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Supplier NameMedChemExpress (MCE)
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Product Name3-Chlorodiphenylamine
Synonyms3-CHLORODIPHENYLAMINE
3-Chlorodiphenylamine
3-Chlorodiphenyl ether
3-chloro-N-phenylaniline
Diphenylamine, 3-chloro-
3-Chloro-N-phenylaniline
n-(3-chlorophenyl)aniline

Synonyms

3-CHLORODIPHENYLAMINE
3-Chlorodiphenylamine
3-Chlorodiphenyl ether
3-chloro-N-phenylaniline
Diphenylamine, 3-chloro-
3-Chloro-N-phenylaniline
n-(3-chlorophenyl)aniline
3-Chloro-N-phenyl-benzenamine
Benzenamine, 3-chloro-N-phenyl-
N-(3-Chlorophenyl)-N-phenylamine
CAS101-17-7
EINECS202-922-0
Chemical FormulaC12H10ClN
Molecular Weight203.67
inchiInChI=1/C12H10ClN/c13-10-5-4-8-12(9-10)14-11-6-2-1-3-7-11/h1-9,14H
Package10 mM * 1 mL;25 mg;50 mg;100 mg
PriceEmail to quote
Descriptions3-Chlorodiphenylamine

3-Chlorodiphenylamine

MedChemExpress (MCE)

HY-131948

101-17-7

98.74%

Pure form -20°C 3 years 4°C 2 years In solvent -80°C 6 months -20°C 1 month

Room temperature in continental US

Descriptions

3-Chlorodiphenylamine

3-Chlorodiphenylamine

MedChemExpress (MCE)

HY-131948

101-17-7

98.74%

Pure form -20°C 3 years 4°C 2 years In solvent -80°C 6 months -20°C 1 month

Room temperature in continental US
may vary elsewhere.

3-Chlorodiphenylamine is a high affinity Ca2+ sensitizer of cardiac muscle. 3-Chlorodiphenylamine is based on diphenylamine and binds to the isolated N-domain of cardiac troponin C (cTnC) (Kd=6 µM). 3-Chlorodiphenylamine is an excellent starting scaffold for the development of more potent Ca2+-sensitizing compounds due to its small size, and can be used for systolic heart failure research.

3-Chlorodiphenylamine is able to bind highly (Kd=10 µM) to a chimeric protein consisting of the regulatory N-domain of cTnC (cNTnC) and the switch region of cTnI (cNTnC–cSp chimera)[1].3-Chlorodiphenylamine (100 µM) results in a 1.5-fold increase in the Ca2+ sensitivity of force development without altering the maximal or resting forces in skinned ventricular trabeculae[1].3-Chlorodiphenylamine (25-100 µM) increases Ca2+ sensitivity of the N-domain of intact cTnC after reconstitution into the cTn complex (cTnC complexed with cTnI and cTnT) in a concentration-dependent manner. It exhibits pCa50s with 6.39±0.01, 6.65±0.01, and 6.73±0.02 in the presence of 25, 50, and 100 µM 3-Chlorodiphenylamine, respectively[1].

Kd: 6 µM (N-domain of cardiac troponin C (cTnC))Kd: 10 µM (cNTnC–cSp chimera)[1] In Vitro 3-Chlorodiphenylamine is able to bind highly (Kd=10 µM) to a chimeric protein consisting of the regulatory N-domain of cTnC (cNTnC) and the switch region of cTnI (cNTnC–cSp chimera)[1].3-Chlorodiphenylamine (100 µM) results in a 1.5-fold increase in the Ca2+ sensitivity of force development without altering the maximal or resting forces in skinned ventricular trabeculae[1].3-Chlorodiphenylamine (25-100 µM) increases Ca2+ sensitivity of the N-domain of intact cTnC after reconstitution into the cTn complex (cTnC complexed with cTnI and cTnT) in a concentration-dependent manner. It exhibits pCa50s with 6.39±0.01, 6.65±0.01, and 6.73±0.02 in the presence of 25, 50, and 100 µM 3-Chlorodiphenylamine, respectively[1]. MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only. 0 --> 3-Chlorodiphenylamine Related Antibodies

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[1]. Svetlana B Tikunova, et al. 3-Chlorodiphenylamine activates cardiac troponin by a mechanism distinct from bepridil or TFP. J Gen Physiol. 2019 Jan 7
151(1):9-17.
[Content Brief]

Supplier Websitehttps://www.medchemexpress.com/3-chlorodiphenylamine.html
Last Update2025-04-01 14:45:47
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