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Targeted therapy! The Capetin Prize winning "Click Chemistry" can be used like this!Targeted therapy! The Nobel Prize winning "Click Chemistry" can be used like this!2025-02-06
13 Results for "
Mandelic Acid
" in MedChemExpress (MCE) Product Catalog:
Products (13)
13 Results for "Mandelic Acid" in MCE Product Catalog:
1
Category:
Ketones, Aldehydes, Acids Other Diseases Rosaceae Armeniaca vulgaris Lam. Plants Endogenous metabolite Disease Research Fields
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1
1 Cited Publications
Cat. No.: HY-W015591
CAS No.: 90-64-2
Synonyms: (±)-Mandelic Acid; DL-Mandelic Acid
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Cat. No.: HY-Y0816
CAS No.: 17199-29-0
Cat. No.: HY-W015591S
CAS No.: 70838-71-0
Synonyms: (±)-Mandelic Acid-2,3,4,5,6-d5; DL-Mandelic Acid-2,3,4,5,6-d5
Cat. No.: HY-W015591R
CAS No.: 90-64-2
Synonyms: (±)-Mandelic Acid (Standard); DL-Mandelic Acid (Standard)
Cat. No.: HY-W654255
CAS No.: 2701643-58-3
Synonyms: (±)-Mandelic Acid-13C8; DL-Mandelic Acid-13C8
Cat. No.: HY-W020655
CAS No.: 97415-09-3
Synonyms: D-(-)-Mandelic Acid Benzyl Ester
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Research Areas:
(R)-Benzyl mandelate (D-(-)-Mandelic Acid Benzyl Ester) is a synthetic intermediate useful for pharmaceutical synthesis.
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Cat. No.: HY-145577A
Purity: 99.95%
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Research Areas:
Lafadofensine D-(-)-Mandelic acid is the monoamines reuptake inhibitor. Lafadofensine D-(-)-Mandelic acid has sufficient effects after short-term administration .
Cat. No.: HY-116252
CAS No.: 131086-22-1
(±)-trans-Lamivudine is separated from the salt of (S)-(+) mandelic acid. (±)-trans-Lamivudine forms cocrystals with (S)-BINOL. (±)-trans-Lamivudine is promising for research of human immunodeficiency virus infection .
Cat. No.: HY-115900
Tuberculosis inhibitor 4 (compound 16), a mandelic acid-based spirothiazolidinone, has potent antimycobacterial activity against Mycobacterium tuberculosis strain H37Rv with the high inhibition value 98% at lower than 6.25 µg/mL concentration .
Cat. No.: HY-E71124
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Research Areas:
(S)-Mandelate dehydrogenase (EC 1.1.99.31) belongs to the FMN-dependent α-hydroxy acid oxidase/dehydrogenase family. (S)-Mandelate dehydrogenase (EC 1.1.99.31) is part of a Pseudomonas metabolic pathway that enables these organisms to utilize mandelic acid (derived from the common soil metabolite amygdalin) as their sole carbon and energy source.
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Protocols
Targeted therapy! The Capetin Prize winning "Click Chemistry" can be used like this!Targeted therapy! The Nobel Prize winning "Click Chemistry" can be used like this!A suitable model is crucial in drug screening experiments. Organs can mimic the three-dimensional functional structure of internal organs, have similar spatial organization to corresponding organs, maintain some key characteristics, and reproduce some physiological functions. They are widely used for modeling and personalized drug screening physiological functions.2025-02-06
