2-(10-Hydroxydec-8-en-2,4,6-triynoylamino)acetic acid

Details

Top
Internal ID ac9975f6-41d4-4647-93e7-078a218e7746
Taxonomy Organic acids and derivatives > Carboxylic acids and derivatives > Amino acids, peptides, and analogues > N-acyl-alpha amino acids
IUPAC Name 2-(10-hydroxydec-8-en-2,4,6-triynoylamino)acetic acid
SMILES (Canonical) C(C=CC#CC#CC#CC(=O)NCC(=O)O)O
SMILES (Isomeric) C(C=CC#CC#CC#CC(=O)NCC(=O)O)O
InChI InChI=1S/C12H9NO4/c14-9-7-5-3-1-2-4-6-8-11(15)13-10-12(16)17/h5,7,14H,9-10H2,(H,13,15)(H,16,17)
InChI Key OCCREIFXNSZZKA-UHFFFAOYSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

Top
Molecular Formula C12H9NO4
Molecular Weight 231.20 g/mol
Exact Mass 231.05315777 g/mol
Topological Polar Surface Area (TPSA) 86.60 Ų
XlogP 0.30
Atomic LogP (AlogP) -1.25
H-Bond Acceptor 3
H-Bond Donor 3
Rotatable Bonds 3

Synonyms

Top
There are no found synonyms.

2D Structure

Top
2D Structure of 2-(10-Hydroxydec-8-en-2,4,6-triynoylamino)acetic acid

3D Structure

Top

ADMET Properties (via admetSAR 2)

Top
Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.5935 59.35%
Caco-2 - 0.8286 82.86%
Blood Brain Barrier + 0.7500 75.00%
Human oral bioavailability - 0.5286 52.86%
Subcellular localzation Mitochondria 0.6727 67.27%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8724 87.24%
OATP1B3 inhibitior + 0.9395 93.95%
MATE1 inhibitior - 0.9200 92.00%
OCT2 inhibitior - 0.9500 95.00%
BSEP inhibitior - 0.9385 93.85%
P-glycoprotein inhibitior - 0.9015 90.15%
P-glycoprotein substrate - 0.8151 81.51%
CYP3A4 substrate - 0.6033 60.33%
CYP2C9 substrate + 0.5962 59.62%
CYP2D6 substrate - 0.8632 86.32%
CYP3A4 inhibition - 0.9152 91.52%
CYP2C9 inhibition - 0.9067 90.67%
CYP2C19 inhibition - 0.8864 88.64%
CYP2D6 inhibition - 0.9188 91.88%
CYP1A2 inhibition - 0.9132 91.32%
CYP2C8 inhibition - 0.9133 91.33%
CYP inhibitory promiscuity - 0.9800 98.00%
UGT catelyzed + 0.9000 90.00%
Carcinogenicity (binary) - 0.7600 76.00%
Carcinogenicity (trinary) Non-required 0.6833 68.33%
Eye corrosion - 0.8956 89.56%
Eye irritation - 0.8182 81.82%
Skin irritation - 0.7881 78.81%
Skin corrosion - 0.9622 96.22%
Ames mutagenesis - 0.6100 61.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7136 71.36%
Micronuclear - 0.5500 55.00%
Hepatotoxicity - 0.6447 64.47%
skin sensitisation - 0.9244 92.44%
Respiratory toxicity - 0.6222 62.22%
Reproductive toxicity - 0.7000 70.00%
Mitochondrial toxicity - 0.7500 75.00%
Nephrotoxicity - 0.5742 57.42%
Acute Oral Toxicity (c) III 0.6958 69.58%
Estrogen receptor binding - 0.8318 83.18%
Androgen receptor binding - 0.6539 65.39%
Thyroid receptor binding - 0.6473 64.73%
Glucocorticoid receptor binding - 0.7103 71.03%
Aromatase binding - 0.5509 55.09%
PPAR gamma - 0.5418 54.18%
Honey bee toxicity - 0.8884 88.84%
Biodegradation - 0.6250 62.50%
Crustacea aquatic toxicity - 0.7700 77.00%
Fish aquatic toxicity - 0.8296 82.96%

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
CHEMBL4040 P28482 MAP kinase ERK2 97.36% 83.82%
CHEMBL2581 P07339 Cathepsin D 89.00% 98.95%
CHEMBL3060 Q9Y345 Glycine transporter 2 88.85% 99.17%
CHEMBL221 P23219 Cyclooxygenase-1 88.47% 90.17%
CHEMBL1293267 Q9HC97 G-protein coupled receptor 35 87.80% 89.34%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 84.12% 96.00%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 83.24% 96.09%
CHEMBL1938211 O15054 Lysine-specific demethylase 6B 81.45% 83.33%
CHEMBL2964 P36507 Dual specificity mitogen-activated protein kinase kinase 2 80.82% 80.00%
CHEMBL1907591 P30926 Neuronal acetylcholine receptor; alpha4/beta4 80.10% 100.00%

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 163039284
LOTUS LTS0232417
wikiData Q105189304