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Chemical Structure| 6018-28-6 Chemical Structure| 6018-28-6

Structure of Arecaidine HCl
CAS No.: 6018-28-6

Chemical Structure| 6018-28-6

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Arecaidine hydrochloride (arecaidine hydrochloride) is a pyridine alkaloid that effectively inhibits GABA uptake. It acts as a substrate for the H+-coupled amino acid transporter 1 (PAT1, SLC36A1), competitively inhibiting L-proline uptake, providing potential value in neurobiological research.

Synonyms: Arecaidine hydrochloride

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Product Details of Arecaidine HCl

CAS No. :6018-28-6
Formula : C7H12ClNO2
M.W : 177.63
SMILES Code : O=C(C1=CCCN(C)C1)O.[H]Cl
Synonyms :
Arecaidine hydrochloride
MDL No. :MFCD00051993
InChI Key :PIVDNPNYIBGXPL-UHFFFAOYSA-N
Pubchem ID :12305194

Safety of Arecaidine HCl

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H315-H319-H335
Precautionary Statements:P261-P305+P351+P338

Isoform Comparison

Biological Activity

In Vitro:

Cell Line
Concentration Treated Time Description References
Feline bladder mucosal cells 50 nM To study the sensitivity of feline interstitial cystitis bladders to muscarinic receptor agonists, results showed that FIC bladder mucosa was significantly more sensitive to arecaidine. J Urol. 2009 Mar;181(3):1415-22
Substantia gelatinosa (SG) neurons in adult rat spinal cord slice 10-100 μM To test the effect of Arecaidine on the frequency of GABAergic inhibitory postsynaptic currents (IPSCs). Results showed that Arecaidine did not mimic the effects of carbachol. J Physiol. 1998 Apr 1;508 ( Pt 1)(Pt 1):83-93
Human dermal fibroblasts 12.5, 25, 50, 100 μM To evaluate the effect of Arecaidine on human dermal fibroblast viability, results showed that Arecaidine did not significantly affect cell viability Cancer Biol Ther. 2014;15(11):1489-98
HT1197 cells 12.5, 25, 50, 100 μM 24 and 48 h To evaluate the effect of Arecaidine on HT1197 cell proliferation, results showed that Arecaidine significantly inhibited HT1197 cell proliferation in a concentration and time-dependent manner Cancer Biol Ther. 2014;15(11):1489-98
5637 cells 12.5, 25, 50, 100 μM 24 and 48 h To evaluate the effect of Arecaidine on 5637 cell proliferation, results showed that Arecaidine significantly inhibited 5637 cell proliferation in a concentration and time-dependent manner Cancer Biol Ther. 2014;15(11):1489-98
T24 cells 12.5, 25, 50, 100 μM 24 and 48 h To evaluate the effect of Arecaidine on T24 cell proliferation, results showed that Arecaidine significantly inhibited T24 cell proliferation in a concentration and time-dependent manner Cancer Biol Ther. 2014;15(11):1489-98
C-nociceptors in rat skin-saphenous nerve preparation 1-10 µM 5 min To test the desensitizing effect of Arecaidine on C-nociceptors. Results showed that Arecaidine dose-dependently reduced sensitivity to heat and mechanical stimulation. J Neurosci. 2001 May 1;21(9):3295-302

In Vivo:

Species
Animal Model
Administration Dosage Frequency Description References
Cats Feline interstitial cystitis model 50 nM To study the sensitivity of feline interstitial cystitis bladders to muscarinic receptor agonists, results showed that FIC bladder mucosa was significantly more sensitive to arecaidine. J Urol. 2009 Mar;181(3):1415-22

Protocol

Bio Calculators
Preparing Stock Solutions 1mg 5mg 10mg

1 mM

5 mM

10 mM

5.63mL

1.13mL

0.56mL

28.15mL

5.63mL

2.81mL

56.30mL

11.26mL

5.63mL

Dissolving Methods
Please choose the appropriate dissolution scheme according to your animal administration guide.For the following dissolution schemes, clear stock solution should be prepared according to in vitro experiments, and then cosolvent should be added in turn:

in order to ensure the reliability of the experimental results, the clarified stock solution can be properly preserved according to the storage conditions; The working fluid for in vivo experiment is recommended to be prepared now and used on the same day;

The percentage shown in front of the following solvent refers to the volume ratio of the solvent in the final solution; If precipitation or precipitation occurs in the preparation process, it can be assisted by heating and/or ultrasound.
Protocol 1
Protocol 2
 

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