Cephalimysin B

Details

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Internal ID 32b05f80-f540-4ce5-aa77-fc8a6cb54c86
Taxonomy Organic oxygen compounds > Organooxygen compounds > Carbonyl compounds > Phenylketones > Alkyl-phenylketones
IUPAC Name (5S,8S,9S)-8-benzoyl-2-(5-ethylfuran-2-yl)-9-hydroxy-8-methoxy-3-methyl-1-oxa-7-azaspiro[4.4]non-2-ene-4,6-dione
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C22H21NO7/c1-4-14-10-11-15(29-14)16-12(2)17(24)21(30-16)19(26)22(28-3,23-20(21)27)18(25)13-8-6-5-7-9-13/h5-11,19,26H,4H2,1-3H3,(H,23,27)/t19-,21+,22+/m0/s1
InChI Key PXIIDWGMSCTXAQ-KSEOMHKRSA-N
Popularity 3 references in papers

Physical and Chemical Properties

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Molecular Formula C22H21NO7
Molecular Weight 411.40 g/mol
Exact Mass 411.13180201 g/mol
Topological Polar Surface Area (TPSA) 115.00 Ų
XlogP 2.30
Atomic LogP (AlogP) 1.63
H-Bond Acceptor 7
H-Bond Donor 2
Rotatable Bonds 5

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of Cephalimysin B

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.8850 88.50%
Caco-2 - 0.6709 67.09%
Blood Brain Barrier - 0.6750 67.50%
Human oral bioavailability - 0.5286 52.86%
Subcellular localzation Mitochondria 0.4445 44.45%
OATP2B1 inhibitior - 0.8580 85.80%
OATP1B1 inhibitior + 0.8977 89.77%
OATP1B3 inhibitior + 0.9322 93.22%
MATE1 inhibitior - 0.7800 78.00%
OCT2 inhibitior - 0.9750 97.50%
BSEP inhibitior + 0.5977 59.77%
P-glycoprotein inhibitior + 0.6913 69.13%
P-glycoprotein substrate - 0.5627 56.27%
CYP3A4 substrate + 0.5726 57.26%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8535 85.35%
CYP3A4 inhibition - 0.8360 83.60%
CYP2C9 inhibition - 0.8460 84.60%
CYP2C19 inhibition - 0.8580 85.80%
CYP2D6 inhibition - 0.9139 91.39%
CYP1A2 inhibition - 0.8527 85.27%
CYP2C8 inhibition + 0.7280 72.80%
CYP inhibitory promiscuity - 0.8029 80.29%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.8243 82.43%
Carcinogenicity (trinary) Non-required 0.5362 53.62%
Eye corrosion - 0.9885 98.85%
Eye irritation - 0.9699 96.99%
Skin irritation - 0.7976 79.76%
Skin corrosion - 0.9381 93.81%
Ames mutagenesis - 0.5500 55.00%
Human Ether-a-go-go-Related Gene inhibition - 0.3814 38.14%
Micronuclear + 0.7759 77.59%
Hepatotoxicity + 0.6728 67.28%
skin sensitisation - 0.8277 82.77%
Respiratory toxicity + 0.8222 82.22%
Reproductive toxicity + 0.7556 75.56%
Mitochondrial toxicity + 0.7500 75.00%
Nephrotoxicity - 0.7882 78.82%
Acute Oral Toxicity (c) III 0.5773 57.73%
Estrogen receptor binding + 0.6297 62.97%
Androgen receptor binding + 0.7129 71.29%
Thyroid receptor binding - 0.5000 50.00%
Glucocorticoid receptor binding + 0.6890 68.90%
Aromatase binding - 0.5152 51.52%
PPAR gamma + 0.7025 70.25%
Honey bee toxicity - 0.8175 81.75%
Biodegradation - 0.9000 90.00%
Crustacea aquatic toxicity - 0.6900 69.00%
Fish aquatic toxicity + 0.6460 64.60%

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
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 94.54% 85.14%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 93.95% 95.56%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 93.54% 91.11%
CHEMBL2581 P07339 Cathepsin D 92.98% 98.95%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 92.81% 96.95%
CHEMBL1293277 O15118 Niemann-Pick C1 protein 92.36% 81.11%
CHEMBL1293249 Q13887 Kruppel-like factor 5 91.40% 86.33%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 91.00% 99.23%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 90.64% 96.09%
CHEMBL221 P23219 Cyclooxygenase-1 86.73% 90.17%
CHEMBL4208 P20618 Proteasome component C5 86.32% 90.00%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 85.35% 94.00%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 83.21% 95.50%
CHEMBL3137262 O60341 LSD1/CoREST complex 82.99% 97.09%
CHEMBL5028 O14672 ADAM10 82.78% 97.50%
CHEMBL4657 Q6V1X1 Dipeptidyl peptidase VIII 82.69% 97.21%
CHEMBL2535 P11166 Glucose transporter 82.10% 98.75%
CHEMBL3401 O75469 Pregnane X receptor 81.88% 94.73%

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 46844969
LOTUS LTS0150456
wikiData Q77372433