L-cysteinesulfinic acid

Details

Top
Internal ID b7adfbdf-0d54-4263-858d-7d75dde3476f
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-sulfinopropanoic acid
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C3H7NO4S/c4-2(3(5)6)1-9(7)8/h2H,1,4H2,(H,5,6)(H,7,8)/t2-/m0/s1
InChI Key ADVPTQAUNPRNPO-REOHCLBHSA-N
Popularity 528 references in papers

Physical and Chemical Properties

Top
Molecular Formula C3H7NO4S
Molecular Weight 153.16 g/mol
Exact Mass 153.00957888 g/mol
Topological Polar Surface Area (TPSA) 120.00 Ų
XlogP -4.20
Atomic LogP (AlogP) -1.38
H-Bond Acceptor 3
H-Bond Donor 3
Rotatable Bonds 3

Synonyms

Top
1115-65-7
3-Sulfino-L-alanine
(2R)-2-amino-3-sulfinopropanoic acid
L-Cysteine sulfinic acid
Cysteinesulfinic acid, L-
56X032NVQL
L-2-Amino-3-sulfinopropionic acid
CHEBI:16345
DTXSID20862546
RefChem:1088156
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

Top
2D Structure of L-cysteinesulfinic acid

3D Structure

Top

ADMET Properties (via admetSAR 2)

Top
Target Value Probability (raw) Probability (%)
Human Intestinal Absorption - 0.6187 61.87%
Caco-2 - 0.9298 92.98%
Blood Brain Barrier + 0.5500 55.00%
Human oral bioavailability + 0.7429 74.29%
Subcellular localzation Lysosomes 0.4956 49.56%
OATP2B1 inhibitior - 0.8545 85.45%
OATP1B1 inhibitior + 0.9636 96.36%
OATP1B3 inhibitior + 0.9371 93.71%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.9500 95.00%
BSEP inhibitior - 0.9493 94.93%
P-glycoprotein inhibitior - 0.9837 98.37%
P-glycoprotein substrate - 0.9807 98.07%
CYP3A4 substrate - 0.7717 77.17%
CYP2C9 substrate - 0.6009 60.09%
CYP2D6 substrate - 0.8130 81.30%
CYP3A4 inhibition - 0.9547 95.47%
CYP2C9 inhibition - 0.9072 90.72%
CYP2C19 inhibition - 0.9026 90.26%
CYP2D6 inhibition - 0.9311 93.11%
CYP1A2 inhibition - 0.9045 90.45%
CYP2C8 inhibition - 0.9766 97.66%
CYP inhibitory promiscuity - 0.9967 99.67%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) + 0.5834 58.34%
Carcinogenicity (trinary) Non-required 0.6850 68.50%
Eye corrosion - 0.9142 91.42%
Eye irritation - 0.7493 74.93%
Skin irritation - 0.7768 77.68%
Skin corrosion - 0.8878 88.78%
Ames mutagenesis - 0.5900 59.00%
Human Ether-a-go-go-Related Gene inhibition - 0.8413 84.13%
Micronuclear + 0.8000 80.00%
Hepatotoxicity + 0.6625 66.25%
skin sensitisation - 0.8769 87.69%
Respiratory toxicity - 0.7111 71.11%
Reproductive toxicity - 0.6778 67.78%
Mitochondrial toxicity - 0.6000 60.00%
Nephrotoxicity - 0.8039 80.39%
Acute Oral Toxicity (c) III 0.6297 62.97%
Estrogen receptor binding - 0.8842 88.42%
Androgen receptor binding - 0.8926 89.26%
Thyroid receptor binding - 0.9082 90.82%
Glucocorticoid receptor binding - 0.8121 81.21%
Aromatase binding - 0.8856 88.56%
PPAR gamma - 0.8421 84.21%
Honey bee toxicity - 0.9152 91.52%
Biodegradation + 0.7750 77.50%
Crustacea aquatic toxicity - 0.7900 79.00%
Fish aquatic toxicity - 0.6965 69.65%

Targets

Top

Proven Targets:

CHEMBL ID UniProt ID Name Min activity Assay type Source
CHEMBL1963 P16473 Thyroid stimulating hormone receptor 794.3 nM
Potency
via Super-PRED

Predicted Targets (via Super-PRED):

CHEMBL ID UniProt ID Name Probability Model accuracy
CHEMBL3976 Q9UHL4 Dipeptidyl peptidase II 94.29% 92.29%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 93.58% 96.09%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 93.56% 96.95%
CHEMBL4657 Q6V1X1 Dipeptidyl peptidase VIII 88.78% 97.21%
CHEMBL3060 Q9Y345 Glycine transporter 2 83.86% 99.17%
CHEMBL204 P00734 Thrombin 81.25% 96.01%

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.
There are no matching plants.

Cross-Links

Top
PubChem 1549098
LOTUS LTS0233804
wikiData Q2823252