research use only
Cat.No.S4542
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In vitro |
DMSO
: 20 mg/mL
(59.18 mM)
Ethanol : 20 mg/mL Water : Insoluble |
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In vivo |
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Step 1: Enter information below (Recommended: An additional animal making an allowance for loss during the experiment)
Step 2: Enter the in vivo formulation (This is only the calculator, not formulation. Please contact us first if there is no in vivo formulation at the solubility Section.)
Calculation results:
Working concentration: mg/ml;
Method for preparing DMSO master liquid: mg drug pre-dissolved in μL DMSO ( Master liquid concentration mg/mL, Please contact us first if the concentration exceeds the DMSO solubility of the batch of drug. )
Method for preparing in vivo formulation: Take μL DMSO master liquid, next addμL PEG300, mix and clarify, next addμL Tween 80, mix and clarify, next add μL ddH2O, mix and clarify.
Method for preparing in vivo formulation: Take μL DMSO master liquid, next add μL Corn oil, mix and clarify.
Note: 1. Please make sure the liquid is clear before adding the next solvent.
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| Molecular Weight | 337.93 | Formula | C20H31NO.HCl |
Storage (From the date of receipt) | |
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| CAS No. | 52-49-3 | Download SDF | Storage of Stock Solutions |
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| Synonyms | Benzhexol hydrochloride, Artane hydrochloride | Smiles | C1CCC(CC1)C(CCN2CCCCC2)(C3=CC=CC=C3)O.Cl | ||
| In vivo |
Trihexyphenidyl-treated rats exhibits significantly extended mean latencies during the initial 3 months of testing; however, this behavioral deficit is restored between the fourth and sixth month of MWM testing. The most significant populations of genes downregulated by THP are the immune response-, antigen processing and presentation-, and major histocompatibility complex (MHC)-related genes, as validated by qRT-PCR. In aging brains, THP treatment decreases expression of MHC class I. Its long-term treatment primes hippocampal and cortical microglia to undergo an inflammatory phenotypic switch, causing microgliosis and microglia activation, which are positively accompanied by pathological misfolded tau lesions.TPH induces dose-dependent structural changes in rat frontal cortex motor area.
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