Colletotrichumine A

Details

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Internal ID f63ad2d2-4a85-4c6b-bd12-f2efe52a3a62
Taxonomy Organoheterocyclic compounds > Indoles and derivatives
IUPAC Name (3E)-3-[(3,5,6-trimethylpyrazin-2-yl)methylidene]-1H-indol-2-one
SMILES (Canonical) CC1=C(N=C(C(=N1)C)C=C2C3=CC=CC=C3NC2=O)C
SMILES (Isomeric) CC1=C(N=C(C(=N1)C)/C=C/2\C3=CC=CC=C3NC2=O)C
InChI InChI=1S/C16H15N3O/c1-9-10(2)18-15(11(3)17-9)8-13-12-6-4-5-7-14(12)19-16(13)20/h4-8H,1-3H3,(H,19,20)/b13-8+
InChI Key UPOJQOAXPUNQHS-MDWZMJQESA-N
Popularity 1 reference in papers

Physical and Chemical Properties

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Molecular Formula C16H15N3O
Molecular Weight 265.31 g/mol
Exact Mass 265.121512110 g/mol
Topological Polar Surface Area (TPSA) 54.90 Ų
XlogP 2.00
Atomic LogP (AlogP) 2.89
H-Bond Acceptor 3
H-Bond Donor 1
Rotatable Bonds 1

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of Colletotrichumine A

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 1.0000 100.00%
Caco-2 + 0.7785 77.85%
Blood Brain Barrier + 0.9500 95.00%
Human oral bioavailability + 0.8286 82.86%
Subcellular localzation Mitochondria 0.5800 58.00%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9219 92.19%
OATP1B3 inhibitior + 0.9498 94.98%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.9000 90.00%
BSEP inhibitior + 0.6445 64.45%
P-glycoprotein inhibitior - 0.6385 63.85%
P-glycoprotein substrate - 0.9180 91.80%
CYP3A4 substrate + 0.5144 51.44%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8975 89.75%
CYP3A4 inhibition + 0.7588 75.88%
CYP2C9 inhibition + 0.8382 83.82%
CYP2C19 inhibition + 0.7972 79.72%
CYP2D6 inhibition + 0.5846 58.46%
CYP1A2 inhibition + 0.9323 93.23%
CYP2C8 inhibition - 0.8510 85.10%
CYP inhibitory promiscuity + 0.9102 91.02%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.9300 93.00%
Carcinogenicity (trinary) Danger 0.4292 42.92%
Eye corrosion - 0.9904 99.04%
Eye irritation - 0.7053 70.53%
Skin irritation - 0.7897 78.97%
Skin corrosion - 0.9647 96.47%
Ames mutagenesis - 0.5554 55.54%
Human Ether-a-go-go-Related Gene inhibition + 0.6951 69.51%
Micronuclear + 0.7500 75.00%
Hepatotoxicity + 0.7750 77.50%
skin sensitisation - 0.8551 85.51%
Respiratory toxicity + 0.6333 63.33%
Reproductive toxicity + 0.5889 58.89%
Mitochondrial toxicity + 0.5125 51.25%
Nephrotoxicity + 0.7337 73.37%
Acute Oral Toxicity (c) III 0.6203 62.03%
Estrogen receptor binding + 0.8635 86.35%
Androgen receptor binding + 0.8304 83.04%
Thyroid receptor binding + 0.8644 86.44%
Glucocorticoid receptor binding + 0.6832 68.32%
Aromatase binding + 0.6221 62.21%
PPAR gamma + 0.7798 77.98%
Honey bee toxicity - 0.9403 94.03%
Biodegradation - 0.9500 95.00%
Crustacea aquatic toxicity + 0.6700 67.00%
Fish aquatic toxicity + 0.8397 83.97%

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
CHEMBL1937 Q92769 Histone deacetylase 2 96.33% 94.75%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 95.87% 95.56%
CHEMBL2581 P07339 Cathepsin D 93.74% 98.95%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 91.29% 99.23%
CHEMBL3524 P56524 Histone deacetylase 4 90.99% 92.97%
CHEMBL230 P35354 Cyclooxygenase-2 90.18% 89.63%
CHEMBL1907600 Q00535 Cyclin-dependent kinase 5/CDK5 activator 1 90.14% 93.03%
CHEMBL1868 P17948 Vascular endothelial growth factor receptor 1 88.74% 96.47%
CHEMBL1951 P21397 Monoamine oxidase A 88.63% 91.49%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 88.02% 85.14%
CHEMBL4237 O75582 Ribosomal protein S6 kinase alpha 5 86.84% 91.00%
CHEMBL1913 P09619 Platelet-derived growth factor receptor beta 86.66% 95.70%
CHEMBL2035 P08912 Muscarinic acetylcholine receptor M5 86.13% 94.62%
CHEMBL1821 P08173 Muscarinic acetylcholine receptor M4 83.98% 94.08%
CHEMBL1293249 Q13887 Kruppel-like factor 5 83.43% 86.33%
CHEMBL2039 P27338 Monoamine oxidase B 83.13% 92.51%
CHEMBL5409 Q8TDU6 G-protein coupled bile acid receptor 1 82.12% 93.65%
CHEMBL2095226 P05556 Integrin alpha-5/beta-1 82.01% 96.39%
CHEMBL2378 P30307 Dual specificity phosphatase Cdc25C 81.77% 96.67%
CHEMBL5805 Q9NR97 Toll-like receptor 8 81.38% 96.25%
CHEMBL4145 Q9UKV0 Histone deacetylase 9 80.52% 85.49%

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 139586214
LOTUS LTS0120421
wikiData Q77501405