(Q27098185)

Gene Ontology release 2020-05-02

Rhea release 113

allantoin racemase activity

1 reference

Gene Ontology release 2020-05-02

Rhea release 113

2-oxo-4-hydroxy-4-carboxy-5-ureidoimidazoline decarboxylase activity

1 reference

reference URL

http://geneontology.org/external2go/rhea2go

1 February 2021

mass

158.044 dalton

1 reference

S-(+)-Allantoin (English)

19 October 2016

1 reference

C₄H₆N₄O₃

1 reference

S-(+)-Allantoin (English)

20 November 2016

canonical SMILES

C1(C(=O)NC(=O)N1)NC(=O)N

1 reference

S-(+)-Allantoin (English)

20 November 2016

isomeric SMILES

[C@H]1(C(=O)NC(=O)N1)NC(=O)N

1 reference

S-(+)-Allantoin (English)

20 November 2016

found in taxon

Achyranthes bidentata

1 reference

Five new oleanolic acid glycosides from Achyranthes bidentata with inhibitory activity on osteoclast formation

Allium tuberosum

1 reference

A steroidal saponin from the seeds of Allium tuberosum.

Anchusa strigosa

1 reference

Pyrrolizidine alkaloids from Anchusa strigosa and their antifeedant activity

Aristolochia kaempferi

1 reference

Constituents from the stem and root of Aristolochia kaempferi

Aristolochia triangularis

1 reference

Terpenes from Aristolochia triangularis

Cordia oncocalyx

1 reference

Cordiachromes from Auxemma oncocalyx

Castela erecta

1 reference

Castelalin, a quassinoid from Castela tortuosa

Castela texana

1 reference

Castelalin, a quassinoid from Castela tortuosa

Castela tortuosa

1 reference

Castelalin, a quassinoid from Castela tortuosa

Cocculus pendulus

1 reference

CONSTITUENTS OF COCCULUS LEAEBA DC--CORRECTION FOR MISTAKEN BOTANICAL IDENTITY

Cordia boissieri

1 reference

Dimethyl-3,4′-kaempferol de Cordia boissieri

Cordia obliqua

1 reference

Chemical Investigation of the Stem Bark of Cordia obliqua

Cynoglossum zeylanicum

1 reference

Allantoin fromParacynoglossum imeretinum

Dioscorea japonica

1 reference

Furostanol saponins from the rhizomes of Dioscorea japonica and their effects on NGF induction

Galega officinalis

1 reference

Studies on the constituents of Goat's Rue (Galega officinalis L.).

Glycine max

1 reference

Nitrogen-containing compounds ofGlycine hispida

Indigofera suffruticosa

1 reference

Immunostimulatory and cytotoxic activities of Indigofera suffruticosa (Fabaceae).

Justicia leonardii

1 reference

An amide of L-threo-gamma-hydroxyglutamic acid from Justicia ghiesbreghtiana

Dolichandra unguis-cati

1 reference

Chemical characterization and biological activity of Macfadyena unguis-cati (Bignoniaceae)

Hypholoma fasciculare

1 reference

Investigation on some compounds biosynthesized by fruitbodies of Naematoloma fasciculare/huds. ex fr./p. Karst

Common rose

1 reference

Aristolochic Acids as a Defensive Substance for the Aristolochiaceous Plant-Feeding Swallowtail Butterfly,Pachliopta aristolochiae interpositus

pea

1 reference

Nitrogen-containing compounds ofPisum sativum

Polyalthia longifolia

2 references

New Antimicrobial Alkaloids from the Roots ofPolyalthia longifoliavar.pendula

Identification of the antioxidant principles of Polyalthia longifolia var. pendula using TEAC assay

Protea compacta

1 reference

Determination of allantoin in Protea seed

Fridericia elegans

1 reference

Inhaltsstoffe aus Pseudocalymma elegans (Vell.) Kuhlm. 1. Isolierung von Allantoin, Lamiid und Sorbarin / Ingredients from Pseudocalymma elegans (Vell.) Kuhlm. 1. Isolation of Allantoin, Lamiide, and Sorbarin

Symphytum orientale

1 reference

Alkaloidal and other constituents of Symphytum orientale

Heliotropium sarmentosum

1 reference

Phenolic compounds from tournefortia sarmentosa

Lathyrus oleraceus

1 reference

Nitrogen-containing compounds ofPisum sativum

Rochelia zeylanica

1 reference

Allantoin fromParacynoglossum imeretinum

Paracynoglossum furcatum

1 reference

Allantoin fromParacynoglossum imeretinum

Isotrema kaempferi

1 reference

Constituents from the stem and root of Aristolochia kaempferi

Identifiers

InChI

InChI=1S/C4H6N4O3/c5-3(10)6-1-2(9)8-4(11)7-1/h1H,(H3,5,6,10)(H2,7,8,9,11)/t1-/m0/s1

1 reference

S-(+)-Allantoin (English)

POJWUDADGALRAB-SFOWXEAESA-N

20 November 2016

InChIKey

2 references

S-(+)-Allantoin (English)

20 November 2016

ChEBI release 2020-09-01

CAS Registry Number

3844-67-5

2 references

Global Substance Registration System

UNII

XDK458E1J9

(+)-allantoin (English)

POJWUDADGALRAB-SFOWXEAESA-N

20 November 2016

InChIKey

8 April 2021

https://commonchemistry.cas.org/detail?cas_rn=3844-67-5

1 reference

(S)-(+)-allantoin (English)

20 November 2016

1 reference

S-(+)-Allantoin (English)

20 November 2016

Reaxys registry number

83513

1 reference

(S)-(+)-allantoin (English)

19 October 2016

ChEBI ID

15678

mapping relation type

1 reference

CHEMBL1230080 (English)

20 November 2016

1 reference

Global Substance Registration System

CHEMBL1230080 (English)

20 November 2016

1 reference

1 reference

UNII

XDK458E1J9

Global Substance Registration System

(+)-allantoin (English)

20 November 2016

1 reference

UNII

XDK458E1J9

(+)-allantoin (English)

20 November 2016

0 references

0 references

0 references

1 reference

2Q37 (English)