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Chemical Structure| 103639-04-9 Chemical Structure| 103639-04-9

Structure of Ondansetron HCl dihydrate
CAS No.: 103639-04-9

Chemical Structure| 103639-04-9

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Ondansetron HCl 2H2O is a competitive 5-HT3 receptor antagonist.

Synonyms: GR 38032 hydrochloride dihydrate; SN 307 hydrochloride dihydrate; Ondansetron (hydrochloride hydrate)

4.5 *For Research Use Only !

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Product Details of Ondansetron HCl dihydrate

CAS No. :103639-04-9
Formula : C18H24ClN3O3
M.W : 365.85
SMILES Code : O=C1C(CN2C=CN=C2C)CCC(N3C)=C1C4=C3C=CC=C4.[H]Cl.[H]O[H].[H]O[H]
Synonyms :
GR 38032 hydrochloride dihydrate; SN 307 hydrochloride dihydrate; Ondansetron (hydrochloride hydrate)
MDL No. :MFCD00374371
InChI Key :VRSLTNZJOUZKLX-UHFFFAOYSA-N
Pubchem ID :59774

Safety of Ondansetron HCl dihydrate

GHS Pictogram:
Signal Word:Danger
Hazard Statements:H301-H318-H410
Precautionary Statements:P273-P280-P301+P310-P305+P351+P338
Class:6.1
UN#:2811
Packing Group:

Related Pathways of Ondansetron HCl dihydrate

GPCR

Isoform Comparison

Biological Activity

Target
  • 5-HT3

    5-HT3 receptor, IC50:810 nM

  • 5-HT3

In Vitro:

Cell Line
Concentration Treated Time Description References
HEK-293 cells overexpressing mMate1 0-50 µM 10 minutes Determine the inhibitory potency of ondansetron on mMate1, Ki value was 0.07 μM Toxicol Appl Pharmacol. 2013 Nov 15;273(1):100-9
HEK-293 cells overexpressing mOct2 0-50 µM 10 minutes Determine the inhibitory potency of ondansetron on mOct2, Ki value was 3.5 μM Toxicol Appl Pharmacol. 2013 Nov 15;273(1):100-9
HEK-293 cells overexpressing hMATE2-K 0-50 µM 10 minutes Determine the inhibitory potency of ondansetron on hMATE2-K, Ki value was 0.015 μM Toxicol Appl Pharmacol. 2013 Nov 15;273(1):100-9
HEK-293 cells overexpressing hMATE1 0-50 µM 10 minutes Determine the inhibitory potency of ondansetron on hMATE1, Ki value was 0.035 μM Toxicol Appl Pharmacol. 2013 Nov 15;273(1):100-9
HEK-293 cells overexpressing hOCT2 0-50 µM 10 minutes Determine the inhibitory potency of ondansetron on hOCT2, Ki value was 3.85 μM Toxicol Appl Pharmacol. 2013 Nov 15;273(1):100-9

In Vivo:

Species
Animal Model
Administration Dosage Frequency Description References
New Zealand white rabbits Heart failure model Perfusion 100 nM Single administration To investigate the effects of Ondansetron on action potential duration (APD) and QT interval in rabbit hearts with heart failure, showing that Ondansetron significantly prolonged APD and QT interval and increased ventricular fibrillation vulnerability. Heart Rhythm. 2020 Feb;17(2):332-340
Mice Wild-type and Mate1−/− mice Intraperitoneal injection 6.4 mg/kg Single dose Evaluate the effect of ondansetron on cisplatin-induced nephrotoxicity, results showed ondansetron enhanced cisplatin nephrotoxicity via inhibition of Mate1 Toxicol Appl Pharmacol. 2013 Nov 15;273(1):100-9

Protocol

Bio Calculators
Preparing Stock Solutions 1mg 5mg 10mg

1 mM

5 mM

10 mM

2.73mL

0.55mL

0.27mL

13.67mL

2.73mL

1.37mL

27.33mL

5.47mL

2.73mL

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

References

 

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