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Record Information

Version

5.0

Status

Detected but not Quantified

Creation Date

2009-04-06 16:22:00 UTC

Update Date

2023-02-21 17:17:47 UTC

HMDB ID

HMDB0012265

Secondary Accession Numbers

HMDB12265

Metabolite Identification

Common Name

N-Carbamoylsarcosine

Description

N-Carbamoylsarcosine is an intermediate in arginine and proline metabolism. It is also involved in a metabolic pathway for the degradation of creatinine. In this pathway, creatinine is not hydrolyzed back to creatine. Instead, it is deaminated to N-methylhydantoin, releasing an amonia molecule, by the action of creatinine deaminase (also known as creatinine iminohydrolase). N-methylhydantoin is then hydrolyzed to N-carbamoylsarcosine, by the action of N-methylhydantoin amidohydrolase, at the expense of one ATP molecule. N-carbamoylsarcosine is deaminated further to sarcosine by N-carbamoylsarcosine amidohydrolase, releasing a second ammonia molecule. In the last step of this pathway, sarcosine is hydrolyzed to glycine and formaldehyde, by either sarcosine dehydrogenase or sarcosine oxidase.

Structure

MOL 3D MOL SDF 3D SDF PDB 3D PDB SMILES InChI

View in JSmol View NMR Assignments View Stereo Labels

Synonyms

Value	Source
Carbamoyl sarcosine	HMDB
Carbamoyl-sarcosine	HMDB
CMS	HMDB
[Carbamoyl(methyl)amino]acetic acid	HMDB

Chemical Formula

C₄H₈N₂O₃

Average Molecular Weight

132.1179

Monoisotopic Molecular Weight

132.053492132

IUPAC Name

2-[(C-hydroxycarbonimidoyl)(methyl)amino]acetic acid

Traditional Name

[C-hydroxycarbonimidoyl(methyl)amino]acetic acid

CAS Registry Number

Not Available

SMILES

CN(CC(O)=O)C(O)=N

InChI Identifier

InChI=1S/C4H8N2O3/c1-6(4(5)9)2-3(7)8/h2H2,1H3,(H2,5,9)(H,7,8)

InChI Key

SREKYKXYSQMOIB-UHFFFAOYSA-N

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as alpha amino acids and derivatives. These are amino acids in which the amino group is attached to the carbon atom immediately adjacent to the carboxylate group (alpha carbon), or a derivative thereof.

Kingdom

Organic compounds

Super Class

Organic acids and derivatives

Class

Carboxylic acids and derivatives

Sub Class

Amino acids, peptides, and analogues

Direct Parent

Alpha amino acids and derivatives

Alternative Parents

Substituents

Alpha-amino acid or derivatives
Urea
Carbonic acid derivative
Monocarboxylic acid or derivatives
Carboxylic acid
Organic nitrogen compound
Organic oxygen compound
Organopnictogen compound
Organic oxide
Hydrocarbon derivative
Organooxygen compound
Organonitrogen compound
Carbonyl group
Aliphatic acyclic compound

Molecular Framework

Aliphatic acyclic compounds

External Descriptors

glycine derivative (CHEBI:15737 )

Ontology

Not Available

Feces (PMID: 29808030)

Source

Endogenous

Endogenous (HMDB: HMDB0012265)

Pheasant (FooDB: FOOD00430)
Squab (FooDB: FOOD00481)
Turkey (FooDB: FOOD00494)
Quail (FooDB: FOOD00541)
Anatidae (FooDB: FOOD00576)
Rock ptarmigan (FooDB: FOOD00597)
Columbidae (Dove, Pigeon) (FooDB: FOOD00610)
Chicken (FooDB: FOOD00329)
Mallard duck (FooDB: FOOD00353)
Emu (FooDB: FOOD00360)
Greylag goose (FooDB: FOOD00368)
Guinea hen (FooDB: FOOD00373)
Ostrich (FooDB: FOOD00422)
Velvet duck (FooDB: FOOD00427)

Lagomorph

Ovis

Sheep (Mutton, Lamb) (FooDB: FOOD00473)

Bovine

Venison

Deer (FooDB: FOOD00524)
Mule deer (FooDB: FOOD00348)
Elk (FooDB: FOOD00359)

Caprae

Domestic goat (FooDB: FOOD00529)

Swine

Domestic pig (FooDB: FOOD00536)
Wild boar (FooDB: FOOD00307)

Equine

Horse (FooDB: FOOD00378)

Process

Not Available

Role

Not Available

Physical Properties

State

Solid

Experimental Molecular Properties

Property	Value	Reference
Melting Point	Not Available	Not Available
Boiling Point	Not Available	Not Available
Water Solubility	Not Available	Not Available
LogP	Not Available	Not Available

Experimental Chromatographic Properties

Not Available

Predicted Molecular Properties

Property	Value	Source
Water Solubility	3.83 g/L	ALOGPS
logP	-1.2	ALOGPS
logP	-2.1	ChemAxon
logS	-1.5	ALOGPS
pKa (Strongest Acidic)	2.64	ChemAxon
pKa (Strongest Basic)	9.38	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	5	ChemAxon
Hydrogen Donor Count	3	ChemAxon
Polar Surface Area	84.62 Å²	ChemAxon
Rotatable Bond Count	2	ChemAxon
Refractivity	40.36 m³·mol⁻¹	ChemAxon
Polarizability	11.78 Å³	ChemAxon
Number of Rings	0	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	Yes	ChemAxon
Ghose Filter	No	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	No	ChemAxon

Predicted Chromatographic Properties

Predicted Collision Cross Sections

Predictor	Adduct Type	CCS Value (Å²)	Reference
DarkChem	[M+H]+	127.987	31661259
DarkChem	[M-H]-	121.125	31661259
DeepCCS	[M+H]+	126.046	30932474
DeepCCS	[M-H]-	123.917	30932474
DeepCCS	[M-2H]-	160.337	30932474
DeepCCS	[M+Na]+	134.957	30932474
AllCCS	[M+H]+	131.2	32859911
AllCCS	[M+H-H2O]+	127.1	32859911
AllCCS	[M+NH4]+	135.0	32859911
AllCCS	[M+Na]+	136.1	32859911
AllCCS	[M-H]-	124.9	32859911
AllCCS	[M+Na-2H]-	127.7	32859911
AllCCS	[M+HCOO]-	130.9	32859911

Predicted Kovats Retention Indices

Underivatized

Metabolite	SMILES	Kovats RI Value	Column Type	Reference
N-Carbamoylsarcosine	CN(CC(O)=O)C(O)=N	2437.4	Standard polar	33892256
N-Carbamoylsarcosine	CN(CC(O)=O)C(O)=N	1384.8	Standard non polar	33892256
N-Carbamoylsarcosine	CN(CC(O)=O)C(O)=N	1605.2	Semi standard non polar	33892256

Derivatized

Derivative Name / Structure	SMILES	Kovats RI Value	Column Type	Reference
N-Carbamoylsarcosine,1TMS,isomer #1	CN(CC(=O)O[Si](C)(C)C)C(=N)O	1546.8	Semi standard non polar	33892256
N-Carbamoylsarcosine,1TMS,isomer #2	CN(CC(=O)O)C(=N)O[Si](C)(C)C	1535.8	Semi standard non polar	33892256
N-Carbamoylsarcosine,1TMS,isomer #3	CN(CC(=O)O)C(O)=N[Si](C)(C)C	1553.7	Semi standard non polar	33892256
N-Carbamoylsarcosine,2TMS,isomer #1	CN(CC(=O)O[Si](C)(C)C)C(=N)O[Si](C)(C)C	1533.6	Semi standard non polar	33892256
N-Carbamoylsarcosine,2TMS,isomer #2	CN(CC(=O)O[Si](C)(C)C)C(O)=N[Si](C)(C)C	1629.8	Semi standard non polar	33892256
N-Carbamoylsarcosine,2TMS,isomer #3	CN(CC(=O)O)C(=N[Si](C)(C)C)O[Si](C)(C)C	1521.4	Semi standard non polar	33892256
N-Carbamoylsarcosine,3TMS,isomer #1	CN(CC(=O)O[Si](C)(C)C)C(=N[Si](C)(C)C)O[Si](C)(C)C	1532.2	Semi standard non polar	33892256
N-Carbamoylsarcosine,3TMS,isomer #1	CN(CC(=O)O[Si](C)(C)C)C(=N[Si](C)(C)C)O[Si](C)(C)C	1478.0	Standard non polar	33892256
N-Carbamoylsarcosine,3TMS,isomer #1	CN(CC(=O)O[Si](C)(C)C)C(=N[Si](C)(C)C)O[Si](C)(C)C	1797.2	Standard polar	33892256
N-Carbamoylsarcosine,1TBDMS,isomer #1	CN(CC(=O)O[Si](C)(C)C(C)(C)C)C(=N)O	1783.6	Semi standard non polar	33892256
N-Carbamoylsarcosine,1TBDMS,isomer #2	CN(CC(=O)O)C(=N)O[Si](C)(C)C(C)(C)C	1780.6	Semi standard non polar	33892256
N-Carbamoylsarcosine,1TBDMS,isomer #3	CN(CC(=O)O)C(O)=N[Si](C)(C)C(C)(C)C	1751.2	Semi standard non polar	33892256
N-Carbamoylsarcosine,2TBDMS,isomer #1	CN(CC(=O)O[Si](C)(C)C(C)(C)C)C(=N)O[Si](C)(C)C(C)(C)C	2000.1	Semi standard non polar	33892256
N-Carbamoylsarcosine,2TBDMS,isomer #2	CN(CC(=O)O[Si](C)(C)C(C)(C)C)C(O)=N[Si](C)(C)C(C)(C)C	2040.3	Semi standard non polar	33892256
N-Carbamoylsarcosine,2TBDMS,isomer #3	CN(CC(=O)O)C(=N[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C	1966.9	Semi standard non polar	33892256
N-Carbamoylsarcosine,3TBDMS,isomer #1	CN(CC(=O)O[Si](C)(C)C(C)(C)C)C(=N[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C	2143.6	Semi standard non polar	33892256
N-Carbamoylsarcosine,3TBDMS,isomer #1	CN(CC(=O)O[Si](C)(C)C(C)(C)C)C(=N[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C	2048.4	Standard non polar	33892256
N-Carbamoylsarcosine,3TBDMS,isomer #1	CN(CC(=O)O[Si](C)(C)C(C)(C)C)C(=N[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C	2123.5	Standard polar	33892256

Spectra

GC-MS Spectra

Spectrum Type	Description	Splash Key	Deposition Date	Source	View
Predicted GC-MS	Predicted GC-MS Spectrum - N-Carbamoylsarcosine GC-MS (2 TMS) - 70eV, Positive	splash10-059l-9420000000-26d7547dadb70ab4fc08	2017-10-06	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - N-Carbamoylsarcosine GC-MS (Non-derivatized) - 70eV, Positive	splash10-0006-9100000000-f7eef7f30a71b2437a21	2017-11-06	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - N-Carbamoylsarcosine GC-MS (Non-derivatized) - 70eV, Positive	Not Available	2021-10-12	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - N-Carbamoylsarcosine GC-MS (Non-derivatized) - 70eV, Positive	Not Available	2021-10-12	Wishart Lab	View Spectrum

MS/MS Spectra

Spectrum Type	Description	Splash Key	Deposition Date	Source	View
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - N-Carbamoylsarcosine 10V, Positive-QTOF	splash10-001i-4900000000-828e01495f55c3ba6112	2015-09-15	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - N-Carbamoylsarcosine 20V, Positive-QTOF	splash10-006x-9100000000-d5aaf1e2016e0db5e1ef	2015-09-15	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - N-Carbamoylsarcosine 40V, Positive-QTOF	splash10-00di-9000000000-7b8ae0e68a69def64830	2015-09-15	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - N-Carbamoylsarcosine 10V, Negative-QTOF	splash10-001c-9300000000-64fe3175ab61247e7c9c	2015-09-15	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - N-Carbamoylsarcosine 20V, Negative-QTOF	splash10-000l-9100000000-3ef98ae24f347887d27a	2015-09-15	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - N-Carbamoylsarcosine 40V, Negative-QTOF	splash10-0006-9000000000-116ba20e6e0fcf01e7db	2015-09-15	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - N-Carbamoylsarcosine 10V, Negative-QTOF	splash10-000i-9000000000-df2ca252dc264c27f09e	2021-09-24	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - N-Carbamoylsarcosine 20V, Negative-QTOF	splash10-000i-9000000000-87f7d4792f3b20ebdd54	2021-09-24	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - N-Carbamoylsarcosine 40V, Negative-QTOF	splash10-006x-9000000000-1e503e67b415a9fae1b0	2021-09-24	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - N-Carbamoylsarcosine 10V, Positive-QTOF	splash10-000f-9100000000-20d310b987c7d3c62e72	2021-09-24	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - N-Carbamoylsarcosine 20V, Positive-QTOF	splash10-0076-9000000000-7debac7e5b881e478ecc	2021-09-24	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - N-Carbamoylsarcosine 40V, Positive-QTOF	splash10-0006-9000000000-a06e49ac0ea6780c12d1	2021-09-24	Wishart Lab	View Spectrum

NMR Spectra

Spectrum Type	Description	Deposition Date	Source	View
Predicted 1D NMR	¹H NMR Spectrum (1D, 100 MHz, D₂O, predicted)	2021-09-25	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 100 MHz, D₂O, predicted)	2021-09-25	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 1000 MHz, D₂O, predicted)	2021-09-25	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 1000 MHz, D₂O, predicted)	2021-09-25	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 200 MHz, D₂O, predicted)	2021-09-25	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 200 MHz, D₂O, predicted)	2021-09-25	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 300 MHz, D₂O, predicted)	2021-09-25	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 300 MHz, D₂O, predicted)	2021-09-25	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 400 MHz, D₂O, predicted)	2021-09-25	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 400 MHz, D₂O, predicted)	2021-09-25	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 500 MHz, D₂O, predicted)	2021-09-25	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 500 MHz, D₂O, predicted)	2021-09-25	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 600 MHz, D₂O, predicted)	2021-09-25	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 600 MHz, D₂O, predicted)	2021-09-25	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 700 MHz, D₂O, predicted)	2021-09-25	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 700 MHz, D₂O, predicted)	2021-09-25	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 800 MHz, D₂O, predicted)	2021-09-25	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 800 MHz, D₂O, predicted)	2021-09-25	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 900 MHz, D₂O, predicted)	2021-09-25	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 900 MHz, D₂O, predicted)	2021-09-25	Wishart Lab	View Spectrum

IR Spectra

Spectrum Type	Description	Deposition Date	Source	View
Predicted IR Spectrum	IR Ion Spectrum (Predicted IRIS Spectrum, Adduct: [M-H]-)	2023-02-03	FELIX lab	View Spectrum
Predicted IR Spectrum	IR Ion Spectrum (Predicted IRIS Spectrum, Adduct: [M+H]+)	2023-02-03	FELIX lab	View Spectrum
Predicted IR Spectrum	IR Ion Spectrum (Predicted IRIS Spectrum, Adduct: [M+Na]+)	2023-02-03	FELIX lab	View Spectrum

Biological Properties

Cellular Locations

Not Available

Biospecimen Locations

Blood
Feces
Urine

Tissue Locations

Not Available

Pathways

Not Available

Name	SMPDB/PathBank	KEGG

Normal Concentrations

Biospecimen	Status	Value	Age	Sex	Condition	Reference	Details
Feces	Detected but not Quantified	Not Quantified	Adult (>18 years old)	Both	Normal	29808030	details

Abnormal Concentrations

Biospecimen	Status	Value	Age	Sex	Condition	Reference	Details
Blood	Expected but not Quantified	Not Quantified	Not Specified	Not Specified	Cancer patients undergoing total body irradiation	31424920	details
Urine	Detected but not Quantified	Not Quantified	Not Specified	Not Specified	Cancer patients undergoing total body irradiation	31424920	details

Associated Disorders and Diseases

Disease References

None

Associated OMIM IDs

None

External Links

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FooDB ID

FDB028903

KNApSAcK ID

Not Available

Chemspider ID

388495

KEGG Compound ID

C01043

BioCyc ID

CARBAMOYL-SARCOSINE

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

439375

PDB ID

Not Available

ChEBI ID

15737

Food Biomarker Ontology

Not Available

VMH ID

Not Available

MarkerDB ID

Not Available

Good Scents ID

Not Available

References

Synthesis Reference

Not Available

Material Safety Data Sheet (MSDS)

Not Available

General References

Jiang S, Sun X, Zhang S: The ycaC-related protein from the amphioxus Branchiostoma belcheri (BbycaCR) interacts with creatine kinase. FEBS J. 2008 Sep;275(18):4597-605. doi: 10.1111/j.1742-4658.2008.06602.x. Epub 2008 Aug 11. [PubMed:18699781 ]
Wang WC, Hsu WH, Chien FT, Chen CY: Crystal structure and site-directed mutagenesis studies of N-carbamoyl-D-amino-acid amidohydrolase from Agrobacterium radiobacter reveals a homotetramer and insight into a catalytic cleft. J Mol Biol. 2001 Feb 16;306(2):251-61. [PubMed:11237598 ]
Lemaitre N, Callebaut I, Frenois F, Jarlier V, Sougakoff W: Study of the structure-activity relationships for the pyrazinamidase (PncA) from Mycobacterium tuberculosis. Biochem J. 2001 Feb 1;353(Pt 3):453-8. [PubMed:11171040 ]
Kim JM, Shimizu S, Yamada H: Purification and characterization of a novel enzyme, N-carbamoylsarcosine amidohydrolase, from Pseudomonas putida 77. J Biol Chem. 1986 Sep 5;261(25):11832-9. [PubMed:3745168 ]
Parsons JF, Calabrese K, Eisenstein E, Ladner JE: Structure and mechanism of Pseudomonas aeruginosa PhzD, an isochorismatase from the phenazine biosynthetic pathway. Biochemistry. 2003 May 20;42(19):5684-93. [PubMed:12741825 ]
Zajc A, Romao MJ, Turk B, Huber R: Crystallographic and fluorescence studies of ligand binding to N-carbamoylsarcosine amidohydrolase from Arthrobacter sp. J Mol Biol. 1996 Oct 25;263(2):269-83. [PubMed:8913306 ]
Kim JM, Shimizu S, Yamada H: Amidohydrolysis of N-methylhydantoin coupled with ATP hydrolysis. Biochem Biophys Res Commun. 1987 Feb 13;142(3):1006-12. [PubMed:3827889 ]
Romao MJ, Turk D, Gomis-Ruth FX, Huber R, Schumacher G, Mollering H, Russmann L: Crystal structure analysis, refinement and enzymatic reaction mechanism of N-carbamoylsarcosine amidohydrolase from Arthrobacter sp. at 2.0 A resolution. J Mol Biol. 1992 Aug 20;226(4):1111-30. [PubMed:1381445 ]
Ogawa J, Nirdnoy W, Tabata M, Yamada H, Shimizu S: A new enzymatic method for the measurement of creatinine involving a novel ATP-dependent enzyme, N-methylhydantoin amidohydrolase. Biosci Biotechnol Biochem. 1995 Dec;59(12):2292-4. [PubMed:8611752 ]
Hermann M, Knerr HJ, Mai N, Gross A, Kaltwasser H: Creatinine and N-methylhydantoin degradation in two newly isolated Clostridium species. Arch Microbiol. 1992;157(5):395-401. [PubMed:1510564 ]
Luo HB, Zheng H, Zimmerman MD, Chruszcz M, Skarina T, Egorova O, Savchenko A, Edwards AM, Minor W: Crystal structure and molecular modeling study of N-carbamoylsarcosine amidase Ta0454 from Thermoplasma acidophilum. J Struct Biol. 2010 Mar;169(3):304-11. doi: 10.1016/j.jsb.2009.11.008. Epub 2009 Nov 20. [PubMed:19932181 ]
Ogawa J, Shimizu S, Yamada H: N-carbamoyl-D-amino acid amidohydrolase from Comamonas sp. E222c purification and characterization. Eur J Biochem. 1993 Mar 15;212(3):685-91. [PubMed:8462543 ]
Caruthers J, Zucker F, Worthey E, Myler PJ, Buckner F, Van Voorhuis W, Mehlin C, Boni E, Feist T, Luft J, Gulde S, Lauricella A, Kaluzhniy O, Anderson L, Le Trong I, Holmes MA, Earnest T, Soltis M, Hodgson KO, Hol WG, Merritt EA: Crystal structures and proposed structural/functional classification of three protozoan proteins from the isochorismatase superfamily. Protein Sci. 2005 Nov;14(11):2887-94. Epub 2005 Sep 30. [PubMed:16199669 ]
Shimizu S, Kim JM, Yamada H: Microbial enzymes for creatinine assay: a review. Clin Chim Acta. 1989 Dec 15;185(3):241-52. [PubMed:2695273 ]

Showing metabocard for N-Carbamoylsarcosine (HMDB0012265)

MOL for HMDB0012265 (N-Carbamoylsarcosine)

3D MOL for HMDB0012265 (N-Carbamoylsarcosine)

3D SDF for HMDB0012265 (N-Carbamoylsarcosine)

3D-SDF for HMDB0012265 (N-Carbamoylsarcosine)

PDB for HMDB0012265 (N-Carbamoylsarcosine)

3D PDB for HMDB0012265 (N-Carbamoylsarcosine)

SMILES for HMDB0012265 (N-Carbamoylsarcosine)

INCHI for HMDB0012265 (N-Carbamoylsarcosine)

Structure for HMDB0012265 (N-Carbamoylsarcosine)

3D Structure for HMDB0012265 (N-Carbamoylsarcosine)

Predicted Collision Cross Sections

Predicted Kovats Retention Indices

Underivatized

Derivatized

GC-MS Spectra

MS/MS Spectra

NMR Spectra

IR Spectra