Rhopaladin C

Details

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Internal ID 4633aa29-db98-41ac-a4b5-3e5b6b584bfe
Taxonomy Organoheterocyclic compounds > Indoles and derivatives > Indolecarboxylic acids and derivatives
IUPAC Name (5-bromo-1H-indol-3-yl)-[4-hydroxy-5-(indol-3-ylidenemethyl)-1H-imidazol-2-yl]methanone
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C21H13BrN4O2/c22-12-5-6-17-14(8-12)15(10-24-17)19(27)20-25-18(21(28)26-20)7-11-9-23-16-4-2-1-3-13(11)16/h1-10,24,28H,(H,25,26)
InChI Key GNXFQJCAILZMRG-UHFFFAOYSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C21H13BrN4O2
Molecular Weight 433.30 g/mol
Exact Mass 432.02219 g/mol
Topological Polar Surface Area (TPSA) 94.10 Ų
XlogP 3.80
Atomic LogP (AlogP) 4.85
H-Bond Acceptor 4
H-Bond Donor 3
Rotatable Bonds 3

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of Rhopaladin C

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9962 99.62%
Caco-2 - 0.7861 78.61%
Blood Brain Barrier + 0.7000 70.00%
Human oral bioavailability + 0.6429 64.29%
Subcellular localzation Mitochondria 0.3862 38.62%
OATP2B1 inhibitior - 0.5702 57.02%
OATP1B1 inhibitior + 0.8615 86.15%
OATP1B3 inhibitior + 0.9403 94.03%
MATE1 inhibitior - 0.9000 90.00%
OCT2 inhibitior - 0.8250 82.50%
BSEP inhibitior + 0.8404 84.04%
P-glycoprotein inhibitior - 0.5657 56.57%
P-glycoprotein substrate - 0.7262 72.62%
CYP3A4 substrate + 0.6116 61.16%
CYP2C9 substrate - 0.8074 80.74%
CYP2D6 substrate - 0.8645 86.45%
CYP3A4 inhibition - 0.6442 64.42%
CYP2C9 inhibition - 0.5321 53.21%
CYP2C19 inhibition + 0.5517 55.17%
CYP2D6 inhibition - 0.7707 77.07%
CYP1A2 inhibition + 0.9043 90.43%
CYP2C8 inhibition + 0.8033 80.33%
CYP inhibitory promiscuity + 0.8113 81.13%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.7276 72.76%
Carcinogenicity (trinary) Non-required 0.5941 59.41%
Eye corrosion - 0.9859 98.59%
Eye irritation - 0.7435 74.35%
Skin irritation - 0.8040 80.40%
Skin corrosion - 0.9475 94.75%
Ames mutagenesis - 0.5100 51.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6931 69.31%
Micronuclear + 0.8600 86.00%
Hepatotoxicity + 0.5302 53.02%
skin sensitisation - 0.8543 85.43%
Respiratory toxicity + 0.6111 61.11%
Reproductive toxicity + 0.7000 70.00%
Mitochondrial toxicity + 0.5375 53.75%
Nephrotoxicity - 0.6571 65.71%
Acute Oral Toxicity (c) III 0.5079 50.79%
Estrogen receptor binding + 0.8221 82.21%
Androgen receptor binding + 0.7746 77.46%
Thyroid receptor binding + 0.5785 57.85%
Glucocorticoid receptor binding + 0.7267 72.67%
Aromatase binding + 0.8084 80.84%
PPAR gamma + 0.8383 83.83%
Honey bee toxicity - 0.8410 84.10%
Biodegradation - 0.9000 90.00%
Crustacea aquatic toxicity - 0.6300 63.00%
Fish aquatic toxicity + 0.9127 91.27%

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
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 97.89% 91.11%
CHEMBL1293255 P15428 15-hydroxyprostaglandin dehydrogenase [NAD+] 97.15% 83.57%
CHEMBL5443 O00311 Cell division cycle 7-related protein kinase 96.49% 96.11%
CHEMBL2535 P11166 Glucose transporter 95.18% 98.75%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 94.70% 95.56%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 94.64% 99.23%
CHEMBL2292 Q13627 Dual-specificity tyrosine-phosphorylation regulated kinase 1A 92.80% 93.24%
CHEMBL5697 Q9GZT9 Egl nine homolog 1 91.74% 93.40%
CHEMBL1907600 Q00535 Cyclin-dependent kinase 5/CDK5 activator 1 90.84% 93.03%
CHEMBL2288 Q13526 Peptidyl-prolyl cis-trans isomerase NIMA-interacting 1 90.22% 91.71%
CHEMBL2581 P07339 Cathepsin D 89.26% 98.95%
CHEMBL2095226 P05556 Integrin alpha-5/beta-1 86.12% 96.39%
CHEMBL2035 P08912 Muscarinic acetylcholine receptor M5 85.46% 94.62%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 85.01% 94.00%
CHEMBL2708 Q16584 Mitogen-activated protein kinase kinase kinase 11 84.28% 81.14%
CHEMBL4208 P20618 Proteasome component C5 83.92% 90.00%
CHEMBL1781 P11387 DNA topoisomerase I 83.72% 97.00%
CHEMBL2095172 P14867 GABA-A receptor; alpha-1/beta-2/gamma-2 83.58% 92.67%
CHEMBL4145 Q9UKV0 Histone deacetylase 9 82.65% 85.49%
CHEMBL213 P08588 Beta-1 adrenergic receptor 81.79% 95.56%
CHEMBL2378 P30307 Dual specificity phosphatase Cdc25C 81.71% 96.67%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 81.62% 95.50%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 81.57% 99.15%
CHEMBL4026 P40763 Signal transducer and activator of transcription 3 81.28% 82.69%
CHEMBL241 Q14432 Phosphodiesterase 3A 81.00% 92.94%
CHEMBL3475 P05121 Plasminogen activator inhibitor-1 80.24% 83.00%

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 136691196
LOTUS LTS0054238
wikiData Q105013424