gamma-Irone

Details

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Internal ID 57a94361-9185-41bc-be33-69244fdb1125
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Sesquiterpenoids
IUPAC Name (E)-4-[(1S,3R)-2,2,3-trimethyl-6-methylidenecyclohexyl]but-3-en-2-one
SMILES (Canonical) CC1CCC(=C)C(C1(C)C)C=CC(=O)C
SMILES (Isomeric) C[C@@H]1CCC(=C)[C@@H](C1(C)C)/C=C/C(=O)C
InChI InChI=1S/C14H22O/c1-10-6-7-11(2)14(4,5)13(10)9-8-12(3)15/h8-9,11,13H,1,6-7H2,2-5H3/b9-8+/t11-,13+/m1/s1
InChI Key MVPDTCQYNRKWJA-UZPJXDOOSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

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Molecular Formula C14H22O
Molecular Weight 206.32 g/mol
Exact Mass 206.167065321 g/mol
Topological Polar Surface Area (TPSA) 17.10 Ų
XlogP 3.50
Atomic LogP (AlogP) 3.76
H-Bond Acceptor 1
H-Bond Donor 0
Rotatable Bonds 2

Synonyms

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IOV6OG0LC8
UNII-IOV6OG0LC8
(+/-)-cis-gamma-Irone
IS4N6X2NA3
gamma-Irone, cis-(+/-)-
79-68-5
(E)-4-[(1S,3R)-2,2,3-trimethyl-6-methylidenecyclohexyl]but-3-en-2-one
3-Buten-2-one, 4-((1R,3S)-2,2,3-trimethyl-6-methylenecyclohexyl)-, (3E)-rel-
117894-47-0
3-Buten-2-one, 4-((1S,3R)-2,2,3-trimethyl-6-methylenecyclohexyl)-, (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 gamma-Irone

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9933 99.33%
Caco-2 + 0.8372 83.72%
Blood Brain Barrier + 0.8750 87.50%
Human oral bioavailability - 0.5429 54.29%
Subcellular localzation Lysosomes 0.4332 43.32%
OATP2B1 inhibitior - 0.8610 86.10%
OATP1B1 inhibitior + 0.9318 93.18%
OATP1B3 inhibitior - 0.3111 31.11%
MATE1 inhibitior - 0.9000 90.00%
OCT2 inhibitior - 0.7250 72.50%
BSEP inhibitior - 0.8858 88.58%
P-glycoprotein inhibitior - 0.9557 95.57%
P-glycoprotein substrate - 0.9045 90.45%
CYP3A4 substrate + 0.5162 51.62%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8845 88.45%
CYP3A4 inhibition - 0.8809 88.09%
CYP2C9 inhibition - 0.8450 84.50%
CYP2C19 inhibition - 0.7527 75.27%
CYP2D6 inhibition - 0.9388 93.88%
CYP1A2 inhibition - 0.6835 68.35%
CYP2C8 inhibition - 0.8900 89.00%
CYP inhibitory promiscuity - 0.6595 65.95%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.6600 66.00%
Carcinogenicity (trinary) Non-required 0.5359 53.59%
Eye corrosion - 0.8518 85.18%
Eye irritation - 0.8289 82.89%
Skin irritation + 0.8865 88.65%
Skin corrosion - 0.9653 96.53%
Ames mutagenesis - 0.8300 83.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5901 59.01%
Micronuclear - 1.0000 100.00%
Hepatotoxicity + 0.5394 53.94%
skin sensitisation + 0.9263 92.63%
Respiratory toxicity - 0.8444 84.44%
Reproductive toxicity - 0.5778 57.78%
Mitochondrial toxicity - 1.0000 100.00%
Nephrotoxicity - 0.5666 56.66%
Acute Oral Toxicity (c) III 0.8421 84.21%
Estrogen receptor binding - 0.8317 83.17%
Androgen receptor binding - 0.7460 74.60%
Thyroid receptor binding - 0.6700 67.00%
Glucocorticoid receptor binding - 0.8342 83.42%
Aromatase binding - 0.7995 79.95%
PPAR gamma - 0.9022 90.22%
Honey bee toxicity - 0.8406 84.06%
Biodegradation - 0.5500 55.00%
Crustacea aquatic toxicity - 0.5700 57.00%
Fish aquatic toxicity + 0.9790 97.90%

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
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 94.01% 91.11%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 90.07% 96.09%
CHEMBL340 P08684 Cytochrome P450 3A4 89.12% 91.19%
CHEMBL1994 P08235 Mineralocorticoid receptor 84.71% 100.00%
CHEMBL325 Q13547 Histone deacetylase 1 82.00% 95.92%

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.
Iris sibirica

Cross-Links

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PubChem 6433146
LOTUS LTS0140105
wikiData Q22077110