Urea - 10mM in DMSO , CAS No.57-13-6

CAS: 57-13-6 Cat. No.: U424822 Fórmula: H₂NCONH₂ Peso molecular: 60.06 Beilstein Registry Number: 635724 Número EC: 200-315-5 PubChem CID: 1176

GRADE & PURITY 10mM in DMSO

Synonyms

urea|carbamide|57-13-6|Carbonyldiamide|Isourea|Ureophil|Carbonyldiamine|Ureaphil|Carbamimidic acid|Urevert|Alphadrate|Aquadrate|Carbaderm|Keratinamin|Pseudourea|Carbonyl diamide|Calmurid|Pastaron|Urepearl|Carbamide resin|Ultra Mide|Varioform ii|Aqua Care|

Storage

Store at -80°C

Shipped In

Dry ice packs + Cold packs

Specifications

Sinónimos

urea | carbamide | 57-13-6 | Carbonyldiamide | Isourea | Ureophil | Carbonyldiamine | Ureaphil | Carbamimidic acid | Urevert | Alphadrate | Aquadrate | Carbaderm | Keratinamin | Pseudourea | Carbonyl diamide | Calmurid | Pastaron | Urepearl | Carbamide resin | Ultra Mide | Varioform ii | Aqua Care |

Especificaciones y pureza

10mM in DMSO

Mecanismos bioquímicos y fisiológicos

Urea participates in the metabolism of nitrogen-containing substances. When used as fertilizer, it can serve as a nitrogen source. Urea is used to manufacture compounds. It is widely used as fertilizer and animal feed additive in the agricultural field, a

Condiciones de almacenamiento de almacenamiento

Store at -80°C

Enviado en

Dry ice packs + Cold packs

Este producto requiere envío en cadena de frío. Los servicios terrestres y otros servicios económicos no están disponibles.

Nombres e identificadores

Pubchem Sid

528771519

Sonrisas canónicas

C(=O)(N)N

IUPAC Name

urea

InChIKey

XSQUKJJJFZCRTK-UHFFFAOYSA-N

INCHI

1S/CH4N2O/c2-1(3)4/h(H4,2,3,4)

Isómeros SMILES

C(=O)(N)N

WGK Alemania

1

RTECS

YR6250000

PubChem CID

1176

Peso molecular

60.06

Beilstein

635724

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Organic acids and derivatives
    • Clase Organic carbonic acids and derivatives
      • Subclass Ureas

• Kingdom: Organic compounds
• Superclass: Organic acids and derivatives
• Clase: Organic carbonic acids and derivatives
• Subclass: Ureas
• Intermediate Tree Nodes: Not available
• Direct Parent: Ureas
• Alternative Parents: Organopnictogen compounds Organonitrogen compounds Organic oxides Hydrocarbon derivatives Carbonyl compounds
• Molecular Framework: Aliphatic acyclic compounds
• Substituents: Urea - Organic nitrogen compound - Organic oxygen compound - Organopnictogen compound - Organic oxide - Hydrocarbon derivative - Organooxygen compound - Organonitrogen compound - Carbonyl group - Aliphatic acyclic compound
• Descripción: This compound belongs to the class of organic compounds known as ureas. These are compounds containing two amine groups joined by a carbonyl (C=O) functional group.
• External Descriptors: a small molecule

Data sources

1. Djoumbou Feunang Y, Eisner R, Knox C, Chepelev L, Hastings J, Owen G, Fahy E, Steinbeck C, Subramanian S, Bolton E, Greiner R, and Wishart DS. ClassyFire: Automated Chemical Classification With A Comprehensive, Computable Taxonomy. Journal of Cheminformatics, 2016, 8:61.

DOI: 10.1186/s13321-016-0174-y

Objetivos asociados (humanos)

OR51E2 Tchem Olfactory receptor 51E2 (2 Activities)

Discover Target: OR51E2

Activity Type	Activity Value -log(M)	Mechanism of Action	Activity Reference	Publications (PubMed IDs)

ALDH1A1 Tchem Aldehyde dehydrogenase 1A1 (77053 Activities)

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Homo sapiens (32628 Activities)

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Caco-2 (12174 Activities)

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POLI Tchem DNA polymerase iota (116820 Activities)

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Skin (286 Activities)

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TDP1 Tchem Tyrosyl-DNA phosphodiesterase 1 (345557 Activities)

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LMNA Tbio Prelamin-A/C (36751 Activities)

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SLCO1B1 Tchem Solute carrier organic anion transporter family member 1B1 (2672 Activities)

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CBX1 Tbio Chromobox protein homolog 1 (92434 Activities)

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SLCO1B3 Tchem Solute carrier organic anion transporter family member 1B3 (2517 Activities)

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RAPGEF3 Tchem Rap guanine nucleotide exchange factor 3 (15528 Activities)

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C5 Tclin Complement C5 (49 Activities)

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Objetivos asociados (no humanos)

Ppard Peroxisome proliferator-activated receptor delta (358 Activities)

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Hdac6 Histone deacetylase 6 (222 Activities)

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Pseudomonas aeruginosa (123386 Activities)

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Staphylococcus aureus (210822 Activities)

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Rattus norvegicus (775804 Activities)

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lef Anthrax lethal factor (7585 Activities)

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rep Replicase polyprotein 1ab (378 Activities)

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Brain (1 Activities)

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Nfe2l2 Nuclear factor erythroid 2-related factor 2 (214 Activities)

Discover Target: Nfe2l2

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

ureB Urease subunit alpha/Urease subunit beta (701 Activities)

Discover Target: ureB

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SARS-CoV-2 (38078 Activities)

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Mecanismos de acción

Propiedades químicas y físicas

• Sensibilidad: Moisture sensitive.
• Punto de fusión (°C): 132-135 °C (lit.)
• Peso molecular: 60.056 g/mol
• XLogP3: -1.400
• Hydrogen Bond Donor Count: 2
• Hydrogen Bond Acceptor Count: 1
• Rotatable Bond Count: 0
• Exact Mass: 60.0324 Da
• Monoisotopic Mass: 60.0324 Da
• Topological Polar Surface Area: 69.100 Ų
• Heavy Atom Count: 4
• Formal Charge: 0
• Complexity: 29.000
• Isotope Atom Count: 0
• Defined Atom Stereocenter Count: 0
• Undefined Atom Stereocenter Count: 0
• Defined Bond Stereocenter Count: 0
• Undefined Bond Stereocenter Count: 0
• The total count of all stereochemical bonds: 0
• Covalently-Bonded Unit Count: 1