Hybrubin A

Details

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Internal ID c13be373-25bd-43ad-b5b7-fd2b6aed8b12
Taxonomy Organic oxygen compounds > Organooxygen compounds > Ethers > Alkyl aryl ethers
IUPAC Name (3E,5Z)-5-ethylidene-3-[[3-methoxy-5-(1H-pyrrol-2-yl)-1H-pyrrol-2-yl]methylidene]pyrrolidine-2,4-dione
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C16H15N3O3/c1-3-10-15(20)9(16(21)19-10)7-13-14(22-2)8-12(18-13)11-5-4-6-17-11/h3-8,17-18H,1-2H3,(H,19,21)/b9-7+,10-3-
InChI Key AZKRVQZEPVBQDN-YJDFGWDTSA-N
Popularity 4 references in papers

Physical and Chemical Properties

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Molecular Formula C16H15N3O3
Molecular Weight 297.31 g/mol
Exact Mass 297.11134135 g/mol
Topological Polar Surface Area (TPSA) 87.00 Ų
XlogP 1.60
Atomic LogP (AlogP) 2.00
H-Bond Acceptor 3
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 Hybrubin A

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9911 99.11%
Caco-2 + 0.6473 64.73%
Blood Brain Barrier + 0.5750 57.50%
Human oral bioavailability + 0.7714 77.14%
Subcellular localzation Mitochondria 0.8441 84.41%
OATP2B1 inhibitior - 0.8565 85.65%
OATP1B1 inhibitior + 0.8988 89.88%
OATP1B3 inhibitior + 0.9425 94.25%
MATE1 inhibitior - 0.9200 92.00%
OCT2 inhibitior - 0.9321 93.21%
BSEP inhibitior + 0.6449 64.49%
P-glycoprotein inhibitior - 0.6362 63.62%
P-glycoprotein substrate - 0.7476 74.76%
CYP3A4 substrate + 0.5731 57.31%
CYP2C9 substrate - 0.5928 59.28%
CYP2D6 substrate - 0.8864 88.64%
CYP3A4 inhibition - 0.8409 84.09%
CYP2C9 inhibition - 0.6819 68.19%
CYP2C19 inhibition - 0.7383 73.83%
CYP2D6 inhibition - 0.9107 91.07%
CYP1A2 inhibition + 0.6138 61.38%
CYP2C8 inhibition - 0.5724 57.24%
CYP inhibitory promiscuity - 0.6491 64.91%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.8283 82.83%
Carcinogenicity (trinary) Non-required 0.5626 56.26%
Eye corrosion - 0.9844 98.44%
Eye irritation - 0.9201 92.01%
Skin irritation - 0.8501 85.01%
Skin corrosion - 0.9394 93.94%
Ames mutagenesis - 0.6300 63.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4174 41.74%
Micronuclear + 0.8600 86.00%
Hepatotoxicity - 0.5000 50.00%
skin sensitisation - 0.8951 89.51%
Respiratory toxicity - 0.5000 50.00%
Reproductive toxicity + 0.7000 70.00%
Mitochondrial toxicity + 0.6500 65.00%
Nephrotoxicity + 0.5392 53.92%
Acute Oral Toxicity (c) III 0.6200 62.00%
Estrogen receptor binding + 0.8264 82.64%
Androgen receptor binding + 0.5788 57.88%
Thyroid receptor binding + 0.6469 64.69%
Glucocorticoid receptor binding + 0.5810 58.10%
Aromatase binding + 0.6146 61.46%
PPAR gamma + 0.6903 69.03%
Honey bee toxicity - 0.7687 76.87%
Biodegradation - 1.0000 100.00%
Crustacea aquatic toxicity + 0.6204 62.04%
Fish aquatic toxicity + 0.7300 73.00%

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
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 97.31% 95.56%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 96.47% 94.45%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 95.20% 91.11%
CHEMBL2581 P07339 Cathepsin D 95.16% 98.95%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 91.56% 96.09%
CHEMBL4224 P49759 Dual specificty protein kinase CLK1 90.90% 85.30%
CHEMBL3192 Q9BY41 Histone deacetylase 8 90.29% 93.99%
CHEMBL1937 Q92769 Histone deacetylase 2 89.19% 94.75%
CHEMBL2535 P11166 Glucose transporter 88.51% 98.75%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 87.64% 94.00%
CHEMBL1293249 Q13887 Kruppel-like factor 5 84.61% 86.33%
CHEMBL2007 P16234 Platelet-derived growth factor receptor alpha 84.17% 91.07%
CHEMBL1255126 O15151 Protein Mdm4 83.59% 90.20%
CHEMBL4578 Q14680 Maternal embryonic leucine zipper kinase 82.70% 81.58%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 82.64% 96.00%
CHEMBL4225 P49760 Dual specificity protein kinase CLK2 81.72% 80.96%
CHEMBL4355 O14976 Serine/threonine-protein kinase GAK 81.64% 89.32%
CHEMBL4145 Q9UKV0 Histone deacetylase 9 81.49% 85.49%
CHEMBL4478 Q00975 Voltage-gated N-type calcium channel alpha-1B subunit 81.30% 97.14%
CHEMBL255 P29275 Adenosine A2b receptor 80.34% 98.59%

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 132559186
LOTUS LTS0016443
wikiData Q104921760