Selagoline

Details

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Internal ID 487cae64-3427-472e-ac98-a24a208392c0
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Sesquiterpenoids
IUPAC Name (1R,2R,10S,11R,13R)-15-methyl-6-azatetracyclo[8.6.0.01,6.02,13]hexadec-14-en-11-ol
SMILES (Canonical) CC1=CC2CC(C3CCCN4C3(C1)C2CCC4)O
SMILES (Isomeric) CC1=C[C@H]2C[C@H]([C@H]3CCCN4[C@]3(C1)[C@@H]2CCC4)O
InChI InChI=1S/C16H25NO/c1-11-8-12-9-15(18)14-5-3-7-17-6-2-4-13(12)16(14,17)10-11/h8,12-15,18H,2-7,9-10H2,1H3/t12-,13+,14+,15+,16+/m0/s1
InChI Key ODKOKIUKHXCUOB-UYJHQMFVSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

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Molecular Formula C16H25NO
Molecular Weight 247.38 g/mol
Exact Mass 247.193614421 g/mol
Topological Polar Surface Area (TPSA) 23.50 Ų
XlogP 2.00
Atomic LogP (AlogP) 2.58
H-Bond Acceptor 2
H-Bond Donor 1
Rotatable Bonds 0

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of Selagoline

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9867 98.67%
Caco-2 + 0.8637 86.37%
Blood Brain Barrier + 0.8949 89.49%
Human oral bioavailability + 0.5286 52.86%
Subcellular localzation Lysosomes 0.4904 49.04%
OATP2B1 inhibitior - 0.8549 85.49%
OATP1B1 inhibitior + 0.9339 93.39%
OATP1B3 inhibitior + 0.9509 95.09%
MATE1 inhibitior - 0.9405 94.05%
OCT2 inhibitior + 0.6500 65.00%
BSEP inhibitior - 0.6852 68.52%
P-glycoprotein inhibitior - 0.9204 92.04%
P-glycoprotein substrate - 0.7556 75.56%
CYP3A4 substrate + 0.5607 56.07%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate + 0.5510 55.10%
CYP3A4 inhibition - 0.8462 84.62%
CYP2C9 inhibition - 0.8469 84.69%
CYP2C19 inhibition - 0.8728 87.28%
CYP2D6 inhibition - 0.5506 55.06%
CYP1A2 inhibition - 0.9001 90.01%
CYP2C8 inhibition - 0.8615 86.15%
CYP inhibitory promiscuity - 0.9663 96.63%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.9700 97.00%
Carcinogenicity (trinary) Non-required 0.5288 52.88%
Eye corrosion - 0.9749 97.49%
Eye irritation - 0.9195 91.95%
Skin irritation - 0.6042 60.42%
Skin corrosion - 0.6893 68.93%
Ames mutagenesis - 0.6700 67.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5294 52.94%
Micronuclear - 0.7200 72.00%
Hepatotoxicity + 0.6000 60.00%
skin sensitisation - 0.7729 77.29%
Respiratory toxicity + 0.7778 77.78%
Reproductive toxicity + 0.8444 84.44%
Mitochondrial toxicity + 0.9125 91.25%
Nephrotoxicity - 0.7056 70.56%
Acute Oral Toxicity (c) III 0.6497 64.97%
Estrogen receptor binding - 0.4911 49.11%
Androgen receptor binding + 0.5426 54.26%
Thyroid receptor binding + 0.5776 57.76%
Glucocorticoid receptor binding - 0.5749 57.49%
Aromatase binding - 0.7563 75.63%
PPAR gamma - 0.7477 74.77%
Honey bee toxicity - 0.9617 96.17%
Biodegradation - 0.8000 80.00%
Crustacea aquatic toxicity + 0.6800 68.00%
Fish aquatic toxicity - 0.7478 74.78%

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
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 93.47% 85.14%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 93.27% 96.09%
CHEMBL3137262 O60341 LSD1/CoREST complex 89.55% 97.09%
CHEMBL5608 Q16288 NT-3 growth factor receptor 89.17% 95.89%
CHEMBL4208 P20618 Proteasome component C5 86.77% 90.00%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 85.22% 95.56%
CHEMBL225 P28335 Serotonin 2c (5-HT2c) receptor 85.20% 89.62%
CHEMBL2581 P07339 Cathepsin D 84.39% 98.95%
CHEMBL1994 P08235 Mineralocorticoid receptor 82.19% 100.00%
CHEMBL1871 P10275 Androgen Receptor 81.69% 96.43%
CHEMBL253 P34972 Cannabinoid CB2 receptor 81.05% 97.25%

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.
Huperzia selago

Cross-Links

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PubChem 139596374
LOTUS LTS0258369
wikiData Q105189891