Thiocysteine

Details

Top
Internal ID be438426-54bd-4458-af30-1f87c675e6a7
Taxonomy Organic acids and derivatives > Carboxylic acids and derivatives > Amino acids, peptides, and analogues > Cysteine and derivatives > L-cysteine-S-conjugates
IUPAC Name (2R)-2-amino-3-(disulfanyl)propanoic acid
SMILES (Canonical) C(C(C(=O)O)N)SS
SMILES (Isomeric) C([C@@H](C(=O)O)N)SS
InChI InChI=1S/C3H7NO2S2/c4-2(1-8-7)3(5)6/h2,7H,1,4H2,(H,5,6)/t2-/m0/s1
InChI Key XBKONSCREBSMCS-REOHCLBHSA-N
Popularity 42 references in papers

Physical and Chemical Properties

Top
Molecular Formula C3H7NO2S2
Molecular Weight 153.23 g/mol
Exact Mass 152.99182081 g/mol
Topological Polar Surface Area (TPSA) 89.60 Ų
XlogP -2.60
Atomic LogP (AlogP) -0.02
H-Bond Acceptor 4
H-Bond Donor 3
Rotatable Bonds 3

Synonyms

Top
S-MERCAPTOCYSTEINE
cysteine perthiol
S-sulfanylcysteine
3-disulfanyl-L-alanine
cysteine persulfide
5652-32-4
L-cysteine persulfide
(R)-2-amino-3-disulfanylpropanoic acid
3-(Thiosulfeno)alanine
3-(thiosulfeno)-alanine
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

Top
2D Structure of Thiocysteine

3D Structure

Top

ADMET Properties (via admetSAR 2)

Top
Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9586 95.86%
Caco-2 - 0.9458 94.58%
Blood Brain Barrier + 0.6750 67.50%
Human oral bioavailability + 0.5714 57.14%
Subcellular localzation Lysosomes 0.6407 64.07%
OATP2B1 inhibitior - 0.8543 85.43%
OATP1B1 inhibitior + 0.9676 96.76%
OATP1B3 inhibitior + 0.9401 94.01%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.8750 87.50%
BSEP inhibitior - 0.9274 92.74%
P-glycoprotein inhibitior - 0.9861 98.61%
P-glycoprotein substrate - 0.9861 98.61%
CYP3A4 substrate - 0.7775 77.75%
CYP2C9 substrate - 0.6012 60.12%
CYP2D6 substrate - 0.8108 81.08%
CYP3A4 inhibition - 0.7694 76.94%
CYP2C9 inhibition - 0.9116 91.16%
CYP2C19 inhibition - 0.9270 92.70%
CYP2D6 inhibition - 0.9304 93.04%
CYP1A2 inhibition - 0.8708 87.08%
CYP2C8 inhibition - 0.9814 98.14%
CYP inhibitory promiscuity - 0.9781 97.81%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.5300 53.00%
Carcinogenicity (trinary) Non-required 0.7056 70.56%
Eye corrosion - 0.9787 97.87%
Eye irritation + 0.5878 58.78%
Skin irritation - 0.6886 68.86%
Skin corrosion - 0.8245 82.45%
Ames mutagenesis - 0.5078 50.78%
Human Ether-a-go-go-Related Gene inhibition - 0.8491 84.91%
Micronuclear + 0.6500 65.00%
Hepatotoxicity + 0.7750 77.50%
skin sensitisation - 0.9251 92.51%
Respiratory toxicity - 0.7000 70.00%
Reproductive toxicity - 0.6778 67.78%
Mitochondrial toxicity - 0.7625 76.25%
Nephrotoxicity - 0.7117 71.17%
Acute Oral Toxicity (c) III 0.7283 72.83%
Estrogen receptor binding - 0.9300 93.00%
Androgen receptor binding - 0.8474 84.74%
Thyroid receptor binding - 0.8915 89.15%
Glucocorticoid receptor binding - 0.8309 83.09%
Aromatase binding - 0.8582 85.82%
PPAR gamma - 0.7962 79.62%
Honey bee toxicity - 0.9357 93.57%
Biodegradation + 0.8000 80.00%
Crustacea aquatic toxicity - 0.8700 87.00%
Fish aquatic toxicity - 0.8232 82.32%

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
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 94.10% 96.09%
CHEMBL3976 Q9UHL4 Dipeptidyl peptidase II 90.42% 92.29%
CHEMBL4040 P28482 MAP kinase ERK2 90.34% 83.82%
CHEMBL221 P23219 Cyclooxygenase-1 87.51% 90.17%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 86.53% 96.95%
CHEMBL3060 Q9Y345 Glycine transporter 2 83.03% 99.17%

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 165331
LOTUS LTS0108890
wikiData Q27093709