Alaremycin

Details

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Internal ID a3fc33f9-b79e-465b-b537-f89300f2caed
Taxonomy Organic acids and derivatives > Keto acids and derivatives > Medium-chain keto acids and derivatives
IUPAC Name 5-acetamido-4-oxohex-5-enoic acid
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C8H11NO4/c1-5(9-6(2)10)7(11)3-4-8(12)13/h1,3-4H2,2H3,(H,9,10)(H,12,13)
InChI Key JRLAQUJSYKXZFV-UHFFFAOYSA-N
Popularity 4 references in papers

Physical and Chemical Properties

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Molecular Formula C8H11NO4
Molecular Weight 185.18 g/mol
Exact Mass 185.06880783 g/mol
Topological Polar Surface Area (TPSA) 83.50 Ų
XlogP -0.60
Atomic LogP (AlogP) 0.07
H-Bond Acceptor 3
H-Bond Donor 2
Rotatable Bonds 5

Synonyms

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SCHEMBL4541809
CHEMBL1213164
5-acetamido-4-oxohex-5-enoic acid

2D Structure

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2D Structure of Alaremycin

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.6673 66.73%
Caco-2 - 0.7121 71.21%
Blood Brain Barrier + 0.7500 75.00%
Human oral bioavailability + 0.7429 74.29%
Subcellular localzation Mitochondria 0.8369 83.69%
OATP2B1 inhibitior - 0.8528 85.28%
OATP1B1 inhibitior + 0.9255 92.55%
OATP1B3 inhibitior + 0.9439 94.39%
MATE1 inhibitior - 0.9200 92.00%
OCT2 inhibitior - 0.9572 95.72%
BSEP inhibitior - 0.9869 98.69%
P-glycoprotein inhibitior - 0.9766 97.66%
P-glycoprotein substrate - 0.9359 93.59%
CYP3A4 substrate - 0.6610 66.10%
CYP2C9 substrate - 0.5905 59.05%
CYP2D6 substrate - 0.8788 87.88%
CYP3A4 inhibition - 0.7999 79.99%
CYP2C9 inhibition - 0.7993 79.93%
CYP2C19 inhibition - 0.8884 88.84%
CYP2D6 inhibition - 0.9300 93.00%
CYP1A2 inhibition - 0.8780 87.80%
CYP2C8 inhibition - 0.9786 97.86%
CYP inhibitory promiscuity - 0.9377 93.77%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.8411 84.11%
Carcinogenicity (trinary) Non-required 0.6426 64.26%
Eye corrosion - 0.9757 97.57%
Eye irritation + 0.7268 72.68%
Skin irritation - 0.8131 81.31%
Skin corrosion - 0.8778 87.78%
Ames mutagenesis - 0.7400 74.00%
Human Ether-a-go-go-Related Gene inhibition - 0.8042 80.42%
Micronuclear + 0.5300 53.00%
Hepatotoxicity + 0.5250 52.50%
skin sensitisation - 0.9257 92.57%
Respiratory toxicity - 0.6222 62.22%
Reproductive toxicity - 0.7941 79.41%
Mitochondrial toxicity - 0.5125 51.25%
Nephrotoxicity + 0.6021 60.21%
Acute Oral Toxicity (c) III 0.6706 67.06%
Estrogen receptor binding - 0.8646 86.46%
Androgen receptor binding - 0.9224 92.24%
Thyroid receptor binding - 0.9159 91.59%
Glucocorticoid receptor binding - 0.8137 81.37%
Aromatase binding - 0.8113 81.13%
PPAR gamma - 0.8495 84.95%
Honey bee toxicity - 0.9658 96.58%
Biodegradation + 0.6000 60.00%
Crustacea aquatic toxicity - 0.9300 93.00%
Fish aquatic toxicity - 0.6144 61.44%

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
CHEMBL4040 P28482 MAP kinase ERK2 99.55% 83.82%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 91.83% 96.09%
CHEMBL2581 P07339 Cathepsin D 90.58% 98.95%
CHEMBL3060 Q9Y345 Glycine transporter 2 86.44% 99.17%
CHEMBL340 P08684 Cytochrome P450 3A4 83.56% 91.19%
CHEMBL2111367 P27986 PI3-kinase p110-alpha/p85-alpha 80.72% 94.33%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 80.12% 91.11%

Plants that contains it

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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

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PubChem 11715298
LOTUS LTS0251835
wikiData Q77519097