Dihydro-beta-ionene

Details

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Internal ID 0fd9838f-8d60-4251-84e2-cf7e77db1a19
Taxonomy Hydrocarbons > Unsaturated hydrocarbons > Branched unsaturated hydrocarbons
IUPAC Name 2-but-3-enyl-1,3,3-trimethylcyclohexene
SMILES (Canonical) CC1=C(C(CCC1)(C)C)CCC=C
SMILES (Isomeric) CC1=C(C(CCC1)(C)C)CCC=C
InChI InChI=1S/C13H22/c1-5-6-9-12-11(2)8-7-10-13(12,3)4/h5H,1,6-10H2,2-4H3
InChI Key KQKAQIOEBKPBEA-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C13H22
Molecular Weight 178.31 g/mol
Exact Mass 178.172150702 g/mol
Topological Polar Surface Area (TPSA) 0.00 Ų
XlogP 4.20
Atomic LogP (AlogP) 4.48
H-Bond Acceptor 0
H-Bond Donor 0
Rotatable Bonds 3

Synonyms

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KQKAQIOEBKPBEA-UHFFFAOYSA-N

2D Structure

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2D Structure of Dihydro-beta-ionene

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 + 0.8900 89.00%
Blood Brain Barrier + 1.0000 100.00%
Human oral bioavailability - 0.5857 58.57%
Subcellular localzation Lysosomes 0.5851 58.51%
OATP2B1 inhibitior - 0.8511 85.11%
OATP1B1 inhibitior + 0.8250 82.50%
OATP1B3 inhibitior - 0.3180 31.80%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.7500 75.00%
BSEP inhibitior - 0.8735 87.35%
P-glycoprotein inhibitior - 0.9758 97.58%
P-glycoprotein substrate - 0.9451 94.51%
CYP3A4 substrate - 0.5258 52.58%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.7625 76.25%
CYP3A4 inhibition - 0.8603 86.03%
CYP2C9 inhibition - 0.8620 86.20%
CYP2C19 inhibition - 0.8554 85.54%
CYP2D6 inhibition - 0.9480 94.80%
CYP1A2 inhibition - 0.8185 81.85%
CYP2C8 inhibition - 0.8582 85.82%
CYP inhibitory promiscuity - 0.6171 61.71%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.7000 70.00%
Carcinogenicity (trinary) Warning 0.4984 49.84%
Eye corrosion - 0.7992 79.92%
Eye irritation + 0.9421 94.21%
Skin irritation + 0.5405 54.05%
Skin corrosion - 0.9888 98.88%
Ames mutagenesis - 0.8040 80.40%
Human Ether-a-go-go-Related Gene inhibition - 0.4684 46.84%
Micronuclear - 1.0000 100.00%
Hepatotoxicity + 0.6357 63.57%
skin sensitisation + 0.9059 90.59%
Respiratory toxicity - 0.5333 53.33%
Reproductive toxicity - 0.5111 51.11%
Mitochondrial toxicity - 0.6125 61.25%
Nephrotoxicity + 0.4819 48.19%
Acute Oral Toxicity (c) III 0.8388 83.88%
Estrogen receptor binding - 0.9715 97.15%
Androgen receptor binding - 0.7237 72.37%
Thyroid receptor binding - 0.8249 82.49%
Glucocorticoid receptor binding - 0.9000 90.00%
Aromatase binding - 0.8391 83.91%
PPAR gamma - 0.8442 84.42%
Honey bee toxicity - 0.8800 88.00%
Biodegradation + 0.5250 52.50%
Crustacea aquatic toxicity - 0.5200 52.00%
Fish aquatic toxicity + 1.0000 100.00%

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
CHEMBL240 Q12809 HERG 97.39% 89.76%
CHEMBL230 P35354 Cyclooxygenase-2 96.78% 89.63%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 92.81% 91.11%
CHEMBL1937 Q92769 Histone deacetylase 2 86.31% 94.75%
CHEMBL253 P34972 Cannabinoid CB2 receptor 85.55% 97.25%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 85.18% 96.09%
CHEMBL1293249 Q13887 Kruppel-like factor 5 84.59% 86.33%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 83.61% 95.56%
CHEMBL5805 Q9NR97 Toll-like receptor 8 83.47% 96.25%
CHEMBL233 P35372 Mu opioid receptor 82.92% 97.93%
CHEMBL1977 P11473 Vitamin D receptor 82.15% 99.43%
CHEMBL2581 P07339 Cathepsin D 81.31% 98.95%

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.
Crocus sativus

Cross-Links

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PubChem 85793089
NPASS NPC262588