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Showing metabocard for D-Cysteine (HMDB0003417)

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Record Information
Version5.0
StatusDetected and Quantified
Creation Date2006-08-12 20:29:18 UTC
Update Date2021-10-13 04:41:39 UTC
HMDB IDHMDB0003417
Secondary Accession Numbers
  • HMDB03417
Metabolite Identification
Common NameD-Cysteine
DescriptionD-cysteine is an optically active form of cysteine having D-configuration. It is a cysteine and a D-alpha-amino acid. It is a conjugate base of a D-cysteinium. It is a conjugate acid of a D-cysteinate(1-). It is an enantiomer of a L-cysteine. It is a tautomer of a D-cysteine zwitterion. D-Cysteine, also known as D-cystein or DCY, belongs to the class of organic compounds known as cysteine and derivatives. Cysteine and derivatives are compounds containing cysteine or a derivative thereof resulting from reaction of cysteine at the amino group or the carboxy group, or from the replacement of any hydrogen of glycine by a heteroatom. It is a non-proteogenic sulfur-containing amino acid. D-Cysteine is known to be toxic to bacteria and several bacteria (and plants) have developed and enzyme called D-cysteine desulfhydrase (EC4.1.99.4). D-cysteine can be generated from D-Cysteine via cysteine racemase. D-Cysteine is a naturally occurring enantiomer of L-Cysteine. Cysteine is named after cystine, which comes from the Greek word kustis meaning bladder -cystine was first isolated from kidney stones. D-Cysteine exists in all living species, ranging from bacteria to humans. Outside of the human body, D-Cysteine has been detected, but not quantified in several different foods, such as chervils, fruits, lichee, nuts, and cherimoya.
Structure
Data?1582752275
MOL3D MOLSDF3D SDFPDB3D PDBSMILESInChI

MOL for HMDB0003417 (D-Cysteine)


  Mrv1652305271900072D          

  7  6  0  0  1  0            999 V2000
    0.6124    0.2357    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1021   -0.1768    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.8165    0.2357    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3269   -0.1768    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.6124    1.0607    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1021   -1.0018    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5310   -0.1768    0.0000 S   0  0  0  0  0  0  0  0  0  0  0  0
  2  1  1  0  0  0  0
  5  1  2  0  0  0  0
  4  1  1  0  0  0  0
  3  2  1  0  0  0  0
  2  6  1  6  0  0  0
  7  3  1  0  0  0  0
M  END
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3D MOL for HMDB0003417 (D-Cysteine)

HMDB0003417
     RDKit          3D
D-Cysteine
 14 13  0  0  0  0  0  0  0  0999 V2000
    0.3079    1.6533   -0.2733 N   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3223    0.5046    0.2970 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.6467   -0.5646    0.7381 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6563   -1.2032   -0.5870 S   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3411   -0.0363   -0.6379 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5335    0.5260   -1.7525 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1041   -1.1537   -0.3326 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.1415    1.6381   -1.3025 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3439    1.6952   -0.0813 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8571    0.8413    1.2283 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2127   -0.2238    1.6283 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0065   -1.4160    1.1165 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9532   -0.6617   -0.6087 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1106   -1.5992    0.5676 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  1  0
  2  5  1  0
  5  6  2  0
  5  7  1  0
  1  8  1  0
  1  9  1  0
  2 10  1  1
  3 11  1  0
  3 12  1  0
  4 13  1  0
  7 14  1  0
M  END
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3D SDF for HMDB0003417 (D-Cysteine)


  Mrv1652305271900072D          

  7  6  0  0  1  0            999 V2000
    0.6124    0.2357    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1021   -0.1768    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.8165    0.2357    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3269   -0.1768    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.6124    1.0607    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1021   -1.0018    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5310   -0.1768    0.0000 S   0  0  0  0  0  0  0  0  0  0  0  0
  2  1  1  0  0  0  0
  5  1  2  0  0  0  0
  4  1  1  0  0  0  0
  3  2  1  0  0  0  0
  2  6  1  6  0  0  0
  7  3  1  0  0  0  0
M  END
> <DATABASE_ID>
HMDB0003417

> <DATABASE_NAME>
hmdb

> <SMILES>
N[C@H](CS)C(O)=O

> <INCHI_IDENTIFIER>
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

> <FORMULA>
C3H7NO2S

> <MOLECULAR_WEIGHT>
121.15

> <EXACT_MASS>
121.019749643

> <JCHEM_ACCEPTOR_COUNT>
3

> <JCHEM_ATOM_COUNT>
14

> <JCHEM_AVERAGE_POLARIZABILITY>
11.401989924934824

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
3

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(2S)-2-amino-3-sulfanylpropanoic acid

> <ALOGPS_LOGP>
-2.57

> <JCHEM_LOGP>
-2.7921332976482773

> <ALOGPS_LOGS>
-0.72

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
0

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
10.171891903949282

> <JCHEM_PKA_STRONGEST_ACIDIC>
2.345995198078135

> <JCHEM_PKA_STRONGEST_BASIC>
9.053809511128133

> <JCHEM_POLAR_SURFACE_AREA>
63.31999999999999

> <JCHEM_REFRACTIVITY>
28.2236

> <JCHEM_ROTATABLE_BOND_COUNT>
2

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
2.31e+01 g/l

> <JCHEM_TRADITIONAL_IUPAC>
L cysteine

> <JCHEM_VEBER_RULE>
0

$$$$
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3D-SDF for HMDB0003417 (D-Cysteine)

HMDB0003417
     RDKit          3D
D-Cysteine
 14 13  0  0  0  0  0  0  0  0999 V2000
    0.3079    1.6533   -0.2733 N   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3223    0.5046    0.2970 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.6467   -0.5646    0.7381 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6563   -1.2032   -0.5870 S   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3411   -0.0363   -0.6379 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5335    0.5260   -1.7525 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1041   -1.1537   -0.3326 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.1415    1.6381   -1.3025 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3439    1.6952   -0.0813 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8571    0.8413    1.2283 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2127   -0.2238    1.6283 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0065   -1.4160    1.1165 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9532   -0.6617   -0.6087 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1106   -1.5992    0.5676 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  1  0
  2  5  1  0
  5  6  2  0
  5  7  1  0
  1  8  1  0
  1  9  1  0
  2 10  1  1
  3 11  1  0
  3 12  1  0
  4 13  1  0
  7 14  1  0
M  END
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PDB for HMDB0003417 (D-Cysteine)

HEADER    PROTEIN                                 27-MAY-19   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   27-MAY-19         0                                  
HETATM    1  C   UNK     0       1.143   0.440   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      -0.191  -0.330   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      -1.524   0.440   0.000  0.00  0.00           C+0
HETATM    4  O   UNK     0       2.477  -0.330   0.000  0.00  0.00           O+0
HETATM    5  O   UNK     0       1.143   1.980   0.000  0.00  0.00           O+0
HETATM    6  N   UNK     0      -0.191  -1.870   0.000  0.00  0.00           N+0
HETATM    7  S   UNK     0      -2.858  -0.330   0.000  0.00  0.00           S+0
CONECT    1    2    5    4                                                  
CONECT    2    1    3    6                                                  
CONECT    3    2    7                                                       
CONECT    4    1                                                            
CONECT    5    1                                                            
CONECT    6    2                                                            
CONECT    7    3                                                            
MASTER        0    0    0    0    0    0    0    0    7    0   12    0
END
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3D PDB for HMDB0003417 (D-Cysteine)

COMPND    HMDB0003417
HETATM    1  N1  UNL     1       0.308   1.653  -0.273  1.00  0.00           N  
HETATM    2  C1  UNL     1      -0.322   0.505   0.297  1.00  0.00           C  
HETATM    3  C2  UNL     1       0.647  -0.565   0.738  1.00  0.00           C  
HETATM    4  S1  UNL     1       1.656  -1.203  -0.587  1.00  0.00           S  
HETATM    5  C3  UNL     1      -1.341  -0.036  -0.638  1.00  0.00           C  
HETATM    6  O1  UNL     1      -1.533   0.526  -1.752  1.00  0.00           O  
HETATM    7  O2  UNL     1      -2.104  -1.154  -0.333  1.00  0.00           O  
HETATM    8  H1  UNL     1       0.142   1.638  -1.302  1.00  0.00           H  
HETATM    9  H2  UNL     1       1.344   1.695  -0.081  1.00  0.00           H  
HETATM   10  H3  UNL     1      -0.857   0.841   1.228  1.00  0.00           H  
HETATM   11  H4  UNL     1       1.213  -0.224   1.628  1.00  0.00           H  
HETATM   12  H5  UNL     1       0.006  -1.416   1.117  1.00  0.00           H  
HETATM   13  H6  UNL     1       2.953  -0.662  -0.609  1.00  0.00           H  
HETATM   14  H7  UNL     1      -2.111  -1.599   0.568  1.00  0.00           H  
CONECT    1    2    8    9
CONECT    2    3    5   10
CONECT    3    4   11   12
CONECT    4   13
CONECT    5    6    6    7
CONECT    7   14
END
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SMILES for HMDB0003417 (D-Cysteine)

N[C@H](CS)C(O)=O
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INCHI for HMDB0003417 (D-Cysteine)

InChI=1S/C3H7NO2S/c4-2(1-7)3(5)6/h2,7H,1,4H2,(H,5,6)/t2-/m1/s1
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View in JSmolView NMR AssignmentsView Stereo Labels
Synonyms
ValueSource
(2S)-2-Amino-3-mercaptopropanoic acidChEBI
(2S)-2-Amino-3-sulfanylpropanoic acidChEBI
(S)-2-Amino-3-mercaptopropanoic acidChEBI
D-Amino-3-mercaptopropionic acidChEBI
D-CysteinChEBI
D-ZysteinChEBI
DCYChEBI
(2S)-2-Amino-3-mercaptopropanoateGenerator
(2S)-2-Amino-3-sulfanylpropanoateGenerator
(2S)-2-Amino-3-sulphanylpropanoateGenerator
(2S)-2-Amino-3-sulphanylpropanoic acidGenerator
(S)-2-Amino-3-mercaptopropanoateGenerator
D-Amino-3-mercaptopropionateGenerator
CysteineMeSH, HMDB
Half cystineMeSH, HMDB
Cysteine hydrochlorideMeSH, HMDB
Half-cystineMeSH, HMDB
L-CysteineMeSH, HMDB
L CysteineMeSH, HMDB
Zinc cysteinateMeSH, HMDB
Chemical FormulaC3H7NO2S
Average Molecular Weight121.15
Monoisotopic Molecular Weight121.019749643
IUPAC Name(2S)-2-amino-3-sulfanylpropanoic acid
Traditional NameL cysteine
CAS Registry Number921-01-7
SMILES
N[C@H](CS)C(O)=O
InChI Identifier
InChI=1S/C3H7NO2S/c4-2(1-7)3(5)6/h2,7H,1,4H2,(H,5,6)/t2-/m1/s1
InChI KeyXUJNEKJLAYXESH-UWTATZPHSA-N
Chemical Taxonomy
Description Belongs to the class of organic compounds known as cysteine and derivatives. Cysteine and derivatives are compounds containing cysteine or a derivative thereof resulting from reaction of cysteine at the amino group or the carboxy group, or from the replacement of any hydrogen of glycine by a heteroatom.
KingdomOrganic compounds
Super ClassOrganic acids and derivatives
ClassCarboxylic acids and derivatives
Sub ClassAmino acids, peptides, and analogues
Direct ParentCysteine and derivatives
Alternative Parents
Substituents
  • Cysteine or derivatives
  • Alpha-amino acid
  • D-alpha-amino acid
  • Amino acid
  • Alkylthiol
  • Carboxylic acid
  • Monocarboxylic acid or derivatives
  • Organic oxygen compound
  • Primary amine
  • Organosulfur compound
  • Organooxygen compound
  • Organonitrogen compound
  • Organic nitrogen compound
  • Primary aliphatic amine
  • Carbonyl group
  • Amine
  • Hydrocarbon derivative
  • Organopnictogen compound
  • Organic oxide
  • Aliphatic acyclic compound
Molecular FrameworkAliphatic acyclic compounds
External Descriptors
Ontology
Not AvailableNot Available
Physical Properties
StateSolid
Experimental Molecular Properties
PropertyValueReference
Melting PointNot AvailableNot Available
Boiling Point293.90 °C. @ 760.00 mm Hg (est)The Good Scents Company Information System
Water Solubility113200 mg/L @ 25 °C (est)The Good Scents Company Information System
LogP0.230 (est)The Good Scents Company Information System
Experimental Chromatographic PropertiesNot Available
Predicted Molecular Properties
PropertyValueSource
Water Solubility23.1 g/LALOGPS
logP-2.6ALOGPS
logP-2.8ChemAxon
logS-0.72ALOGPS
pKa (Strongest Acidic)2.35ChemAxon
pKa (Strongest Basic)9.05ChemAxon
Physiological Charge0ChemAxon
Hydrogen Acceptor Count3ChemAxon
Hydrogen Donor Count3ChemAxon
Polar Surface Area63.32 ŲChemAxon
Rotatable Bond Count2ChemAxon
Refractivity28.22 m³·mol⁻¹ChemAxon
Polarizability11.4 ųChemAxon
Number of Rings0ChemAxon
BioavailabilityYesChemAxon
Rule of FiveYesChemAxon
Ghose FilterNoChemAxon
Veber's RuleNoChemAxon
MDDR-like RuleNoChemAxon
Predicted Chromatographic Properties

Predicted Collision Cross Sections

PredictorAdduct TypeCCS Value (Å2)Reference
DarkChem[M+H]+123.25531661259
DarkChem[M-H]-119.15731661259
DeepCCS[M+H]+122.90830932474
DeepCCS[M-H]-120.01230932474
DeepCCS[M-2H]-156.50730932474
DeepCCS[M+Na]+131.46730932474
AllCCS[M+H]+130.132859911
AllCCS[M+H-H2O]+126.032859911
AllCCS[M+NH4]+134.032859911
AllCCS[M+Na]+135.132859911
AllCCS[M-H]-128.732859911
AllCCS[M+Na-2H]-132.632859911
AllCCS[M+HCOO]-136.932859911

Predicted Retention Times

Underivatized

Chromatographic MethodRetention TimeReference
Measured using a Waters Acquity ultraperformance liquid chromatography (UPLC) ethylene-bridged hybrid (BEH) C18 column (100 mm × 2.1 mm; 1.7 μmparticle diameter). Predicted by Afia on May 17, 2022. Predicted by Afia on May 17, 2022.0.95 minutes32390414
Predicted by Siyang on May 30, 20229.9987 minutes33406817
Predicted by Siyang using ReTip algorithm on June 8, 20226.63 minutes32390414
AjsUoB = Accucore 150 Amide HILIC with 10mM Ammonium Formate, 0.1% Formic Acid366.0 seconds40023050
Fem_Long = Waters ACQUITY UPLC HSS T3 C18 with Water:MeOH and 0.1% Formic Acid1059.2 seconds40023050
Fem_Lipids = Ascentis Express C18 with (60:40 water:ACN):(90:10 IPA:ACN) and 10mM NH4COOH + 0.1% Formic Acid386.5 seconds40023050
Life_Old = Waters ACQUITY UPLC BEH C18 with Water:(20:80 acetone:ACN) and 0.1% Formic Acid51.6 seconds40023050
Life_New = RP Waters ACQUITY UPLC HSS T3 C18 with Water:(30:70 MeOH:ACN) and 0.1% Formic Acid255.6 seconds40023050
RIKEN = Waters ACQUITY UPLC BEH C18 with Water:ACN and 0.1% Formic Acid99.6 seconds40023050
Eawag_XBridgeC18 = XBridge C18 3.5u 2.1x50 mm with Water:MeOH and 0.1% Formic Acid303.3 seconds40023050
BfG_NTS_RP1 =Agilent Zorbax Eclipse Plus C18 (2.1 mm x 150 mm, 3.5 um) with Water:ACN and 0.1% Formic Acid273.2 seconds40023050
HILIC_BDD_2 = Merck SeQuant ZIC-HILIC with ACN(0.1% formic acid):water(16 mM ammonium formate)843.8 seconds40023050
UniToyama_Atlantis = RP Waters Atlantis T3 (2.1 x 150 mm, 5 um) with ACN:Water and 0.1% Formic Acid647.0 seconds40023050
BDD_C18 = Hypersil Gold 1.9µm C18 with Water:ACN and 0.1% Formic Acid37.3 seconds40023050
UFZ_Phenomenex = Kinetex Core-Shell C18 2.6 um, 3.0 x 100 mm, Phenomenex with Water:MeOH and 0.1% Formic Acid884.4 seconds40023050
SNU_RIKEN_POS = Waters ACQUITY UPLC BEH C18 with Water:ACN and 0.1% Formic Acid237.7 seconds40023050
RPMMFDA = Waters ACQUITY UPLC BEH C18 with Water:ACN and 0.1% Formic Acid278.2 seconds40023050
MTBLS87 = Merck SeQuant ZIC-pHILIC column with ACN:Water and :ammonium carbonate694.0 seconds40023050
KI_GIAR_zic_HILIC_pH2_7 = Merck SeQuant ZIC-HILIC with ACN:Water and 0.1% FA365.5 seconds40023050
Meister zic-pHILIC pH9.3 = Merck SeQuant ZIC-pHILIC column with ACN:Water 5mM NH4Ac pH9.3 and 5mM ammonium acetate in water399.6 seconds40023050

Predicted Kovats Retention Indices

Underivatized

MetaboliteSMILESKovats RI ValueColumn TypeReference
D-CysteineN[C@H](CS)C(O)=O2227.2Standard polar33892256
D-CysteineN[C@H](CS)C(O)=O1161.7Standard non polar33892256
D-CysteineN[C@H](CS)C(O)=O1654.4Semi standard non polar33892256

Derivatized

Derivative Name / StructureSMILESKovats RI ValueColumn TypeReference
D-Cysteine,1TMS,isomer #1C[Si](C)(C)OC(=O)[C@H](N)CS1232.3Semi standard non polar33892256
D-Cysteine,1TMS,isomer #2C[Si](C)(C)SC[C@@H](N)C(=O)O1396.7Semi standard non polar33892256
D-Cysteine,1TMS,isomer #3C[Si](C)(C)N[C@H](CS)C(=O)O1356.8Semi standard non polar33892256
D-Cysteine,2TMS,isomer #1C[Si](C)(C)OC(=O)[C@H](N)CS[Si](C)(C)C1430.6Semi standard non polar33892256
D-Cysteine,2TMS,isomer #1C[Si](C)(C)OC(=O)[C@H](N)CS[Si](C)(C)C1483.2Standard non polar33892256
D-Cysteine,2TMS,isomer #1C[Si](C)(C)OC(=O)[C@H](N)CS[Si](C)(C)C1966.7Standard polar33892256
D-Cysteine,2TMS,isomer #2C[Si](C)(C)N[C@H](CS)C(=O)O[Si](C)(C)C1373.0Semi standard non polar33892256
D-Cysteine,2TMS,isomer #2C[Si](C)(C)N[C@H](CS)C(=O)O[Si](C)(C)C1346.7Standard non polar33892256
D-Cysteine,2TMS,isomer #2C[Si](C)(C)N[C@H](CS)C(=O)O[Si](C)(C)C1622.8Standard polar33892256
D-Cysteine,2TMS,isomer #3C[Si](C)(C)N[C@H](CS[Si](C)(C)C)C(=O)O1507.3Semi standard non polar33892256
D-Cysteine,2TMS,isomer #3C[Si](C)(C)N[C@H](CS[Si](C)(C)C)C(=O)O1480.2Standard non polar33892256
D-Cysteine,2TMS,isomer #3C[Si](C)(C)N[C@H](CS[Si](C)(C)C)C(=O)O1939.2Standard polar33892256
D-Cysteine,2TMS,isomer #4C[Si](C)(C)N([C@H](CS)C(=O)O)[Si](C)(C)C1542.8Semi standard non polar33892256
D-Cysteine,2TMS,isomer #4C[Si](C)(C)N([C@H](CS)C(=O)O)[Si](C)(C)C1433.3Standard non polar33892256
D-Cysteine,2TMS,isomer #4C[Si](C)(C)N([C@H](CS)C(=O)O)[Si](C)(C)C1777.1Standard polar33892256
D-Cysteine,3TMS,isomer #1C[Si](C)(C)N[C@H](CS[Si](C)(C)C)C(=O)O[Si](C)(C)C1547.8Semi standard non polar33892256
D-Cysteine,3TMS,isomer #1C[Si](C)(C)N[C@H](CS[Si](C)(C)C)C(=O)O[Si](C)(C)C1544.9Standard non polar33892256
D-Cysteine,3TMS,isomer #1C[Si](C)(C)N[C@H](CS[Si](C)(C)C)C(=O)O[Si](C)(C)C1647.5Standard polar33892256
D-Cysteine,3TMS,isomer #2C[Si](C)(C)OC(=O)[C@@H](CS)N([Si](C)(C)C)[Si](C)(C)C1560.2Semi standard non polar33892256
D-Cysteine,3TMS,isomer #2C[Si](C)(C)OC(=O)[C@@H](CS)N([Si](C)(C)C)[Si](C)(C)C1545.0Standard non polar33892256
D-Cysteine,3TMS,isomer #2C[Si](C)(C)OC(=O)[C@@H](CS)N([Si](C)(C)C)[Si](C)(C)C1630.8Standard polar33892256
D-Cysteine,3TMS,isomer #3C[Si](C)(C)SC[C@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C1674.3Semi standard non polar33892256
D-Cysteine,3TMS,isomer #3C[Si](C)(C)SC[C@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C1640.0Standard non polar33892256
D-Cysteine,3TMS,isomer #3C[Si](C)(C)SC[C@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C1769.1Standard polar33892256
D-Cysteine,4TMS,isomer #1C[Si](C)(C)OC(=O)[C@@H](CS[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C1709.4Semi standard non polar33892256
D-Cysteine,4TMS,isomer #1C[Si](C)(C)OC(=O)[C@@H](CS[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C1691.1Standard non polar33892256
D-Cysteine,4TMS,isomer #1C[Si](C)(C)OC(=O)[C@@H](CS[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C1597.8Standard polar33892256
D-Cysteine,1TBDMS,isomer #1CC(C)(C)[Si](C)(C)OC(=O)[C@H](N)CS1477.3Semi standard non polar33892256
D-Cysteine,1TBDMS,isomer #2CC(C)(C)[Si](C)(C)SC[C@@H](N)C(=O)O1634.9Semi standard non polar33892256
D-Cysteine,1TBDMS,isomer #3CC(C)(C)[Si](C)(C)N[C@H](CS)C(=O)O1628.9Semi standard non polar33892256
D-Cysteine,2TBDMS,isomer #1CC(C)(C)[Si](C)(C)OC(=O)[C@H](N)CS[Si](C)(C)C(C)(C)C1910.9Semi standard non polar33892256
D-Cysteine,2TBDMS,isomer #1CC(C)(C)[Si](C)(C)OC(=O)[C@H](N)CS[Si](C)(C)C(C)(C)C1945.2Standard non polar33892256
D-Cysteine,2TBDMS,isomer #1CC(C)(C)[Si](C)(C)OC(=O)[C@H](N)CS[Si](C)(C)C(C)(C)C2095.6Standard polar33892256
D-Cysteine,2TBDMS,isomer #2CC(C)(C)[Si](C)(C)N[C@H](CS)C(=O)O[Si](C)(C)C(C)(C)C1841.2Semi standard non polar33892256
D-Cysteine,2TBDMS,isomer #2CC(C)(C)[Si](C)(C)N[C@H](CS)C(=O)O[Si](C)(C)C(C)(C)C1804.2Standard non polar33892256
D-Cysteine,2TBDMS,isomer #2CC(C)(C)[Si](C)(C)N[C@H](CS)C(=O)O[Si](C)(C)C(C)(C)C1889.6Standard polar33892256
D-Cysteine,2TBDMS,isomer #3CC(C)(C)[Si](C)(C)N[C@H](CS[Si](C)(C)C(C)(C)C)C(=O)O1997.9Semi standard non polar33892256
D-Cysteine,2TBDMS,isomer #3CC(C)(C)[Si](C)(C)N[C@H](CS[Si](C)(C)C(C)(C)C)C(=O)O1935.6Standard non polar33892256
D-Cysteine,2TBDMS,isomer #3CC(C)(C)[Si](C)(C)N[C@H](CS[Si](C)(C)C(C)(C)C)C(=O)O2068.0Standard polar33892256
D-Cysteine,2TBDMS,isomer #4CC(C)(C)[Si](C)(C)N([C@H](CS)C(=O)O)[Si](C)(C)C(C)(C)C2011.1Semi standard non polar33892256
D-Cysteine,2TBDMS,isomer #4CC(C)(C)[Si](C)(C)N([C@H](CS)C(=O)O)[Si](C)(C)C(C)(C)C1890.2Standard non polar33892256
D-Cysteine,2TBDMS,isomer #4CC(C)(C)[Si](C)(C)N([C@H](CS)C(=O)O)[Si](C)(C)C(C)(C)C1926.0Standard polar33892256
D-Cysteine,3TBDMS,isomer #1CC(C)(C)[Si](C)(C)N[C@H](CS[Si](C)(C)C(C)(C)C)C(=O)O[Si](C)(C)C(C)(C)C2209.4Semi standard non polar33892256
D-Cysteine,3TBDMS,isomer #1CC(C)(C)[Si](C)(C)N[C@H](CS[Si](C)(C)C(C)(C)C)C(=O)O[Si](C)(C)C(C)(C)C2208.7Standard non polar33892256
D-Cysteine,3TBDMS,isomer #1CC(C)(C)[Si](C)(C)N[C@H](CS[Si](C)(C)C(C)(C)C)C(=O)O[Si](C)(C)C(C)(C)C2038.9Standard polar33892256
D-Cysteine,3TBDMS,isomer #2CC(C)(C)[Si](C)(C)OC(=O)[C@@H](CS)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C2226.0Semi standard non polar33892256
D-Cysteine,3TBDMS,isomer #2CC(C)(C)[Si](C)(C)OC(=O)[C@@H](CS)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C2211.8Standard non polar33892256
D-Cysteine,3TBDMS,isomer #2CC(C)(C)[Si](C)(C)OC(=O)[C@@H](CS)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C1954.6Standard polar33892256
D-Cysteine,3TBDMS,isomer #3CC(C)(C)[Si](C)(C)SC[C@H](C(=O)O)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C2354.4Semi standard non polar33892256
D-Cysteine,3TBDMS,isomer #3CC(C)(C)[Si](C)(C)SC[C@H](C(=O)O)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C2283.6Standard non polar33892256
D-Cysteine,3TBDMS,isomer #3CC(C)(C)[Si](C)(C)SC[C@H](C(=O)O)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C2091.4Standard polar33892256
D-Cysteine,4TBDMS,isomer #1CC(C)(C)[Si](C)(C)OC(=O)[C@@H](CS[Si](C)(C)C(C)(C)C)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C2581.8Semi standard non polar33892256
D-Cysteine,4TBDMS,isomer #1CC(C)(C)[Si](C)(C)OC(=O)[C@@H](CS[Si](C)(C)C(C)(C)C)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C2504.1Standard non polar33892256
D-Cysteine,4TBDMS,isomer #1CC(C)(C)[Si](C)(C)OC(=O)[C@@H](CS[Si](C)(C)C(C)(C)C)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C2105.3Standard polar33892256
Spectra
Biological Properties
Cellular Locations
  • Cytoplasm (predicted from logP)
Biospecimen Locations
  • Saliva
Tissue LocationsNot Available
Pathways
Normal Concentrations
BiospecimenStatusValueAgeSexConditionReferenceDetails
SalivaDetected and Quantified8.643 +/- 2.11 uMAdult (>18 years old)BothNormal
    • Zerihun T. Dame, ...
 details
Abnormal Concentrations
Not Available
Associated Disorders and Diseases
Disease ReferencesNone
Associated OMIM IDsNone
DrugBank IDDB03201
Phenol Explorer Compound IDNot Available
FooDB IDFDB023168
KNApSAcK IDC00007323
Chemspider ID83819
KEGG Compound IDC00793
BioCyc IDNot Available
BiGG IDNot Available
Wikipedia LinkCysteine
METLIN IDNot Available
PubChem Compound92851
PDB IDNot Available
ChEBI ID16375
Food Biomarker OntologyNot Available
VMH IDNot Available
MarkerDB IDNot Available
Good Scents IDrw1353141
References
Synthesis ReferenceNot Available
Material Safety Data Sheet (MSDS)Download (PDF)
General References
  1. Tsukamoto S, Kanegae T, Nagoya T, Shimamura M, Mieda Y, Nomura M, Hojo K, Okubo H: Effects of amino acids on acute alcohol intoxication in mice--concentrations of ethanol, acetaldehyde, acetate and acetone in blood and tissues. Arukoru Kenkyuto Yakubutsu Ison. 1990 Oct;25(5):429-40. [PubMed:2275637 ]
  2. Riemenschneider A, Wegele R, Schmidt A, Papenbrock J: Isolation and characterization of a D-cysteine desulfhydrase protein from Arabidopsis thaliana. FEBS J. 2005 Mar;272(5):1291-304. [PubMed:15720402 ]