L-Cysteic acid

Details

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Internal ID 80a49c6c-c5a0-4010-909c-426c25f53949
Taxonomy Organic acids and derivatives > Carboxylic acids and derivatives > Amino acids, peptides, and analogues > Alpha amino acids and derivatives > Alpha amino acids > L-alpha-amino acids
IUPAC Name (2R)-2-amino-3-sulfopropanoic acid
SMILES (Canonical) C(C(C(=O)O)N)S(=O)(=O)O
SMILES (Isomeric) C([C@@H](C(=O)O)N)S(=O)(=O)O
InChI InChI=1S/C3H7NO5S/c4-2(3(5)6)1-10(7,8)9/h2H,1,4H2,(H,5,6)(H,7,8,9)/t2-/m0/s1
InChI Key XVOYSCVBGLVSOL-REOHCLBHSA-N
Popularity 1,672 references in papers

Physical and Chemical Properties

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Molecular Formula C3H7NO5S
Molecular Weight 169.16 g/mol
Exact Mass 169.00449350 g/mol
Topological Polar Surface Area (TPSA) 126.00 Ų
XlogP -4.50
Atomic LogP (AlogP) -1.71
H-Bond Acceptor 4
H-Bond Donor 3
Rotatable Bonds 3

Synonyms

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498-40-8
Cysteinesulfonic acid
Cysteic acid, L-
(R)-2-Amino-3-sulfopropanoic acid
Cysteric acid
L-Alanine, 3-sulfo-
(2R)-2-amino-3-sulfopropanoic acid
3-sulfo-L-alanine
Alanine, 3-sulfo-, L-
Cysteic acid (VAN)
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of L-Cysteic acid

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption - 0.8236 82.36%
Caco-2 - 0.9342 93.42%
Blood Brain Barrier + 0.5750 57.50%
Human oral bioavailability + 0.7571 75.71%
Subcellular localzation Lysosomes 0.4512 45.12%
OATP2B1 inhibitior - 0.8564 85.64%
OATP1B1 inhibitior + 0.9754 97.54%
OATP1B3 inhibitior + 0.9394 93.94%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.9000 90.00%
BSEP inhibitior - 0.9647 96.47%
P-glycoprotein inhibitior - 0.9800 98.00%
P-glycoprotein substrate - 0.9878 98.78%
CYP3A4 substrate - 0.7897 78.97%
CYP2C9 substrate - 0.6009 60.09%
CYP2D6 substrate - 0.8203 82.03%
CYP3A4 inhibition - 0.9733 97.33%
CYP2C9 inhibition - 0.8328 83.28%
CYP2C19 inhibition - 0.8213 82.13%
CYP2D6 inhibition - 0.9313 93.13%
CYP1A2 inhibition - 0.8059 80.59%
CYP2C8 inhibition - 0.9832 98.32%
CYP inhibitory promiscuity - 0.9969 99.69%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) + 0.7034 70.34%
Carcinogenicity (trinary) Non-required 0.6818 68.18%
Eye corrosion - 0.7913 79.13%
Eye irritation - 0.8734 87.34%
Skin irritation - 0.7672 76.72%
Skin corrosion - 0.8360 83.60%
Ames mutagenesis - 0.6300 63.00%
Human Ether-a-go-go-Related Gene inhibition - 0.8538 85.38%
Micronuclear + 0.8500 85.00%
Hepatotoxicity + 0.7055 70.55%
skin sensitisation - 0.8552 85.52%
Respiratory toxicity - 0.6111 61.11%
Reproductive toxicity - 0.6556 65.56%
Mitochondrial toxicity - 0.5000 50.00%
Nephrotoxicity - 0.7401 74.01%
Acute Oral Toxicity (c) III 0.6306 63.06%
Estrogen receptor binding - 0.9296 92.96%
Androgen receptor binding - 0.7801 78.01%
Thyroid receptor binding - 0.8544 85.44%
Glucocorticoid receptor binding - 0.8503 85.03%
Aromatase binding - 0.9265 92.65%
PPAR gamma - 0.8221 82.21%
Honey bee toxicity - 0.9276 92.76%
Biodegradation + 0.6250 62.50%
Crustacea aquatic toxicity - 0.8700 87.00%
Fish aquatic toxicity - 0.5840 58.40%

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 91.96% 96.09%
CHEMBL3976 Q9UHL4 Dipeptidyl peptidase II 89.85% 92.29%
CHEMBL4040 P28482 MAP kinase ERK2 87.54% 83.82%
CHEMBL4657 Q6V1X1 Dipeptidyl peptidase VIII 84.43% 97.21%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 82.84% 95.56%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 82.70% 96.95%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 80.27% 96.00%
CHEMBL2581 P07339 Cathepsin D 80.03% 98.95%

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.
Lilium hansonii
Picea glauca
Shorea uliginosa
Sonchus microcarpus
Strychnos diplotricha

Cross-Links

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PubChem 72886
NPASS NPC265829
LOTUS LTS0133011
wikiData Q29743881