(Z)-lanceol

Details

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Internal ID 7a7ef87d-d72c-4283-854c-be9ccffcb215
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Sesquiterpenoids
IUPAC Name (2E)-2-methyl-6-[(1S)-4-methylcyclohex-3-en-1-yl]hepta-2,6-dien-1-ol
SMILES (Canonical) CC1=CCC(CC1)C(=C)CCC=C(C)CO
SMILES (Isomeric) CC1=CC[C@H](CC1)C(=C)CC/C=C(\C)/CO
InChI InChI=1S/C15H24O/c1-12-7-9-15(10-8-12)14(3)6-4-5-13(2)11-16/h5,7,15-16H,3-4,6,8-11H2,1-2H3/b13-5+/t15-/m1/s1
InChI Key HBVOEGGRCJCMLG-DTHCKZEYSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

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Molecular Formula C15H24O
Molecular Weight 220.35 g/mol
Exact Mass 220.182715385 g/mol
Topological Polar Surface Area (TPSA) 20.20 Ų
XlogP 4.00
Atomic LogP (AlogP) 4.01
H-Bond Acceptor 1
H-Bond Donor 1
Rotatable Bonds 5

Synonyms

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Lanceol
10067-29-5
(2E)-2-methyl-6-[(1S)-4-methylcyclohex-3-en-1-yl]hepta-2,6-dien-1-ol
CHEMBL443875
Q67866092

2D Structure

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2D Structure of (Z)-lanceol

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9846 98.46%
Caco-2 + 0.7940 79.40%
Blood Brain Barrier + 0.9250 92.50%
Human oral bioavailability - 0.5000 50.00%
Subcellular localzation Lysosomes 0.7312 73.12%
OATP2B1 inhibitior - 0.8516 85.16%
OATP1B1 inhibitior + 0.9268 92.68%
OATP1B3 inhibitior + 0.9295 92.95%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.6250 62.50%
BSEP inhibitior - 0.8389 83.89%
P-glycoprotein inhibitior - 0.9477 94.77%
P-glycoprotein substrate - 0.8410 84.10%
CYP3A4 substrate + 0.5088 50.88%
CYP2C9 substrate - 0.6591 65.91%
CYP2D6 substrate - 0.7543 75.43%
CYP3A4 inhibition - 0.7193 71.93%
CYP2C9 inhibition - 0.8864 88.64%
CYP2C19 inhibition - 0.8495 84.95%
CYP2D6 inhibition - 0.8909 89.09%
CYP1A2 inhibition - 0.7969 79.69%
CYP2C8 inhibition - 0.7322 73.22%
CYP inhibitory promiscuity - 0.7575 75.75%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.8228 82.28%
Carcinogenicity (trinary) Non-required 0.6631 66.31%
Eye corrosion - 0.5839 58.39%
Eye irritation + 0.7040 70.40%
Skin irritation - 0.5671 56.71%
Skin corrosion - 0.9751 97.51%
Ames mutagenesis - 0.8800 88.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4487 44.87%
Micronuclear - 1.0000 100.00%
Hepatotoxicity - 0.5324 53.24%
skin sensitisation + 0.8949 89.49%
Respiratory toxicity - 0.7444 74.44%
Reproductive toxicity - 0.6889 68.89%
Mitochondrial toxicity - 0.9000 90.00%
Nephrotoxicity - 0.6031 60.31%
Acute Oral Toxicity (c) III 0.9152 91.52%
Estrogen receptor binding - 0.7485 74.85%
Androgen receptor binding - 0.7201 72.01%
Thyroid receptor binding - 0.6538 65.38%
Glucocorticoid receptor binding - 0.5356 53.56%
Aromatase binding - 0.7065 70.65%
PPAR gamma + 0.5916 59.16%
Honey bee toxicity - 0.9148 91.48%
Biodegradation - 0.5500 55.00%
Crustacea aquatic toxicity - 0.6000 60.00%
Fish aquatic toxicity + 0.9887 98.87%

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 96.05% 91.11%
CHEMBL2581 P07339 Cathepsin D 89.53% 98.95%
CHEMBL1994 P08235 Mineralocorticoid receptor 86.07% 100.00%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 83.06% 95.56%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 82.54% 96.09%
CHEMBL253 P34972 Cannabinoid CB2 receptor 82.34% 97.25%
CHEMBL3137262 O60341 LSD1/CoREST complex 81.41% 97.09%

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.
Avena fatua
Santalum album
Wurfbainia neoaurantiaca

Cross-Links

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PubChem 15560069
NPASS NPC244038
LOTUS LTS0148391
wikiData Q67866092