Microsporin A

Details

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Internal ID 5d313d19-0839-4d6e-9953-e556059d3741
Taxonomy Organic acids and derivatives > Carboxylic acids and derivatives > Amino acids, peptides, and analogues > Peptides > Oligopeptides
IUPAC Name (3S,6S,9S,12R)-3-benzyl-6-methyl-9-(6-oxooctyl)-1,4,7,10-tetrazabicyclo[10.4.0]hexadecane-2,5,8,11-tetrone
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C28H40N4O5/c1-3-21(33)14-8-5-9-15-22-26(35)29-19(2)25(34)31-23(18-20-12-6-4-7-13-20)28(37)32-17-11-10-16-24(32)27(36)30-22/h4,6-7,12-13,19,22-24H,3,5,8-11,14-18H2,1-2H3,(H,29,35)(H,30,36)(H,31,34)/t19-,22-,23-,24+/m0/s1
InChI Key DEUCVOIWOGPZGS-ZNEWLNCYSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

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Molecular Formula C28H40N4O5
Molecular Weight 512.60 g/mol
Exact Mass 512.29987039 g/mol
Topological Polar Surface Area (TPSA) 125.00 Ų
XlogP 2.60
Atomic LogP (AlogP) 2.03
H-Bond Acceptor 5
H-Bond Donor 3
Rotatable Bonds 9

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of Microsporin A

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.8467 84.67%
Caco-2 - 0.8487 84.87%
Blood Brain Barrier - 0.5250 52.50%
Human oral bioavailability - 0.6286 62.86%
Subcellular localzation Mitochondria 0.7006 70.06%
OATP2B1 inhibitior - 0.7230 72.30%
OATP1B1 inhibitior + 0.8615 86.15%
OATP1B3 inhibitior + 0.9316 93.16%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.8064 80.64%
BSEP inhibitior + 0.7718 77.18%
P-glycoprotein inhibitior + 0.8348 83.48%
P-glycoprotein substrate + 0.7965 79.65%
CYP3A4 substrate + 0.6423 64.23%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.7938 79.38%
CYP3A4 inhibition - 0.6434 64.34%
CYP2C9 inhibition - 0.8567 85.67%
CYP2C19 inhibition - 0.6719 67.19%
CYP2D6 inhibition - 0.8865 88.65%
CYP1A2 inhibition - 0.9691 96.91%
CYP2C8 inhibition + 0.5431 54.31%
CYP inhibitory promiscuity - 0.9035 90.35%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.9200 92.00%
Carcinogenicity (trinary) Non-required 0.6932 69.32%
Eye corrosion - 0.9931 99.31%
Eye irritation - 0.9662 96.62%
Skin irritation - 0.8016 80.16%
Skin corrosion - 0.9400 94.00%
Ames mutagenesis - 0.7700 77.00%
Human Ether-a-go-go-Related Gene inhibition + 0.7667 76.67%
Micronuclear + 0.8100 81.00%
Hepatotoxicity + 0.5625 56.25%
skin sensitisation - 0.9155 91.55%
Respiratory toxicity + 0.8667 86.67%
Reproductive toxicity + 0.9333 93.33%
Mitochondrial toxicity + 0.9625 96.25%
Nephrotoxicity - 0.7079 70.79%
Acute Oral Toxicity (c) III 0.6572 65.72%
Estrogen receptor binding + 0.5558 55.58%
Androgen receptor binding - 0.5434 54.34%
Thyroid receptor binding - 0.6194 61.94%
Glucocorticoid receptor binding - 0.5121 51.21%
Aromatase binding - 0.6226 62.26%
PPAR gamma - 0.5078 50.78%
Honey bee toxicity - 0.9260 92.60%
Biodegradation - 0.6750 67.50%
Crustacea aquatic toxicity + 0.6400 64.00%
Fish aquatic toxicity + 0.7056 70.56%

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 99.72% 98.95%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 98.95% 96.09%
CHEMBL2693 Q9UIQ6 Cystinyl aminopeptidase 95.89% 97.64%
CHEMBL3524 P56524 Histone deacetylase 4 94.48% 92.97%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 92.80% 95.56%
CHEMBL1907600 Q00535 Cyclin-dependent kinase 5/CDK5 activator 1 91.49% 93.03%
CHEMBL1902 P62942 FK506-binding protein 1A 90.90% 97.05%
CHEMBL2288 Q13526 Peptidyl-prolyl cis-trans isomerase NIMA-interacting 1 90.01% 91.71%
CHEMBL3807 P17706 T-cell protein-tyrosine phosphatase 89.98% 93.00%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 89.81% 91.11%
CHEMBL2069156 Q14145 Kelch-like ECH-associated protein 1 89.42% 82.38%
CHEMBL1293249 Q13887 Kruppel-like factor 5 85.81% 86.33%
CHEMBL5608 Q16288 NT-3 growth factor receptor 85.66% 95.89%
CHEMBL325 Q13547 Histone deacetylase 1 85.24% 95.92%
CHEMBL4026 P40763 Signal transducer and activator of transcription 3 83.74% 82.69%
CHEMBL3137262 O60341 LSD1/CoREST complex 83.72% 97.09%
CHEMBL5103 Q969S8 Histone deacetylase 10 83.69% 90.08%
CHEMBL4040 P28482 MAP kinase ERK2 82.74% 83.82%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 82.27% 99.23%
CHEMBL253 P34972 Cannabinoid CB2 receptor 81.88% 97.25%
CHEMBL3060 Q9Y345 Glycine transporter 2 80.82% 99.17%
CHEMBL2095172 P14867 GABA-A receptor; alpha-1/beta-2/gamma-2 80.73% 92.67%
CHEMBL5805 Q9NR97 Toll-like receptor 8 80.31% 96.25%

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 132596108
LOTUS LTS0101127
wikiData Q104977531