2,5-Dimethyl-1,6-heptadiene

Details

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Internal ID 285793ae-de40-4115-8714-2a7a72a22689
Taxonomy Hydrocarbons > Unsaturated hydrocarbons > Branched unsaturated hydrocarbons
IUPAC Name 2,5-dimethylhepta-1,6-diene
SMILES (Canonical) CC(CCC(=C)C)C=C
SMILES (Isomeric) CC(CCC(=C)C)C=C
InChI InChI=1S/C9H16/c1-5-9(4)7-6-8(2)3/h5,9H,1-2,6-7H2,3-4H3
InChI Key QDURDEDFGSDOQY-UHFFFAOYSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C9H16
Molecular Weight 124.22 g/mol
Exact Mass 124.125200510 g/mol
Topological Polar Surface Area (TPSA) 0.00 Ų
XlogP 3.90
Atomic LogP (AlogP) 3.16
H-Bond Acceptor 0
H-Bond Donor 0
Rotatable Bonds 4

Synonyms

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1,6-Heptadiene, 2,5-dimethyl-
2,5-dimethylhepta-1,6-diene
QDURDEDFGSDOQY-UHFFFAOYSA-N
2,5-Dimethyl-1,6-heptadiene #
68701-90-6

2D Structure

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2D Structure of 2,5-Dimethyl-1,6-heptadiene

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9860 98.60%
Caco-2 + 0.6409 64.09%
Blood Brain Barrier + 1.0000 100.00%
Human oral bioavailability - 0.5571 55.71%
Subcellular localzation Nucleus 0.4512 45.12%
OATP2B1 inhibitior - 0.8580 85.80%
OATP1B1 inhibitior + 0.9331 93.31%
OATP1B3 inhibitior + 0.9385 93.85%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.7750 77.50%
BSEP inhibitior - 0.9427 94.27%
P-glycoprotein inhibitior - 0.9800 98.00%
P-glycoprotein substrate - 0.9561 95.61%
CYP3A4 substrate - 0.6900 69.00%
CYP2C9 substrate - 0.8110 81.10%
CYP2D6 substrate - 0.7415 74.15%
CYP3A4 inhibition - 0.9585 95.85%
CYP2C9 inhibition - 0.9413 94.13%
CYP2C19 inhibition - 0.8949 89.49%
CYP2D6 inhibition - 0.9245 92.45%
CYP1A2 inhibition - 0.7571 75.71%
CYP2C8 inhibition - 0.9928 99.28%
CYP inhibitory promiscuity - 0.7267 72.67%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.5100 51.00%
Carcinogenicity (trinary) Warning 0.4848 48.48%
Eye corrosion + 0.8976 89.76%
Eye irritation + 0.9845 98.45%
Skin irritation + 0.8036 80.36%
Skin corrosion - 0.9377 93.77%
Ames mutagenesis - 0.8500 85.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5654 56.54%
Micronuclear - 1.0000 100.00%
Hepatotoxicity + 0.6875 68.75%
skin sensitisation + 0.9350 93.50%
Respiratory toxicity - 0.8000 80.00%
Reproductive toxicity - 0.8889 88.89%
Mitochondrial toxicity - 0.8500 85.00%
Nephrotoxicity + 0.6091 60.91%
Acute Oral Toxicity (c) III 0.8232 82.32%
Estrogen receptor binding - 0.9392 93.92%
Androgen receptor binding - 0.9245 92.45%
Thyroid receptor binding - 0.8856 88.56%
Glucocorticoid receptor binding - 0.9279 92.79%
Aromatase binding - 0.8818 88.18%
PPAR gamma - 0.9103 91.03%
Honey bee toxicity - 0.8313 83.13%
Biodegradation + 0.8500 85.00%
Crustacea aquatic toxicity - 0.8000 80.00%
Fish aquatic toxicity + 0.9622 96.22%

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 88.16% 96.09%
CHEMBL203 P00533 Epidermal growth factor receptor erbB1 86.99% 97.34%
CHEMBL2581 P07339 Cathepsin D 85.80% 98.95%
CHEMBL3892 Q99500 Sphingosine 1-phosphate receptor Edg-3 83.46% 97.29%
CHEMBL2885 P07451 Carbonic anhydrase III 81.34% 87.45%
CHEMBL3401 O75469 Pregnane X receptor 80.25% 94.73%
CHEMBL253 P34972 Cannabinoid CB2 receptor 80.18% 97.25%

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
Citrus deliciosa

Cross-Links

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PubChem 534896
NPASS NPC20536