Bacillamidin E

Details

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Internal ID d6a9f7d5-e480-473b-8035-6252d0aa130e
Taxonomy Organoheterocyclic compounds > Benzopyrans > 2-benzopyrans
IUPAC Name N-[(2S,3S)-2-[(1S)-1-hydroxy-2-[[(1S)-1-[(3S)-8-hydroxy-1-oxo-3,4-dihydroisochromen-3-yl]-3-methylbutyl]amino]-2-oxoethyl]-5-oxooxolan-3-yl]-13-methyltetradecanamide
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C35H54N2O8/c1-22(2)15-12-10-8-6-5-7-9-11-13-18-29(39)36-26-21-30(40)45-33(26)32(41)34(42)37-25(19-23(3)4)28-20-24-16-14-17-27(38)31(24)35(43)44-28/h14,16-17,22-23,25-26,28,32-33,38,41H,5-13,15,18-21H2,1-4H3,(H,36,39)(H,37,42)/t25-,26-,28-,32-,33-/m0/s1
InChI Key BERAGSAGTUCEKR-MHMCFALESA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C35H54N2O8
Molecular Weight 630.80 g/mol
Exact Mass 630.38801669 g/mol
Topological Polar Surface Area (TPSA) 151.00 Ų
XlogP 8.60
Atomic LogP (AlogP) 5.11
H-Bond Acceptor 8
H-Bond Donor 4
Rotatable Bonds 19

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of Bacillamidin E

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.5655 56.55%
Caco-2 - 0.8509 85.09%
Blood Brain Barrier - 0.9500 95.00%
Human oral bioavailability - 0.7429 74.29%
Subcellular localzation Mitochondria 0.6181 61.81%
OATP2B1 inhibitior + 0.7149 71.49%
OATP1B1 inhibitior + 0.8902 89.02%
OATP1B3 inhibitior + 0.8745 87.45%
MATE1 inhibitior - 0.8846 88.46%
OCT2 inhibitior - 0.8572 85.72%
BSEP inhibitior + 0.9437 94.37%
P-glycoprotein inhibitior + 0.7270 72.70%
P-glycoprotein substrate + 0.7824 78.24%
CYP3A4 substrate + 0.6968 69.68%
CYP2C9 substrate + 0.6154 61.54%
CYP2D6 substrate - 0.8429 84.29%
CYP3A4 inhibition - 0.7514 75.14%
CYP2C9 inhibition - 0.8940 89.40%
CYP2C19 inhibition - 0.8612 86.12%
CYP2D6 inhibition - 0.9157 91.57%
CYP1A2 inhibition - 0.9150 91.50%
CYP2C8 inhibition - 0.5684 56.84%
CYP inhibitory promiscuity - 0.7697 76.97%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.9800 98.00%
Carcinogenicity (trinary) Non-required 0.5718 57.18%
Eye corrosion - 0.9895 98.95%
Eye irritation - 0.9185 91.85%
Skin irritation - 0.7810 78.10%
Skin corrosion - 0.9346 93.46%
Ames mutagenesis - 0.6500 65.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5906 59.06%
Micronuclear + 0.7600 76.00%
Hepatotoxicity + 0.5625 56.25%
skin sensitisation - 0.8690 86.90%
Respiratory toxicity + 0.8111 81.11%
Reproductive toxicity + 0.9667 96.67%
Mitochondrial toxicity + 0.9500 95.00%
Nephrotoxicity + 0.7275 72.75%
Acute Oral Toxicity (c) III 0.5965 59.65%
Estrogen receptor binding + 0.8216 82.16%
Androgen receptor binding + 0.6842 68.42%
Thyroid receptor binding - 0.5525 55.25%
Glucocorticoid receptor binding + 0.6454 64.54%
Aromatase binding + 0.5503 55.03%
PPAR gamma + 0.6661 66.61%
Honey bee toxicity - 0.8766 87.66%
Biodegradation - 0.7750 77.50%
Crustacea aquatic toxicity + 0.5771 57.71%
Fish aquatic toxicity + 0.9628 96.28%

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 99.44% 98.95%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 98.77% 91.11%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 96.34% 94.45%
CHEMBL3359 P21462 Formyl peptide receptor 1 96.31% 93.56%
CHEMBL3060 Q9Y345 Glycine transporter 2 95.24% 99.17%
CHEMBL2094135 Q96BI3 Gamma-secretase 93.81% 98.05%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 92.60% 96.09%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 91.93% 90.71%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 91.91% 95.56%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 90.05% 99.23%
CHEMBL3401 O75469 Pregnane X receptor 89.86% 94.73%
CHEMBL3192 Q9BY41 Histone deacetylase 8 89.58% 93.99%
CHEMBL2996 Q05655 Protein kinase C delta 89.31% 97.79%
CHEMBL1806 P11388 DNA topoisomerase II alpha 88.12% 89.00%
CHEMBL3976 Q9UHL4 Dipeptidyl peptidase II 86.70% 92.29%
CHEMBL4478 Q00975 Voltage-gated N-type calcium channel alpha-1B subunit 85.41% 97.14%
CHEMBL1907 P15144 Aminopeptidase N 83.89% 93.31%
CHEMBL220 P22303 Acetylcholinesterase 82.89% 94.45%
CHEMBL3137262 O60341 LSD1/CoREST complex 82.57% 97.09%
CHEMBL4227 P25090 Lipoxin A4 receptor 82.38% 100.00%
CHEMBL4657 Q6V1X1 Dipeptidyl peptidase VIII 82.11% 97.21%
CHEMBL2179 P04062 Beta-glucocerebrosidase 80.63% 85.31%
CHEMBL1795139 Q8IU80 Transmembrane protease serine 6 80.63% 98.33%
CHEMBL2535 P11166 Glucose transporter 80.59% 98.75%
CHEMBL5028 O14672 ADAM10 80.53% 97.50%

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 139590721
LOTUS LTS0060489
wikiData Q104933405