Neocryptolepine

Details

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Internal ID a65e66d7-b736-4616-8c89-f7c5d3253584
Taxonomy Organoheterocyclic compounds > Quinolines and derivatives > Pyrroloquinolines
IUPAC Name 5-methylindolo[2,3-b]quinoline
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C16H12N2/c1-18-15-9-5-2-6-11(15)10-13-12-7-3-4-8-14(12)17-16(13)18/h2-10H,1H3
InChI Key PZIIKMBOSNKNFZ-UHFFFAOYSA-N
Popularity 67 references in papers

Physical and Chemical Properties

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Molecular Formula C16H12N2
Molecular Weight 232.28 g/mol
Exact Mass 232.100048391 g/mol
Topological Polar Surface Area (TPSA) 17.80 Ų
XlogP 3.70
Atomic LogP (AlogP) 3.83
H-Bond Acceptor 2
H-Bond Donor 0
Rotatable Bonds 0

Synonyms

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5-methylindolo[2,3-b]quinoline
5-Methylindolo(2,3-b)quinoline
RefChem:927602
114414-78-7
5H-Quinindoline, 5-methyl-
5H-Quinodoline, 5-methyl-
5-Methyl-5H-quinindoline
NSC-687967
CHEMBL465591
NSC687967
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of Neocryptolepine

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9923 99.23%
Caco-2 + 0.7821 78.21%
Blood Brain Barrier + 0.9250 92.50%
Human oral bioavailability + 0.6714 67.14%
Subcellular localzation Mitochondria 0.6306 63.06%
OATP2B1 inhibitior - 0.8613 86.13%
OATP1B1 inhibitior + 0.9569 95.69%
OATP1B3 inhibitior + 0.9556 95.56%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.6069 60.69%
BSEP inhibitior + 0.7541 75.41%
P-glycoprotein inhibitior - 0.8518 85.18%
P-glycoprotein substrate - 0.9044 90.44%
CYP3A4 substrate - 0.5107 51.07%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.7700 77.00%
CYP3A4 inhibition - 0.5667 56.67%
CYP2C9 inhibition - 0.9386 93.86%
CYP2C19 inhibition + 0.5240 52.40%
CYP2D6 inhibition - 0.5385 53.85%
CYP1A2 inhibition + 0.7081 70.81%
CYP2C8 inhibition - 0.6981 69.81%
CYP inhibitory promiscuity + 0.5906 59.06%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.9600 96.00%
Carcinogenicity (trinary) Danger 0.3631 36.31%
Eye corrosion - 0.9642 96.42%
Eye irritation + 0.5483 54.83%
Skin irritation + 0.5287 52.87%
Skin corrosion - 0.8991 89.91%
Ames mutagenesis + 0.8400 84.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5158 51.58%
Micronuclear + 0.8559 85.59%
Hepatotoxicity + 0.6875 68.75%
skin sensitisation - 0.8968 89.68%
Respiratory toxicity - 0.5000 50.00%
Reproductive toxicity + 0.6667 66.67%
Mitochondrial toxicity + 0.6500 65.00%
Nephrotoxicity - 0.7221 72.21%
Acute Oral Toxicity (c) III 0.6819 68.19%
Estrogen receptor binding + 0.9227 92.27%
Androgen receptor binding + 0.7870 78.70%
Thyroid receptor binding + 0.7523 75.23%
Glucocorticoid receptor binding + 0.9356 93.56%
Aromatase binding + 0.8897 88.97%
PPAR gamma + 0.6981 69.81%
Honey bee toxicity - 0.9674 96.74%
Biodegradation - 0.9500 95.00%
Crustacea aquatic toxicity + 0.8400 84.00%
Fish aquatic toxicity - 0.6550 65.50%

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
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 95.99% 95.56%
CHEMBL2581 P07339 Cathepsin D 93.63% 98.95%
CHEMBL1951 P21397 Monoamine oxidase A 93.37% 91.49%
CHEMBL1293249 Q13887 Kruppel-like factor 5 91.75% 86.33%
CHEMBL5805 Q9NR97 Toll-like receptor 8 91.62% 96.25%
CHEMBL1899 P46098 Serotonin 3a (5-HT3a) receptor 91.32% 100.00%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 88.21% 85.14%
CHEMBL3192 Q9BY41 Histone deacetylase 8 87.81% 93.99%
CHEMBL1868 P17948 Vascular endothelial growth factor receptor 1 86.87% 96.47%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 86.02% 96.09%
CHEMBL2378 P30307 Dual specificity phosphatase Cdc25C 85.83% 96.67%
CHEMBL4145 Q9UKV0 Histone deacetylase 9 84.06% 85.49%
CHEMBL3761 Q9HCG7 Beta-glucosidase 83.88% 99.00%
CHEMBL1936 P10721 Stem cell growth factor receptor 83.48% 84.17%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 82.88% 94.00%
CHEMBL1806 P11388 DNA topoisomerase II alpha 82.35% 89.00%
CHEMBL2035 P08912 Muscarinic acetylcholine receptor M5 82.09% 94.62%
CHEMBL5409 Q8TDU6 G-protein coupled bile acid receptor 1 81.53% 93.65%
CHEMBL3401 O75469 Pregnane X receptor 80.96% 94.73%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 80.64% 99.23%
CHEMBL2335 P42785 Lysosomal Pro-X carboxypeptidase 80.47% 100.00%
CHEMBL2716 Q8WUI4 Histone deacetylase 7 80.45% 89.44%

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
Wisteria brachybotrys

Cross-Links

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PubChem 390526
NPASS NPC288232
ChEMBL CHEMBL115585
LOTUS LTS0033067
wikiData Q83016911