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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
84 Results for "
carbon source
" in MedChemExpress (MCE) Product Catalog:
Products (84)
84 Results for "carbon source" in MCE Product Catalog:
Cat. No.: HY-N2024AS2
Cat. No.: HY-130778R
CAS No.: 35061-50-8
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Cat. No.: HY-N3686S
Cat. No.: HY-N3686S1
Cat. No.: HY-N3686S2
Cat. No.: HY-W010062R
CAS No.: 1878-66-6
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Cat. No.: HY-W127434A
CAS No.: 1466461-81-3
Synonyms: (12R)-Octadecane-1,12-diol
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(12R)-1,12-Octadecanediol ((12R)-Octadecane-1,12-diol) is a compound characterized by a linear chain of 18 carbon atoms with two hydroxyl groups (C18H38O2). This colorless substance has unique properties owing to the presence of two hydroxyl groups in its molecular structure.
Whether derived from natural sources or synthesized chemically, 12-Octadecanediol finds applications in various industries. It is often utilized in the formulation of cosmetics, personal care products, and pharmaceuticals due to its emollient properties, enhancing moisturization and conditioning effects in different formulations. The compound's distinctive structure may make it suitable for specific uses in research or industrial processes.
In industrial contexts, 12-Octadecanediol serves as a valuable chemical intermediate for synthesizing other compounds. Its specialized structure and adaptability in formulations make it a significant component across diverse industries, contributing to the development of products for various purposes.
Cat. No.: HY-N16496
CAS No.: 136514-33-5
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Cat. No.: HY-189512
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Simmon's Citrate Agar is a synthetic differential medium that uses sodium citrate as the sole carbon source. Simmon's Citrate Agar can determine the ability of bacteria to utilize citrate as a carbon source. Bacterial metabolism of citrate produces bicarbonate, which causes bromothymol blue to change from blue to deep blue. Simmon's Citrate Agar can be used for bacterial identification and isolation-related research .
Cat. No.: HY-E71567
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2-Hydroxymethylglutarate dehydrogenase (EC 1.1.1.291) is an NADPH-dependent D-ribulose reductase—a type of oxidoreductase—that catalyzes the reduction of D-ribulose to D-arabitol. It plays a key role in pentose metabolism, sugar alcohol metabolism, and carbon source utilization in microorganisms and fungi.
Cat. No.: HY-178398S
Cat. No.: HY-W004303S
CAS No.: 1809273-36-6
Synonyms: Tetradecyl Aldehyde-d27
Cat. No.: HY-E71124
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(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.
Cat. No.: HY-W708332
Cat. No.: HY-N21558
CAS No.: 135463-09-1
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Cat. No.: HY-W415856
CAS No.: 7296-64-2
Synonyms: Beta-D-galactose
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β-D-galactose (Beta-D-galactose) is one of the two anomers of D-Galactose (HY-N0210). β-D-galactose efficiently binds to and inhibits the galactose repressor (GalR), thereby inducing the expression of the gal regulon. β-D-galactose acts as a persistent induction signal to trigger the synthesis of UDP-galactose for the biosynthetic glycosylation pathway, rather than serving as a carbon source in Yersinia pestis with inactivated GalM .
Cat. No.: HY-179649
CAS No.: 484026-63-3
sALT629 is an orally active antitubercular agent with potent intramacrophage activity (EC50 = 1.5 μM). sALT629 shows broad-spectrum anti-Mycobacterium tuberculosis (Mtb) activities across four carbon sources, equipotent efficacy against drug-resistant Mtb, and activity against both slow-replicating and nonreplicating Mtb. sALT629 exhibits synergistic activity when combined with oxazolidinone drugs, such as Linezolid (HY-10394) and Sutezolid (HY-10392). sALT629 can be used for the research of tuberculosis .
Cat. No.: HY-W587486A
CAS No.: 75350-40-2
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N-Acetyltaurine hemimagnesium is an orally active endogenous sulfonate that is synthesized from taurine and acetate in the renal cortex. N-Acetyltaurine hemimagnesium supports bacterial growth as a sole fixed nitrogen or carbon source. N-Acetyltaurine hemimagnesium buffers acetyl moieties of mitochondrial acetyl‑CoA in skeletal muscle. N-Acetyltaurine hemimagnesium reduces food intake and body weight in obese and lean wild‑type mice in a GFRAL‑dependent manner. N-Acetyltaurine hemimagnesium can be used for the research of diet‑induced obesity, hyperacetatemia and diabetes .
Cat. No.: HY-W779018
CAS No.: 201741-00-6
Synonyms: D-(+)-Xylose-13C2; (+)-Xylose-13C2; Wood sugar-13C2
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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
