Collismycin M6

Details

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Internal ID 91ede2fb-4d6e-4b57-9c6a-117a8c9d98d4
Taxonomy Organoheterocyclic compounds > Pyridines and derivatives > Bipyridines and oligopyridines
IUPAC Name N-[[4-methoxy-6-(6-methylpyridin-2-yl)-3-methylsulfanylpyridin-2-yl]methylidene]hydroxylamine
SMILES (Canonical) CC1=NC(=CC=C1)C2=NC(=C(C(=C2)OC)SC)C=NO
SMILES (Isomeric) CC1=NC(=CC=C1)C2=NC(=C(C(=C2)OC)SC)C=NO
InChI InChI=1S/C14H15N3O2S/c1-9-5-4-6-10(16-9)11-7-13(19-2)14(20-3)12(17-11)8-15-18/h4-8,18H,1-3H3
InChI Key UFSZPVKXDNGQHJ-UHFFFAOYSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

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Molecular Formula C14H15N3O2S
Molecular Weight 289.35 g/mol
Exact Mass 289.08849790 g/mol
Topological Polar Surface Area (TPSA) 92.90 Ų
XlogP 2.40
Atomic LogP (AlogP) 2.99
H-Bond Acceptor 6
H-Bond Donor 1
Rotatable Bonds 4

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of Collismycin M6

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9636 96.36%
Caco-2 - 0.5955 59.55%
Blood Brain Barrier + 0.8250 82.50%
Human oral bioavailability + 0.5571 55.71%
Subcellular localzation Mitochondria 0.8328 83.28%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9394 93.94%
OATP1B3 inhibitior + 0.9431 94.31%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.7500 75.00%
BSEP inhibitior - 0.5079 50.79%
P-glycoprotein inhibitior - 0.8599 85.99%
P-glycoprotein substrate - 0.7917 79.17%
CYP3A4 substrate + 0.5250 52.50%
CYP2C9 substrate + 0.6085 60.85%
CYP2D6 substrate - 0.8410 84.10%
CYP3A4 inhibition + 0.6091 60.91%
CYP2C9 inhibition - 0.5367 53.67%
CYP2C19 inhibition + 0.7399 73.99%
CYP2D6 inhibition - 0.8657 86.57%
CYP1A2 inhibition + 0.5972 59.72%
CYP2C8 inhibition + 0.7308 73.08%
CYP inhibitory promiscuity + 0.8098 80.98%
UGT catelyzed + 0.8000 80.00%
Carcinogenicity (binary) - 0.7600 76.00%
Carcinogenicity (trinary) Non-required 0.4736 47.36%
Eye corrosion - 0.9819 98.19%
Eye irritation + 0.6877 68.77%
Skin irritation - 0.7775 77.75%
Skin corrosion - 0.9364 93.64%
Ames mutagenesis + 0.5600 56.00%
Human Ether-a-go-go-Related Gene inhibition + 0.7450 74.50%
Micronuclear + 0.7574 75.74%
Hepatotoxicity + 0.5656 56.56%
skin sensitisation - 0.8270 82.70%
Respiratory toxicity - 0.5556 55.56%
Reproductive toxicity + 0.5556 55.56%
Mitochondrial toxicity + 0.6125 61.25%
Nephrotoxicity + 0.4567 45.67%
Acute Oral Toxicity (c) III 0.6344 63.44%
Estrogen receptor binding + 0.8021 80.21%
Androgen receptor binding + 0.6182 61.82%
Thyroid receptor binding + 0.8451 84.51%
Glucocorticoid receptor binding + 0.8563 85.63%
Aromatase binding + 0.9006 90.06%
PPAR gamma + 0.7436 74.36%
Honey bee toxicity - 0.7744 77.44%
Biodegradation - 0.8250 82.50%
Crustacea aquatic toxicity + 0.6300 63.00%
Fish aquatic toxicity + 0.7071 70.71%

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
CHEMBL1293249 Q13887 Kruppel-like factor 5 96.25% 86.33%
CHEMBL230 P35354 Cyclooxygenase-2 93.11% 89.63%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 92.27% 95.56%
CHEMBL4040 P28482 MAP kinase ERK2 90.89% 83.82%
CHEMBL3401 O75469 Pregnane X receptor 88.89% 94.73%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 88.00% 96.09%
CHEMBL3227 P41594 Metabotropic glutamate receptor 5 87.85% 96.42%
CHEMBL2535 P11166 Glucose transporter 86.70% 98.75%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 86.51% 96.00%
CHEMBL3060 Q9Y345 Glycine transporter 2 84.79% 99.17%
CHEMBL225 P28335 Serotonin 2c (5-HT2c) receptor 84.75% 89.62%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 83.95% 94.00%
CHEMBL2581 P07339 Cathepsin D 82.52% 98.95%
CHEMBL290 Q13370 Phosphodiesterase 3B 81.80% 94.00%
CHEMBL240 Q12809 HERG 81.30% 89.76%
CHEMBL1255126 O15151 Protein Mdm4 80.67% 90.20%
CHEMBL5409 Q8TDU6 G-protein coupled bile acid receptor 1 80.59% 93.65%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 80.01% 91.11%

Plants that contains it

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Below are displayed all the plants proven (via scientific papers) to contain this compound!
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There are no matching plants.

Cross-Links

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PubChem 139588721
LOTUS LTS0215198
wikiData Q105272090