Gusanlung D

Details

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Internal ID 341b73b3-837e-4162-aa31-7bc5e3d99eff
Taxonomy Alkaloids and derivatives > Protoberberine alkaloids and derivatives
IUPAC Name (1S)-5,7-dioxa-13-azapentacyclo[11.8.0.02,10.04,8.015,20]henicosa-2,4(8),9,15,17,19-hexaen-14-one
SMILES (Canonical) C1CN2C(CC3=CC=CC=C3C2=O)C4=CC5=C(C=C41)OCO5
SMILES (Isomeric) C1CN2[C@@H](CC3=CC=CC=C3C2=O)C4=CC5=C(C=C41)OCO5
InChI InChI=1S/C18H15NO3/c20-18-13-4-2-1-3-11(13)7-15-14-9-17-16(21-10-22-17)8-12(14)5-6-19(15)18/h1-4,8-9,15H,5-7,10H2/t15-/m0/s1
InChI Key PUJMLVRTJXBOER-HNNXBMFYSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C18H15NO3
Molecular Weight 293.30 g/mol
Exact Mass 293.10519334 g/mol
Topological Polar Surface Area (TPSA) 38.80 Ų
XlogP 2.80
Atomic LogP (AlogP) 2.71
H-Bond Acceptor 3
H-Bond Donor 0
Rotatable Bonds 0

Synonyms

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SCHEMBL30473246
(1S)-5,7-Dioxa-13-azapentacyclo[11.8.0.02,10.04,8.015,20]henicosa-2,4(8),9,15,17,19-hexaen-14-one
(S)-(-)-2,3-methylenedioxy-8-oxoberbine

2D Structure

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2D Structure of Gusanlung D

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9922 99.22%
Caco-2 + 0.8384 83.84%
Blood Brain Barrier + 0.8250 82.50%
Human oral bioavailability - 0.6143 61.43%
Subcellular localzation Mitochondria 0.6719 67.19%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9377 93.77%
OATP1B3 inhibitior + 0.9511 95.11%
MATE1 inhibitior - 0.9200 92.00%
OCT2 inhibitior - 0.6250 62.50%
BSEP inhibitior + 0.9005 90.05%
P-glycoprotein inhibitior - 0.5707 57.07%
P-glycoprotein substrate - 0.8465 84.65%
CYP3A4 substrate + 0.5394 53.94%
CYP2C9 substrate - 0.8070 80.70%
CYP2D6 substrate - 0.8241 82.41%
CYP3A4 inhibition + 0.6284 62.84%
CYP2C9 inhibition - 0.8321 83.21%
CYP2C19 inhibition + 0.6137 61.37%
CYP2D6 inhibition + 0.7765 77.65%
CYP1A2 inhibition + 0.9178 91.78%
CYP2C8 inhibition - 0.9326 93.26%
CYP inhibitory promiscuity + 0.7354 73.54%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.9700 97.00%
Carcinogenicity (trinary) Non-required 0.5864 58.64%
Eye corrosion - 0.9859 98.59%
Eye irritation - 0.8967 89.67%
Skin irritation - 0.7660 76.60%
Skin corrosion - 0.9329 93.29%
Ames mutagenesis + 0.5100 51.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5996 59.96%
Micronuclear + 0.6100 61.00%
Hepatotoxicity - 0.5750 57.50%
skin sensitisation - 0.8426 84.26%
Respiratory toxicity + 0.8556 85.56%
Reproductive toxicity + 0.8000 80.00%
Mitochondrial toxicity + 0.8625 86.25%
Nephrotoxicity + 0.7033 70.33%
Acute Oral Toxicity (c) III 0.6605 66.05%
Estrogen receptor binding + 0.8469 84.69%
Androgen receptor binding + 0.5223 52.23%
Thyroid receptor binding - 0.5000 50.00%
Glucocorticoid receptor binding + 0.7808 78.08%
Aromatase binding + 0.5916 59.16%
PPAR gamma + 0.6840 68.40%
Honey bee toxicity - 0.8234 82.34%
Biodegradation - 0.7250 72.50%
Crustacea aquatic toxicity + 0.6200 62.00%
Fish aquatic toxicity + 0.8079 80.79%

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
CHEMBL2581 P07339 Cathepsin D 98.65% 98.95%
CHEMBL5697 Q9GZT9 Egl nine homolog 1 96.59% 93.40%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 96.28% 91.11%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 94.66% 95.56%
CHEMBL1951 P21397 Monoamine oxidase A 94.40% 91.49%
CHEMBL4303 P08238 Heat shock protein HSP 90-beta 92.09% 96.77%
CHEMBL1293249 Q13887 Kruppel-like factor 5 91.50% 86.33%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 89.64% 96.09%
CHEMBL1806 P11388 DNA topoisomerase II alpha 88.52% 89.00%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 86.14% 85.14%
CHEMBL1902 P62942 FK506-binding protein 1A 85.94% 97.05%
CHEMBL6007 O75762 Transient receptor potential cation channel subfamily A member 1 85.14% 92.17%
CHEMBL1994 P08235 Mineralocorticoid receptor 84.57% 100.00%
CHEMBL217 P14416 Dopamine D2 receptor 84.40% 95.62%
CHEMBL2056 P21728 Dopamine D1 receptor 84.39% 91.00%
CHEMBL4296 Q15858 Sodium channel protein type IX alpha subunit 84.18% 96.11%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 83.50% 90.71%
CHEMBL4040 P28482 MAP kinase ERK2 82.70% 83.82%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 82.29% 99.23%

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.
Arcangelisia gusanlung

Cross-Links

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PubChem 11380814
LOTUS LTS0173084
wikiData Q105215128