3,5-Dimethyl-1-hexene

Details

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Internal ID 5b730250-fe40-480a-9751-4169aa5076e9
Taxonomy Hydrocarbons > Unsaturated hydrocarbons > Unsaturated aliphatic hydrocarbons
IUPAC Name 3,5-dimethylhex-1-ene
SMILES (Canonical) CC(C)CC(C)C=C
SMILES (Isomeric) CC(C)CC(C)C=C
InChI InChI=1S/C8H16/c1-5-8(4)6-7(2)3/h5,7-8H,1,6H2,2-4H3
InChI Key FEZKAPRRVNNJTK-UHFFFAOYSA-N
Popularity 5 references in papers

Physical and Chemical Properties

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Molecular Formula C8H16
Molecular Weight 112.21 g/mol
Exact Mass 112.125200510 g/mol
Topological Polar Surface Area (TPSA) 0.00 Ų
XlogP 3.50
Atomic LogP (AlogP) 2.85
H-Bond Acceptor 0
H-Bond Donor 0
Rotatable Bonds 3

Synonyms

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3,5-dimethylhex-1-ene
7423-69-0
1-Hexene, 3,5-dimethyl-
DTXSID40334977
FEZKAPRRVNNJTK-UHFFFAOYSA-N
AKOS006274876
FT-0692011

2D Structure

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2D Structure of 3,5-Dimethyl-1-hexene

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9879 98.79%
Caco-2 + 0.6749 67.49%
Blood Brain Barrier + 1.0000 100.00%
Human oral bioavailability + 0.7143 71.43%
Subcellular localzation Lysosomes 0.3788 37.88%
OATP2B1 inhibitior - 0.8634 86.34%
OATP1B1 inhibitior + 0.9406 94.06%
OATP1B3 inhibitior + 0.9498 94.98%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.9250 92.50%
BSEP inhibitior - 0.9325 93.25%
P-glycoprotein inhibitior - 0.9829 98.29%
P-glycoprotein substrate - 0.9447 94.47%
CYP3A4 substrate - 0.7481 74.81%
CYP2C9 substrate - 0.8110 81.10%
CYP2D6 substrate - 0.7415 74.15%
CYP3A4 inhibition - 0.9279 92.79%
CYP2C9 inhibition - 0.9183 91.83%
CYP2C19 inhibition - 0.9196 91.96%
CYP2D6 inhibition - 0.9311 93.11%
CYP1A2 inhibition - 0.8476 84.76%
CYP2C8 inhibition - 0.9871 98.71%
CYP inhibitory promiscuity - 0.8210 82.10%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) + 0.6483 64.83%
Carcinogenicity (trinary) Warning 0.5632 56.32%
Eye corrosion + 0.9895 98.95%
Eye irritation + 0.9923 99.23%
Skin irritation + 0.8235 82.35%
Skin corrosion - 0.9618 96.18%
Ames mutagenesis - 0.8500 85.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6922 69.22%
Micronuclear - 0.9900 99.00%
Hepatotoxicity + 0.8266 82.66%
skin sensitisation + 0.8958 89.58%
Respiratory toxicity - 0.5111 51.11%
Reproductive toxicity - 0.9889 98.89%
Mitochondrial toxicity + 0.8125 81.25%
Nephrotoxicity + 0.5743 57.43%
Acute Oral Toxicity (c) III 0.7084 70.84%
Estrogen receptor binding - 0.9501 95.01%
Androgen receptor binding - 0.8882 88.82%
Thyroid receptor binding - 0.9054 90.54%
Glucocorticoid receptor binding - 0.8633 86.33%
Aromatase binding - 0.8430 84.30%
PPAR gamma - 0.9384 93.84%
Honey bee toxicity - 0.8189 81.89%
Biodegradation + 0.6250 62.50%
Crustacea aquatic toxicity - 0.7800 78.00%
Fish aquatic toxicity + 0.9504 95.04%

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 91.24% 98.95%
CHEMBL1907 P15144 Aminopeptidase N 86.44% 93.31%
CHEMBL2885 P07451 Carbonic anhydrase III 84.68% 87.45%
CHEMBL3837 P07711 Cathepsin L 82.30% 96.61%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 82.19% 96.09%
CHEMBL221 P23219 Cyclooxygenase-1 81.70% 90.17%
CHEMBL253 P34972 Cannabinoid CB2 receptor 81.56% 97.25%
CHEMBL3130 O00329 PI3-kinase p110-delta subunit 80.10% 96.47%

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 522526
NPASS NPC69348