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D7441

Sigma-Aldrich

Daltroban

>98% (HPLC)

Synonym(s):

4-[2-[(4-Chlorophenylsulfonyl)amino]ethyl]benzeneacetic acid, BM-13505, SKF-96148

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About This Item

Empirical Formula (Hill Notation):
C16H16ClNO4S
CAS Number:
79094-20-5
Molecular Weight:
353.82
MDL number:
MFCD00868295
UNSPSC Code:
12352200
PubChem Substance ID:
24724468
NACRES:
NA.77

Assay

>98% (HPLC)

form

solid

color

white

mp

132.5-137.4 °C (lit.)

solubility

DMSO: soluble 22 mg/mL

SMILES string

OC(=O)Cc1ccc(CCNS(=O)(=O)c2ccc(Cl)cc2)cc1

InChI

1S/C16H16ClNO4S/c17-14-5-7-15(8-6-14)23(21,22)18-10-9-12-1-3-13(4-2-12)11-16(19)20/h1-8,18H,9-11H2,(H,19,20)

InChI key

IULOBWFWYDMECP-UHFFFAOYSA-N

Gene Information

human ... TBXA2R(6915)

General description

Exerts protective effects on brain infarction, heart cell injury due to hypoxia and hypoglycemia and lowers serum CPK activity.

Biochem/physiol Actions

Selective thromboxane A2 receptor antagonist

Features and Benefits

This compound is featured on the Prostanoid Receptors page of the Handbook of Receptor Classification and Signal Transduction. To browse other handbook pages, click here.

Pictograms

Exclamation mark
GHS07

Signal Word

Warning

Hazard Statements

H315,H319,H335

Hazard Classifications

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

Target Organs

Respiratory system

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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U Grandel et al.
Circulation, 102(22), 2758-2764 (2000-11-30)
Although endotoxin (lipopolysaccharides, LPS) is recognized as a mediator of septic cardiodepression, its cardiac effects are still not fully elucidated. Perfusion of isolated rat hearts with LPS for 180 minutes resulted in a decline of left ventricular contractility after 90
Growth inhibitory effects of thromboxane antagonists on breast cancer cell lines: a preliminary study.
K Marshall et al.
Advances in experimental medicine and biology, 400A, 455-460 (1997-01-01)
Anna K Leal et al.
American journal of physiology. Heart and circulatory physiology, 301(5), H2140-H2146 (2011-08-23)
Cyclooxygenase metabolites stimulate or sensitize group III and IV muscle afferents, which comprise the sensory arm of the exercise pressor reflex. The thromboxane (TP) receptor binds several of these metabolites, whose concentrations in the muscle interstitium are increased by exercise
T Tanaka et al.
European journal of pharmacology, 357(1), 53-60 (1998-10-27)
We investigated the pharmacological characteristics of Z-335 ((+/-)-sodium[2-[4-(chlorophenylsulfonylaminomethyl)indan-5-yl]ace tate monohydrate), a new indan derivative. Z-335 inhibited the specific binding of [3H]SQ-29548 to human platelets and guinea pig platelet membranes. The IC50 values of Z-335 for human platelets and guinea pig
Sabine Pestel et al.
Biochemical pharmacology, 66(4), 643-652 (2003-08-09)
Prostanoids, i.e. prostaglandins and thromboxane, regulate liver-specific functions both in homeostasis and during defense reactions. For example, prostanoids are released from Kupffer cells, the resident liver macrophages, in response to the inflammatory mediator anaphylatoxin C5a, and mediate an enhanced glucose
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