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Brc1cnc(nc1)C
Pyrimidine, 5-bromo-2-methyl-
CCCP1(=O)OP(=O)(CCC)OP(=O)(O1)CCC
1,3,5,2,4,6-Trioxatriphosphorinane, 2,4,6-tripropyl-, 2,4,6-trioxide
CC1(C)OB(OC1(C)C)B1OC(C(O1)(C)C)(C)C
2,2'-Bi-1,3,2-dioxaborolane, 4,4,4',4',5,5,5',5'-octamethyl-
O=C(C=Cc1ccccc1)C=Cc1ccccc1.O=C(C=Cc1ccccc1)C=Cc1ccccc1.O=C(C=Cc1ccccc1)C=Cc1ccccc1.[Pd].[Pd]
Tris(dibenzylideneacetone)dipalladium
C1CCC(CC1)P(C1CCCCC1)C1CCCCC1.Cc1cc(C)c(c(c1)C)N1CCN(C1=[Ru](=Cc1ccccc1)(Cl)Cl)c1c(C)cc(cc1C)C
Ruthenium,[1,3-bis(2,4,6-trimethylphenyl)-2-imidazolidinylidene]dichloro(phenylmethylene)(tricyclohexylphosphine)-, (SP-5-41)-

(S)-HDAC-42

ONC(=O)c1ccc(cc1)NC(=O)[C@H](c1ccccc1)C(C)C Request for Quotation
Chemical Name: (S)-HDAC-42
CAS Number: 935881-37-1
Product Number: AG0061ZH(AGN-PC-0W36BA)
Synonyms:
MDL No: MFCD17676151
Molecular Formula: C18H20N2O3
Molecular Weight: 312.3630

Identification/Properties

Properties
Storage:
Inert atmosphere;-10 ℃;
Form:
Solid
Computed Properties
Molecular Weight:
312.369g/mol
XLogP3:
2.8
Hydrogen Bond Donor Count:
3
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
5
Exact Mass:
312.147g/mol
Monoisotopic Mass:
312.147g/mol
Topological Polar Surface Area:
78.4A^2
Heavy Atom Count:
23
Formal Charge:
0
Complexity:
397
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
1
Undefined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
Covalently-Bonded Unit Count:
1
Compound Is Canonicalized:
Yes

Safety Information

NMR Spectrum

Other Analytical Data

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Chemical Structure


AR-42, a novel histone deacetylase inhibitor, has found extensive application in chemical synthesis. Its unique properties make it a valuable tool for researchers in the field. AR-42 is known for its ability to modulate gene expression by affecting histone acetylation, thereby influencing various cellular processes. In the realm of chemical synthesis, this compound is particularly useful in the creation of novel drug candidates, as its impact on gene regulation can lead to the development of new therapeutic agents. Additionally, AR-42's role in epigenetic modifications makes it a key player in the study of gene function and regulation, offering insights into potential targets for drug discovery. By leveraging the capabilities of AR-42 in chemical synthesis, researchers can explore innovative pathways for the creation of compounds with diverse pharmacological activities.