2-Isopropenyl-5-methylhex-4-enal

Details

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Internal ID 1e2eb488-b24d-4892-81fe-b44e19773113
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Monoterpenoids > Acyclic monoterpenoids
IUPAC Name 5-methyl-2-prop-1-en-2-ylhex-4-enal
SMILES (Canonical) CC(=CCC(C=O)C(=C)C)C
SMILES (Isomeric) CC(=CCC(C=O)C(=C)C)C
InChI InChI=1S/C10H16O/c1-8(2)5-6-10(7-11)9(3)4/h5,7,10H,3,6H2,1-2,4H3
InChI Key PAIVGFRXYIGODL-UHFFFAOYSA-N
Popularity 4 references in papers

Physical and Chemical Properties

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Molecular Formula C10H16O
Molecular Weight 152.23 g/mol
Exact Mass 152.120115130 g/mol
Topological Polar Surface Area (TPSA) 17.10 Ų
XlogP 3.10
Atomic LogP (AlogP) 2.73
H-Bond Acceptor 1
H-Bond Donor 0
Rotatable Bonds 4

Synonyms

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EINECS 229-462-3
5-Methyl-2-isopropenyl-4-hexenal
(R)-5-Methyl-2-(1-methylvinyl)hex-4-enal
2-Isopropenyl-5-methylhex-4-enal
4-Hexenal, 5-methyl-2-(1-methylethenyl)-, (R)-
SCHEMBL336894
2-Isopropenyl-5-methyl-4-hexenal #

2D Structure

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2D Structure of 2-Isopropenyl-5-methylhex-4-enal

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9944 99.44%
Caco-2 + 0.6186 61.86%
Blood Brain Barrier + 1.0000 100.00%
Human oral bioavailability - 0.5571 55.71%
Subcellular localzation Nucleus 0.3305 33.05%
OATP2B1 inhibitior - 0.8643 86.43%
OATP1B1 inhibitior + 0.9315 93.15%
OATP1B3 inhibitior + 0.9385 93.85%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.8500 85.00%
BSEP inhibitior - 0.9144 91.44%
P-glycoprotein inhibitior - 0.9838 98.38%
P-glycoprotein substrate - 0.9512 95.12%
CYP3A4 substrate - 0.6443 64.43%
CYP2C9 substrate - 0.5888 58.88%
CYP2D6 substrate - 0.7942 79.42%
CYP3A4 inhibition - 0.9532 95.32%
CYP2C9 inhibition - 0.8970 89.70%
CYP2C19 inhibition - 0.8595 85.95%
CYP2D6 inhibition - 0.9354 93.54%
CYP1A2 inhibition - 0.8377 83.77%
CYP2C8 inhibition - 0.9818 98.18%
CYP inhibitory promiscuity - 0.7200 72.00%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) + 0.6283 62.83%
Carcinogenicity (trinary) Non-required 0.6138 61.38%
Eye corrosion + 0.9663 96.63%
Eye irritation + 0.9865 98.65%
Skin irritation + 0.8952 89.52%
Skin corrosion + 0.7361 73.61%
Ames mutagenesis - 0.7400 74.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5723 57.23%
Micronuclear - 0.9400 94.00%
Hepatotoxicity + 0.7250 72.50%
skin sensitisation + 0.9418 94.18%
Respiratory toxicity - 0.8000 80.00%
Reproductive toxicity - 0.9667 96.67%
Mitochondrial toxicity - 0.8875 88.75%
Nephrotoxicity + 0.7508 75.08%
Acute Oral Toxicity (c) III 0.4848 48.48%
Estrogen receptor binding - 0.9564 95.64%
Androgen receptor binding - 0.8931 89.31%
Thyroid receptor binding - 0.8944 89.44%
Glucocorticoid receptor binding - 0.9432 94.32%
Aromatase binding - 0.8728 87.28%
PPAR gamma - 0.9039 90.39%
Honey bee toxicity - 0.8569 85.69%
Biodegradation + 0.6000 60.00%
Crustacea aquatic toxicity - 0.8500 85.00%
Fish aquatic toxicity + 0.9366 93.66%

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
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 86.43% 94.45%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 85.46% 96.09%
CHEMBL2581 P07339 Cathepsin D 83.29% 98.95%
CHEMBL3401 O75469 Pregnane X receptor 81.75% 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.
Rhodiola crenulata

Cross-Links

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PubChem 110898
NPASS NPC106106