2-Amino-5-chlorohex-4-enoic acid

Details

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Internal ID 69799ef3-1284-4350-8c3a-75de7e724702
Taxonomy Organic acids and derivatives > Carboxylic acids and derivatives > Amino acids, peptides, and analogues > Alpha amino acids and derivatives > Alpha amino acids
IUPAC Name 2-amino-5-chlorohex-4-enoic acid
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C6H10ClNO2/c1-4(7)2-3-5(8)6(9)10/h2,5H,3,8H2,1H3,(H,9,10)
InChI Key AVAZRPNRSUVNKU-UHFFFAOYSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

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Molecular Formula C6H10ClNO2
Molecular Weight 163.60 g/mol
Exact Mass 163.0400063 g/mol
Topological Polar Surface Area (TPSA) 63.30 Ų
XlogP -1.60
Atomic LogP (AlogP) 0.93
H-Bond Acceptor 2
H-Bond Donor 2
Rotatable Bonds 3

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 2-Amino-5-chlorohex-4-enoic acid

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 1.0000 100.00%
Caco-2 - 0.8237 82.37%
Blood Brain Barrier + 0.7500 75.00%
Human oral bioavailability + 0.5571 55.71%
Subcellular localzation Lysosomes 0.6612 66.12%
OATP2B1 inhibitior - 0.8528 85.28%
OATP1B1 inhibitior + 0.9486 94.86%
OATP1B3 inhibitior + 0.9421 94.21%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.8000 80.00%
BSEP inhibitior - 0.8890 88.90%
P-glycoprotein inhibitior - 0.9877 98.77%
P-glycoprotein substrate - 0.9757 97.57%
CYP3A4 substrate - 0.6829 68.29%
CYP2C9 substrate - 0.5888 58.88%
CYP2D6 substrate - 0.8074 80.74%
CYP3A4 inhibition - 0.8786 87.86%
CYP2C9 inhibition - 0.8794 87.94%
CYP2C19 inhibition - 0.8940 89.40%
CYP2D6 inhibition - 0.9218 92.18%
CYP1A2 inhibition - 0.7157 71.57%
CYP2C8 inhibition - 0.9690 96.90%
CYP inhibitory promiscuity - 0.9715 97.15%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.5813 58.13%
Carcinogenicity (trinary) Non-required 0.6516 65.16%
Eye corrosion - 0.9503 95.03%
Eye irritation + 0.5510 55.10%
Skin irritation - 0.6302 63.02%
Skin corrosion - 0.5000 50.00%
Ames mutagenesis + 0.5500 55.00%
Human Ether-a-go-go-Related Gene inhibition - 0.8595 85.95%
Micronuclear - 0.6026 60.26%
Hepatotoxicity + 0.6750 67.50%
skin sensitisation - 0.8490 84.90%
Respiratory toxicity - 0.7667 76.67%
Reproductive toxicity - 0.5889 58.89%
Mitochondrial toxicity + 0.5125 51.25%
Nephrotoxicity - 0.6947 69.47%
Acute Oral Toxicity (c) III 0.6475 64.75%
Estrogen receptor binding - 0.9293 92.93%
Androgen receptor binding - 0.8604 86.04%
Thyroid receptor binding - 0.9172 91.72%
Glucocorticoid receptor binding - 0.8350 83.50%
Aromatase binding - 0.8926 89.26%
PPAR gamma - 0.8346 83.46%
Honey bee toxicity - 0.9007 90.07%
Biodegradation + 0.5750 57.50%
Crustacea aquatic toxicity - 0.8152 81.52%
Fish aquatic toxicity - 0.4013 40.13%

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
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 95.69% 96.95%
CHEMBL4040 P28482 MAP kinase ERK2 94.69% 83.82%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 93.52% 96.09%
CHEMBL3976 Q9UHL4 Dipeptidyl peptidase II 93.37% 92.29%
CHEMBL4657 Q6V1X1 Dipeptidyl peptidase VIII 90.41% 97.21%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 83.72% 94.45%
CHEMBL3060 Q9Y345 Glycine transporter 2 82.86% 99.17%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 81.00% 91.11%
CHEMBL340 P08684 Cytochrome P450 3A4 80.95% 91.19%
CHEMBL221 P23219 Cyclooxygenase-1 80.27% 90.17%

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 3016757
LOTUS LTS0009275
wikiData Q104919285