Benthocyanin A

Details

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Internal ID 17de0a97-6123-48b2-b6db-d8a6239d49c8
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Terpene lactones
IUPAC Name 5-(3,7-dimethylocta-2,6-dienyl)-2-oxo-3-phenylfuro[3,2-i]phenazine-9-carboxylic acid
SMILES (Canonical) CC(=CCCC(=CCN1C2=CC=CC(=C2N=C3C1=CC4=C(C(=O)OC4=C3)C5=CC=CC=C5)C(=O)O)C)C
SMILES (Isomeric) CC(=CCCC(=CCN1C2=CC=CC(=C2N=C3C1=CC4=C(C(=O)OC4=C3)C5=CC=CC=C5)C(=O)O)C)C
InChI InChI=1S/C31H28N2O4/c1-19(2)9-7-10-20(3)15-16-33-25-14-8-13-22(30(34)35)29(25)32-24-18-27-23(17-26(24)33)28(31(36)37-27)21-11-5-4-6-12-21/h4-6,8-9,11-15,17-18H,7,10,16H2,1-3H3,(H,34,35)
InChI Key KRDKFSFTOURVBO-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C31H28N2O4
Molecular Weight 492.60 g/mol
Exact Mass 492.20490738 g/mol
Topological Polar Surface Area (TPSA) 79.20 Ų
XlogP 6.20
Atomic LogP (AlogP) 7.35
H-Bond Acceptor 5
H-Bond Donor 1
Rotatable Bonds 7

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of Benthocyanin A

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9309 93.09%
Caco-2 - 0.8716 87.16%
Blood Brain Barrier + 0.7250 72.50%
Human oral bioavailability - 0.5000 50.00%
Subcellular localzation Mitochondria 0.8160 81.60%
OATP2B1 inhibitior - 0.8434 84.34%
OATP1B1 inhibitior + 0.9104 91.04%
OATP1B3 inhibitior + 0.9011 90.11%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.6750 67.50%
BSEP inhibitior + 0.9905 99.05%
P-glycoprotein inhibitior + 0.8466 84.66%
P-glycoprotein substrate + 0.5314 53.14%
CYP3A4 substrate + 0.5927 59.27%
CYP2C9 substrate - 0.6277 62.77%
CYP2D6 substrate - 0.9088 90.88%
CYP3A4 inhibition + 0.5457 54.57%
CYP2C9 inhibition - 0.6022 60.22%
CYP2C19 inhibition - 0.6535 65.35%
CYP2D6 inhibition - 0.7738 77.38%
CYP1A2 inhibition + 0.5147 51.47%
CYP2C8 inhibition + 0.7573 75.73%
CYP inhibitory promiscuity + 0.5102 51.02%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.9500 95.00%
Carcinogenicity (trinary) Non-required 0.5871 58.71%
Eye corrosion - 0.9889 98.89%
Eye irritation - 0.9157 91.57%
Skin irritation - 0.7878 78.78%
Skin corrosion - 0.9389 93.89%
Ames mutagenesis - 0.5100 51.00%
Human Ether-a-go-go-Related Gene inhibition + 0.8140 81.40%
Micronuclear + 0.6200 62.00%
Hepatotoxicity + 0.5426 54.26%
skin sensitisation - 0.8675 86.75%
Respiratory toxicity + 0.7333 73.33%
Reproductive toxicity + 0.7556 75.56%
Mitochondrial toxicity + 0.7625 76.25%
Nephrotoxicity - 0.6811 68.11%
Acute Oral Toxicity (c) III 0.7480 74.80%
Estrogen receptor binding + 0.8786 87.86%
Androgen receptor binding + 0.7983 79.83%
Thyroid receptor binding + 0.6736 67.36%
Glucocorticoid receptor binding + 0.8372 83.72%
Aromatase binding + 0.7265 72.65%
PPAR gamma + 0.8325 83.25%
Honey bee toxicity - 0.8413 84.13%
Biodegradation - 0.9250 92.50%
Crustacea aquatic toxicity - 0.7200 72.00%
Fish aquatic toxicity + 1.0000 100.00%

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
CHEMBL2581 P07339 Cathepsin D 98.89% 98.95%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 98.24% 85.14%
CHEMBL4769 O95749 Geranylgeranyl pyrophosphate synthetase 98.19% 92.08%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 97.24% 99.23%
CHEMBL1293249 Q13887 Kruppel-like factor 5 96.87% 86.33%
CHEMBL3401 O75469 Pregnane X receptor 95.16% 94.73%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 94.47% 95.56%
CHEMBL1293294 P51151 Ras-related protein Rab-9A 92.48% 87.67%
CHEMBL1811 P34995 Prostanoid EP1 receptor 92.14% 95.71%
CHEMBL1806 P11388 DNA topoisomerase II alpha 91.78% 89.00%
CHEMBL3807 P17706 T-cell protein-tyrosine phosphatase 91.72% 93.00%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 88.71% 91.11%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 88.51% 95.50%
CHEMBL2716 Q8WUI4 Histone deacetylase 7 86.31% 89.44%
CHEMBL2107 P61073 C-X-C chemokine receptor type 4 86.23% 93.10%
CHEMBL3864 Q06124 Protein-tyrosine phosphatase 2C 86.13% 94.42%
CHEMBL3060 Q9Y345 Glycine transporter 2 85.27% 99.17%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 84.07% 96.00%
CHEMBL2378 P30307 Dual specificity phosphatase Cdc25C 83.42% 96.67%
CHEMBL1293277 O15118 Niemann-Pick C1 protein 81.74% 81.11%
CHEMBL3891 P07384 Calpain 1 81.67% 93.04%

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 73817716
LOTUS LTS0174814
wikiData Q77375256