Print…

Procurou por: 3-Pyrroline


159  resultados encontrados

SearchResultCount:"159"

Sort Results

Visualização em Lista Easy View (new)

Classifique os resultados da pesquisa

Código de Artigo: (ACRO371690050)
Fornecedor: Thermo Fisher Scientific
Descrição: Benzyl-2,5-dihydro-1H-pyrrole-1-carboxylate 98%
UOM: 1 * 5 g

MSDS


Código de Artigo: (TCIAD3825-100MG)
Fornecedor: TCI
Descrição: 3,4-Dehydro-L-proline ≥99.0% (by HPLC)
UOM: 1 * 100 mg


Código de Artigo: (BOSSBS-5813R-CY5.5)
Fornecedor: Bioss
Descrição: Proline oxidase catalyzes the conversion of proline to pyrroline-5-carboxylate, or P5C during the degradation of the amino acid Proline. Defects in PRODH are the cause of hyperprolinemia type 1, a disorder characterized by elevated serum proline levels. Defective PRODH may be involved in the psychiatric and behavioral phenotypes associated with the 22q11 velocardiofacial and DiGeorge syndrome and may be associated with susceptibility to schizophrenia 4 (SCZD4).
UOM: 1 * 100 µl


Código de Artigo: (BOSSBS-5813R-CY3)
Fornecedor: Bioss
Descrição: Proline oxidase catalyzes the conversion of proline to pyrroline-5-carboxylate, or P5C during the degradation of the amino acid Proline. Defects in PRODH are the cause of hyperprolinemia type 1, a disorder characterized by elevated serum proline levels. Defective PRODH may be involved in the psychiatric and behavioral phenotypes associated with the 22q11 velocardiofacial and DiGeorge syndrome and may be associated with susceptibility to schizophrenia 4 (SCZD4).
UOM: 1 * 100 µl


Fornecedor: Apollo Scientific
Descrição: tert-Butyl-2,5-dihydro-1H-pyrrole-1-carboxylate

Código de Artigo: (BOSSBS-5813R-HRP)
Fornecedor: Bioss
Descrição: Proline oxidase catalyzes the conversion of proline to pyrroline-5-carboxylate, or P5C during the degradation of the amino acid Proline. Defects in PRODH are the cause of hyperprolinemia type 1, a disorder characterized by elevated serum proline levels. Defective PRODH may be involved in the psychiatric and behavioral phenotypes associated with the 22q11 velocardiofacial and DiGeorge syndrome and may be associated with susceptibility to schizophrenia 4 (SCZD4).
UOM: 1 * 100 µl


Código de Artigo: (BOSSBS-5813R-CY7)
Fornecedor: Bioss
Descrição: Proline oxidase catalyzes the conversion of proline to pyrroline-5-carboxylate, or P5C during the degradation of the amino acid Proline. Defects in PRODH are the cause of hyperprolinemia type 1, a disorder characterized by elevated serum proline levels. Defective PRODH may be involved in the psychiatric and behavioral phenotypes associated with the 22q11 velocardiofacial and DiGeorge syndrome and may be associated with susceptibility to schizophrenia 4 (SCZD4).
UOM: 1 * 100 µl


Código de Artigo: (BOSSBS-5813R-A555)
Fornecedor: Bioss
Descrição: Proline oxidase catalyzes the conversion of proline to pyrroline-5-carboxylate, or P5C during the degradation of the amino acid Proline. Defects in PRODH are the cause of hyperprolinemia type 1, a disorder characterized by elevated serum proline levels. Defective PRODH may be involved in the psychiatric and behavioral phenotypes associated with the 22q11 velocardiofacial and DiGeorge syndrome and may be associated with susceptibility to schizophrenia 4 (SCZD4).
UOM: 1 * 100 µl


Código de Artigo: (BOSSBS-5813R-A647)
Fornecedor: Bioss
Descrição: Proline oxidase catalyzes the conversion of proline to pyrroline-5-carboxylate, or P5C during the degradation of the amino acid Proline. Defects in PRODH are the cause of hyperprolinemia type 1, a disorder characterized by elevated serum proline levels. Defective PRODH may be involved in the psychiatric and behavioral phenotypes associated with the 22q11 velocardiofacial and DiGeorge syndrome and may be associated with susceptibility to schizophrenia 4 (SCZD4).
UOM: 1 * 100 µl


Código de Artigo: (BOSSBS-5813R-A350)
Fornecedor: Bioss
Descrição: Proline oxidase catalyzes the conversion of proline to pyrroline-5-carboxylate, or P5C during the degradation of the amino acid Proline. Defects in PRODH are the cause of hyperprolinemia type 1, a disorder characterized by elevated serum proline levels. Defective PRODH may be involved in the psychiatric and behavioral phenotypes associated with the 22q11 velocardiofacial and DiGeorge syndrome and may be associated with susceptibility to schizophrenia 4 (SCZD4).
UOM: 1 * 100 µl


Fornecedor: TCI
Descrição: tert-Butyl-2,5-dihydro-1H-pyrrole-1-carboxylate ≥98.0% (by GC)

Código de Artigo: (BOSSBS-5813R-CY5)
Fornecedor: Bioss
Descrição: Proline oxidase catalyzes the conversion of proline to pyrroline-5-carboxylate, or P5C during the degradation of the amino acid Proline. Defects in PRODH are the cause of hyperprolinemia type 1, a disorder characterized by elevated serum proline levels. Defective PRODH may be involved in the psychiatric and behavioral phenotypes associated with the 22q11 velocardiofacial and DiGeorge syndrome and may be associated with susceptibility to schizophrenia 4 (SCZD4).
UOM: 1 * 100 µl


Fornecedor: TCI
Descrição: Benzyl-2,5-dihydro-1H-pyrrole-1-carboxylate ≥97.0% (by GC)

Código de Artigo: (BOSSBS-5813R-A750)
Fornecedor: Bioss
Descrição: Proline oxidase catalyses the conversion of proline to pyrroline-5-carboxylate, or P5C during the degradation of the amino acid Proline. Defects in PRODH are the cause of hyperprolinemia type 1, a disorder characterised by elevated serum proline levels. Defective PRODH may be involved in the psychiatric and behavioral phenotypes associated with the 22q11 velocardiofacial and DiGeorge syndrome and may be associated with susceptibility to schizophrenia 4 (SCZD4).
UOM: 1 * 100 µl


Código de Artigo: (BOSSBS-5813R-FITC)
Fornecedor: Bioss
Descrição: Proline oxidase catalyzes the conversion of proline to pyrroline-5-carboxylate, or P5C during the degradation of the amino acid Proline. Defects in PRODH are the cause of hyperprolinemia type 1, a disorder characterized by elevated serum proline levels. Defective PRODH may be involved in the psychiatric and behavioral phenotypes associated with the 22q11 velocardiofacial and DiGeorge syndrome and may be associated with susceptibility to schizophrenia 4 (SCZD4).
UOM: 1 * 100 µl


Código de Artigo: (BOSSBS-5813R-A680)
Fornecedor: Bioss
Descrição: Proline oxidase catalyses the conversion of proline to pyrroline-5-carboxylate, or P5C during the degradation of the amino acid Proline. Defects in PRODH are the cause of hyperprolinemia type 1, a disorder characterised by elevated serum proline levels. Defective PRODH may be involved in the psychiatric and behavioral phenotypes associated with the 22q11 velocardiofacial and DiGeorge syndrome and may be associated with susceptibility to schizophrenia 4 (SCZD4).
UOM: 1 * 100 µl


Preço sob consulta
O stock para este item é limitado. Por favor, certifique-se de que efetuou o seu login para visualizar o stock disponível. Se a call ainda é exibida e precisar de ajuda, por favor, ligue para 213 600 770
O stock para este item é limitado. Por favor, certifique-se de que efetuou o seu login para visualizar o stock disponível. Se a call está visível e precisar de ajuda, por favor, ligue para 213 600 770
Este produto é sujeito a regulamentação especifica.
Em caso de encomenda, será contactado a solicitar documentação complementar necessária e/ou obrigatória (licença, autorização ou declaração de uso final) para a continuidade do pedido. Agradecemos a vossa compreensão
Este produto é sujeito a regulamentação especifica.
Em caso de encomenda, será contactado a solicitar documentação complementar necessária e/ou obrigatória (licença, autorização ou declaração de uso final) para a continuidade do pedido. Agradecemos a vossa compreensão.
Este produto está bloqueado. Para obter mais informações, contacte a VWR através do número 213 600 770.
O produto pretendido já não se encontra disponível. O produto indicado é um substituto.
Este produto encontra-se em rutura de stock. Poderá encontrar alternativas pesquisando pelo código de artigo indicado acima. Se precisar de ajuda, por favor contacte a VWR através do 213 600 770.
33 - 48 of 159
no targeter for Bottom