Microansamycin A

Details

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Internal ID def6c2e2-0041-4f1e-acf9-abe944ead080
Taxonomy Organoheterocyclic compounds > Indoles and derivatives > Indolines
IUPAC Name (4S,6S,8S,9R,12R,16S)-8-hydroxy-4,6-dimethyl-17-oxa-2-azatetracyclo[7.6.2.04,16.012,16]heptadec-1(15)-ene-3,5,14-trione
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C17H21NO5/c1-8-5-11(20)12-4-3-9-6-10(19)7-13-17(9,23-12)16(2,14(8)21)15(22)18-13/h7-9,11-12,20H,3-6H2,1-2H3,(H,18,22)/t8-,9+,11-,12+,16-,17+/m0/s1
InChI Key DMESAMBFWVWMAL-RXPMBABLSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C17H21NO5
Molecular Weight 319.40 g/mol
Exact Mass 319.14197277 g/mol
Topological Polar Surface Area (TPSA) 92.70 Ų
XlogP -0.40
Atomic LogP (AlogP) 0.48
H-Bond Acceptor 5
H-Bond Donor 2
Rotatable Bonds 0

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of Microansamycin A

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9624 96.24%
Caco-2 + 0.5576 55.76%
Blood Brain Barrier + 0.6500 65.00%
Human oral bioavailability + 0.5286 52.86%
Subcellular localzation Mitochondria 0.7657 76.57%
OATP2B1 inhibitior - 0.8605 86.05%
OATP1B1 inhibitior + 0.8855 88.55%
OATP1B3 inhibitior + 0.9451 94.51%
MATE1 inhibitior - 0.9200 92.00%
OCT2 inhibitior - 0.8029 80.29%
BSEP inhibitior - 0.9118 91.18%
P-glycoprotein inhibitior - 0.9012 90.12%
P-glycoprotein substrate - 0.5051 50.51%
CYP3A4 substrate + 0.6479 64.79%
CYP2C9 substrate - 0.7878 78.78%
CYP2D6 substrate - 0.8730 87.30%
CYP3A4 inhibition - 0.9600 96.00%
CYP2C9 inhibition - 0.8855 88.55%
CYP2C19 inhibition - 0.8605 86.05%
CYP2D6 inhibition - 0.9441 94.41%
CYP1A2 inhibition - 0.8444 84.44%
CYP2C8 inhibition - 0.7317 73.17%
CYP inhibitory promiscuity - 0.8953 89.53%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.9500 95.00%
Carcinogenicity (trinary) Danger 0.4324 43.24%
Eye corrosion - 0.9881 98.81%
Eye irritation - 0.9940 99.40%
Skin irritation - 0.7139 71.39%
Skin corrosion - 0.9158 91.58%
Ames mutagenesis - 0.7600 76.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6709 67.09%
Micronuclear + 0.6700 67.00%
Hepatotoxicity + 0.6427 64.27%
skin sensitisation - 0.8313 83.13%
Respiratory toxicity + 0.7889 78.89%
Reproductive toxicity + 0.9556 95.56%
Mitochondrial toxicity + 0.8250 82.50%
Nephrotoxicity - 0.6361 63.61%
Acute Oral Toxicity (c) III 0.4997 49.97%
Estrogen receptor binding + 0.5884 58.84%
Androgen receptor binding + 0.7118 71.18%
Thyroid receptor binding - 0.5078 50.78%
Glucocorticoid receptor binding + 0.7025 70.25%
Aromatase binding - 0.6016 60.16%
PPAR gamma - 0.7017 70.17%
Honey bee toxicity - 0.8796 87.96%
Biodegradation - 0.8000 80.00%
Crustacea aquatic toxicity + 0.6000 60.00%
Fish aquatic toxicity + 0.7398 73.98%

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
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 97.96% 91.11%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 96.49% 85.14%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 94.29% 96.09%
CHEMBL3137262 O60341 LSD1/CoREST complex 93.07% 97.09%
CHEMBL1994 P08235 Mineralocorticoid receptor 90.67% 100.00%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 89.82% 95.56%
CHEMBL253 P34972 Cannabinoid CB2 receptor 88.76% 97.25%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 87.66% 94.45%
CHEMBL241 Q14432 Phosphodiesterase 3A 86.84% 92.94%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 85.70% 99.23%
CHEMBL5608 Q16288 NT-3 growth factor receptor 84.49% 95.89%
CHEMBL1902 P62942 FK506-binding protein 1A 83.93% 97.05%
CHEMBL2581 P07339 Cathepsin D 82.71% 98.95%
CHEMBL1806 P11388 DNA topoisomerase II alpha 81.06% 89.00%
CHEMBL4303 P08238 Heat shock protein HSP 90-beta 80.94% 96.77%
CHEMBL2553 Q15418 Ribosomal protein S6 kinase alpha 1 80.85% 85.11%
CHEMBL1937 Q92769 Histone deacetylase 2 80.03% 94.75%

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 139591124
LOTUS LTS0258164
wikiData Q104985046