N-(3-Carboxy-3-hydroxypropyl)-L-homoserine, 9CI

Details

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Internal ID 7f1e2633-cf63-4f28-819d-1e58c4aff474
Taxonomy Organic acids and derivatives > Carboxylic acids and derivatives > Amino acids, peptides, and analogues > Amino acids and derivatives > Gamma amino acids and derivatives
IUPAC Name 4-[(1-carboxy-3-hydroxypropyl)amino]-2-hydroxybutanoic acid
SMILES (Canonical) C(CNC(CCO)C(=O)O)C(C(=O)O)O
SMILES (Isomeric) C(CNC(CCO)C(=O)O)C(C(=O)O)O
InChI InChI=1S/C8H15NO6/c10-4-2-5(7(12)13)9-3-1-6(11)8(14)15/h5-6,9-11H,1-4H2,(H,12,13)(H,14,15)
InChI Key YVTYLIZWVFUUMH-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C8H15NO6
Molecular Weight 221.21 g/mol
Exact Mass 221.08993720 g/mol
Topological Polar Surface Area (TPSA) 127.00 Ų
XlogP -3.90
Atomic LogP (AlogP) -1.75
H-Bond Acceptor 5
H-Bond Donor 5
Rotatable Bonds 8

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of N-(3-Carboxy-3-hydroxypropyl)-L-homoserine, 9CI

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption - 0.7552 75.52%
Caco-2 - 0.9222 92.22%
Blood Brain Barrier - 0.5500 55.00%
Human oral bioavailability - 0.5714 57.14%
Subcellular localzation Mitochondria 0.7158 71.58%
OATP2B1 inhibitior - 0.8425 84.25%
OATP1B1 inhibitior + 0.9369 93.69%
OATP1B3 inhibitior + 0.9082 90.82%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.9000 90.00%
BSEP inhibitior - 0.9786 97.86%
P-glycoprotein inhibitior - 0.9846 98.46%
P-glycoprotein substrate - 0.8979 89.79%
CYP3A4 substrate - 0.6644 66.44%
CYP2C9 substrate - 0.6000 60.00%
CYP2D6 substrate - 0.7587 75.87%
CYP3A4 inhibition - 0.9776 97.76%
CYP2C9 inhibition - 0.9325 93.25%
CYP2C19 inhibition - 0.9364 93.64%
CYP2D6 inhibition - 0.9554 95.54%
CYP1A2 inhibition - 0.6996 69.96%
CYP2C8 inhibition - 0.9867 98.67%
CYP inhibitory promiscuity - 0.9879 98.79%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.9200 92.00%
Carcinogenicity (trinary) Non-required 0.7616 76.16%
Eye corrosion - 0.9575 95.75%
Eye irritation + 0.7094 70.94%
Skin irritation - 0.8708 87.08%
Skin corrosion - 0.9803 98.03%
Ames mutagenesis - 0.6700 67.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6918 69.18%
Micronuclear - 0.5900 59.00%
Hepatotoxicity - 0.5664 56.64%
skin sensitisation - 0.9337 93.37%
Respiratory toxicity - 0.5333 53.33%
Reproductive toxicity - 0.7778 77.78%
Mitochondrial toxicity + 0.5250 52.50%
Nephrotoxicity + 0.4800 48.00%
Acute Oral Toxicity (c) IV 0.5095 50.95%
Estrogen receptor binding - 0.8003 80.03%
Androgen receptor binding - 0.6652 66.52%
Thyroid receptor binding - 0.7019 70.19%
Glucocorticoid receptor binding - 0.5824 58.24%
Aromatase binding - 0.7594 75.94%
PPAR gamma - 0.6794 67.94%
Honey bee toxicity - 0.9381 93.81%
Biodegradation - 0.5750 57.50%
Crustacea aquatic toxicity - 0.8900 89.00%
Fish aquatic toxicity - 0.9219 92.19%

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
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 92.32% 96.09%
CHEMBL3060 Q9Y345 Glycine transporter 2 91.28% 99.17%
CHEMBL2581 P07339 Cathepsin D 90.34% 98.95%
CHEMBL1907591 P30926 Neuronal acetylcholine receptor; alpha4/beta4 85.44% 100.00%
CHEMBL221 P23219 Cyclooxygenase-1 84.97% 90.17%
CHEMBL3976 Q9UHL4 Dipeptidyl peptidase II 84.74% 92.29%
CHEMBL340 P08684 Cytochrome P450 3A4 80.89% 91.19%

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.
Avena sativa

Cross-Links

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PubChem 73232334
LOTUS LTS0109657
wikiData Q105365982