4-Hydroxy-methylprolin

Details

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Internal ID 252538dd-bd21-4f36-a198-eb136018966e
Taxonomy Organic acids and derivatives > Carboxylic acids and derivatives > Amino acids, peptides, and analogues > Alpha amino acids and derivatives > Proline and derivatives
IUPAC Name (2S)-4-hydroxy-1-methylpyrrolidine-2-carboxylic acid
SMILES (Canonical) CN1CC(CC1C(=O)O)O
SMILES (Isomeric) CN1CC(C[C@H]1C(=O)O)O
InChI InChI=1S/C6H11NO3/c1-7-3-4(8)2-5(7)6(9)10/h4-5,8H,2-3H2,1H3,(H,9,10)/t4?,5-/m0/s1
InChI Key FMIPNAUMSPFTHK-AKGZTFGVSA-N
Popularity 11 references in papers

Physical and Chemical Properties

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Molecular Formula C6H11NO3
Molecular Weight 145.16 g/mol
Exact Mass 145.07389321 g/mol
Topological Polar Surface Area (TPSA) 60.80 Ų
XlogP -2.90
Atomic LogP (AlogP) -0.86
H-Bond Acceptor 3
H-Bond Donor 2
Rotatable Bonds 1

Synonyms

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SCHEMBL3674503

2D Structure

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2D Structure of 4-Hydroxy-methylprolin

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.8987 89.87%
Caco-2 + 0.5000 50.00%
Blood Brain Barrier + 0.5750 57.50%
Human oral bioavailability + 0.5571 55.71%
Subcellular localzation Lysosomes 0.5601 56.01%
OATP2B1 inhibitior - 0.8392 83.92%
OATP1B1 inhibitior + 0.9780 97.80%
OATP1B3 inhibitior + 0.9418 94.18%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.7500 75.00%
BSEP inhibitior - 0.9418 94.18%
P-glycoprotein inhibitior - 0.9933 99.33%
P-glycoprotein substrate - 0.8894 88.94%
CYP3A4 substrate - 0.5719 57.19%
CYP2C9 substrate - 0.8119 81.19%
CYP2D6 substrate + 0.3617 36.17%
CYP3A4 inhibition - 0.9807 98.07%
CYP2C9 inhibition - 0.9481 94.81%
CYP2C19 inhibition - 0.9392 93.92%
CYP2D6 inhibition - 0.9468 94.68%
CYP1A2 inhibition - 0.8726 87.26%
CYP2C8 inhibition - 0.9983 99.83%
CYP inhibitory promiscuity - 0.9934 99.34%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.9500 95.00%
Carcinogenicity (trinary) Non-required 0.6461 64.61%
Eye corrosion - 0.9727 97.27%
Eye irritation + 0.7375 73.75%
Skin irritation - 0.7149 71.49%
Skin corrosion - 0.8401 84.01%
Ames mutagenesis - 0.7200 72.00%
Human Ether-a-go-go-Related Gene inhibition - 0.8331 83.31%
Micronuclear - 0.6400 64.00%
Hepatotoxicity + 0.6520 65.20%
skin sensitisation - 0.8868 88.68%
Respiratory toxicity + 0.5889 58.89%
Reproductive toxicity + 0.6333 63.33%
Mitochondrial toxicity + 0.7500 75.00%
Nephrotoxicity - 0.6721 67.21%
Acute Oral Toxicity (c) III 0.6204 62.04%
Estrogen receptor binding - 0.9348 93.48%
Androgen receptor binding - 0.7798 77.98%
Thyroid receptor binding - 0.9133 91.33%
Glucocorticoid receptor binding - 0.8827 88.27%
Aromatase binding - 0.9192 91.92%
PPAR gamma - 0.8793 87.93%
Honey bee toxicity - 0.9135 91.35%
Biodegradation + 0.8250 82.50%
Crustacea aquatic toxicity - 0.7600 76.00%
Fish aquatic toxicity - 0.7711 77.11%

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 95.18% 83.82%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 95.03% 96.09%
CHEMBL253 P34972 Cannabinoid CB2 receptor 83.17% 97.25%
CHEMBL340 P08684 Cytochrome P450 3A4 81.78% 91.19%
CHEMBL3807 P17706 T-cell protein-tyrosine phosphatase 81.62% 93.00%
CHEMBL1907598 P05106 Integrin alpha-V/beta-3 80.42% 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.
Erythroxylum argentinum
Lonchocarpus guatemalensis
Melaleuca uncinata
Moquiniastrum polymorphum subsp. polymorphum
Trichilia claussenii
Trichilia lepidota

Cross-Links

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PubChem 11499239
LOTUS LTS0003406
wikiData Q104375377