Lycorenan

Details

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Internal ID b2d7e066-833d-490a-b62a-dd118b94234f
Taxonomy Organoheterocyclic compounds > Benzopyrans > 2-benzopyrans
IUPAC Name (5aR,11bS,11cS)-1,2,3,5,5a,7,11b,11c-octahydroisochromeno[3,4-g]indole
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C15H17NO/c1-2-4-12-11(3-1)9-17-13-6-5-10-7-8-16-15(10)14(12)13/h1-5,13-16H,6-9H2/t13-,14-,15-/m1/s1
InChI Key QPRHCMLXIWSVGT-RBSFLKMASA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C15H17NO
Molecular Weight 227.30 g/mol
Exact Mass 227.131014166 g/mol
Topological Polar Surface Area (TPSA) 21.30 Ų
XlogP 1.30
Atomic LogP (AlogP) 2.36
H-Bond Acceptor 2
H-Bond Donor 1
Rotatable Bonds 0

Synonyms

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CHEBI:36282
Q27116770
(5aR,11bS,11cS)-1,2,3,5,5a,7,11b,11c-octahydroisochromeno[3,4-g]indole

2D Structure

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2D Structure of Lycorenan

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 1.0000 100.00%
Caco-2 + 0.8392 83.92%
Blood Brain Barrier + 0.9379 93.79%
Human oral bioavailability + 0.5143 51.43%
Subcellular localzation Mitochondria 0.4368 43.68%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9385 93.85%
OATP1B3 inhibitior + 0.9493 94.93%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior + 0.6000 60.00%
BSEP inhibitior - 0.8184 81.84%
P-glycoprotein inhibitior - 0.9327 93.27%
P-glycoprotein substrate - 0.7355 73.55%
CYP3A4 substrate + 0.5298 52.98%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate + 0.6082 60.82%
CYP3A4 inhibition - 0.9303 93.03%
CYP2C9 inhibition - 0.8254 82.54%
CYP2C19 inhibition - 0.7911 79.11%
CYP2D6 inhibition + 0.5854 58.54%
CYP1A2 inhibition + 0.5417 54.17%
CYP2C8 inhibition - 0.6554 65.54%
CYP inhibitory promiscuity - 0.7830 78.30%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.9100 91.00%
Carcinogenicity (trinary) Non-required 0.6810 68.10%
Eye corrosion - 0.9747 97.47%
Eye irritation - 0.9822 98.22%
Skin irritation - 0.6874 68.74%
Skin corrosion - 0.8642 86.42%
Ames mutagenesis + 0.6663 66.63%
Human Ether-a-go-go-Related Gene inhibition + 0.8669 86.69%
Micronuclear - 0.6300 63.00%
Hepatotoxicity + 0.6125 61.25%
skin sensitisation - 0.8024 80.24%
Respiratory toxicity + 0.7556 75.56%
Reproductive toxicity + 0.8778 87.78%
Mitochondrial toxicity + 0.8625 86.25%
Nephrotoxicity - 0.6706 67.06%
Acute Oral Toxicity (c) III 0.5673 56.73%
Estrogen receptor binding - 0.5750 57.50%
Androgen receptor binding - 0.4854 48.54%
Thyroid receptor binding - 0.6899 68.99%
Glucocorticoid receptor binding - 0.8622 86.22%
Aromatase binding - 0.6268 62.68%
PPAR gamma - 0.4891 48.91%
Honey bee toxicity - 0.8200 82.00%
Biodegradation - 0.9000 90.00%
Crustacea aquatic toxicity + 0.5500 55.00%
Fish aquatic toxicity - 0.6303 63.03%

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
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 96.96% 91.11%
CHEMBL3137262 O60341 LSD1/CoREST complex 94.59% 97.09%
CHEMBL253 P34972 Cannabinoid CB2 receptor 90.29% 97.25%
CHEMBL3192 Q9BY41 Histone deacetylase 8 87.38% 93.99%
CHEMBL3227 P41594 Metabotropic glutamate receptor 5 84.71% 96.42%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 83.45% 96.09%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 82.29% 95.56%
CHEMBL3401 O75469 Pregnane X receptor 80.70% 94.73%
CHEMBL2581 P07339 Cathepsin D 80.10% 98.95%

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.
Crinum asiaticum

Cross-Links

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PubChem 9548788
NPASS NPC250