Rhinocladin B

Details

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Internal ID a899a21e-3886-48b4-bf98-2b9c8cee4a3e
Taxonomy Organoheterocyclic compounds > Indoles and derivatives > Indoles > 3-alkylindoles
IUPAC Name (3S,6S)-3-[[5-(3-methylbut-2-enyl)-1H-indol-3-yl]methyl]-6-(2-methylpropyl)piperazine-2,5-dione
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C22H29N3O2/c1-13(2)5-6-15-7-8-18-17(10-15)16(12-23-18)11-20-22(27)24-19(9-14(3)4)21(26)25-20/h5,7-8,10,12,14,19-20,23H,6,9,11H2,1-4H3,(H,24,27)(H,25,26)/t19-,20-/m0/s1
InChI Key OPJDHMQJVPIBCH-PMACEKPBSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C22H29N3O2
Molecular Weight 367.50 g/mol
Exact Mass 367.22597718 g/mol
Topological Polar Surface Area (TPSA) 74.00 Ų
XlogP 4.50
Atomic LogP (AlogP) 3.25
H-Bond Acceptor 2
H-Bond Donor 3
Rotatable Bonds 6

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of Rhinocladin B

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9967 99.67%
Caco-2 - 0.7013 70.13%
Blood Brain Barrier + 0.7250 72.50%
Human oral bioavailability - 0.6571 65.71%
Subcellular localzation Mitochondria 0.4409 44.09%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9101 91.01%
OATP1B3 inhibitior + 0.9373 93.73%
MATE1 inhibitior - 0.7868 78.68%
OCT2 inhibitior - 0.7399 73.99%
BSEP inhibitior + 0.9782 97.82%
P-glycoprotein inhibitior - 0.4312 43.12%
P-glycoprotein substrate + 0.7164 71.64%
CYP3A4 substrate + 0.5527 55.27%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8213 82.13%
CYP3A4 inhibition + 0.5676 56.76%
CYP2C9 inhibition + 0.5076 50.76%
CYP2C19 inhibition + 0.6158 61.58%
CYP2D6 inhibition - 0.8221 82.21%
CYP1A2 inhibition - 0.5620 56.20%
CYP2C8 inhibition - 0.8545 85.45%
CYP inhibitory promiscuity + 0.7919 79.19%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.9000 90.00%
Carcinogenicity (trinary) Non-required 0.5944 59.44%
Eye corrosion - 0.9899 98.99%
Eye irritation - 0.9921 99.21%
Skin irritation - 0.7906 79.06%
Skin corrosion - 0.9331 93.31%
Ames mutagenesis - 0.7500 75.00%
Human Ether-a-go-go-Related Gene inhibition + 0.8954 89.54%
Micronuclear + 0.7300 73.00%
Hepatotoxicity - 0.6625 66.25%
skin sensitisation - 0.8593 85.93%
Respiratory toxicity + 0.7556 75.56%
Reproductive toxicity + 0.8667 86.67%
Mitochondrial toxicity + 0.7375 73.75%
Nephrotoxicity - 0.8313 83.13%
Acute Oral Toxicity (c) III 0.5005 50.05%
Estrogen receptor binding - 0.4884 48.84%
Androgen receptor binding + 0.5292 52.92%
Thyroid receptor binding + 0.5813 58.13%
Glucocorticoid receptor binding - 0.4769 47.69%
Aromatase binding - 0.6049 60.49%
PPAR gamma + 0.6869 68.69%
Honey bee toxicity - 0.8113 81.13%
Biodegradation - 0.8750 87.50%
Crustacea aquatic toxicity - 0.6800 68.00%
Fish aquatic toxicity + 0.9303 93.03%

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
CHEMBL4040 P28482 MAP kinase ERK2 99.74% 83.82%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 99.01% 91.11%
CHEMBL2581 P07339 Cathepsin D 98.75% 98.95%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 98.36% 94.45%
CHEMBL3830 Q2M2I8 Adaptor-associated kinase 96.27% 83.10%
CHEMBL1951 P21397 Monoamine oxidase A 95.29% 91.49%
CHEMBL1937 Q92769 Histone deacetylase 2 94.02% 94.75%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 92.29% 96.09%
CHEMBL3837 P07711 Cathepsin L 92.08% 96.61%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 90.27% 92.62%
CHEMBL2535 P11166 Glucose transporter 88.47% 98.75%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 87.45% 95.56%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 87.04% 85.14%
CHEMBL255 P29275 Adenosine A2b receptor 86.74% 98.59%
CHEMBL5163 Q9NY46 Sodium channel protein type III alpha subunit 86.63% 96.90%
CHEMBL3401 O75469 Pregnane X receptor 86.45% 94.73%
CHEMBL1907605 P24864 Cyclin-dependent kinase 2/cyclin E1 85.44% 92.88%
CHEMBL3310 Q96DB2 Histone deacetylase 11 85.00% 88.56%
CHEMBL1829 O15379 Histone deacetylase 3 84.54% 95.00%
CHEMBL5103 Q969S8 Histone deacetylase 10 83.80% 90.08%
CHEMBL213 P08588 Beta-1 adrenergic receptor 82.90% 95.56%
CHEMBL5608 Q16288 NT-3 growth factor receptor 82.76% 95.89%
CHEMBL4051 P13569 Cystic fibrosis transmembrane conductance regulator 82.38% 95.71%
CHEMBL3155 P34969 Serotonin 7 (5-HT7) receptor 81.73% 90.71%
CHEMBL3492 P49721 Proteasome Macropain subunit 81.38% 90.24%
CHEMBL1255126 O15151 Protein Mdm4 80.19% 90.20%
CHEMBL1806 P11388 DNA topoisomerase II alpha 80.14% 89.00%

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 139584593
LOTUS LTS0031731
wikiData Q77372024