cis-Dracunculifoliol

Details

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Internal ID ac50f0df-6157-4585-b00e-ba50b869649a
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Sesquiterpenoids
IUPAC Name (1R)-1-[(1S,3aS,7aS)-1,3a-dimethyl-7-methylidene-2,3,4,5,6,7a-hexahydroinden-1-yl]-2-methylpropan-1-ol
SMILES (Canonical) CC(C)C(C1(CCC2(C1C(=C)CCC2)C)C)O
SMILES (Isomeric) CC(C)[C@H]([C@]1(CC[C@]2([C@@H]1C(=C)CCC2)C)C)O
InChI InChI=1S/C16H28O/c1-11(2)14(17)16(5)10-9-15(4)8-6-7-12(3)13(15)16/h11,13-14,17H,3,6-10H2,1-2,4-5H3/t13-,14+,15-,16-/m0/s1
InChI Key XOCDJJVJLDUYLX-FZKCQIBNSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C16H28O
Molecular Weight 236.39 g/mol
Exact Mass 236.214015512 g/mol
Topological Polar Surface Area (TPSA) 20.20 Ų
XlogP 4.60
Atomic LogP (AlogP) 4.17
H-Bond Acceptor 1
H-Bond Donor 1
Rotatable Bonds 2

Synonyms

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XOCDJJVJLDUYLX-FZKCQIBNSA-N

2D Structure

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2D Structure of cis-Dracunculifoliol

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9943 99.43%
Caco-2 + 0.7747 77.47%
Blood Brain Barrier + 0.8250 82.50%
Human oral bioavailability + 0.5571 55.71%
Subcellular localzation Lysosomes 0.6030 60.30%
OATP2B1 inhibitior - 0.8482 84.82%
OATP1B1 inhibitior + 0.8989 89.89%
OATP1B3 inhibitior - 0.2447 24.47%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.7500 75.00%
BSEP inhibitior - 0.9051 90.51%
P-glycoprotein inhibitior - 0.8934 89.34%
P-glycoprotein substrate - 0.9011 90.11%
CYP3A4 substrate - 0.5414 54.14%
CYP2C9 substrate - 0.6499 64.99%
CYP2D6 substrate - 0.6843 68.43%
CYP3A4 inhibition - 0.8194 81.94%
CYP2C9 inhibition + 0.5119 51.19%
CYP2C19 inhibition - 0.5476 54.76%
CYP2D6 inhibition - 0.9279 92.79%
CYP1A2 inhibition - 0.7264 72.64%
CYP2C8 inhibition - 0.9130 91.30%
CYP inhibitory promiscuity - 0.6919 69.19%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.8100 81.00%
Carcinogenicity (trinary) Non-required 0.5743 57.43%
Eye corrosion - 0.9502 95.02%
Eye irritation + 0.7064 70.64%
Skin irritation + 0.6454 64.54%
Skin corrosion - 0.9698 96.98%
Ames mutagenesis - 0.7000 70.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6837 68.37%
Micronuclear - 0.9900 99.00%
Hepatotoxicity + 0.5409 54.09%
skin sensitisation + 0.8025 80.25%
Respiratory toxicity - 0.5889 58.89%
Reproductive toxicity - 0.7333 73.33%
Mitochondrial toxicity + 0.5875 58.75%
Nephrotoxicity - 0.7347 73.47%
Acute Oral Toxicity (c) III 0.6613 66.13%
Estrogen receptor binding - 0.7333 73.33%
Androgen receptor binding + 0.5285 52.85%
Thyroid receptor binding - 0.5698 56.98%
Glucocorticoid receptor binding + 0.5489 54.89%
Aromatase binding - 0.6712 67.12%
PPAR gamma - 0.8020 80.20%
Honey bee toxicity - 0.8643 86.43%
Biodegradation - 0.7000 70.00%
Crustacea aquatic toxicity - 0.6900 69.00%
Fish aquatic toxicity + 0.9944 99.44%

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
CHEMBL253 P34972 Cannabinoid CB2 receptor 98.01% 97.25%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 96.44% 94.45%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 94.12% 91.11%
CHEMBL221 P23219 Cyclooxygenase-1 90.45% 90.17%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 88.66% 96.09%
CHEMBL2581 P07339 Cathepsin D 86.46% 98.95%
CHEMBL3137262 O60341 LSD1/CoREST complex 84.52% 97.09%
CHEMBL3130 O00329 PI3-kinase p110-delta subunit 83.94% 96.47%
CHEMBL1977 P11473 Vitamin D receptor 83.57% 99.43%
CHEMBL237 P41145 Kappa opioid receptor 81.93% 98.10%
CHEMBL5608 Q16288 NT-3 growth factor receptor 81.33% 95.89%
CHEMBL3430907 Q96GD4 Aurora kinase B/Inner centromere protein 80.06% 97.50%

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.
Baccharis dracunculifolia

Cross-Links

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PubChem 91749998
LOTUS LTS0231670
wikiData Q104375465