Neolymphostinol B

Details

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Internal ID fbe56d61-bb3c-4f84-9aa7-4da8271816b0
Taxonomy Organoheterocyclic compounds > Quinolines and derivatives > Pyrroloquinolines > Pyrrolo[4,3,2-de]quinolines
IUPAC Name N-[6-(3-hydroxypropanoyl)-11-imino-2,7-diazatricyclo[6.3.1.04,12]dodeca-1,3,5,8(12),9-pentaen-9-yl]propanamide
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C16H16N4O3/c1-2-13(23)19-11-6-9(17)15-14-8(7-18-15)5-10(20-16(11)14)12(22)3-4-21/h5-7,17,20-21H,2-4H2,1H3,(H,19,23)
InChI Key HPWURPWOHPLBEV-UHFFFAOYSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C16H16N4O3
Molecular Weight 312.32 g/mol
Exact Mass 312.12224039 g/mol
Topological Polar Surface Area (TPSA) 119.00 Ų
XlogP -0.30
Atomic LogP (AlogP) 1.55
H-Bond Acceptor 5
H-Bond Donor 4
Rotatable Bonds 5

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of Neolymphostinol B

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9209 92.09%
Caco-2 - 0.7353 73.53%
Blood Brain Barrier + 0.5750 57.50%
Human oral bioavailability + 0.5143 51.43%
Subcellular localzation Mitochondria 0.6203 62.03%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8944 89.44%
OATP1B3 inhibitior + 0.9455 94.55%
MATE1 inhibitior - 0.9041 90.41%
OCT2 inhibitior - 0.7399 73.99%
BSEP inhibitior + 0.7240 72.40%
P-glycoprotein inhibitior - 0.8767 87.67%
P-glycoprotein substrate + 0.5054 50.54%
CYP3A4 substrate + 0.5347 53.47%
CYP2C9 substrate - 0.8046 80.46%
CYP2D6 substrate - 0.8566 85.66%
CYP3A4 inhibition - 0.7467 74.67%
CYP2C9 inhibition - 0.7015 70.15%
CYP2C19 inhibition - 0.7973 79.73%
CYP2D6 inhibition - 0.8602 86.02%
CYP1A2 inhibition - 0.7028 70.28%
CYP2C8 inhibition + 0.6759 67.59%
CYP inhibitory promiscuity - 0.7436 74.36%
UGT catelyzed - 0.6000 60.00%
Carcinogenicity (binary) - 0.8400 84.00%
Carcinogenicity (trinary) Non-required 0.6726 67.26%
Eye corrosion - 0.9892 98.92%
Eye irritation - 0.9438 94.38%
Skin irritation - 0.8005 80.05%
Skin corrosion - 0.9394 93.94%
Ames mutagenesis + 0.5600 56.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4169 41.69%
Micronuclear + 0.7400 74.00%
Hepatotoxicity + 0.6658 66.58%
skin sensitisation - 0.8827 88.27%
Respiratory toxicity + 0.7111 71.11%
Reproductive toxicity + 0.9556 95.56%
Mitochondrial toxicity + 0.8250 82.50%
Nephrotoxicity - 0.6386 63.86%
Acute Oral Toxicity (c) III 0.6441 64.41%
Estrogen receptor binding + 0.6371 63.71%
Androgen receptor binding + 0.5207 52.07%
Thyroid receptor binding + 0.6281 62.81%
Glucocorticoid receptor binding + 0.8026 80.26%
Aromatase binding + 0.6498 64.98%
PPAR gamma + 0.8248 82.48%
Honey bee toxicity - 0.9088 90.88%
Biodegradation - 0.8500 85.00%
Crustacea aquatic toxicity - 0.6900 69.00%
Fish aquatic toxicity - 0.8372 83.72%

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
CHEMBL230 P35354 Cyclooxygenase-2 99.85% 89.63%
CHEMBL1293267 Q9HC97 G-protein coupled receptor 35 97.86% 89.34%
CHEMBL2292 Q13627 Dual-specificity tyrosine-phosphorylation regulated kinase 1A 94.43% 93.24%
CHEMBL3060 Q9Y345 Glycine transporter 2 94.31% 99.17%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 93.09% 96.09%
CHEMBL2535 P11166 Glucose transporter 92.37% 98.75%
CHEMBL2581 P07339 Cathepsin D 89.97% 98.95%
CHEMBL3401 O75469 Pregnane X receptor 89.25% 94.73%
CHEMBL1293277 O15118 Niemann-Pick C1 protein 88.33% 81.11%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 88.29% 91.11%
CHEMBL2107 P61073 C-X-C chemokine receptor type 4 87.94% 93.10%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 87.62% 96.00%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 87.02% 99.23%
CHEMBL1781 P11387 DNA topoisomerase I 86.55% 97.00%
CHEMBL5163 Q9NY46 Sodium channel protein type III alpha subunit 85.16% 96.90%
CHEMBL4208 P20618 Proteasome component C5 83.40% 90.00%
CHEMBL221 P23219 Cyclooxygenase-1 83.12% 90.17%
CHEMBL2243 O00519 Anandamide amidohydrolase 82.92% 97.53%
CHEMBL255 P29275 Adenosine A2b receptor 82.21% 98.59%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 81.30% 90.71%
CHEMBL5994 O00574 C-X-C chemokine receptor type 6 81.16% 90.00%
CHEMBL3864 Q06124 Protein-tyrosine phosphatase 2C 80.54% 94.42%
CHEMBL1944495 P28065 Proteasome subunit beta type-9 80.41% 97.50%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 80.32% 94.45%

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.
There are no matching plants.

Cross-Links

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PubChem 139587399
LOTUS LTS0101051
wikiData Q77565164