9 Results for "

2-HBA

" in MedChemExpress (MCE) Product Catalog:
Products (9)

9 Results for "2-HBA" in MCE Product Catalog:

3
3 Cited Publications
Cat. No.: HY-103667
CAS No.: 131359-24-5
Purity:  99.46%
Research Areas:  

Cancer

2-HBA is a potent inducer of NAD(P)H:quinone acceptor oxidoreductase 1 (NQO1) which can also activate caspase-3 and caspase-10.
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Cat. No.: HY-103667R
CAS No.: 131359-24-5
Research Areas:  

Cancer

2-HBA (Standard) is the analytical standard of 2-HBA (HY-103667). This product is intended for research and analytical applications. 2-HBA is a potent inducer of NAD(P)H:quinone acceptor oxidoreductase 1 (NQO1) which can also activate caspase-3 and caspase-10.
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Cat. No.: HY-187269S
[U- 15N]-HbA2 is the 15N-labeled HbA2. HbA2 plays a critical role in the prevention and diagnosis of hereditary hemoglobinopathies. This isotope can be used in NMR studies of disease mechanisms and in mass spectrometry analysis. The marker is utilized in clinical mass spectrometry testing.
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Cat. No.: HY-P84094
Synonyms: MIC2; HBA71; MIC2X; MIC2Y; MSK5X

Host:  

Mouse

Application:  

WB, IHC-P, FC, ELISA

Reactivity:  

Human, Mouse

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Cat. No.: HY-P84095
Synonyms: MIC2; HBA71; MIC2X; MIC2Y; MSK5X

Host:  

Mouse

Application:  

WB, IHC-P, ICC/IF, FC, ELISA

Reactivity:  

Human

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Cat. No.: HY-P87961
Synonyms: HBA2, HBA1, Hemoglobin subunit alpha, Alpha-globin, Hemoglobin alpha chain

Host:  

Rabbit

Application:  

IHC-P, IHC-F, IF-Tissue, WB, FC, IP

Reactivity:  

Human, Mouse, Rat

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Cat. No.: HY-P84094A
Synonyms: MIC2; HBA71; MIC2X; MIC2Y; MSK5X

Host:  

Mouse

Application:  

WB, IHC-P, FC, ELISA

Reactivity:  

Human, Mouse

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Cat. No.: HY-P84095A
Synonyms: MIC2; HBA71; MIC2X; MIC2Y; MSK5X

Host:  

Mouse

Application:  

WB, IHC-P, ICC/IF, FC, ELISA

Reactivity:  

Human

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Cat. No.: HY-L942
1,632 compounds

Unlike highly conserved orthosteric sites, allosteric sites exhibit low conservation, high hydrophobicity, weak polarity, confined geometry, and dynamic cryptic properties. Rather than rigid keyhole-like cavities, they typically appear as flexible grooves, subunit interface clefts, or shallow depressions formed by protein conformational changes.

Based on the dynamic, hydrophobic, and elongated nature of allosteric pockets, MCE has carried out targeted fragment modification and screening under strict physicochemical criteria: MW 120–280 Da, HBD ≤ 2, HBA ≤ 3, PSA 30–80 Ų, rotatable bonds ≤ 2, cLogP 1–3.5. High 3D diversity was further ensured by PMI analysis, yielding fragments with excellent shape complementarity to allosteric pockets.

This library contains 1,800 structurally diverse, drug-like fragments, this library supports allosteric drug development and pocket optimization. It significantly improves screening hit rates and enables efficient, precise early-stage R&D of allosteric drugs.