Lunacrine, (A+-)-

Details

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Internal ID 5fed3f4a-3d43-409d-8cb5-a0628457315a
Taxonomy Organoheterocyclic compounds > Quinolines and derivatives > Dihydrofuranoquinolines
IUPAC Name 8-methoxy-9-methyl-2-propan-2-yl-2,3-dihydrofuro[2,3-b]quinolin-4-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C16H19NO3/c1-9(2)13-8-11-15(18)10-6-5-7-12(19-4)14(10)17(3)16(11)20-13/h5-7,9,13H,8H2,1-4H3
InChI Key FMEKJMQGMONLTQ-UHFFFAOYSA-N
Popularity 3 references in papers

Physical and Chemical Properties

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Molecular Formula C16H19NO3
Molecular Weight 273.33 g/mol
Exact Mass 273.13649347 g/mol
Topological Polar Surface Area (TPSA) 38.80 Ų
XlogP 3.30
Atomic LogP (AlogP) 2.51
H-Bond Acceptor 4
H-Bond Donor 0
Rotatable Bonds 2

Synonyms

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NSC 77152
2-Isopropyl-8-methoxy-9-methyl-3,9-dihydrofuro[2,3-b]quinolin-4(2H)-one
(+/-)-lunacrine
NSC77152
Lunacrine, (+/-)-
3,9-Dihydro-8-methoxy-9-methyl-2-(1-methylethyl)furo(2,3-b)quinolin-4(2H)-one
934E1B70FS
NSC-77152
Furo(2,3-b)quinolin-4(2H)-one, 3,9-dihydro-8-methoxy-9-methyl-2-(1-methylethyl)-
[2r,(-)]-3,9-Dihydro-8-methoxy-9-methyl-2-isopropylfuro[2,3-b]quinoline-4(2H)-one
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of Lunacrine, (A+-)-

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9798 97.98%
Caco-2 + 0.9081 90.81%
Blood Brain Barrier + 0.8250 82.50%
Human oral bioavailability + 0.5286 52.86%
Subcellular localzation Mitochondria 0.5473 54.73%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9600 96.00%
OATP1B3 inhibitior + 0.9493 94.93%
MATE1 inhibitior - 0.7000 70.00%
OCT2 inhibitior - 0.8500 85.00%
BSEP inhibitior - 0.7533 75.33%
P-glycoprotein inhibitior - 0.7812 78.12%
P-glycoprotein substrate - 0.5247 52.47%
CYP3A4 substrate + 0.6468 64.68%
CYP2C9 substrate - 0.6141 61.41%
CYP2D6 substrate - 0.7862 78.62%
CYP3A4 inhibition - 0.7930 79.30%
CYP2C9 inhibition - 0.8333 83.33%
CYP2C19 inhibition + 0.5888 58.88%
CYP2D6 inhibition - 0.8996 89.96%
CYP1A2 inhibition + 0.9130 91.30%
CYP2C8 inhibition - 0.8778 87.78%
CYP inhibitory promiscuity - 0.5756 57.56%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.9200 92.00%
Carcinogenicity (trinary) Non-required 0.4889 48.89%
Eye corrosion - 0.9903 99.03%
Eye irritation - 0.5313 53.13%
Skin irritation - 0.8458 84.58%
Skin corrosion - 0.9503 95.03%
Ames mutagenesis - 0.5300 53.00%
Human Ether-a-go-go-Related Gene inhibition + 0.6700 67.00%
Micronuclear + 0.5800 58.00%
Hepatotoxicity + 0.6034 60.34%
skin sensitisation - 0.8873 88.73%
Respiratory toxicity + 0.7778 77.78%
Reproductive toxicity + 0.8000 80.00%
Mitochondrial toxicity + 0.7250 72.50%
Nephrotoxicity - 0.5985 59.85%
Acute Oral Toxicity (c) III 0.6731 67.31%
Estrogen receptor binding + 0.7179 71.79%
Androgen receptor binding - 0.5759 57.59%
Thyroid receptor binding + 0.5458 54.58%
Glucocorticoid receptor binding - 0.5880 58.80%
Aromatase binding - 0.5330 53.30%
PPAR gamma - 0.5995 59.95%
Honey bee toxicity - 0.8144 81.44%
Biodegradation - 0.8750 87.50%
Crustacea aquatic toxicity + 0.6300 63.00%
Fish aquatic toxicity - 0.4892 48.92%

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 98.09% 98.95%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 97.84% 95.56%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 97.20% 96.09%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 95.80% 85.14%
CHEMBL2535 P11166 Glucose transporter 95.35% 98.75%
CHEMBL5608 Q16288 NT-3 growth factor receptor 93.29% 95.89%
CHEMBL253 P34972 Cannabinoid CB2 receptor 91.13% 97.25%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 89.76% 94.00%
CHEMBL4478 Q00975 Voltage-gated N-type calcium channel alpha-1B subunit 89.02% 97.14%
CHEMBL1293249 Q13887 Kruppel-like factor 5 86.95% 86.33%
CHEMBL1806 P11388 DNA topoisomerase II alpha 85.41% 89.00%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 85.02% 99.23%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 83.92% 94.45%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 83.61% 92.62%
CHEMBL3192 Q9BY41 Histone deacetylase 8 80.96% 93.99%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 80.77% 96.00%
CHEMBL4306 P22460 Voltage-gated potassium channel subunit Kv1.5 80.77% 94.03%
CHEMBL2335 P42785 Lysosomal Pro-X carboxypeptidase 80.66% 100.00%

Plants that contains it

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Below are displayed all the plants proven (via scientific papers) to contain this compound!
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There are no matching plants.

Cross-Links

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PubChem 96511
LOTUS LTS0063716
wikiData Q27271556