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4-Oxohexahydrocyclopenta[c]pyrrole-2-carboxylic+acid+tert-butyl+e
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4-Oxohexahydrocyclopenta[c]pyrrole-2-carboxylic+acid+tert-butyl+e
Artikel-Nr:
(APOSOR904283-25G)
Lieferant:
APOLLO SCIENTIFIC
Hersteller-Artikelnummer::
OR904283-25G
Lokale Artikelnummer::
APOSOR904283-25G
Beschreibung:
1-Furfurylpyrrol 95%
VE:
1 * 25 g
Artikel-Nr:
(BOSSBS-5813R-CY7)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-5813R-CY7
Lokale Artikelnummer::
BOSSBS-5813R-CY7
Beschreibung:
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).
VE:
1 * 100 µl
Lieferant:
APOLLO SCIENTIFIC
Beschreibung:
Inhibitor of protein kinase C.
Artikel-Nr:
(APOSOR53182-100G)
Lieferant:
APOLLO SCIENTIFIC
Hersteller-Artikelnummer::
OR53182-100G
Lokale Artikelnummer::
APOSOR53182-100G
Beschreibung:
3-Azabicyclo[3.3.0]octane hydrochloride
VE:
1 * 100 g
Lieferant:
APOLLO SCIENTIFIC
Beschreibung:
Gö 6983 is a potent, cell-permeable, ATP-competitive inhibitor of protein kinase C (PKC).
Artikel-Nr:
(F9926-250UG)
Lieferant:
SIGMA ALDRICH MICROSCOPY
Hersteller-Artikelnummer::
F9926-250UG
Lokale Artikelnummer::
SIAMF9926-250UG
Beschreibung:
A fluorescent conjugate of bisindolylmaleimide that specifically binds phosphokinase C at the active site. Can monitor enzyme activation and translocation. This reagent is not membrane permeable. The diacetate form (Sigma No. F9801) is membrane permeable.
VE:
1 * 250 µG
Lieferant:
APOLLO SCIENTIFIC
Beschreibung:
Chiral intermediate for pharmaceuticals and agrochemicals.
Artikel-Nr:
(BOSSBS-5813R-A647)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-5813R-A647
Lokale Artikelnummer::
BOSSBS-5813R-A647
Beschreibung:
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).
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-5813R-A555)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-5813R-A555
Lokale Artikelnummer::
BOSSBS-5813R-A555
Beschreibung:
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).
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-5813R-A350)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-5813R-A350
Lokale Artikelnummer::
BOSSBS-5813R-A350
Beschreibung:
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).
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-5813R-CY5)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-5813R-CY5
Lokale Artikelnummer::
BOSSBS-5813R-CY5
Beschreibung:
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).
VE:
1 * 100 µl
Lieferant:
Thermo Scientific
Beschreibung:
L(-)-Prolin 99+%
Artikel-Nr:
(APOSOR900851-1G)
Lieferant:
APOLLO SCIENTIFIC
Hersteller-Artikelnummer::
OR900851-1G
Lokale Artikelnummer::
APOSOR900851-1G
Beschreibung:
3,4-Diethylpyrrole 98%
VE:
1 * 1 g
Artikel-Nr:
(BOSSBS-4225R-CY5)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-4225R-CY5
Lokale Artikelnummer::
BOSSBS-4225R-CY5
Beschreibung:
The UDP-Glucuronosyltransferases (UGT) comprise a family of enzymes that detoxify and enhance the urinary excretion of a wide variety of xenobiotic and endogenous substrates by transferring glucuronic acid to sulfhydryl, hydroxyl, aromatic amino, or carboxylic acid groups. They have been subdivided into two families, UGT1 and UGT2, based on the evolutionary divergence of their genes. The enzymes of the UGT1A family play an important role in the metabolism of dietary constituents, phenols, and therapeutic drugs, and also the glucuronidation of bilirubin and iodothyronines. The enzymes of the UGT2B family are involved in the metabolism of bile acids, phenol derivatives, catecholestrogens and steroids. Although it is widely recognized that the liver is the major site of glucuronidation, it is now clear that UGT enzymes are also found in extra-hepatic tissues.
VE:
1 * 100 µl
Artikel-Nr:
(BOSSBS-4225R-CY3)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-4225R-CY3
Lokale Artikelnummer::
BOSSBS-4225R-CY3
Beschreibung:
The UDP-Glucuronosyltransferases (UGT) comprise a family of enzymes that detoxify and enhance the urinary excretion of a wide variety of xenobiotic and endogenous substrates by transferring glucuronic acid to sulfhydryl, hydroxyl, aromatic amino, or carboxylic acid groups. They have been subdivided into two families, UGT1 and UGT2, based on the evolutionary divergence of their genes. The enzymes of the UGT1A family play an important role in the metabolism of dietary constituents, phenols, and therapeutic drugs, and also the glucuronidation of bilirubin and iodothyronines. The enzymes of the UGT2B family are involved in the metabolism of bile acids, phenol derivatives, catecholestrogens and steroids. Although it is widely recognized that the liver is the major site of glucuronidation, it is now clear that UGT enzymes are also found in extra-hepatic tissues.
VE:
1 * 100 µl
Preis auf Anfrage
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 noch angezeigt wird und Sie Hilfe benötigen, rufen Sie uns an 1-800-932 - 5000.
Lager für diesen Artikel ist begrenzt, kann aber in einem Lagerhaus in Ihrer Nähe zur Verfügung. Bitte stellen Sie sicher, dass Sie in sind angemeldet auf dieser Seite, so dass verfügbare Bestand angezeigt werden können. Wenn das
noch angezeigt wird und Sie Hilfe benötigen, rufen Sie uns an 1-800-932 - 5000.
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