Acinetobactin

Details

Top
Internal ID 9135f50d-fa0a-412e-a891-39d61280484f
Taxonomy Organic acids and derivatives > Carboxylic acids and derivatives > Amino acids, peptides, and analogues > N-acyl-alpha amino acids and derivatives
IUPAC Name 2,3-dihydroxy-N-[(4S,5S)-2-[2-(1H-imidazol-5-yl)ethyl]-5-methyl-3-oxo-1,2-oxazolidin-4-yl]benzamide
SMILES (Canonical) CC1C(C(=O)N(O1)CCC2=CN=CN2)NC(=O)C3=C(C(=CC=C3)O)O
SMILES (Isomeric) C[C@H]1[C@@H](C(=O)N(O1)CCC2=CN=CN2)NC(=O)C3=C(C(=CC=C3)O)O
InChI InChI=1S/C16H18N4O5/c1-9-13(19-15(23)11-3-2-4-12(21)14(11)22)16(24)20(25-9)6-5-10-7-17-8-18-10/h2-4,7-9,13,21-22H,5-6H2,1H3,(H,17,18)(H,19,23)/t9-,13-/m0/s1
InChI Key YQXURFXJBIFMOA-ZANVPECISA-N
Popularity 27 references in papers

Physical and Chemical Properties

Top
Molecular Formula C16H18N4O5
Molecular Weight 346.34 g/mol
Exact Mass 346.12771969 g/mol
Topological Polar Surface Area (TPSA) 128.00 Ų
XlogP 1.00
Atomic LogP (AlogP) 0.32
H-Bond Acceptor 6
H-Bond Donor 4
Rotatable Bonds 5

Synonyms

Top
OPV
SCHEMBL31261766

2D Structure

Top
2D Structure of Acinetobactin

3D Structure

Top

ADMET Properties (via admetSAR 2)

Top
Target Value Probability (raw) Probability (%)
Human Intestinal Absorption - 0.5515 55.15%
Caco-2 + 0.5208 52.08%
Blood Brain Barrier - 0.5250 52.50%
Human oral bioavailability + 0.5429 54.29%
Subcellular localzation Mitochondria 0.4923 49.23%
OATP2B1 inhibitior - 0.8575 85.75%
OATP1B1 inhibitior + 0.8196 81.96%
OATP1B3 inhibitior + 0.9340 93.40%
MATE1 inhibitior - 0.9009 90.09%
OCT2 inhibitior - 0.8787 87.87%
BSEP inhibitior - 0.6159 61.59%
P-glycoprotein inhibitior - 0.7630 76.30%
P-glycoprotein substrate + 0.6550 65.50%
CYP3A4 substrate + 0.5879 58.79%
CYP2C9 substrate + 0.5815 58.15%
CYP2D6 substrate - 0.8742 87.42%
CYP3A4 inhibition + 0.6451 64.51%
CYP2C9 inhibition - 0.7624 76.24%
CYP2C19 inhibition - 0.7897 78.97%
CYP2D6 inhibition - 0.8990 89.90%
CYP1A2 inhibition - 0.8879 88.79%
CYP2C8 inhibition + 0.5000 50.00%
CYP inhibitory promiscuity - 0.8017 80.17%
UGT catelyzed + 0.8000 80.00%
Carcinogenicity (binary) - 0.7900 79.00%
Carcinogenicity (trinary) Non-required 0.5167 51.67%
Eye corrosion - 0.9862 98.62%
Eye irritation - 0.9919 99.19%
Skin irritation - 0.7822 78.22%
Skin corrosion - 0.9323 93.23%
Ames mutagenesis + 0.5500 55.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4855 48.55%
Micronuclear + 0.8800 88.00%
Hepatotoxicity + 0.6159 61.59%
skin sensitisation - 0.8630 86.30%
Respiratory toxicity + 0.9333 93.33%
Reproductive toxicity + 0.9778 97.78%
Mitochondrial toxicity + 0.9125 91.25%
Nephrotoxicity - 0.7927 79.27%
Acute Oral Toxicity (c) III 0.6658 66.58%
Estrogen receptor binding + 0.6143 61.43%
Androgen receptor binding + 0.6427 64.27%
Thyroid receptor binding - 0.6266 62.66%
Glucocorticoid receptor binding + 0.6238 62.38%
Aromatase binding + 0.5301 53.01%
PPAR gamma - 0.5512 55.12%
Honey bee toxicity - 0.8787 87.87%
Biodegradation - 0.8250 82.50%
Crustacea aquatic toxicity - 0.5900 59.00%
Fish aquatic toxicity - 0.5986 59.86%

Targets

Top

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 97.28% 96.09%
CHEMBL1293277 O15118 Niemann-Pick C1 protein 95.97% 81.11%
CHEMBL2581 P07339 Cathepsin D 94.81% 98.95%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 94.77% 99.23%
CHEMBL2096618 P11274 Bcr/Abl fusion protein 92.41% 85.83%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 92.41% 85.14%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 88.41% 95.56%
CHEMBL3038469 P24941 CDK2/Cyclin A 88.25% 91.38%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 88.10% 94.00%
CHEMBL1907600 Q00535 Cyclin-dependent kinase 5/CDK5 activator 1 86.53% 93.03%
CHEMBL255 P29275 Adenosine A2b receptor 86.19% 98.59%
CHEMBL1293267 Q9HC97 G-protein coupled receptor 35 84.13% 89.34%
CHEMBL3401 O75469 Pregnane X receptor 83.41% 94.73%
CHEMBL253 P34972 Cannabinoid CB2 receptor 83.23% 97.25%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 82.11% 91.11%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 81.93% 90.71%
CHEMBL1293249 Q13887 Kruppel-like factor 5 81.64% 86.33%
CHEMBL2535 P11166 Glucose transporter 80.03% 98.75%

Plants that contains it

Top
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

Top
PubChem 49802052
LOTUS LTS0086149
wikiData Q105269850