Antibiotic FR 29038

Details

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Internal ID a1ba9cdb-37bf-44e1-8481-651cd0854910
Taxonomy Organic acids and derivatives > Carboxylic acids and derivatives > Amino acids, peptides, and analogues > Peptides > Oligopeptides
IUPAC Name (2R)-2-amino-4-[4-[(1R)-1-amino-2-[[(3S)-1-[(R)-carboxy-(4-hydroxyphenyl)methyl]-2-oxoazetidin-3-yl]amino]-2-oxoethyl]phenoxy]butanoic acid
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C23H26N4O8/c24-16(22(31)32)9-10-35-15-7-3-12(4-8-15)18(25)20(29)26-17-11-27(21(17)30)19(23(33)34)13-1-5-14(28)6-2-13/h1-8,16-19,28H,9-11,24-25H2,(H,26,29)(H,31,32)(H,33,34)/t16-,17+,18-,19-/m1/s1
InChI Key CWTCWGGPTVMMLT-FCGDIQPGSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C23H26N4O8
Molecular Weight 486.50 g/mol
Exact Mass 486.17506380 g/mol
Topological Polar Surface Area (TPSA) 206.00 Ų
XlogP -4.90
Atomic LogP (AlogP) -0.27
H-Bond Acceptor 8
H-Bond Donor 6
Rotatable Bonds 11

Synonyms

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(-)-nocardicin C
C17351
Q27154979
(2R)-2-amino-4-[4-[(1R)-1-amino-2-[[(3S)-1-[(R)-carboxy-(4-hydroxyphenyl)methyl]-2-oxoazetidin-3-yl]amino]-2-oxoethyl]phenoxy]butanoic acid
O-{4-[(1R)-1-amino-2-({(3S)-1-[(R)-carboxy(4-hydroxyphenyl)methyl]-2-oxoazetidin-3-yl}amino)-2-oxoethyl]phenyl}-D-homoserine

2D Structure

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2D Structure of Antibiotic FR 29038

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption - 0.7172 71.72%
Caco-2 - 0.9052 90.52%
Blood Brain Barrier - 0.8500 85.00%
Human oral bioavailability + 0.5714 57.14%
Subcellular localzation Mitochondria 0.5671 56.71%
OATP2B1 inhibitior - 0.8599 85.99%
OATP1B1 inhibitior + 0.9304 93.04%
OATP1B3 inhibitior + 0.9334 93.34%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.9317 93.17%
BSEP inhibitior + 0.5814 58.14%
P-glycoprotein inhibitior + 0.6347 63.47%
P-glycoprotein substrate + 0.6734 67.34%
CYP3A4 substrate + 0.6205 62.05%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.7770 77.70%
CYP3A4 inhibition - 0.7871 78.71%
CYP2C9 inhibition - 0.8677 86.77%
CYP2C19 inhibition - 0.6542 65.42%
CYP2D6 inhibition - 0.8268 82.68%
CYP1A2 inhibition - 0.9230 92.30%
CYP2C8 inhibition - 0.6335 63.35%
CYP inhibitory promiscuity - 0.9035 90.35%
UGT catelyzed + 0.6362 63.62%
Carcinogenicity (binary) - 0.8300 83.00%
Carcinogenicity (trinary) Non-required 0.6192 61.92%
Eye corrosion - 0.9894 98.94%
Eye irritation - 0.9645 96.45%
Skin irritation - 0.7723 77.23%
Skin corrosion - 0.9388 93.88%
Ames mutagenesis - 0.6700 67.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4807 48.07%
Micronuclear + 0.9400 94.00%
Hepatotoxicity + 0.5920 59.20%
skin sensitisation - 0.8986 89.86%
Respiratory toxicity + 0.8889 88.89%
Reproductive toxicity + 0.8556 85.56%
Mitochondrial toxicity + 0.9125 91.25%
Nephrotoxicity - 0.6968 69.68%
Acute Oral Toxicity (c) III 0.5812 58.12%
Estrogen receptor binding + 0.6629 66.29%
Androgen receptor binding + 0.8453 84.53%
Thyroid receptor binding - 0.5000 50.00%
Glucocorticoid receptor binding + 0.6149 61.49%
Aromatase binding - 0.6382 63.82%
PPAR gamma + 0.6380 63.80%
Honey bee toxicity - 0.8819 88.19%
Biodegradation - 0.8000 80.00%
Crustacea aquatic toxicity - 0.7150 71.50%
Fish aquatic toxicity - 0.4429 44.29%

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
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 98.67% 96.09%
CHEMBL2581 P07339 Cathepsin D 96.01% 98.95%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 96.01% 91.11%
CHEMBL3060 Q9Y345 Glycine transporter 2 95.80% 99.17%
CHEMBL3137262 O60341 LSD1/CoREST complex 94.27% 97.09%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 93.76% 99.15%
CHEMBL4208 P20618 Proteasome component C5 93.08% 90.00%
CHEMBL3437 Q16853 Amine oxidase, copper containing 92.55% 94.00%
CHEMBL2035 P08912 Muscarinic acetylcholine receptor M5 91.71% 94.62%
CHEMBL236 P41143 Delta opioid receptor 91.36% 99.35%
CHEMBL226 P30542 Adenosine A1 receptor 89.12% 95.93%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 88.47% 94.45%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 87.91% 90.71%
CHEMBL211 P08172 Muscarinic acetylcholine receptor M2 87.18% 94.97%
CHEMBL2107 P61073 C-X-C chemokine receptor type 4 86.94% 93.10%
CHEMBL5608 Q16288 NT-3 growth factor receptor 86.50% 95.89%
CHEMBL1907603 Q05586 Glutamate NMDA receptor; GRIN1/GRIN2B 85.65% 95.89%
CHEMBL3359 P21462 Formyl peptide receptor 1 84.17% 93.56%
CHEMBL242 Q92731 Estrogen receptor beta 84.08% 98.35%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 83.16% 95.56%
CHEMBL3891 P07384 Calpain 1 82.00% 93.04%
CHEMBL2563 Q9UQL6 Histone deacetylase 5 81.81% 89.67%
CHEMBL4330 Q9NS75 Cysteinyl leukotriene receptor 2 81.21% 98.00%
CHEMBL2335 P42785 Lysosomal Pro-X carboxypeptidase 81.07% 100.00%
CHEMBL3976 Q9UHL4 Dipeptidyl peptidase II 80.44% 92.29%

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 13770100
LOTUS LTS0171692
wikiData Q27154979