5-(4-Hydroxyphenyl)thiophene-2-carboxylic+acid
Lieferant:
APOLLO SCIENTIFIC
Beschreibung:
4-[(Trifluoromethyl)sulphonyl]phenol 97%
Lieferant:
Thermo Scientific
Beschreibung:
CAS No.: 932-30-9
Lieferant:
Thermo Scientific
Beschreibung:
5-Brom-2-hydroxybenzylalkohol 98%
Lieferant:
APOLLO SCIENTIFIC
Beschreibung:
trans-4-Hydroxy-L(-)-prolin
Lieferant:
APOLLO SCIENTIFIC
Beschreibung:
2-Thiophenmethanol 99%
Lieferant:
Thermo Scientific
Beschreibung:
Appearance: White to off-white Crystalline powder
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
Lieferant:
APOLLO SCIENTIFIC
Beschreibung:
2,6-Dibromo-4-[(trifluoromethyl)sulphonyl]phenol
Lieferant:
APOLLO SCIENTIFIC
Beschreibung:
4,4'-(Hexafluorisopropyliden)diphenol 98%
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
Artikel-Nr:
(BLDPBD01097200-100)
Lieferant:
BLD PHARMATECH GMBH
Hersteller-Artikelnummer::
BD01097200-100
Lokale Artikelnummer::
BLDPBD01097200-100
Beschreibung:
2,5-Dioctyl-3,6-bis(5-(trimethylstannyl)thiophen-2-yl)pyrrolo[3,4-c]pyrrole-1,4(2H,5H)-dione 99%
VE:
1 * 100 mg
Lieferant:
Alfa Aesar
Beschreibung:
3-Chlor-2-benzo[b]thiophencarbonylchlorid 95%
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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