D-cysteine

Details

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Internal ID 98f97218-0810-4ad9-8778-8c324038d0fb
Taxonomy Organic acids and derivatives > Carboxylic acids and derivatives > Amino acids, peptides, and analogues > Cysteine and derivatives
IUPAC Name (2S)-2-amino-3-sulfanylpropanoic acid
SMILES (Canonical) C(C(C(=O)O)N)S
SMILES (Isomeric) C([C@H](C(=O)O)N)S
InChI InChI=1S/C3H7NO2S/c4-2(1-7)3(5)6/h2,7H,1,4H2,(H,5,6)/t2-/m1/s1
InChI Key XUJNEKJLAYXESH-UWTATZPHSA-N
Popularity 58,960 references in papers

Physical and Chemical Properties

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Molecular Formula C3H7NO2S
Molecular Weight 121.16 g/mol
Exact Mass 121.01974964 g/mol
Topological Polar Surface Area (TPSA) 64.30 Ų
XlogP -2.50
Atomic LogP (AlogP) -0.67
H-Bond Acceptor 3
H-Bond Donor 3
Rotatable Bonds 2

Synonyms

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921-01-7
(2S)-2-amino-3-sulfanylpropanoic acid
D-Cystein
(S)-2-amino-3-mercaptopropanoic acid
Cysteine, D-
D-Zystein
D-Amino-3-mercaptopropionic acid
D-Cys
(S)-2-Amino-3-mercaptopropionic acid
(S)-Cysteine
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of D-cysteine

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9799 97.99%
Caco-2 - 0.9491 94.91%
Blood Brain Barrier + 0.6250 62.50%
Human oral bioavailability + 0.6571 65.71%
Subcellular localzation Lysosomes 0.7697 76.97%
OATP2B1 inhibitior - 0.8523 85.23%
OATP1B1 inhibitior + 0.9709 97.09%
OATP1B3 inhibitior + 0.9340 93.40%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.8750 87.50%
BSEP inhibitior - 0.9113 91.13%
P-glycoprotein inhibitior - 0.9888 98.88%
P-glycoprotein substrate - 0.9906 99.06%
CYP3A4 substrate - 0.8263 82.63%
CYP2C9 substrate - 0.6012 60.12%
CYP2D6 substrate - 0.8053 80.53%
CYP3A4 inhibition - 0.9602 96.02%
CYP2C9 inhibition - 0.9584 95.84%
CYP2C19 inhibition - 0.9634 96.34%
CYP2D6 inhibition - 0.9665 96.65%
CYP1A2 inhibition - 0.9400 94.00%
CYP2C8 inhibition - 0.9901 99.01%
CYP inhibitory promiscuity - 0.9888 98.88%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.7000 70.00%
Carcinogenicity (trinary) Non-required 0.7251 72.51%
Eye corrosion - 0.9886 98.86%
Eye irritation - 0.7937 79.37%
Skin irritation - 0.6261 62.61%
Skin corrosion - 0.7796 77.96%
Ames mutagenesis + 0.9500 95.00%
Human Ether-a-go-go-Related Gene inhibition - 0.8623 86.23%
Micronuclear + 0.5500 55.00%
Hepatotoxicity + 0.6125 61.25%
skin sensitisation - 0.9436 94.36%
Respiratory toxicity - 0.8889 88.89%
Reproductive toxicity - 0.7778 77.78%
Mitochondrial toxicity - 0.8250 82.50%
Nephrotoxicity - 0.7273 72.73%
Acute Oral Toxicity (c) III 0.8014 80.14%
Estrogen receptor binding - 0.9310 93.10%
Androgen receptor binding - 0.8773 87.73%
Thyroid receptor binding - 0.9171 91.71%
Glucocorticoid receptor binding - 0.8954 89.54%
Aromatase binding - 0.9003 90.03%
PPAR gamma - 0.8315 83.15%
Honey bee toxicity - 0.9568 95.68%
Biodegradation + 0.8000 80.00%
Crustacea aquatic toxicity - 0.9000 90.00%
Fish aquatic toxicity - 0.9439 94.39%

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 93.50% 96.09%
CHEMBL4040 P28482 MAP kinase ERK2 92.60% 83.82%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 87.88% 96.95%
CHEMBL3976 Q9UHL4 Dipeptidyl peptidase II 85.05% 92.29%
CHEMBL3060 Q9Y345 Glycine transporter 2 84.04% 99.17%
CHEMBL1907591 P30926 Neuronal acetylcholine receptor; alpha4/beta4 81.11% 100.00%

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.
Allium cepa
Arabidopsis thaliana
Cucurbita foetidissima
Gossypium hirsutum
Indigofera hirsuta
Nicotiana tabacum
Prunus domestica
Ripariosida hermaphrodita
Telekia speciosa
Treculia africana

Cross-Links

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PubChem 92851
NPASS NPC110533
ChEMBL CHEMBL171281
LOTUS LTS0095991
wikiData Q16633812