Quindoline

Details

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Internal ID cb9e7863-812b-4f99-8c4e-7d5a4bc169a5
Taxonomy Organoheterocyclic compounds > Quinolines and derivatives > Indoloquinolines
IUPAC Name 10H-indolo[3,2-b]quinoline
SMILES (Canonical) C1=CC=C2C(=C1)C=C3C(=N2)C4=CC=CC=C4N3
SMILES (Isomeric) C1=CC=C2C(=C1)C=C3C(=N2)C4=CC=CC=C4N3
InChI InChI=1S/C15H10N2/c1-3-7-12-10(5-1)9-14-15(17-12)11-6-2-4-8-13(11)16-14/h1-9,16H
InChI Key QOAKRWLMTKEDDL-UHFFFAOYSA-N
Popularity 108 references in papers

Physical and Chemical Properties

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Molecular Formula C15H10N2
Molecular Weight 218.25 g/mol
Exact Mass 218.084398327 g/mol
Topological Polar Surface Area (TPSA) 28.70 Ų
XlogP 3.40
Atomic LogP (AlogP) 3.87
H-Bond Acceptor 1
H-Bond Donor 1
Rotatable Bonds 0

Synonyms

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10H-Quindoline
10H-indolo[3,2-b]quinoline
243-58-3
NSC177394
NSC647766
NSC 177394
NSC 647766
5H-Quindoline
indolo[3,2-b]quinoline
c12nc3ccccc3cc2Nc4c1cccc4
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of Quindoline

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9968 99.68%
Caco-2 + 0.6866 68.66%
Blood Brain Barrier + 0.9250 92.50%
Human oral bioavailability + 0.5714 57.14%
Subcellular localzation Mitochondria 0.5918 59.18%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9310 93.10%
OATP1B3 inhibitior + 0.9583 95.83%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.6000 60.00%
BSEP inhibitior + 0.7091 70.91%
P-glycoprotein inhibitior - 0.8947 89.47%
P-glycoprotein substrate - 0.9667 96.67%
CYP3A4 substrate - 0.5454 54.54%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.7923 79.23%
CYP3A4 inhibition - 0.5168 51.68%
CYP2C9 inhibition - 0.8076 80.76%
CYP2C19 inhibition - 0.9131 91.31%
CYP2D6 inhibition + 0.5489 54.89%
CYP1A2 inhibition + 0.9380 93.80%
CYP2C8 inhibition + 0.7300 73.00%
CYP inhibitory promiscuity + 0.6643 66.43%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.9600 96.00%
Carcinogenicity (trinary) Non-required 0.7174 71.74%
Eye corrosion - 0.9740 97.40%
Eye irritation + 0.9277 92.77%
Skin irritation + 0.6572 65.72%
Skin corrosion - 0.9297 92.97%
Ames mutagenesis + 0.8600 86.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6686 66.86%
Micronuclear + 0.8400 84.00%
Hepatotoxicity + 0.6699 66.99%
skin sensitisation - 0.8528 85.28%
Respiratory toxicity - 0.7667 76.67%
Reproductive toxicity + 0.7333 73.33%
Mitochondrial toxicity - 0.7375 73.75%
Nephrotoxicity - 0.5655 56.55%
Acute Oral Toxicity (c) III 0.8078 80.78%
Estrogen receptor binding + 0.9776 97.76%
Androgen receptor binding + 0.8064 80.64%
Thyroid receptor binding + 0.8711 87.11%
Glucocorticoid receptor binding + 0.9494 94.94%
Aromatase binding + 0.9661 96.61%
PPAR gamma + 0.9135 91.35%
Honey bee toxicity - 0.9113 91.13%
Biodegradation - 1.0000 100.00%
Crustacea aquatic toxicity + 0.7900 79.00%
Fish aquatic toxicity - 0.5000 50.00%

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 95.41% 91.11%
CHEMBL2035 P08912 Muscarinic acetylcholine receptor M5 92.30% 94.62%
CHEMBL4145 Q9UKV0 Histone deacetylase 9 91.75% 85.49%
CHEMBL2716 Q8WUI4 Histone deacetylase 7 91.41% 89.44%
CHEMBL4302 P08183 P-glycoprotein 1 90.20% 92.98%
CHEMBL1937 Q92769 Histone deacetylase 2 89.24% 94.75%
CHEMBL2288 Q13526 Peptidyl-prolyl cis-trans isomerase NIMA-interacting 1 88.11% 91.71%
CHEMBL3192 Q9BY41 Histone deacetylase 8 87.96% 93.99%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 87.15% 94.00%
CHEMBL1781 P11387 DNA topoisomerase I 86.65% 97.00%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 86.09% 95.56%
CHEMBL2581 P07339 Cathepsin D 85.67% 98.95%
CHEMBL1951 P21397 Monoamine oxidase A 85.47% 91.49%
CHEMBL2708 Q16584 Mitogen-activated protein kinase kinase kinase 11 84.78% 81.14%
CHEMBL3401 O75469 Pregnane X receptor 83.94% 94.73%
CHEMBL3902 P09211 Glutathione S-transferase Pi 83.28% 93.81%
CHEMBL2095172 P14867 GABA-A receptor; alpha-1/beta-2/gamma-2 82.82% 92.67%
CHEMBL2535 P11166 Glucose transporter 82.69% 98.75%
CHEMBL1293249 Q13887 Kruppel-like factor 5 82.43% 86.33%
CHEMBL3524 P56524 Histone deacetylase 4 82.12% 92.97%
CHEMBL216 P11229 Muscarinic acetylcholine receptor M1 81.89% 94.23%
CHEMBL4225 P49760 Dual specificity protein kinase CLK2 81.81% 80.96%
CHEMBL1952 P04818 Thymidylate synthase 81.42% 93.53%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 81.41% 99.23%
CHEMBL2378 P30307 Dual specificity phosphatase Cdc25C 81.12% 96.67%
CHEMBL1806 P11388 DNA topoisomerase II alpha 80.71% 89.00%
CHEMBL2885 P07451 Carbonic anhydrase III 80.28% 87.45%

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.
Cryptolepis sanguinolenta
Isatis tinctoria
Persicaria tinctoria
Wisteria brachybotrys

Cross-Links

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PubChem 98912
NPASS NPC284635
ChEMBL CHEMBL224248
LOTUS LTS0007392
wikiData Q6095002