Sarcosine

Details

Top
Internal ID d6eea3d8-1a93-4f5c-b3d2-4a71cf01cd77
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-(methylamino)acetic acid
SMILES (Canonical) CNCC(=O)O
SMILES (Isomeric) CNCC(=O)O
InChI InChI=1S/C3H7NO2/c1-4-2-3(5)6/h4H,2H2,1H3,(H,5,6)
InChI Key FSYKKLYZXJSNPZ-UHFFFAOYSA-N
Popularity 5,479 references in papers

Physical and Chemical Properties

Top
Molecular Formula C3H7NO2
Molecular Weight 89.09 g/mol
Exact Mass 89.047678466 g/mol
Topological Polar Surface Area (TPSA) 49.30 Ų
XlogP -2.80
Atomic LogP (AlogP) -0.71
H-Bond Acceptor 2
H-Bond Donor 2
Rotatable Bonds 2

Synonyms

Top
107-97-1
N-methylglycine
Sarcosinic acid
Methylglycine
2-(methylamino)acetic acid
N-Methylaminoacetic acid
Sarcosin
Glycine, N-methyl-
Methylaminoacetic acid
(Methylamino)acetic acid
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

Top
2D Structure of Sarcosine

3D Structure

Top

ADMET Properties (via admetSAR 2)

Top
Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9464 94.64%
Caco-2 + 0.7496 74.96%
Blood Brain Barrier + 0.6000 60.00%
Human oral bioavailability + 0.7143 71.43%
Subcellular localzation Lysosomes 0.6161 61.61%
OATP2B1 inhibitior - 0.8674 86.74%
OATP1B1 inhibitior + 0.9387 93.87%
OATP1B3 inhibitior + 0.9523 95.23%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.8500 85.00%
BSEP inhibitior - 0.9681 96.81%
P-glycoprotein inhibitior - 0.9847 98.47%
P-glycoprotein substrate - 0.9856 98.56%
CYP3A4 substrate - 0.7849 78.49%
CYP2C9 substrate - 0.5814 58.14%
CYP2D6 substrate - 0.7810 78.10%
CYP3A4 inhibition - 0.9724 97.24%
CYP2C9 inhibition - 0.9667 96.67%
CYP2C19 inhibition - 0.9650 96.50%
CYP2D6 inhibition - 0.9675 96.75%
CYP1A2 inhibition - 0.9394 93.94%
CYP2C8 inhibition - 0.9935 99.35%
CYP inhibitory promiscuity - 0.9937 99.37%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.6120 61.20%
Carcinogenicity (trinary) Non-required 0.6840 68.40%
Eye corrosion + 0.7881 78.81%
Eye irritation + 0.9817 98.17%
Skin irritation - 0.6826 68.26%
Skin corrosion - 0.6074 60.74%
Ames mutagenesis - 0.9800 98.00%
Human Ether-a-go-go-Related Gene inhibition - 0.8628 86.28%
Micronuclear - 0.8900 89.00%
Hepatotoxicity + 0.5250 52.50%
skin sensitisation - 0.9073 90.73%
Respiratory toxicity - 0.8000 80.00%
Reproductive toxicity - 0.7333 73.33%
Mitochondrial toxicity + 0.6625 66.25%
Nephrotoxicity + 0.4502 45.02%
Acute Oral Toxicity (c) III 0.7123 71.23%
Estrogen receptor binding - 0.9602 96.02%
Androgen receptor binding - 0.9266 92.66%
Thyroid receptor binding - 0.9111 91.11%
Glucocorticoid receptor binding - 0.9268 92.68%
Aromatase binding - 0.8981 89.81%
PPAR gamma - 0.9300 93.00%
Honey bee toxicity - 0.9854 98.54%
Biodegradation + 0.9250 92.50%
Crustacea aquatic toxicity - 0.8400 84.00%
Fish aquatic toxicity - 0.9766 97.66%

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 91.68% 83.82%
CHEMBL221 P23219 Cyclooxygenase-1 90.24% 90.17%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 89.54% 96.09%
CHEMBL2581 P07339 Cathepsin D 87.45% 98.95%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 87.45% 85.14%
CHEMBL3060 Q9Y345 Glycine transporter 2 81.01% 99.17%
CHEMBL2111367 P27986 PI3-kinase p110-alpha/p85-alpha 80.35% 94.33%

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.
Juncus roemerianus
Sarcococca saligna

Cross-Links

Top
PubChem 1088
NPASS NPC134570
LOTUS LTS0202877
wikiData Q414157