Marinocyanin C

Details

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Internal ID 2002c1b1-6fdc-4699-8c55-b50dc4f05730
Taxonomy Organoheterocyclic compounds > Diazanaphthalenes > Benzodiazines > Quinoxalines > Phenazines and derivatives
IUPAC Name [2-[(2-bromo-1-oxophenazin-5-yl)methyl]-5,5-dimethylcyclohexen-1-yl]methyl 3-methylbut-2-enoate
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C27H29BrN2O3/c1-17(2)13-24(31)33-16-19-14-27(3,4)12-11-18(19)15-30-22-8-6-5-7-21(22)29-25-23(30)10-9-20(28)26(25)32/h5-10,13H,11-12,14-16H2,1-4H3
InChI Key GSMIEZJYRUIRNY-UHFFFAOYSA-N
Popularity 3 references in papers

Physical and Chemical Properties

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Molecular Formula C27H29BrN2O3
Molecular Weight 509.40 g/mol
Exact Mass 508.13616 g/mol
Topological Polar Surface Area (TPSA) 59.00 Ų
XlogP 5.80
Atomic LogP (AlogP) 6.28
H-Bond Acceptor 5
H-Bond Donor 0
Rotatable Bonds 5

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of Marinocyanin C

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9671 96.71%
Caco-2 - 0.6858 68.58%
Blood Brain Barrier + 0.5750 57.50%
Human oral bioavailability - 0.7143 71.43%
Subcellular localzation Mitochondria 0.6547 65.47%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8967 89.67%
OATP1B3 inhibitior + 0.9275 92.75%
MATE1 inhibitior - 0.8200 82.00%
OCT2 inhibitior - 0.6500 65.00%
BSEP inhibitior + 0.9943 99.43%
P-glycoprotein inhibitior + 0.8785 87.85%
P-glycoprotein substrate - 0.6280 62.80%
CYP3A4 substrate + 0.6860 68.60%
CYP2C9 substrate - 0.7795 77.95%
CYP2D6 substrate - 0.9021 90.21%
CYP3A4 inhibition - 0.5704 57.04%
CYP2C9 inhibition - 0.6396 63.96%
CYP2C19 inhibition + 0.5082 50.82%
CYP2D6 inhibition - 0.7164 71.64%
CYP1A2 inhibition + 0.6166 61.66%
CYP2C8 inhibition + 0.7339 73.39%
CYP inhibitory promiscuity + 0.8845 88.45%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.8648 86.48%
Carcinogenicity (trinary) Non-required 0.5252 52.52%
Eye corrosion - 0.9857 98.57%
Eye irritation - 0.9456 94.56%
Skin irritation - 0.7683 76.83%
Skin corrosion - 0.9317 93.17%
Ames mutagenesis - 0.5700 57.00%
Human Ether-a-go-go-Related Gene inhibition + 0.9303 93.03%
Micronuclear + 0.6000 60.00%
Hepatotoxicity + 0.6182 61.82%
skin sensitisation - 0.8225 82.25%
Respiratory toxicity + 0.7556 75.56%
Reproductive toxicity + 0.8111 81.11%
Mitochondrial toxicity + 0.8375 83.75%
Nephrotoxicity - 0.6544 65.44%
Acute Oral Toxicity (c) III 0.6924 69.24%
Estrogen receptor binding + 0.8235 82.35%
Androgen receptor binding + 0.7290 72.90%
Thyroid receptor binding + 0.6111 61.11%
Glucocorticoid receptor binding + 0.8225 82.25%
Aromatase binding + 0.7544 75.44%
PPAR gamma + 0.6915 69.15%
Honey bee toxicity - 0.8290 82.90%
Biodegradation - 0.9250 92.50%
Crustacea aquatic toxicity - 0.6200 62.00%
Fish aquatic toxicity + 0.9963 99.63%

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 98.59% 96.09%
CHEMBL240 Q12809 HERG 98.46% 89.76%
CHEMBL2581 P07339 Cathepsin D 97.10% 98.95%
CHEMBL1293249 Q13887 Kruppel-like factor 5 96.78% 86.33%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 95.69% 91.11%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 95.03% 85.14%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 94.18% 95.56%
CHEMBL4145 Q9UKV0 Histone deacetylase 9 93.34% 85.49%
CHEMBL1806 P11388 DNA topoisomerase II alpha 92.04% 89.00%
CHEMBL1937 Q92769 Histone deacetylase 2 90.21% 94.75%
CHEMBL2716 Q8WUI4 Histone deacetylase 7 90.14% 89.44%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 89.59% 99.23%
CHEMBL230 P35354 Cyclooxygenase-2 87.99% 89.63%
CHEMBL3807 P17706 T-cell protein-tyrosine phosphatase 86.67% 93.00%
CHEMBL301 P24941 Cyclin-dependent kinase 2 86.13% 91.23%
CHEMBL2288 Q13526 Peptidyl-prolyl cis-trans isomerase NIMA-interacting 1 85.72% 91.71%
CHEMBL255 P29275 Adenosine A2b receptor 85.56% 98.59%
CHEMBL2007 P16234 Platelet-derived growth factor receptor alpha 85.20% 91.07%
CHEMBL2563 Q9UQL6 Histone deacetylase 5 83.83% 89.67%
CHEMBL2378 P30307 Dual specificity phosphatase Cdc25C 83.15% 96.67%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 82.74% 94.00%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 82.65% 96.00%
CHEMBL3524 P56524 Histone deacetylase 4 82.61% 92.97%
CHEMBL5028 O14672 ADAM10 81.96% 97.50%
CHEMBL5103 Q969S8 Histone deacetylase 10 81.41% 90.08%

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 132570351
LOTUS LTS0266957
wikiData Q105017363