neolabuanine A

Details

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Internal ID 737b877a-ab03-4b2f-b4e6-3673c4117f9e
Taxonomy Organoheterocyclic compounds > Quinolines and derivatives > Benzoquinolines > Pyridoacridines > Pyrido[2,3,4-kl]acridines
IUPAC Name 8-hydroxy-3,10,20-triazapentacyclo[11.7.1.02,7.09,21.014,19]henicosa-1(20),2,7,9,11,13(21),14,16,18-nonaen-6-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C18H11N3O2/c22-12-6-8-19-15-14(12)18(23)17-13-10(5-7-20-17)9-3-1-2-4-11(9)21-16(13)15/h1-5,7,23H,6,8H2
InChI Key HECBXFITOWBQFA-UHFFFAOYSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

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Molecular Formula C18H11N3O2
Molecular Weight 301.30 g/mol
Exact Mass 301.085126602 g/mol
Topological Polar Surface Area (TPSA) 75.40 Ų
XlogP 2.30
Atomic LogP (AlogP) 2.57
H-Bond Acceptor 5
H-Bond Donor 1
Rotatable Bonds 0

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of neolabuanine A

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9890 98.90%
Caco-2 - 0.6796 67.96%
Blood Brain Barrier + 0.8379 83.79%
Human oral bioavailability + 0.5857 58.57%
Subcellular localzation Mitochondria 0.8099 80.99%
OATP2B1 inhibitior - 0.7178 71.78%
OATP1B1 inhibitior + 0.9249 92.49%
OATP1B3 inhibitior + 0.9531 95.31%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.5567 55.67%
BSEP inhibitior + 0.6599 65.99%
P-glycoprotein inhibitior - 0.7703 77.03%
P-glycoprotein substrate - 0.8492 84.92%
CYP3A4 substrate + 0.5908 59.08%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate + 0.3796 37.96%
CYP3A4 inhibition - 0.8924 89.24%
CYP2C9 inhibition - 0.7951 79.51%
CYP2C19 inhibition - 0.6916 69.16%
CYP2D6 inhibition - 0.8069 80.69%
CYP1A2 inhibition + 0.8598 85.98%
CYP2C8 inhibition + 0.5714 57.14%
CYP inhibitory promiscuity - 0.8002 80.02%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.9000 90.00%
Carcinogenicity (trinary) Non-required 0.6718 67.18%
Eye corrosion - 0.9883 98.83%
Eye irritation - 0.8488 84.88%
Skin irritation - 0.7582 75.82%
Skin corrosion - 0.9454 94.54%
Ames mutagenesis + 0.6700 67.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6158 61.58%
Micronuclear + 0.6200 62.00%
Hepatotoxicity + 0.6125 61.25%
skin sensitisation - 0.8425 84.25%
Respiratory toxicity + 0.7444 74.44%
Reproductive toxicity + 0.7111 71.11%
Mitochondrial toxicity + 0.8875 88.75%
Nephrotoxicity - 0.7044 70.44%
Acute Oral Toxicity (c) III 0.6911 69.11%
Estrogen receptor binding + 0.8798 87.98%
Androgen receptor binding + 0.6586 65.86%
Thyroid receptor binding + 0.6173 61.73%
Glucocorticoid receptor binding + 0.8146 81.46%
Aromatase binding + 0.8006 80.06%
PPAR gamma + 0.9467 94.67%
Honey bee toxicity - 0.9171 91.71%
Biodegradation - 1.0000 100.00%
Crustacea aquatic toxicity - 0.5600 56.00%
Fish aquatic toxicity - 0.9155 91.55%

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 99.37% 91.11%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 96.16% 99.23%
CHEMBL1806 P11388 DNA topoisomerase II alpha 95.92% 89.00%
CHEMBL1868 P17948 Vascular endothelial growth factor receptor 1 95.15% 96.47%
CHEMBL2581 P07339 Cathepsin D 93.27% 98.95%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 92.73% 95.56%
CHEMBL1951 P21397 Monoamine oxidase A 91.95% 91.49%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 91.39% 85.14%
CHEMBL2378 P30307 Dual specificity phosphatase Cdc25C 86.16% 96.67%
CHEMBL3192 Q9BY41 Histone deacetylase 8 85.34% 93.99%
CHEMBL1293249 Q13887 Kruppel-like factor 5 85.14% 86.33%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 83.34% 94.00%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 82.77% 99.15%
CHEMBL2535 P11166 Glucose transporter 82.51% 98.75%
CHEMBL2095172 P14867 GABA-A receptor; alpha-1/beta-2/gamma-2 82.37% 92.67%
CHEMBL1907598 P05106 Integrin alpha-V/beta-3 81.72% 95.71%
CHEMBL1781 P11387 DNA topoisomerase I 80.97% 97.00%

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 135800554
LOTUS LTS0000602
wikiData Q105026735