Dubinine

Details

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Internal ID 7ed5e65f-e980-490e-9407-107e2ab66fb7
Taxonomy Organoheterocyclic compounds > Quinolines and derivatives > Dihydrofuranoquinolines
IUPAC Name [2-hydroxy-2-(4-methoxy-2,3-dihydrofuro[2,3-b]quinolin-2-yl)propyl] acetate
SMILES (Canonical) CC(=O)OCC(C)(C1CC2=C(C3=CC=CC=C3N=C2O1)OC)O
SMILES (Isomeric) CC(=O)OCC(C)(C1CC2=C(C3=CC=CC=C3N=C2O1)OC)O
InChI InChI=1S/C17H19NO5/c1-10(19)22-9-17(2,20)14-8-12-15(21-3)11-6-4-5-7-13(11)18-16(12)23-14/h4-7,14,20H,8-9H2,1-3H3
InChI Key ICXADQHBWHLSCI-UHFFFAOYSA-N
Popularity 8 references in papers

Physical and Chemical Properties

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Molecular Formula C17H19NO5
Molecular Weight 317.34 g/mol
Exact Mass 317.12632271 g/mol
Topological Polar Surface Area (TPSA) 77.90 Ų
XlogP 2.00
Atomic LogP (AlogP) 1.86
H-Bond Acceptor 6
H-Bond Donor 1
Rotatable Bonds 4

Synonyms

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23092-72-0
CBMicro_021740
Oprea1_383863
Oprea1_621330
MLS000106956
CHEMBL1374297
DTXSID101346561
HMS1607G11
HMS2480C14
CCG-9155
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of Dubinine

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9816 98.16%
Caco-2 - 0.5780 57.80%
Blood Brain Barrier + 0.6250 62.50%
Human oral bioavailability - 0.5571 55.71%
Subcellular localzation Mitochondria 0.5557 55.57%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9155 91.55%
OATP1B3 inhibitior + 0.9211 92.11%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.9250 92.50%
BSEP inhibitior - 0.5605 56.05%
P-glycoprotein inhibitior - 0.8240 82.40%
P-glycoprotein substrate - 0.7946 79.46%
CYP3A4 substrate + 0.6240 62.40%
CYP2C9 substrate - 0.8027 80.27%
CYP2D6 substrate - 0.8041 80.41%
CYP3A4 inhibition - 0.7917 79.17%
CYP2C9 inhibition - 0.8454 84.54%
CYP2C19 inhibition - 0.8665 86.65%
CYP2D6 inhibition - 0.9337 93.37%
CYP1A2 inhibition + 0.7473 74.73%
CYP2C8 inhibition + 0.5871 58.71%
CYP inhibitory promiscuity - 0.7686 76.86%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.9700 97.00%
Carcinogenicity (trinary) Non-required 0.5459 54.59%
Eye corrosion - 0.9894 98.94%
Eye irritation - 0.8869 88.69%
Skin irritation - 0.8116 81.16%
Skin corrosion - 0.9493 94.93%
Ames mutagenesis + 0.5200 52.00%
Human Ether-a-go-go-Related Gene inhibition + 0.7129 71.29%
Micronuclear + 0.5500 55.00%
Hepatotoxicity + 0.6198 61.98%
skin sensitisation - 0.8350 83.50%
Respiratory toxicity + 0.7556 75.56%
Reproductive toxicity + 0.9000 90.00%
Mitochondrial toxicity + 0.8625 86.25%
Nephrotoxicity - 0.6130 61.30%
Acute Oral Toxicity (c) III 0.5669 56.69%
Estrogen receptor binding + 0.8659 86.59%
Androgen receptor binding + 0.5545 55.45%
Thyroid receptor binding + 0.5409 54.09%
Glucocorticoid receptor binding + 0.5696 56.96%
Aromatase binding - 0.5984 59.84%
PPAR gamma + 0.6598 65.98%
Honey bee toxicity - 0.8849 88.49%
Biodegradation - 0.7500 75.00%
Crustacea aquatic toxicity - 0.5600 56.00%
Fish aquatic toxicity + 0.8044 80.44%

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
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 99.45% 85.14%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 97.87% 91.11%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 96.72% 96.09%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 93.03% 99.23%
CHEMBL1293249 Q13887 Kruppel-like factor 5 91.97% 86.33%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 89.18% 92.62%
CHEMBL3060 Q9Y345 Glycine transporter 2 89.17% 99.17%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 88.88% 95.56%
CHEMBL3401 O75469 Pregnane X receptor 87.21% 94.73%
CHEMBL5028 O14672 ADAM10 84.40% 97.50%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 84.04% 96.00%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 83.98% 94.00%
CHEMBL2095226 P05556 Integrin alpha-5/beta-1 83.73% 96.39%
CHEMBL2535 P11166 Glucose transporter 82.77% 98.75%
CHEMBL2581 P07339 Cathepsin D 80.71% 98.95%

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.
There are no matching plants.

Cross-Links

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PubChem 3107433
LOTUS LTS0238623
wikiData Q105111211