1. Metabolic Enzyme/Protease Neuronal Signaling
  2. Carbonic Anhydrase Cholinesterase (ChE)
  3. hCAI/II-IN-8

hCAI/II-IN-8 (Compound 8) is a hydrazide derivative based on 4-hydroxybenzaldehyde. hCAI/II-IN-8 primarily targets human carbonic anhydrase isomerase I (hCA I) and II (hCA II) for inhibition (IC50 = 21.35 ± 0.39 nM (hCA I); 7.12 ± 0.12 nM (hCA II)). hCAI/II-IN-8 inhibits AChE and BChE as well(IC50 = 46.27 ±0.75 nM (AChE); 43.38 ± 0.83 nM (BChE)). ..

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hCAI/II-IN-8 Chemical Structure

hCAI/II-IN-8 Chemical Structure

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Description

hCAI/II-IN-8 (Compound 8) is a hydrazide derivative based on 4-hydroxybenzaldehyde. hCAI/II-IN-8 primarily targets human carbonic anhydrase isomerase I (hCA I) and II (hCA II) for inhibition (IC50 = 21.35 ± 0.39 nM (hCA I); 7.12 ± 0.12 nM (hCA II)). hCAI/II-IN-8 inhibits AChE and BChE as well(IC50 = 46.27 ±0.75 nM (AChE); 43.38 ± 0.83 nM (BChE)). [1].[1].

IC50 & Target

hCA I

21.35 nM (IC50)

hCA II

7.12 nM (IC50)

AChE

46.27 ±0.7 nM (IC50)

BChE

43.38 ± 0. nM (IC50)

In Vitro

hCAI/II-IN-8 is an efficient activity inhibitor by forming multiple hydrogen bonds and hydrophobic interactions with key residues in hCA I and hCA II. hCAI/II-IN-8 also has high stability in binding to the enzyme[1].

MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only.

Molecular Weight

388.42

Formula

C22H20N4O3

Unlabeled Cas

SMILES

CN(C)C1=CC=C(C(OC2=CC=C(/C=N/NC(C3=CN=CC=C3)=O)C=C2)=O)C=C1

Shipping

Room temperature in continental US; may vary elsewhere.

Storage

Please store the product under the recommended conditions in the Certificate of Analysis.

Purity & Documentation
References
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hCAI/II-IN-8
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HY-161507
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