2,3,3-Trimethyl-1,4-pentadiene

Details

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Internal ID 589bd178-dbe3-42ab-90dd-055f7a041d52
Taxonomy Hydrocarbons > Unsaturated hydrocarbons > Branched unsaturated hydrocarbons
IUPAC Name 2,3,3-trimethylpenta-1,4-diene
SMILES (Canonical) CC(=C)C(C)(C)C=C
SMILES (Isomeric) CC(=C)C(C)(C)C=C
InChI InChI=1S/C8H14/c1-6-8(4,5)7(2)3/h6H,1-2H2,3-5H3
InChI Key OXYDHUPSYIQGAP-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C8H14
Molecular Weight 110.20 g/mol
Exact Mass 110.109550447 g/mol
Topological Polar Surface Area (TPSA) 0.00 Ų
XlogP 3.60
Atomic LogP (AlogP) 2.77
H-Bond Acceptor 0
H-Bond Donor 0
Rotatable Bonds 2

Synonyms

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756-02-5
1,4-Pentadiene, 2,3,3-trimethyl-
2,3,3-trimethylpenta-1,4-diene
NSC157574
1, 2,3,3-trimethyl-
2,3-Trimethyl-1,4-pentadiene
DTXSID40226505
OXYDHUPSYIQGAP-UHFFFAOYSA-N
AKOS006274055
NSC 157574
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of 2,3,3-Trimethyl-1,4-pentadiene

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9838 98.38%
Caco-2 + 0.7505 75.05%
Blood Brain Barrier + 0.9750 97.50%
Human oral bioavailability + 0.5143 51.43%
Subcellular localzation Lysosomes 0.5779 57.79%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9637 96.37%
OATP1B3 inhibitior + 0.9436 94.36%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.9000 90.00%
BSEP inhibitior - 0.8898 88.98%
P-glycoprotein inhibitior - 0.9766 97.66%
P-glycoprotein substrate - 0.9768 97.68%
CYP3A4 substrate - 0.7027 70.27%
CYP2C9 substrate - 0.8132 81.32%
CYP2D6 substrate - 0.7975 79.75%
CYP3A4 inhibition - 0.8112 81.12%
CYP2C9 inhibition - 0.8357 83.57%
CYP2C19 inhibition - 0.8357 83.57%
CYP2D6 inhibition - 0.9364 93.64%
CYP1A2 inhibition - 0.8831 88.31%
CYP2C8 inhibition - 0.9792 97.92%
CYP inhibitory promiscuity - 0.7068 70.68%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) + 0.6783 67.83%
Carcinogenicity (trinary) Warning 0.6085 60.85%
Eye corrosion + 0.9247 92.47%
Eye irritation + 0.9786 97.86%
Skin irritation + 0.7734 77.34%
Skin corrosion - 0.9646 96.46%
Ames mutagenesis - 0.6700 67.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7432 74.32%
Micronuclear - 0.9800 98.00%
Hepatotoxicity + 0.8875 88.75%
skin sensitisation + 0.8887 88.87%
Respiratory toxicity - 0.8889 88.89%
Reproductive toxicity - 0.9778 97.78%
Mitochondrial toxicity + 0.5331 53.31%
Nephrotoxicity + 0.6699 66.99%
Acute Oral Toxicity (c) III 0.7916 79.16%
Estrogen receptor binding - 0.8610 86.10%
Androgen receptor binding - 0.9055 90.55%
Thyroid receptor binding - 0.8003 80.03%
Glucocorticoid receptor binding - 0.9326 93.26%
Aromatase binding - 0.8088 80.88%
PPAR gamma - 0.8774 87.74%
Honey bee toxicity - 0.7366 73.66%
Biodegradation - 0.5250 52.50%
Crustacea aquatic toxicity - 0.6900 69.00%
Fish aquatic toxicity + 0.9348 93.48%

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
CHEMBL253 P34972 Cannabinoid CB2 receptor 80.71% 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.
Elsholtzia ciliata
Mentha arvensis
Mentha canadensis
Mosla chinensis

Cross-Links

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PubChem 136569
NPASS NPC299001