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(R)-2-amino-3-cyclohexylpropanoic acid

Cat. No. M39306
(R)-2-amino-3-cyclohexylpropanoic acid Structure
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Biological Activity

(R)-2-amino-3-cyclohexylpropanoic acid is an alanine derivative.

Chemical Information
Molecular Weight 171.24
Formula C9H17NO2
CAS Number 58717-02-5
Form Solid
Storage Powder          -20°C   3 years ;  4°C   2 years
In solvent       -80°C   6 months ;  -20°C   1 month
Conversion of different model animals based on BSA (PMID: 27057123)
Species Mouse Rat Rabbit Guinea pig Hamster Dog
Weight (kg) 0.02 0.15 1.8 0.4 0.08 10
Body Surface Area (m2) 0.007 0.025 0.15 0.05 0.02 0.5
Km factor 3 6 12 8 5 20
Animal A (mg/kg) = Animal B (mg/kg) multiplied by  Animal B Km
Animal A Km

For example, to modify the dose of Compound A used for a mouse (20 mg/kg) to a dose based on the BSA for a rat, multiply 20 mg/kg by the Km factor for a mouse and then divide by the Km factor for a rat. This calculation results in a rat equivalent dose for Compound A of 10 mg/kg.

References

[1] Srinivas Chandrasekaran et al. Molecules. Enantioseparation of 3-Hydroxycarboxylic Acids via Diastereomeric Salt Formation by 2-Amino-1,2-diphenylethanol (ADPE) and Cinchonidine

[2] Zenghui Sun et al. Org Lett. λ3-Iodane/Lewis Acid Mediated Intramolecular Cross-Nucleophile Coupling of β-Amino Acrylates: Chemodivergent Syntheses of Indole Alkaloidal Frameworks

[3] Alexander Müller et al. Int J Environ Res Public Health. A Vegan Diet Is Associated with a Significant Reduction in Dietary Acid Load: Post Hoc Analysis of a Randomized Controlled Trial in Healthy Individuals

[4] K Pallitsch et al. Org Biomol Chem. Towards the biodegradation pathway of fosfomycin

[5] Yubo Wu et al. J Org Chem. Enantioselective recognition of mandelic acid by a 3,6-dithiophen-2-yl-9H-carbazole-based chiral fluorescent bisboronic acid sensor

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