uracil (Q182990)

uracil catabolic process

reactant

1 reference

1 reference

uracil biosynthetic process

product

1 reference

uracil transmembrane transport

1 reference

uracil transmembrane transporter activity

1 reference

uracil:cation symporter activity

1 reference

1 reference

uracil import across plasma membrane

1 reference

uracil metabolic process

participant

1 reference

cytosine deaminase activity

1 reference

dihydropyrimidine dehydrogenase (NAD+) activity

1 reference

pseudouridylate synthase activity

1 reference

uracil phosphoribosyltransferase activity

1 reference

uridine phosphorylase activity

1 reference

dihydropyrimidine dehydrogenase (NADP+) activity

1 reference

uridine nucleosidase activity

1 reference

deoxyuridine 1'-dioxygenase activity

1 reference

deoxyuridine phosphorylase activity

1 reference

dihydrouracil oxidase activity

1 reference

uracil-5-carboxylate decarboxylase activity

1 reference

uracilylalanine synthase activity

1 reference

uracil oxygenase activity

1 reference

http://geneontology.org/external2go/rhea2go

uracil dehydrogenase activity

1 February 2021

1 reference

http://geneontology.org/external2go/rhea2go

1 February 2021

chemical structure

Uracil.svg
112 × 154; 4 KB

1 reference

German Wikipedia

mass

112.027 dalton

1 reference

uracil (English)

17 November 2016

C₄H₄N₂O₂

1 reference

uracil (English)

17 November 2016

C1=CNC(=O)NC1=O

1 reference

uncertainty corresponds to

uracil (English)

17 November 2016

339±1 degree Celsius

expanded uncertainty

1 reference

CRC Handbook of Chemistry and Physics (97th edition)

page(s)

3-546

330 degree Celsius

1 reference

Jean-Claude Bradley Open Melting Point Dataset

solubility

4.62 gram per kilogram

25 degree Celsius

1 reference

CRC Handbook of Chemistry and Physics (97th edition)

page(s)

5-166

pKa

9.45

temperature

25 degree Celsius

1 reference

CRC Handbook of Chemistry and Physics (97th edition)

page(s)

5-97

safety classification and labelling

NFPA 704: Standard System for the Identification of the Hazards of Materials for Emergency Response

0

0

0

no value

1 reference

https://www.sigmaaldrich.com/MSDS/MSDS/DisplayMSDSPage.do?country=US&language=en&productNumber=U0750&brand=SIGMA&PageToGoToURL=https%3A%2F%2Fwww.sigmaaldrich.com%2Fcatalog%2Fproduct%2Fsigma%2Fu0750%3Flang%3Dpl

Uracil (English)

30 January 2015

10 July 2018

Regulation (EC) No. 1272/2008

GHS hazard pictogram

no value

GHS signal word

no value

GHS hazard statement

no value

GHS precautionary statement

no value

1 reference

https://www.sigmaaldrich.com/MSDS/MSDS/DisplayMSDSPage.do?country=PL&language=EN-generic&productNumber=U0750&brand=SIGMA&PageToGoToURL=https%3A%2F%2Fwww.sigmaaldrich.com%2Fcatalog%2Fproduct%2Fsigma%2Fu0750%3Flang%3Dpl

Uracil (English)

12 June 2015

10 July 2018

Recon 2.2: from reconstruction to model of human metabolism

3 references

The human saliva metabolome

A community-driven global reconstruction of human metabolism.

3 references

Copper = Leslie M. Klevay

Escherichia coli

3 references

Chimeras between single-stranded DNA-binding proteins from Escherichia coli and Mycobacterium tuberculosis reveal that their C-terminal domains interact with uracil DNA glycosylases.

Metabolic Profiling of Escherichia coli-based Cell-Free Expression Systems for Process Optimization

A comprehensive genome-scale reconstruction of Escherichia coli metabolism--2011.

Penicillium

1 reference

Bioactive metabolites produced by Penicillium sp. 1 and sp. 2, two endophytes associated with Alibertia macrophylla (Rubiaceae).

Begonia nantoensis

2 references

Cytotoxic and anti-HIV principles from the rhizomes of Begonia nantoensis.

Cytotoxic and anti-HIV Principles from the Rhizomes of Begonia nantoensis.

Crocus sativus

3 references

Constituents of the stigmas of Crocus sativus and their tyrosinase inhibitory activity

Constituents of the pollen of Crocus sativus L. and their tyrosinase inhibitory activity.

Constituents of the Pollen of Crocus sativus L. and Their Tyrosinase Inhibitory Activity.

Ficus septica

2 references

Ficus spp. (fig): ethnobotany and potential as anticancer and anti-inflammatory agents

Phenanthroindolizidine Alkaloids and Their Cytotoxicity from the Leaves of Ficus septica

Herpetospermum pedunculosum

1 reference

Two new coumarins from Herpetospermum caudigerum.

Junceella juncea

1 reference

Study on the chemical constituents of the South China Sea gorgonian Junceella juncea.

Subergorgia suberosa

1 reference

Purine and pyrimidine derivatives from the South China Sea gorgonian Subergorgia suberosa.

Viscum coloratum

1 reference

The inhibition of superoxide anion generation in human neutrophils by Viscum coloratum

maize

1 reference

Chemical constituents of the style of Zea mays L. with glycation inhibitory activity

Arabidopsis thaliana

4 references

Unbiased characterization of genotype-dependent metabolic regulations by metabolomic approach in Arabidopsis thaliana

Decreased abundance of type III secretion system-inducing signals in Arabidopsis mkp1 enhances resistance against Pseudomonas syringae

Balancing of B6 Vitamers Is Essential for Plant Development and Metabolism in Arabidopsis.

Arabidopsis thaliana nucleosidase mutants provide new insights into nucleoside degradation

Whistling tree frog

1 reference

Survival, gene and metabolite responses of Litoria verreauxii alpina frogs to fungal disease chytridiomycosis.

Lotus corniculatus

2 references

Integrative functional genomics of salt acclimatization in the model legume Lotus japonicus

Mining for robust transcriptional and metabolic responses to long-term salt stress: a case study on the model legume Lotus japonicus

Mycoplasma bovis

1 reference

Comparative Metabolomics of Mycoplasma bovis and Mycoplasma gallisepticum Reveals Fundamental Differences in Active Metabolic Pathways and Suggests Novel Gene Annotations.

Mycoplasma gallisepticum

1 reference

Comparative Metabolomics of Mycoplasma bovis and Mycoplasma gallisepticum Reveals Fundamental Differences in Active Metabolic Pathways and Suggests Novel Gene Annotations.

Populus tremula

1 reference

A metabolite roadmap of the wood-forming tissue in Populus tremula

Pseudomonas aeruginosa

1 reference

Transcriptomic and Metabolomics Profiling of Phage-Host Interactions between Phage PaP1 and Pseudomonas aeruginosa

Pseudomonas putida

1 reference

Metabolomics Analysis Reveals the Participation of Efflux Pumps and Ornithine in the Response of Pseudomonas putida DOT-T1E Cells to Challenge with Propranolol

Salmonella enterica

2 references

Salmonella modulates metabolism during growth under conditions that induce expression of virulence genes

The impact of slyA on cell metabolism of Salmonella Typhimurium: a joint study of transcriptomics and metabolomics

Trypanosoma brucei

1 reference

Untargeted metabolomics reveals a lack of synergy between nifurtimox and eflornithine against Trypanosoma brucei

Echinoclathria gibbosa

1 reference

New compounds from the Red Sea marine sponge Echinoclathria gibbosa

Eleutherococcus giraldii

1 reference

Chemical constituents from Acanthopanax brachypus

Aristolochia heterophylla

1 reference

The Constituents of the Leaves of Aristolochia heterophylla HEMSL.

Aristolochia kaempferi

1 reference

The Constituents of the Leaves of Aristolochia heterophylla HEMSL.

Carteriospongia

1 reference

Hydrophilic metabolites from the tropical marine sponge Carteriospongia sp.

Senna didymobotrya

1 reference

PHYTOCHEMICAL STUDY OF CASSIA DIDYMOBOTRYA FRES. CULTIVATED IN EGYPT PART 1: STUDY OF QUINONES AND URACIL

Leptochilus hemionitideus

1 reference

Chemical and Chemotaxonomical Studies on Filices. LVII. Chemical Studies on the Constituents of Colysis hemionitidea (WALL) PRESL. and Microsorium fortunei (MOORE) CHING

Paraphaeosphaeria minitans

1 reference

3(2H)-Benzofuranones and chromanes from liquid cultures of the mycoparasitic fungus Coniothyrium minitans

Ophiocordyceps sinensis

2 references

Medicinal Value of Cordyceps sinensis

Anti-inflammatory principles from Cordyceps sinensis

Coriandrum sativum

1 reference

Water-soluble constituents of coriander

Cuminum cyminum

1 reference

Sesquiterpene lactone glucosides and alkyl glycosides from the fruit of cumin.

Tetradium daniellii

1 reference

Constituents of the fruits and leaves of Euodia daniellii.

Euphorbia altotibetica

1 reference

Chemical Constituents from the Whole Plant of Euphorbia altotibetic

fennel

1 reference

Water-Soluble Constituents of Fennel. IX. Glucides and Nucleosides.

Ganoderma japonicum

1 reference

Identification and quantification of base and nucleoside markers in extracts of Ganoderma lucidum, Ganoderma japonicum and Ganoderma capsules by micellar electrokinetic chromatography.

Ganoderma lucidum

1 reference

Identification and quantification of base and nucleoside markers in extracts of Ganoderma lucidum, Ganoderma japonicum and Ganoderma capsules by micellar electrokinetic chromatography.

Geodia japonica

1 reference

Isomalabaricane-type nortriterpenoids and other constituents of the marine sponge Geodia japonica.

Jatropha curcas

1 reference

A complex of 5-hydroxypyrrolidin-2-one and pyrimidine-2,4-dione isolated from Jatropha curcas

Lathyrus davidii

1 reference

[Chemical constituents from Sinacalia davidii].

Conioselinum anthriscoides

1 reference

Ligusticum chuanxiong

1 reference

Neocheiropteris fortunei

1 reference

Chemical and Chemotaxonomical Studies on Filices. LVII. Chemical Studies on the Constituents of Colysis hemionitidea (WALL) PRESL. and Microsorium fortunei (MOORE) CHING

Momordica charantia

1 reference

Novel Active Constituents of Momordica Charantia L.

Muscari neglectum

1 reference

Homoisoflavanones and other constituents from Muscari racemosum

Muscari racemosum

1 reference

Homoisoflavanones and other constituents from Muscari racemosum

Nothapodytes nimmoniana

1 reference

Constituents and cytotoxic principles of Nothapodytes foetida

Panax ginseng

1 reference

Application of high-speed liquid chromatography and dual wave-length thin-layer chromatograph-densitometry to analysis of crude drugs: Nucleosides and free bases of nucleic acids in Ginseng roots (author's transl)

Pancratium maritimum

1 reference

Alkaloids of the flowers of Pancratium maritimum

Procris repens

1 reference

A new glucoceramide from the watermelon Begonia, Pellionia repens.

Petasites formosanus

1 reference

Constituents of the Leaves of Petasites formosanus and Their Antioxidative Activity

Rehmannia glutinosa

1 reference

Five cyclopentanoid monoterpenes from Rehmannia glutinosa

Scaphium affine

1 reference

Alkaloids from the Seeds of Sterculia lychnophora (Pangdahai).

Trichoderma koningii

2 references

Studies on Metabolites of Mycoparasitic Fungi. III. New Sesquiterpene Alcohol from Trichoderma koningii.

Studies on metabolites of mycoparasitic fungi. IV. Minor peptaibols of Trichoderma koningii

Aspergillus fumigatus

1 reference

Metabolites from Aspergillus fumigatus, an endophytic fungus associated with Melia azedarach, and their antifungal, antifeedant, and toxic activities.

Daphnia magna

1 reference

Streptomyces xanthophaeus

1 reference

α-Glucosidase inhibitors and phytotoxins from Streptomyces xanthophaeus

Actinidia chinensis

1 reference

Chemical constituents from the roots of Actinidia chinensis

Colletotrichum gloeosporioides

1 reference

Metabolites of Colletotrichum gloeosporioides, an endophytic fungus in Artemisia mongolica

Hamigera avellanea

1 reference

Hamigeromycins C–G, 14-membered macrolides from the fungus Hamigera avellanea BCC 17816

Mandragora officinarum

1 reference

New withanolides from Mandragora officinarum: first report of withanolides from the Genus Mandragora.

Oryza aristata

1 reference

Anti-inflammatory and antioxidant components from Hygroryza aristata

Oxytropis racemosa

1 reference

3-Hydroxymethylglutaryl flavonol glycosides from a Mongolian and Tibetan medicine, Oxytropis racemosa

Peucedanum japonicum

1 reference

Antioxidant compounds from the leaves of Peucedanum japonicum thunb.

Kali collinum

1 reference

Chemical and biologically active constituents of Salsola collina

Salsola collina

1 reference

Chemical and biologically active constituents of Salsola collina

Tuber indicum

1 reference

Chemical constituents from the ascomycetous fungus Tuber indicum

Ulva pertusa

1 reference

Secondary metabolites from green algae Ulva pertusa

Xanthium sibiricum

1 reference

Chemical constituents from the roots of Xanthium sibiricum

Xanthium strumarium

1 reference

Chemical constituents from the roots of Xanthium sibiricum

Phyllospongia

1 reference

Hydrophilic metabolites from the tropical marine sponge Carteriospongia sp.

Cordyceps militaris

1 reference

Anti-inflammatory principles from Cordyceps sinensis

Petrosiidae

1 reference

New manzamine alkaloids with activity against infectious and tropical parasitic diseases from an Indonesian sponge.

Neolepisorus fortunei

1 reference

Chemical and Chemotaxonomical Studies on Filices. LVII. Chemical Studies on the Constituents of Colysis hemionitidea (WALL) PRESL. and Microsorium fortunei (MOORE) CHING

Fritillaria cirrhosa

1 reference

Identification and Quantitative Analysis of Nucleosides and Nucleobases in Aqueous Extracts ofFritillaria CirrhosaD. Don. Using HPLC–DAD and HPLC-ESI-MS

Drosophila melanogaster

1 reference

Rapid metabolic shifts occur during the transition between hunger and satiety in Drosophila melanogaster

Ensifer meliloti

1 reference

Creation and Characterization of a Genomically Hybrid Strain in the Nitrogen-Fixing Symbiotic Bacterium Sinorhizobium meliloti

Sinorhizobium meliloti

1 reference

Creation and Characterization of a Genomically Hybrid Strain in the Nitrogen-Fixing Symbiotic Bacterium Sinorhizobium meliloti

Penicillium commune

1 reference

Chemical constituents of a marine-derived endophytic fungus Penicillium commune G2M.

Nocardia alba

1 reference

(1)H and (13)C NMR assignments of eight nitrogen containing compounds from Nocardia alba sp.nov (YIM 30243(T)).

Polyporus umbellatus

1 reference

1β-hydroxylfriedelin, a new natural pentacylic triterpene from the sclerotia of <I>Polyporus umbellatus</I>

Ulva australis

1 reference

Secondary metabolites from green algae Ulva pertusa

Ligusticum striatum

1 reference

Oreocome striata

1 reference

Lepisorus fortunei

1 reference

Chemical and Chemotaxonomical Studies on Filices. LVII. Chemical Studies on the Constituents of Colysis hemionitidea (WALL) PRESL. and Microsorium fortunei (MOORE) CHING

Aeromonas veronii

1 reference

Absence of tmRNA Increases the Persistence to Cefotaxime and the Intercellular Accumulation of Metabolite GlcNAc in Aeromonas veronii

Isotrema kaempferi

1 reference

The Constituents of the Leaves of Aristolochia heterophylla HEMSL.

1 reference

1 reference

Anti-inflammatory and antioxidant components from Hygroryza aristata

Euglena gracilis

1 reference

Metabolic Responses of a Model Green Microalga Euglena gracilis to Different Environmental Stresses

Lotus japonicus

2 references

Mining for robust transcriptional and metabolic responses to long-term salt stress: a case study on the model legume Lotus japonicus

Integrative functional genomics of salt acclimatization in the model legume Lotus japonicus

Saccharomyces cerevisiae

1 reference

Proteome allocations change linearly with the specific growth rate of Saccharomyces cerevisiae under glucose limitation

Caenorhabditis elegans

1 reference

Modeling Meets Metabolomics-The WormJam Consensus Model as Basis for Metabolic Studies in the Model Organism

Sauromatum giganteum

1 reference

Chemical constituents of Typhonium giganteum Engl.

Streptococcus pneumoniae

1 reference

Dysregulation of Streptococcus pneumoniae zinc homeostasis breaks ampicillin resistance in a pneumonia infection model

Leishmania donovani

1 reference

Integrated genomic and metabolomic profiling of ISC1, an emerging Leishmania donovani population in the Indian subcontinent

0 references

0 references

0 references

0 references

Uracil

0 references

Identifiers

GND ID

4187149-2

1 reference

InChI=1S/C4H4N2O2/c7-3-1-2-5-4(8)6-3/h1-2H,(H2,5,6)

German Wikipedia

InChI

1 reference

ISAKRJDGNUQOIC-UHFFFAOYSA-N

uracil (English)

17 November 2016

2 references

uracil (English)

17 November 2016

ChEBI release 2020-09-01

CAS Registry Number

66-22-8

2 references

ISAKRJDGNUQOIC-UHFFFAOYSA-N

uracil (English)

17 November 2016

8 April 2021

https://commonchemistry.cas.org/detail?cas_rn=66-22-8

1 reference

Uracil (English)

17 November 2016

1 reference

uracil (English)

17 November 2016

Reaxys registry number

606623

1 reference

uracil (English)

19 October 2016

2896

0 references

ChEBI ID

17568

mapping relation type

2 references

URACIL (English)

17 November 2016

ChEBI release 2019-10-02

1 reference

URACIL (English)

MSBNK-Fac_Eng_Univ_Tokyo-JP009498

17 November 2016

MassBank accession ID

0 references

MSBNK-Osaka_Univ-OUF00483

0 references

MSBNK-RIKEN-PR010100

0 references

MSBNK-RIKEN-PR100037

0 references

MSBNK-RIKEN-PR100501

0 references

MSBNK-Fac_Eng_Univ_Tokyo-JP008282

0 references

MSBNK-Keio_Univ-KO001973

0 references

MSBNK-Keio_Univ-KO001974

0 references

MSBNK-Keio_Univ-KO001975

0 references

MSBNK-Keio_Univ-KO001976

0 references

MSBNK-Keio_Univ-KO001977

0 references

SPLASH

splash10-03xu-9400000000-1c29f070a8135b06f88b

0 references

splash10-03di-0900000000-309fe212c929f3c6a930

0 references

splash10-03di-6900000000-55a7de75a40eab61da8b

0 references

splash10-0006-9000000000-1c3caab26eb7e359db92

0 references

splash10-0006-9000000000-7494d4e611a73ecb79ea

0 references

splash10-0006-9000000000-ed4046b040337db620d8

0 references

splash10-0002-5950000000-18425875415ad150c4fc

0 references

splash10-006t-9740000000-e884a4b98e7e9dc75e5f

0 references

splash10-03di-0900000000-ff54f3083ce4ccccfd95

0 references

splash10-03di-0900000000-6728c1eb6f68b40c09f8

0 references

splash10-00di-4139010000-b46eda05ead5c72a303a

0 references

splash10-03di-0900000000-a21102c708f8d5eaf262

0 references

splash10-03di-0900000000-411568a56aeb7f4159b3

0 references

splash10-03di-6900000000-cb61fa5fde57a0693b89

0 references

splash10-03di-0900000000-a26776164618a601ad62

0 references

splash10-0002-6940000000-a726178341f6443e60cc

0 references

splash10-03xu-9400000000-d7ffe72f606f1af3349b

0 references

splash10-006y-9000000000-130eb5f4414426e03667

0 references

splash10-052e-7790000000-026cb6beb5cde6a61b80

0 references

splash10-03di-3900000000-e422eda255a4b6414f86

0 references

splash10-0006-9100000000-c096d08ca715d97cd732

0 references

RTECS number

YQ8650000

2 references

Russian Wikipedia

Mapping file of InChIStrings, InChIKeys and DTXSIDs for the EPA CompTox Dashboard

1 reference

DSSTOX compound identifier

0 references

0 references

0 references

200-621-9

1 reference

uracil (English)

ECHA Substance Infocard ID

17 November 2016

100.000.565

1 reference

ECHA Substance Infocard database

ECHA Substance Infocard ID

27 December 2018

Uracil (English)

CAS no.: 66-22-8 (English)

1 reference

28 December 2019

URACIL (English)

CAS no.: 66-22-8 (English)

AICS Chemical ID (BEING DELETED)

735

0 references

Guide to Pharmacology Ligand ID

4560

1 reference

IUPHAR/BPS Guide to PHARMACOLOGY

Guide to Pharmacology Ligand ID

4560

uracil (English)

17 November 2016

Uracil

0 references

0 references

1 reference

uracil (English)

17 November 2016

1 reference

Uracil (English)

Human Metabolome Database ID

17 November 2016

0 references

1 reference

uracil (English)

19 October 2016

1 reference

uracil (English)

17 November 2016

1 reference

Immune Epitope Database and Analysis Resource

uracil (English)

19 October 2016

0 references

1 reference

1 March 2022

0 references

1 reference

6 April 2020

1 reference

0 references

0 references

Dizionario delle Scienze Fisiche ID

uracile

subject named as

uracile

publication date

1996

0 references

Dizionario di Medicina ID

uracile

subject named as

uracile

publication date

2010

0 references

Elhuyar ZTH ID

031750

0 references

Encyclopædia Britannica Online ID

0 references

1 reference

28 October 2013

Gran Enciclopèdia Catalana ID

0149362

0 references

Great Russian Encyclopedia Online ID

4700847

0 references

JSTOR topic ID

uracil-nucleotides

0 references

1 reference

9 July 2020

Microsoft Academic ID

0 references

0 references

0 references

1 reference

26 January 2022

https://docs.openalex.org/download-snapshot/snapshot-data-format

1 reference

2EUG (English)

19 October 2016

1 reference

4HK7 (English)

19 October 2016

1 reference

4WPL (English)

19 October 2016

1 reference

3QPB (English)

19 October 2016

1 reference

4YGM (English)

19 October 2016

1 reference

1TGY (English)

19 October 2016

1 reference

3KVY (English)

19 October 2016

1 reference

1KSL (English)

19 October 2016

1 reference

3BJE (English)

19 October 2016

1 reference

1BD4 (English)

19 October 2016

1 reference

4JYK (English)

19 October 2016

1 reference

2RJ3 (English)

19 October 2016

1 reference

1BRW (English)

19 October 2016

1 reference

1WS3 (English)

19 October 2016

1 reference

3QE7 (English)

19 October 2016

1 reference

1OE5 (English)

19 October 2016

1 reference

4YIG (English)

19 October 2016

1 reference

1UDH (English)

19 October 2016

1 reference

1UCD (English)

19 October 2016

1 reference

1GTH (English)

19 October 2016

1 reference

3LOC (English)

19 October 2016

1 reference

4YJK (English)

19 October 2016

1 reference

1UI0 (English)

19 October 2016

1 reference

1EMJ (English)

19 October 2016

1 reference

4ZBY (English)

19 October 2016

1 reference

1KSK (English)

19 October 2016

1 reference

4OEH (English)

19 October 2016

1 reference

4LZB (English)

19 October 2016

1 reference

3SLF (English)

19 October 2016

1 reference

1Y1S (English)

19 October 2016

1 reference

3PNS (English)

19 October 2016

1 reference

1SSP (English)

19 October 2016

1 reference

3CXM (English)

19 October 2016

1 reference

4WRU (English)

19 October 2016

1 reference

4WRV (English)

19 October 2016

1 reference

4KPV (English)

19 October 2016

1 reference

1JLS (English)

19 October 2016

1 reference

1FLZ (English)

19 October 2016

1 reference

1Q3F (English)

19 October 2016

1 reference

4TXL (English)

19 October 2016

1 reference

5ILX (English)

19 October 2016

1 reference

2XRF (English)

19 October 2016

1 reference

5EUG (English)

19 October 2016

1 reference

4SKN (English)

19 October 2016

0 references

0 references

Store norske leksikon ID

0 references

uracile

0 references

WordNet 3.1 Synset ID

15108924-n

1 reference