Anhydrolycodoline

Details

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Internal ID 61aa2085-b3fc-4196-9cc5-891ac18e68f8
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Sesquiterpenoids
IUPAC Name (1S,10S,13R,15S)-15-methyl-6-azatetracyclo[8.6.0.01,6.02,13]hexadec-2-en-11-one
SMILES (Canonical) CC1CC2CC(=O)C3CCCN4C3(C1)C2=CCC4
SMILES (Isomeric) C[C@H]1C[C@@H]2CC(=O)[C@H]3CCCN4[C@]3(C1)C2=CCC4
InChI InChI=1S/C16H23NO/c1-11-8-12-9-15(18)14-5-3-7-17-6-2-4-13(12)16(14,17)10-11/h4,11-12,14H,2-3,5-10H2,1H3/t11-,12+,14+,16+/m0/s1
InChI Key XZMYQBCMWCZCML-KLZCAUPSSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C16H23NO
Molecular Weight 245.36 g/mol
Exact Mass 245.177964357 g/mol
Topological Polar Surface Area (TPSA) 20.30 Ų
XlogP 1.90
Atomic LogP (AlogP) 2.79
H-Bond Acceptor 2
H-Bond Donor 0
Rotatable Bonds 0

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of Anhydrolycodoline

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9869 98.69%
Caco-2 + 0.8757 87.57%
Blood Brain Barrier + 0.9129 91.29%
Human oral bioavailability + 0.6429 64.29%
Subcellular localzation Mitochondria 0.4985 49.85%
OATP2B1 inhibitior - 0.8515 85.15%
OATP1B1 inhibitior + 0.9219 92.19%
OATP1B3 inhibitior + 0.9554 95.54%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior + 0.7500 75.00%
BSEP inhibitior - 0.5723 57.23%
P-glycoprotein inhibitior - 0.9061 90.61%
P-glycoprotein substrate - 0.6229 62.29%
CYP3A4 substrate + 0.5390 53.90%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate + 0.4392 43.92%
CYP3A4 inhibition - 0.8227 82.27%
CYP2C9 inhibition - 0.8101 81.01%
CYP2C19 inhibition - 0.8118 81.18%
CYP2D6 inhibition - 0.7451 74.51%
CYP1A2 inhibition - 0.8824 88.24%
CYP2C8 inhibition - 0.8638 86.38%
CYP inhibitory promiscuity - 0.8402 84.02%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.9300 93.00%
Carcinogenicity (trinary) Non-required 0.4947 49.47%
Eye corrosion - 0.9723 97.23%
Eye irritation - 0.8528 85.28%
Skin irritation - 0.6615 66.15%
Skin corrosion - 0.7923 79.23%
Ames mutagenesis - 0.7200 72.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4337 43.37%
Micronuclear - 0.7200 72.00%
Hepatotoxicity + 0.7000 70.00%
skin sensitisation - 0.7280 72.80%
Respiratory toxicity + 0.7556 75.56%
Reproductive toxicity + 0.6889 68.89%
Mitochondrial toxicity + 0.9125 91.25%
Nephrotoxicity + 0.5675 56.75%
Acute Oral Toxicity (c) III 0.7375 73.75%
Estrogen receptor binding - 0.7721 77.21%
Androgen receptor binding + 0.5517 55.17%
Thyroid receptor binding - 0.5437 54.37%
Glucocorticoid receptor binding - 0.6130 61.30%
Aromatase binding - 0.6135 61.35%
PPAR gamma - 0.7403 74.03%
Honey bee toxicity - 0.8998 89.98%
Biodegradation - 0.7750 77.50%
Crustacea aquatic toxicity + 0.7500 75.00%
Fish aquatic toxicity - 0.6446 64.46%

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
CHEMBL3137262 O60341 LSD1/CoREST complex 94.45% 97.09%
CHEMBL4303 P08238 Heat shock protein HSP 90-beta 94.35% 96.77%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 94.21% 96.09%
CHEMBL5697 Q9GZT9 Egl nine homolog 1 94.03% 93.40%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 93.21% 85.14%
CHEMBL253 P34972 Cannabinoid CB2 receptor 91.99% 97.25%
CHEMBL2581 P07339 Cathepsin D 91.64% 98.95%
CHEMBL4588 P22894 Matrix metalloproteinase 8 88.77% 94.66%
CHEMBL5608 Q16288 NT-3 growth factor receptor 87.30% 95.89%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 87.21% 95.56%
CHEMBL4208 P20618 Proteasome component C5 86.48% 90.00%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 85.74% 99.23%
CHEMBL241 Q14432 Phosphodiesterase 3A 85.02% 92.94%
CHEMBL3746 P80365 11-beta-hydroxysteroid dehydrogenase 2 84.57% 94.78%
CHEMBL2781 P19634 Sodium/hydrogen exchanger 1 84.43% 90.24%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 83.54% 91.11%
CHEMBL5255 O00206 Toll-like receptor 4 83.33% 92.50%
CHEMBL1293249 Q13887 Kruppel-like factor 5 82.10% 86.33%
CHEMBL228 P31645 Serotonin transporter 80.65% 95.51%

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.
Lycopodium japonicum

Cross-Links

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PubChem 102442792
NPASS NPC216996