(1S,3aR,5S,8aS)-1-methyl-4-methylidene-7-propan-2-yl-2,3,3a,5,6,8a-hexahydro-1H-azulen-5-ol

Details

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Internal ID 98cba7d7-834e-48b6-bbca-d8b528c71574
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Sesquiterpenoids > Guaianes
IUPAC Name (1S,3aR,5S,8aS)-1-methyl-4-methylidene-7-propan-2-yl-2,3,3a,5,6,8a-hexahydro-1H-azulen-5-ol
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C15H24O/c1-9(2)12-7-14-10(3)5-6-13(14)11(4)15(16)8-12/h7,9-10,13-16H,4-6,8H2,1-3H3/t10-,13-,14+,15-/m0/s1
InChI Key WFAWAGJRGJHCLR-HPEDKQMDSA-N
Popularity 2 references 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 3.20
Atomic LogP (AlogP) 3.55
H-Bond Acceptor 1
H-Bond Donor 1
Rotatable Bonds 1

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of (1S,3aR,5S,8aS)-1-methyl-4-methylidene-7-propan-2-yl-2,3,3a,5,6,8a-hexahydro-1H-azulen-5-ol

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9941 99.41%
Caco-2 + 0.7432 74.32%
Blood Brain Barrier + 0.5500 55.00%
Human oral bioavailability + 0.5857 58.57%
Subcellular localzation Lysosomes 0.6266 62.66%
OATP2B1 inhibitior - 0.8505 85.05%
OATP1B1 inhibitior + 0.9137 91.37%
OATP1B3 inhibitior + 0.8621 86.21%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.8250 82.50%
BSEP inhibitior - 0.9686 96.86%
P-glycoprotein inhibitior - 0.9002 90.02%
P-glycoprotein substrate - 0.7960 79.60%
CYP3A4 substrate - 0.5240 52.40%
CYP2C9 substrate - 0.6284 62.84%
CYP2D6 substrate + 0.3479 34.79%
CYP3A4 inhibition - 0.9309 93.09%
CYP2C9 inhibition - 0.8274 82.74%
CYP2C19 inhibition - 0.8131 81.31%
CYP2D6 inhibition - 0.9228 92.28%
CYP1A2 inhibition - 0.6078 60.78%
CYP2C8 inhibition - 0.8793 87.93%
CYP inhibitory promiscuity - 0.8630 86.30%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.8700 87.00%
Carcinogenicity (trinary) Non-required 0.6333 63.33%
Eye corrosion - 0.9527 95.27%
Eye irritation - 0.5330 53.30%
Skin irritation + 0.6757 67.57%
Skin corrosion - 0.9002 90.02%
Ames mutagenesis - 0.7800 78.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4536 45.36%
Micronuclear - 0.9800 98.00%
Hepatotoxicity + 0.6928 69.28%
skin sensitisation + 0.6639 66.39%
Respiratory toxicity - 0.5111 51.11%
Reproductive toxicity + 0.6333 63.33%
Mitochondrial toxicity + 0.7000 70.00%
Nephrotoxicity - 0.6998 69.98%
Acute Oral Toxicity (c) III 0.7200 72.00%
Estrogen receptor binding - 0.8414 84.14%
Androgen receptor binding - 0.6030 60.30%
Thyroid receptor binding - 0.5451 54.51%
Glucocorticoid receptor binding - 0.7333 73.33%
Aromatase binding - 0.8308 83.08%
PPAR gamma - 0.8832 88.32%
Honey bee toxicity - 0.8667 86.67%
Biodegradation - 0.5500 55.00%
Crustacea aquatic toxicity + 0.5500 55.00%
Fish aquatic toxicity + 0.9450 94.50%

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
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 93.52% 96.09%
CHEMBL2581 P07339 Cathepsin D 90.72% 98.95%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 89.41% 91.11%
CHEMBL3359 P21462 Formyl peptide receptor 1 86.29% 93.56%
CHEMBL3137262 O60341 LSD1/CoREST complex 85.11% 97.09%
CHEMBL4040 P28482 MAP kinase ERK2 84.25% 83.82%
CHEMBL4481 P35228 Nitric oxide synthase, inducible 83.99% 94.80%
CHEMBL1907594 P30926 Neuronal acetylcholine receptor; alpha3/beta4 83.05% 97.23%
CHEMBL4803 P29474 Nitric-oxide synthase, endothelial 82.73% 86.00%
CHEMBL226 P30542 Adenosine A1 receptor 81.83% 95.93%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 81.75% 90.71%
CHEMBL5608 Q16288 NT-3 growth factor receptor 81.19% 95.89%

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.
Ligularia macrophylla

Cross-Links

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PubChem 24778006
LOTUS LTS0099944
wikiData Q105303743