Guai-11-en-10-ol

Details

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Internal ID 214c3d58-f5ad-440f-a04e-7c9848f4500d
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Sesquiterpenoids > Guaianes
IUPAC Name 1,4-dimethyl-7-prop-1-en-2-yl-2,3,4,5,6,7,8,8a-octahydro-1H-azulen-3a-ol
SMILES (Canonical) CC1CCC2(C1CC(CCC2C)C(=C)C)O
SMILES (Isomeric) CC1CCC2(C1CC(CCC2C)C(=C)C)O
InChI InChI=1S/C15H26O/c1-10(2)13-6-5-12(4)15(16)8-7-11(3)14(15)9-13/h11-14,16H,1,5-9H2,2-4H3
InChI Key YCHDRKAWJJJVIH-UHFFFAOYSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

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Molecular Formula C15H26O
Molecular Weight 222.37 g/mol
Exact Mass 222.198365449 g/mol
Topological Polar Surface Area (TPSA) 20.20 Ų
XlogP 4.30
Atomic LogP (AlogP) 3.78
H-Bond Acceptor 1
H-Bond Donor 1
Rotatable Bonds 1

Synonyms

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YCHDRKAWJJJVIH-UHFFFAOYSA-N

2D Structure

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2D Structure of Guai-11-en-10-ol

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9944 99.44%
Caco-2 + 0.7842 78.42%
Blood Brain Barrier + 0.5250 52.50%
Human oral bioavailability - 0.5286 52.86%
Subcellular localzation Lysosomes 0.7002 70.02%
OATP2B1 inhibitior - 0.8468 84.68%
OATP1B1 inhibitior + 0.9565 95.65%
OATP1B3 inhibitior + 0.8314 83.14%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.7250 72.50%
BSEP inhibitior - 0.8343 83.43%
P-glycoprotein inhibitior - 0.9416 94.16%
P-glycoprotein substrate - 0.7719 77.19%
CYP3A4 substrate + 0.5544 55.44%
CYP2C9 substrate - 0.5471 54.71%
CYP2D6 substrate - 0.7267 72.67%
CYP3A4 inhibition - 0.8449 84.49%
CYP2C9 inhibition - 0.6986 69.86%
CYP2C19 inhibition - 0.7237 72.37%
CYP2D6 inhibition - 0.9448 94.48%
CYP1A2 inhibition - 0.6072 60.72%
CYP2C8 inhibition - 0.8763 87.63%
CYP inhibitory promiscuity - 0.8954 89.54%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.8600 86.00%
Carcinogenicity (trinary) Non-required 0.5578 55.78%
Eye corrosion - 0.9754 97.54%
Eye irritation + 0.7253 72.53%
Skin irritation + 0.6892 68.92%
Skin corrosion - 0.9379 93.79%
Ames mutagenesis - 0.8900 89.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5305 53.05%
Micronuclear - 0.9800 98.00%
Hepatotoxicity - 0.5913 59.13%
skin sensitisation + 0.5365 53.65%
Respiratory toxicity - 0.6333 63.33%
Reproductive toxicity + 0.7889 78.89%
Mitochondrial toxicity + 0.7875 78.75%
Nephrotoxicity - 0.7320 73.20%
Acute Oral Toxicity (c) III 0.7441 74.41%
Estrogen receptor binding - 0.6620 66.20%
Androgen receptor binding - 0.6137 61.37%
Thyroid receptor binding - 0.6020 60.20%
Glucocorticoid receptor binding - 0.6160 61.60%
Aromatase binding - 0.7437 74.37%
PPAR gamma - 0.7738 77.38%
Honey bee toxicity - 0.7792 77.92%
Biodegradation + 0.5750 57.50%
Crustacea aquatic toxicity + 0.5100 51.00%
Fish aquatic toxicity + 0.9733 97.33%

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 97.84% 97.25%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 92.83% 96.09%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 90.70% 91.11%
CHEMBL241 Q14432 Phosphodiesterase 3A 86.87% 92.94%
CHEMBL3137262 O60341 LSD1/CoREST complex 86.72% 97.09%
CHEMBL4026 P40763 Signal transducer and activator of transcription 3 86.00% 82.69%
CHEMBL206 P03372 Estrogen receptor alpha 85.98% 97.64%
CHEMBL218 P21554 Cannabinoid CB1 receptor 85.40% 96.61%
CHEMBL1994 P08235 Mineralocorticoid receptor 85.31% 100.00%
CHEMBL1951 P21397 Monoamine oxidase A 81.43% 91.49%
CHEMBL4187 Q99250 Sodium channel protein type II alpha subunit 80.52% 95.50%
CHEMBL238 Q01959 Dopamine transporter 80.04% 95.88%
CHEMBL1902 P62942 FK506-binding protein 1A 80.01% 97.05%

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.
Laggera crispata

Cross-Links

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PubChem 91747158
NPASS NPC55024