DL-Serine

Details

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Internal ID 8f289c6d-5032-4ce9-bd3f-17fec3d857b7
Taxonomy Organic acids and derivatives > Carboxylic acids and derivatives > Amino acids, peptides, and analogues > Alpha amino acids and derivatives > Serine and derivatives
IUPAC Name 2-amino-3-hydroxypropanoic acid
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C3H7NO3/c4-2(1-5)3(6)7/h2,5H,1,4H2,(H,6,7)
InChI Key MTCFGRXMJLQNBG-UHFFFAOYSA-N
Popularity 857 references in papers

Physical and Chemical Properties

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Molecular Formula C3H7NO3
Molecular Weight 105.09 g/mol
Exact Mass 105.042593085 g/mol
Topological Polar Surface Area (TPSA) 83.60 Ų
XlogP -3.10
Atomic LogP (AlogP) -1.61
H-Bond Acceptor 3
H-Bond Donor 3
Rotatable Bonds 2

Synonyms

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302-84-1
Serine, DL-
00PAR1C66F
NSC-9960
DTXSID70859325
NSC9960
2-azaniumyl-3-hydroxypropanoate
Serine DL-
RefChem:1083916
DTXCID20202802
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of DL-Serine

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9675 96.75%
Caco-2 - 0.9411 94.11%
Blood Brain Barrier - 0.5500 55.00%
Human oral bioavailability + 0.6286 62.86%
Subcellular localzation Lysosomes 0.6959 69.59%
OATP2B1 inhibitior - 0.8532 85.32%
OATP1B1 inhibitior + 0.9778 97.78%
OATP1B3 inhibitior + 0.8997 89.97%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.9500 95.00%
BSEP inhibitior - 0.9272 92.72%
P-glycoprotein inhibitior - 0.9871 98.71%
P-glycoprotein substrate - 0.9942 99.42%
CYP3A4 substrate - 0.8366 83.66%
CYP2C9 substrate - 0.8024 80.24%
CYP2D6 substrate - 0.7943 79.43%
CYP3A4 inhibition - 0.9080 90.80%
CYP2C9 inhibition - 0.9512 95.12%
CYP2C19 inhibition - 0.9450 94.50%
CYP2D6 inhibition - 0.9349 93.49%
CYP1A2 inhibition - 0.9087 90.87%
CYP2C8 inhibition - 0.9942 99.42%
CYP inhibitory promiscuity - 0.9914 99.14%
UGT catelyzed + 0.9000 90.00%
Carcinogenicity (binary) - 0.7900 79.00%
Carcinogenicity (trinary) Non-required 0.7108 71.08%
Eye corrosion - 0.9415 94.15%
Eye irritation + 0.7445 74.45%
Skin irritation - 0.6313 63.13%
Skin corrosion - 0.8378 83.78%
Ames mutagenesis - 0.9200 92.00%
Human Ether-a-go-go-Related Gene inhibition - 0.8509 85.09%
Micronuclear + 0.5474 54.74%
Hepatotoxicity - 0.5125 51.25%
skin sensitisation - 0.9742 97.42%
Respiratory toxicity - 0.7889 78.89%
Reproductive toxicity - 0.8111 81.11%
Mitochondrial toxicity - 0.6375 63.75%
Nephrotoxicity - 0.7170 71.70%
Acute Oral Toxicity (c) III 0.5142 51.42%
Estrogen receptor binding - 0.9562 95.62%
Androgen receptor binding - 0.8910 89.10%
Thyroid receptor binding - 0.8897 88.97%
Glucocorticoid receptor binding - 0.9282 92.82%
Aromatase binding - 0.9033 90.33%
PPAR gamma - 0.8563 85.63%
Honey bee toxicity - 0.9672 96.72%
Biodegradation + 0.8500 85.00%
Crustacea aquatic toxicity - 0.9700 97.00%
Fish aquatic toxicity - 0.9578 95.78%

Targets

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Proven Targets:

CHEMBL ID UniProt ID Name Min activity Assay type Source
CHEMBL1293237 P54132 Bloom syndrome protein 2.5 nM
Potency
via Super-PRED

Predicted Targets (via Super-PRED):

CHEMBL ID UniProt ID Name Probability Model accuracy
CHEMBL4040 P28482 MAP kinase ERK2 98.11% 83.82%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 93.52% 96.09%
CHEMBL3976 Q9UHL4 Dipeptidyl peptidase II 85.96% 92.29%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 85.93% 96.95%
CHEMBL3060 Q9Y345 Glycine transporter 2 84.14% 99.17%

Plants that contains it

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Cross-Links

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PubChem 617
LOTUS LTS0138133
wikiData Q26997410