChem 5320249
NPASS NPC198198
LOTUS LTS0276186
wikiData Q26776996