Lycojaponicumin D

Details

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Internal ID 9853c79a-9f85-4645-840a-11eb759bdbdc
Taxonomy Organoheterocyclic compounds > Azaspirodecane derivatives
IUPAC Name (1S,2S,13R,15R)-2,10-dihydroxy-15-methyl-6-azatetracyclo[7.7.0.01,6.02,13]hexadec-9-en-11-one
SMILES (Canonical) CC1CC2CC(=O)C(=C3CCN4C3(C1)C2(CCC4)O)O
SMILES (Isomeric) C[C@@H]1C[C@@H]2CC(=O)C(=C3CCN4[C@]3(C1)[C@@]2(CCC4)O)O
InChI InChI=1S/C16H23NO3/c1-10-7-11-8-13(18)14(19)12-3-6-17-5-2-4-16(11,20)15(12,17)9-10/h10-11,19-20H,2-9H2,1H3/t10-,11-,15+,16+/m1/s1
InChI Key GUHDXXGJMVTAEM-XYPYXGAPSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C16H23NO3
Molecular Weight 277.36 g/mol
Exact Mass 277.16779360 g/mol
Topological Polar Surface Area (TPSA) 60.80 Ų
XlogP 0.60
Atomic LogP (AlogP) 1.79
H-Bond Acceptor 4
H-Bond Donor 2
Rotatable Bonds 0

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of Lycojaponicumin D

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9784 97.84%
Caco-2 + 0.7828 78.28%
Blood Brain Barrier + 0.7750 77.50%
Human oral bioavailability - 0.5571 55.71%
Subcellular localzation Mitochondria 0.6529 65.29%
OATP2B1 inhibitior - 0.8530 85.30%
OATP1B1 inhibitior + 0.9197 91.97%
OATP1B3 inhibitior + 0.9577 95.77%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.5250 52.50%
BSEP inhibitior - 0.8091 80.91%
P-glycoprotein inhibitior - 0.9503 95.03%
P-glycoprotein substrate - 0.7322 73.22%
CYP3A4 substrate + 0.5991 59.91%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.7573 75.73%
CYP3A4 inhibition - 0.9113 91.13%
CYP2C9 inhibition - 0.8714 87.14%
CYP2C19 inhibition - 0.8594 85.94%
CYP2D6 inhibition - 0.7963 79.63%
CYP1A2 inhibition - 0.8877 88.77%
CYP2C8 inhibition - 0.9325 93.25%
CYP inhibitory promiscuity - 0.9447 94.47%
UGT catelyzed + 1.0000 100.00%
Carcinogenicity (binary) - 0.9800 98.00%
Carcinogenicity (trinary) Non-required 0.4384 43.84%
Eye corrosion - 0.9861 98.61%
Eye irritation - 0.7293 72.93%
Skin irritation - 0.7254 72.54%
Skin corrosion - 0.8986 89.86%
Ames mutagenesis - 0.5600 56.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5399 53.99%
Micronuclear - 0.5000 50.00%
Hepatotoxicity + 0.5098 50.98%
skin sensitisation - 0.8169 81.69%
Respiratory toxicity + 0.6778 67.78%
Reproductive toxicity + 0.9667 96.67%
Mitochondrial toxicity + 0.9875 98.75%
Nephrotoxicity - 0.5691 56.91%
Acute Oral Toxicity (c) III 0.5359 53.59%
Estrogen receptor binding - 0.5403 54.03%
Androgen receptor binding + 0.6428 64.28%
Thyroid receptor binding + 0.5897 58.97%
Glucocorticoid receptor binding + 0.7445 74.45%
Aromatase binding - 0.5918 59.18%
PPAR gamma - 0.5429 54.29%
Honey bee toxicity - 0.8533 85.33%
Biodegradation - 0.7750 77.50%
Crustacea aquatic toxicity + 0.5900 59.00%
Fish aquatic toxicity - 0.4287 42.87%

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 94.60% 97.25%
CHEMBL3137262 O60341 LSD1/CoREST complex 93.66% 97.09%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 92.27% 96.09%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 89.99% 91.11%
CHEMBL5697 Q9GZT9 Egl nine homolog 1 89.23% 93.40%
CHEMBL2581 P07339 Cathepsin D 88.81% 98.95%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 88.11% 95.56%
CHEMBL3351 Q13085 Acetyl-CoA carboxylase 1 86.71% 93.04%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 86.03% 85.14%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 85.93% 90.71%
CHEMBL4026 P40763 Signal transducer and activator of transcription 3 85.56% 82.69%
CHEMBL1293249 Q13887 Kruppel-like factor 5 84.58% 86.33%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 84.10% 99.23%
CHEMBL4208 P20618 Proteasome component C5 83.83% 90.00%
CHEMBL2781 P19634 Sodium/hydrogen exchanger 1 81.86% 90.24%
CHEMBL321 P14780 Matrix metalloproteinase 9 80.51% 92.12%

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 102306584
NPASS NPC299787