Nardoguaianone E

Details

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Internal ID 59bd838f-d2a9-477f-bf4c-21471bfa9030
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Sesquiterpenoids
IUPAC Name (3R,6S,8R)-6,8-dihydroxy-3,8-dimethyl-5-propan-2-yl-2,3,6,7-tetrahydroazulen-1-one
SMILES (Canonical) CC1CC(=O)C2=C1C=C(C(CC2(C)O)O)C(C)C
SMILES (Isomeric) C[C@@H]1CC(=O)C2=C1C=C([C@H](C[C@@]2(C)O)O)C(C)C
InChI InChI=1S/C15H22O3/c1-8(2)10-6-11-9(3)5-12(16)14(11)15(4,18)7-13(10)17/h6,8-9,13,17-18H,5,7H2,1-4H3/t9-,13+,15-/m1/s1
InChI Key WLVFIKBXIVYVEO-ZDBHGNHJSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C15H22O3
Molecular Weight 250.33 g/mol
Exact Mass 250.15689456 g/mol
Topological Polar Surface Area (TPSA) 57.50 Ų
XlogP 0.50
Atomic LogP (AlogP) 1.99
H-Bond Acceptor 3
H-Bond Donor 2
Rotatable Bonds 1

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of Nardoguaianone E

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9913 99.13%
Caco-2 + 0.7804 78.04%
Blood Brain Barrier - 0.5000 50.00%
Human oral bioavailability + 0.5143 51.43%
Subcellular localzation Mitochondria 0.4980 49.80%
OATP2B1 inhibitior - 0.8544 85.44%
OATP1B1 inhibitior + 0.9397 93.97%
OATP1B3 inhibitior + 0.9648 96.48%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.8250 82.50%
BSEP inhibitior - 0.8443 84.43%
P-glycoprotein inhibitior - 0.9388 93.88%
P-glycoprotein substrate - 0.6924 69.24%
CYP3A4 substrate + 0.5340 53.40%
CYP2C9 substrate - 0.8086 80.86%
CYP2D6 substrate - 0.8738 87.38%
CYP3A4 inhibition - 0.8619 86.19%
CYP2C9 inhibition - 0.7403 74.03%
CYP2C19 inhibition - 0.7503 75.03%
CYP2D6 inhibition - 0.9311 93.11%
CYP1A2 inhibition - 0.7516 75.16%
CYP2C8 inhibition - 0.9455 94.55%
CYP inhibitory promiscuity - 0.7750 77.50%
UGT catelyzed + 0.8000 80.00%
Carcinogenicity (binary) - 0.9100 91.00%
Carcinogenicity (trinary) Non-required 0.4817 48.17%
Eye corrosion - 0.9803 98.03%
Eye irritation + 0.5565 55.65%
Skin irritation + 0.5000 50.00%
Skin corrosion - 0.9004 90.04%
Ames mutagenesis - 0.7100 71.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6865 68.65%
Micronuclear - 0.8300 83.00%
Hepatotoxicity + 0.6411 64.11%
skin sensitisation - 0.5755 57.55%
Respiratory toxicity + 0.7222 72.22%
Reproductive toxicity + 0.7000 70.00%
Mitochondrial toxicity + 0.7750 77.50%
Nephrotoxicity + 0.5331 53.31%
Acute Oral Toxicity (c) I 0.3426 34.26%
Estrogen receptor binding - 0.7020 70.20%
Androgen receptor binding - 0.7590 75.90%
Thyroid receptor binding + 0.7187 71.87%
Glucocorticoid receptor binding + 0.5532 55.32%
Aromatase binding - 0.7396 73.96%
PPAR gamma - 0.7622 76.22%
Honey bee toxicity - 0.8125 81.25%
Biodegradation - 0.7750 77.50%
Crustacea aquatic toxicity - 0.5100 51.00%
Fish aquatic toxicity + 0.8996 89.96%

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 94.54% 96.09%
CHEMBL2581 P07339 Cathepsin D 93.10% 98.95%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 92.14% 85.14%
CHEMBL253 P34972 Cannabinoid CB2 receptor 91.73% 97.25%
CHEMBL1937 Q92769 Histone deacetylase 2 90.45% 94.75%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 89.72% 91.11%
CHEMBL221 P23219 Cyclooxygenase-1 88.91% 90.17%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 87.68% 94.45%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 87.34% 95.56%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 86.86% 90.71%
CHEMBL4026 P40763 Signal transducer and activator of transcription 3 85.04% 82.69%
CHEMBL3137262 O60341 LSD1/CoREST complex 84.19% 97.09%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 84.09% 99.23%
CHEMBL1994 P08235 Mineralocorticoid receptor 82.60% 100.00%
CHEMBL5608 Q16288 NT-3 growth factor receptor 82.11% 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.
Humulus scandens
Kopsia flavida
Ribes sanguineum
Stachys chinensis

Cross-Links

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PubChem 15884945
NPASS NPC39619
LOTUS LTS0249070
wikiData Q105308246