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667730

3-(2-Furyl)propionic acid

Name: 3-(2-Furyl)propionic acid
Brand: ALDRICH

97%

Synonym(s):

2-Furanpropanoic acid, 2-Furanpropionic acid

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About This Item

Empirical Formula (Hill Notation):

C₇H₈O₃

CAS Number:

935-13-7

Molecular Weight:

140.14

NACRES:

NA.22

PubChem Substance ID:

24884939

UNSPSC Code:

12352100

EC Number:

213-298-4

MDL number:

MFCD00005346

Assay:

97%

Form:

solid

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Properties

Quality Level

200

assay

97%

form

solid

mp

56-60 °C

functional group

carboxylic acid

SMILES string

OC(=O)CCc1ccco1

InChI

1S/C7H8O3/c8-7(9)4-3-6-2-1-5-10-6/h1-2,5H,3-4H2,(H,8,9)

InChI key

XLTJXJJMUFDQEZ-UHFFFAOYSA-N

Description

pictograms

GHS05,GHS07

signalword

Danger

hcodes

H315,H318,H335

pcodes

P261 - P264 - P271 - P280 - P302 + P352 - P305 + P351 + P338

Hazard Classifications

Eye Dam. 1 - Skin Irrit. 2 - STOT SE 3

target_organs

Respiratory system

Storage Class

11 - Combustible Solids

wgk

WGK 3

ppe

dust mask type N95 (US), Eyeshields, Gloves

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Mechanisms of Metabolism Interaction Between p-Cresol and Mycophenolic Acid.

Yan Rong et al.

Toxicological sciences : an official journal of the Society of Toxicology, 173(2), 267-279 (2019-11-20)

Mycophenolic acid (MPA) is commonly prescribed for preventing graft rejection after kidney transplantation. The primary metabolic pathways of MPA are hepatic glucuronidation through UDP-glucuronosyltransferase (UGT) enzymes in the formation of MPA-glucuronide (MPAG, major pathway) and MPA-acyl glucuronide (AcMPAG). p-Cresol, a

Organic anion transporting polypeptides 1B1 and 1B3 play an important role in uremic toxin handling and drug-uremic toxin interactions in the liver.

Toshihiro Sato et al.

Journal of pharmacy & pharmaceutical sciences : a publication of the Canadian Society for Pharmaceutical Sciences, Societe canadienne des sciences pharmaceutiques, 17(4), 475-484 (2015-01-13)

Organic anion-transporting polypeptide (OATP) 1B1 and OATP1B3 contribute to hepatic uptake of numerous drugs. Thus, reduced OATP1B1 and OATP1B3 activity in chronic kidney disease (CKD) may have a major impact on the hepatic clearance of drugs. The effect of drug-uremic

Diels-Alder hydrogels with enhanced stability: First step toward controlled release of bevacizumab.

Susanne Kirchhof et al.

European journal of pharmaceutics and biopharmaceutics : official journal of Arbeitsgemeinschaft fur Pharmazeutische Verfahrenstechnik e.V, 96, 217-225 (2015-08-09)

Eight-armed PEG was functionalized with furyl and maleimide groups (8armPEG20k-Fur and 8armPEG20k-Mal); degradable hydrogels were obtained by cross-linking via Diels-Alder chemistry. To increase the stability to degradation, the macromonomers were modified by introducing a hydrophobic 6-aminohexanoic acid spacer between PEG

Global Trade Item Number

SKU	GTIN
667730-5G	04061833358108