(2S,4R)-4-acetamidopiperidine-2-carboxylic acid

Details

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Internal ID b7298064-caf3-48ed-8c03-fec19a2b1073
Taxonomy Organic acids and derivatives > Carboxylic acids and derivatives > Amino acids, peptides, and analogues > Alpha amino acids and derivatives > Alpha amino acids > L-alpha-amino acids
IUPAC Name (2S,4R)-4-acetamidopiperidine-2-carboxylic acid
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C8H14N2O3/c1-5(11)10-6-2-3-9-7(4-6)8(12)13/h6-7,9H,2-4H2,1H3,(H,10,11)(H,12,13)/t6-,7+/m1/s1
InChI Key GOIIOCZFZDAMIJ-RQJHMYQMSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C8H14N2O3
Molecular Weight 186.21 g/mol
Exact Mass 186.10044231 g/mol
Topological Polar Surface Area (TPSA) 78.40 Ų
XlogP -3.00
Atomic LogP (AlogP) -0.67
H-Bond Acceptor 3
H-Bond Donor 3
Rotatable Bonds 2

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of (2S,4R)-4-acetamidopiperidine-2-carboxylic acid

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption - 0.6330 63.30%
Caco-2 - 0.8720 87.20%
Blood Brain Barrier - 0.5000 50.00%
Human oral bioavailability + 0.6143 61.43%
Subcellular localzation Mitochondria 0.7641 76.41%
OATP2B1 inhibitior - 0.8358 83.58%
OATP1B1 inhibitior + 0.9275 92.75%
OATP1B3 inhibitior + 0.9502 95.02%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.9750 97.50%
BSEP inhibitior - 0.9660 96.60%
P-glycoprotein inhibitior - 0.9921 99.21%
P-glycoprotein substrate - 0.6990 69.90%
CYP3A4 substrate - 0.5519 55.19%
CYP2C9 substrate - 0.8074 80.74%
CYP2D6 substrate - 0.7820 78.20%
CYP3A4 inhibition - 0.9689 96.89%
CYP2C9 inhibition - 0.9510 95.10%
CYP2C19 inhibition - 0.9606 96.06%
CYP2D6 inhibition - 0.9723 97.23%
CYP1A2 inhibition - 0.9391 93.91%
CYP2C8 inhibition - 0.9660 96.60%
CYP inhibitory promiscuity - 0.9958 99.58%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.9100 91.00%
Carcinogenicity (trinary) Non-required 0.7403 74.03%
Eye corrosion - 0.9734 97.34%
Eye irritation - 0.8834 88.34%
Skin irritation - 0.7760 77.60%
Skin corrosion - 0.9566 95.66%
Ames mutagenesis - 0.7000 70.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7661 76.61%
Micronuclear + 0.5800 58.00%
Hepatotoxicity + 0.8050 80.50%
skin sensitisation - 0.9203 92.03%
Respiratory toxicity - 0.5778 57.78%
Reproductive toxicity + 0.6556 65.56%
Mitochondrial toxicity + 0.5375 53.75%
Nephrotoxicity + 0.5558 55.58%
Acute Oral Toxicity (c) III 0.5997 59.97%
Estrogen receptor binding - 0.9086 90.86%
Androgen receptor binding - 0.7618 76.18%
Thyroid receptor binding - 0.7320 73.20%
Glucocorticoid receptor binding - 0.8506 85.06%
Aromatase binding - 0.8244 82.44%
PPAR gamma - 0.7665 76.65%
Honey bee toxicity - 0.9132 91.32%
Biodegradation + 0.6500 65.00%
Crustacea aquatic toxicity - 0.7300 73.00%
Fish aquatic toxicity - 0.7619 76.19%

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
CHEMBL4657 Q6V1X1 Dipeptidyl peptidase VIII 93.14% 97.21%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 93.12% 96.95%
CHEMBL4040 P28482 MAP kinase ERK2 91.93% 83.82%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 91.55% 96.09%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 91.21% 85.14%
CHEMBL340 P08684 Cytochrome P450 3A4 90.16% 91.19%
CHEMBL3137262 O60341 LSD1/CoREST complex 89.15% 97.09%
CHEMBL4979 P13866 Sodium/glucose cotransporter 1 84.93% 98.24%
CHEMBL2693 Q9UIQ6 Cystinyl aminopeptidase 82.37% 97.64%
CHEMBL2581 P07339 Cathepsin D 81.41% 98.95%
CHEMBL5255 O00206 Toll-like receptor 4 81.20% 92.50%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 80.27% 99.23%
CHEMBL2111367 P27986 PI3-kinase p110-alpha/p85-alpha 80.23% 94.33%
CHEMBL1907598 P05106 Integrin alpha-V/beta-3 80.01% 95.71%

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.
Calliandra haematocephala

Cross-Links

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PubChem 15607348
LOTUS LTS0141636
wikiData Q105013990