Communesin C

Details

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Internal ID b4cd7d84-5b5c-4644-84d9-3b5f58d5f0ab
Taxonomy Organoheterocyclic compounds > Indoles and derivatives > Pyridoindoles > Alpha carbolines
IUPAC Name (2E,4E)-1-[(2S,6R,14R,22R,25S)-25-[(2R)-3,3-dimethyloxiran-2-yl]-1,3,13,15-tetrazaheptacyclo[18.4.1.02,6.06,22.07,12.014,22.016,21]pentacosa-7,9,11,16,18,20-hexaen-3-yl]hexa-2,4-dien-1-one
SMILES (Canonical) CC=CC=CC(=O)N1CCC23C1N4CCC25C(NC6=CC=CC=C36)NC7=CC=CC(=C57)C4C8C(O8)(C)C
SMILES (Isomeric) C/C=C/C=C/C(=O)N1CC[C@]23[C@H]1N4CC[C@]25[C@H](NC6=CC=CC=C36)NC7=CC=CC(=C57)[C@H]4[C@@H]8C(O8)(C)C
InChI InChI=1S/C31H34N4O2/c1-4-5-6-14-23(36)34-17-15-30-20-11-7-8-12-21(20)32-27-31(30)16-18-35(28(30)34)25(26-29(2,3)37-26)19-10-9-13-22(33-27)24(19)31/h4-14,25-28,32-33H,15-18H2,1-3H3/b5-4+,14-6+/t25-,26+,27+,28+,30-,31-/m0/s1
InChI Key NGWRTMWKLOPVRM-SNBYXLDTSA-N
Popularity 3 references in papers

Physical and Chemical Properties

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Molecular Formula C31H34N4O2
Molecular Weight 494.60 g/mol
Exact Mass 494.26817634 g/mol
Topological Polar Surface Area (TPSA) 60.10 Ų
XlogP 4.80
Atomic LogP (AlogP) 4.67
H-Bond Acceptor 5
H-Bond Donor 2
Rotatable Bonds 3

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of Communesin C

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9827 98.27%
Caco-2 - 0.5748 57.48%
Blood Brain Barrier + 0.5750 57.50%
Human oral bioavailability - 0.6286 62.86%
Subcellular localzation Mitochondria 0.6973 69.73%
OATP2B1 inhibitior - 0.8555 85.55%
OATP1B1 inhibitior + 0.8487 84.87%
OATP1B3 inhibitior + 0.9391 93.91%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.7000 70.00%
BSEP inhibitior + 0.9578 95.78%
P-glycoprotein inhibitior + 0.8965 89.65%
P-glycoprotein substrate + 0.6482 64.82%
CYP3A4 substrate + 0.6813 68.13%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8682 86.82%
CYP3A4 inhibition - 0.5246 52.46%
CYP2C9 inhibition + 0.5064 50.64%
CYP2C19 inhibition + 0.5896 58.96%
CYP2D6 inhibition - 0.7616 76.16%
CYP1A2 inhibition - 0.6363 63.63%
CYP2C8 inhibition + 0.6216 62.16%
CYP inhibitory promiscuity + 0.7809 78.09%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.8600 86.00%
Carcinogenicity (trinary) Non-required 0.6250 62.50%
Eye corrosion - 0.9852 98.52%
Eye irritation - 0.9606 96.06%
Skin irritation - 0.7870 78.70%
Skin corrosion - 0.9255 92.55%
Ames mutagenesis - 0.6300 63.00%
Human Ether-a-go-go-Related Gene inhibition + 0.9350 93.50%
Micronuclear + 0.7900 79.00%
Hepatotoxicity + 0.5500 55.00%
skin sensitisation - 0.8453 84.53%
Respiratory toxicity + 0.7667 76.67%
Reproductive toxicity + 0.9111 91.11%
Mitochondrial toxicity + 0.8875 88.75%
Nephrotoxicity + 0.5999 59.99%
Acute Oral Toxicity (c) III 0.5483 54.83%
Estrogen receptor binding + 0.8047 80.47%
Androgen receptor binding + 0.7769 77.69%
Thyroid receptor binding + 0.6723 67.23%
Glucocorticoid receptor binding + 0.6952 69.52%
Aromatase binding + 0.5607 56.07%
PPAR gamma + 0.6980 69.80%
Honey bee toxicity - 0.8535 85.35%
Biodegradation - 0.9750 97.50%
Crustacea aquatic toxicity + 0.5200 52.00%
Fish aquatic toxicity + 0.9531 95.31%

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
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 98.72% 96.09%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 95.71% 91.11%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 91.96% 95.56%
CHEMBL1293249 Q13887 Kruppel-like factor 5 91.86% 86.33%
CHEMBL5028 O14672 ADAM10 90.66% 97.50%
CHEMBL221 P23219 Cyclooxygenase-1 89.69% 90.17%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 88.79% 99.23%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 86.27% 85.14%
CHEMBL3524 P56524 Histone deacetylase 4 85.99% 92.97%
CHEMBL1907600 Q00535 Cyclin-dependent kinase 5/CDK5 activator 1 85.94% 93.03%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 85.36% 94.45%
CHEMBL233 P35372 Mu opioid receptor 84.94% 97.93%
CHEMBL1806 P11388 DNA topoisomerase II alpha 83.87% 89.00%
CHEMBL2035 P08912 Muscarinic acetylcholine receptor M5 83.21% 94.62%
CHEMBL2581 P07339 Cathepsin D 83.00% 98.95%
CHEMBL3359 P21462 Formyl peptide receptor 1 82.48% 93.56%
CHEMBL5805 Q9NR97 Toll-like receptor 8 80.14% 96.25%

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.
Krameria bicolor
Krameria erecta

Cross-Links

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PubChem 44575538
LOTUS LTS0266209
wikiData Q104993494