beta-Ocimene

Details

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Internal ID c656c63e-3673-47da-b8e4-5bdd62373187
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Monoterpenoids > Acyclic monoterpenoids
IUPAC Name 3,7-dimethylocta-1,3,6-triene
SMILES (Canonical) CC(=CCC=C(C)C=C)C
SMILES (Isomeric) CC(=CCC=C(C)C=C)C
InChI InChI=1S/C10H16/c1-5-10(4)8-6-7-9(2)3/h5,7-8H,1,6H2,2-4H3
InChI Key IHPKGUQCSIINRJ-UHFFFAOYSA-N
Popularity 1,132 references in papers

Physical and Chemical Properties

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Molecular Formula C10H16
Molecular Weight 136.23 g/mol
Exact Mass 136.125200510 g/mol
Topological Polar Surface Area (TPSA) 0.00 Ų
XlogP 4.30
Atomic LogP (AlogP) 3.48
H-Bond Acceptor 0
H-Bond Donor 0
Rotatable Bonds 3

Synonyms

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13877-91-3
3,7-Dimethylocta-1,3,6-triene
OCIMENE
CHEBI:10436
DSSTox_CID_27051
DSSTox_RID_82069
DSSTox_GSID_47051
beta-Ocimene (>90per cent)
CHEMBL3187449
DTXSID70274135
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of beta-Ocimene

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9910 99.10%
Caco-2 + 0.8971 89.71%
Blood Brain Barrier + 1.0000 100.00%
Human oral bioavailability - 0.5857 58.57%
Subcellular localzation Nucleus 0.4245 42.45%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9406 94.06%
OATP1B3 inhibitior + 0.9461 94.61%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.8000 80.00%
BSEP inhibitior - 0.8706 87.06%
P-glycoprotein inhibitior - 0.9881 98.81%
P-glycoprotein substrate - 0.9755 97.55%
CYP3A4 substrate - 0.7119 71.19%
CYP2C9 substrate - 0.8209 82.09%
CYP2D6 substrate - 0.7550 75.50%
CYP3A4 inhibition - 0.9316 93.16%
CYP2C9 inhibition - 0.8890 88.90%
CYP2C19 inhibition - 0.8582 85.82%
CYP2D6 inhibition - 0.9160 91.60%
CYP1A2 inhibition - 0.8436 84.36%
CYP2C8 inhibition - 0.9845 98.45%
CYP inhibitory promiscuity - 0.6734 67.34%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) + 0.6483 64.83%
Carcinogenicity (trinary) Warning 0.5264 52.64%
Eye corrosion + 0.9237 92.37%
Eye irritation + 0.9914 99.14%
Skin irritation + 0.8497 84.97%
Skin corrosion - 0.8708 87.08%
Ames mutagenesis - 0.8100 81.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6498 64.98%
Micronuclear - 0.9900 99.00%
Hepatotoxicity + 0.6625 66.25%
skin sensitisation + 0.8987 89.87%
Respiratory toxicity - 0.7667 76.67%
Reproductive toxicity - 0.9333 93.33%
Mitochondrial toxicity - 0.5250 52.50%
Nephrotoxicity + 0.4659 46.59%
Acute Oral Toxicity (c) III 0.6148 61.48%
Estrogen receptor binding - 0.9644 96.44%
Androgen receptor binding - 0.9270 92.70%
Thyroid receptor binding - 0.9197 91.97%
Glucocorticoid receptor binding - 0.8330 83.30%
Aromatase binding - 0.8595 85.95%
PPAR gamma - 0.7901 79.01%
Honey bee toxicity - 0.9010 90.10%
Biodegradation + 0.7000 70.00%
Crustacea aquatic toxicity - 0.7100 71.00%
Fish aquatic toxicity + 0.9659 96.59%

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
CHEMBL4040 P28482 MAP kinase ERK2 89.83% 83.82%
CHEMBL2581 P07339 Cathepsin D 87.77% 98.95%
CHEMBL3401 O75469 Pregnane X receptor 83.04% 94.73%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 83.03% 91.11%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 82.27% 96.09%

Cross-Links

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PubChem 18756
NPASS NPC262789