8-Hydroxyeupolauridine

Details

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Internal ID 3012ea4c-5b30-47d0-a671-412f264b896b
Taxonomy Organoheterocyclic compounds > Diazanaphthalenes > Naphthyridines
IUPAC Name 2,8-diazatetracyclo[7.6.1.05,16.010,15]hexadeca-1,3,5(16),6,8,10(15),11,13-octaen-12-ol
SMILES (Canonical) C1=CC2=C(C=C1O)C3=NC=CC4=C3C2=NC=C4
SMILES (Isomeric) C1=CC2=C(C=C1O)C3=NC=CC4=C3C2=NC=C4
InChI InChI=1S/C14H8N2O/c17-9-1-2-10-11(7-9)14-12-8(4-6-16-14)3-5-15-13(10)12/h1-7,17H
InChI Key CTGUKNNRGTZRCB-UHFFFAOYSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

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Molecular Formula C14H8N2O
Molecular Weight 220.23 g/mol
Exact Mass 220.063662883 g/mol
Topological Polar Surface Area (TPSA) 46.00 Ų
XlogP 2.10
Atomic LogP (AlogP) 2.98
H-Bond Acceptor 3
H-Bond Donor 1
Rotatable Bonds 0

Synonyms

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CHEBI:67601
CHEMBL1801763
Q27136071

2D Structure

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2D Structure of 8-Hydroxyeupolauridine

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9972 99.72%
Caco-2 - 0.7411 74.11%
Blood Brain Barrier + 0.6379 63.79%
Human oral bioavailability - 0.5429 54.29%
Subcellular localzation Mitochondria 0.6857 68.57%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9157 91.57%
OATP1B3 inhibitior + 0.9601 96.01%
MATE1 inhibitior - 0.9000 90.00%
OCT2 inhibitior - 0.9000 90.00%
BSEP inhibitior - 0.6441 64.41%
P-glycoprotein inhibitior - 0.9556 95.56%
P-glycoprotein substrate - 0.8291 82.91%
CYP3A4 substrate - 0.6152 61.52%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.7428 74.28%
CYP3A4 inhibition - 0.7045 70.45%
CYP2C9 inhibition + 0.5097 50.97%
CYP2C19 inhibition - 0.5665 56.65%
CYP2D6 inhibition + 0.7332 73.32%
CYP1A2 inhibition + 0.9794 97.94%
CYP2C8 inhibition + 0.6989 69.89%
CYP inhibitory promiscuity + 0.5186 51.86%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.9430 94.30%
Carcinogenicity (trinary) Non-required 0.6956 69.56%
Eye corrosion - 0.9933 99.33%
Eye irritation + 0.9734 97.34%
Skin irritation - 0.6109 61.09%
Skin corrosion - 0.9772 97.72%
Ames mutagenesis + 0.7300 73.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7884 78.84%
Micronuclear + 0.7300 73.00%
Hepatotoxicity + 0.7657 76.57%
skin sensitisation - 0.7767 77.67%
Respiratory toxicity + 0.5111 51.11%
Reproductive toxicity + 0.7333 73.33%
Mitochondrial toxicity - 0.7250 72.50%
Nephrotoxicity + 0.4759 47.59%
Acute Oral Toxicity (c) III 0.6472 64.72%
Estrogen receptor binding + 0.9464 94.64%
Androgen receptor binding + 0.8935 89.35%
Thyroid receptor binding + 0.8479 84.79%
Glucocorticoid receptor binding + 0.9450 94.50%
Aromatase binding + 0.9260 92.60%
PPAR gamma + 0.8552 85.52%
Honey bee toxicity - 0.9359 93.59%
Biodegradation - 0.9250 92.50%
Crustacea aquatic toxicity + 0.6300 63.00%
Fish aquatic toxicity - 0.6983 69.83%

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
CHEMBL1951 P21397 Monoamine oxidase A 98.60% 91.49%
CHEMBL2107 P61073 C-X-C chemokine receptor type 4 96.77% 93.10%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 91.14% 91.11%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 87.89% 99.15%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 87.57% 94.00%
CHEMBL2292 Q13627 Dual-specificity tyrosine-phosphorylation regulated kinase 1A 86.57% 93.24%
CHEMBL1293249 Q13887 Kruppel-like factor 5 86.37% 86.33%
CHEMBL242 Q92731 Estrogen receptor beta 86.34% 98.35%
CHEMBL2581 P07339 Cathepsin D 84.99% 98.95%
CHEMBL5145 P15056 Serine/threonine-protein kinase B-raf 84.91% 97.90%
CHEMBL2378 P30307 Dual specificity phosphatase Cdc25C 84.64% 96.67%
CHEMBL4208 P20618 Proteasome component C5 84.52% 90.00%
CHEMBL301 P24941 Cyclin-dependent kinase 2 83.36% 91.23%
CHEMBL5014 O43353 Serine/threonine-protein kinase RIPK2 83.10% 86.79%
CHEMBL1806 P11388 DNA topoisomerase II alpha 82.72% 89.00%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 82.02% 96.09%
CHEMBL2535 P11166 Glucose transporter 81.82% 98.75%
CHEMBL5339 Q5NUL3 G-protein coupled receptor 120 81.57% 95.78%
CHEMBL3060 Q9Y345 Glycine transporter 2 81.27% 99.17%
CHEMBL1293255 P15428 15-hydroxyprostaglandin dehydrogenase [NAD+] 80.68% 83.57%

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.
Ambavia gerrardii

Cross-Links

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PubChem 136026143
LOTUS LTS0200353
wikiData Q27136071