모든 사진(2)

문서

35389

Triclabendazole sulfone

Name: Triclabendazole sulfone
Brand: SIAL

VETRANAL^®, analytical standard

동의어(들):

5-Chloro-6-(2,3-dichlorophenoxy)-2-(methylsulfonyl)-1H-benzimidazole

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모든 사진(2)

About This Item

실험식(Hill 표기법):

C₁₄H₉Cl₃N₂O₃S

CAS Number:

106791-37-1

Molecular Weight:

391.66

Beilstein:

18516857

UNSPSC 코드:

41116107

NACRES:

NA.24

추천 제품

Slide 1 of 10

1 of 10

USP

1681611

Triclabendazole

Supelco

35391

Triclabendazole sulfoxide

Sigma-Aldrich

741752

Dienestrol-3′,3",5′,5"-d₄

20693

Hamilton^® syringe, 1000 series GASTIGHT^®, LTN (fixed needle)

Supelco

32802

Triclabendazole

USP

1681633

Triclabendazole Related Compound B

Supelco

PHR1448

Sulfadimethoxine

Supelco

32162

Ketotriclabendazole

Y0001737

Triclabendazole

Supelco

50648-U

Ascentis^® Express 90 Å PCS-C18, 2.7 µm HPLC Column

Grade

analytical standard

Quality Level

100

제품 라인

VETRANAL^®

기술

HPLC: suitable
gas chromatography (GC): suitable

응용 분야

forensics and toxicology
pharmaceutical (small molecule)

형식

neat

SMILES string

CS(=O)(=O)c1nc2cc(Cl)c(Oc3cccc(Cl)c3Cl)cc2[nH]1

InChI

1S/C14H9Cl3N2O3S/c1-23(20,21)14-18-9-5-8(16)12(6-10(9)19-14)22-11-4-2-3-7(15)13(11)17/h2-6H,1H3,(H,18,19)

InChI key

ZEIHWBIRYIXBSV-UHFFFAOYSA-N

애플리케이션

Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.

법적 정보

VETRANAL is a registered trademark of Merck KGaA, Darmstadt, Germany

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

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문서 라이브러리 방문

The small molecule triclabendazole decreases the intracellular level of cyclic AMP and increases resistance to stress in Saccharomyces cerevisiae.

Yong Joo Lee et al.

PloS one, 8(5), e64337-e64337 (2013-05-15)

The Ras-adenylyl cyclase-protein kinase A nutrient-sensing pathway controls metabolism, proliferation and resistance to stress in Saccharomyces cerevisiae. The genetic disruption of this pathway increases resistance to a variety of stresses. We show here that the pharmacological inhibition of this pathway

Assessment of the pharmacological interactions between the nematodicidal fenbendazole and the flukicidal triclabendazole: In vitro studies with bovine liver microsomes and slices.

P Viviani et al.

Journal of veterinary pharmacology and therapeutics, 41(3), 476-484 (2018-02-22)

Parasitic diseases have a significant impact on livestock production. Nematodicidal drugs, such as fenbendazole (FBZ) or its oxidized metabolite oxfendazole (OFZ), can be used along with the trematodicidal triclabendazole (TCBZ), to broaden the spectrum of anthelmintic activity. However, co-exposure to

Using In Silico Fragmentation to Improve Routine Residue Screening in Complex Matrices.

Anton Kaufmann et al.

Journal of the American Society for Mass Spectrometry, 28(12), 2705-2715 (2017-09-14)

Targeted residue screening requires the use of reference substances in order to identify potential residues. This becomes a difficult issue when using multi-residue methods capable of analyzing several hundreds of analytes. Therefore, the capability of in silico fragmentation based on

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문서

Triclabendazole sulfone