MB-3 - Moligand™ , Inhibitor of lysine acetyltransferase 2B, CAS No.M611752, Inhibitor of lysine acetyltransferase 2B

CAS: M611752 Cat. No.: M611752 PubChem CID: 91827357

GRADE & PURITY Moligand™

Synonyms

α-methylene-γ-butyrolactone 3

Storage

Room temperature

Specifications

Synonyms

α-methylene-γ-butyrolactone 3

Specifications & Purity

Moligand™

Storage

Room temperature

Grade

Moligand™

Action Type

INHIBITOR

Mechanism of action

Inhibitor of lysine acetyltransferase 2B

Names and Identifiers

• Canonical Smiles: CCC[C@@H]1OC(=O)C(=O)[C@H]1C(=O)O
• IUPAC Name: (2S,3S)-4,5-dioxo-2-propyloxolane-3-carboxylic acid
• InChIKey: AKWJFOMNTDKSRR-WHFBIAKZSA-N
• INCHI: 1S/C8H10O5/c1-2-3-4-5(7(10)11)6(9)8(12)13-4/h4-5H,2-3H2,1H3,(H,10,11)/t4-,5-/m0/s1
• Isomeric SMILES: CCC[C@H]1[C@@H](C(=O)C(=O)O1)C(=O)O
• PubChem CID: 91827357

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Organoheterocyclic compounds
    • Class Lactones
      • Subclass Gamma butyrolactones

• Kingdom: Organic compounds
• Superclass: Organoheterocyclic compounds
• Class: Lactones
• Subclass: Gamma butyrolactones
• Intermediate Tree Nodes: Not available
• Direct Parent: Gamma butyrolactones
• Alternative Parents: Furanones Dicarboxylic acids and derivatives 1,3-dicarbonyl compounds Oxolanes Cyclic ketones Carboxylic acid esters Oxacyclic compounds Carboxylic acids Organic oxides Hydrocarbon derivatives
• Molecular Framework: Aliphatic heteromonocyclic compounds
• Substituents: Dicarboxylic acid or derivatives - 3-furanone - Gamma butyrolactone - 1,3-dicarbonyl compound - Oxolane - Carboxylic acid ester - Ketone - Cyclic ketone - Carboxylic acid - Oxacycle - Carboxylic acid derivative - Carbonyl group - Hydrocarbon derivative - Organic oxide - Organic oxygen compound - Organooxygen compound - Aliphatic heteromonocyclic compound
• Description: This compound belongs to the class of organic compounds known as gamma butyrolactones. These are compounds containing a gamma butyrolactone moiety, which consists of an aliphatic five-member ring with four carbon atoms, one oxygen atom, and bears a ketone group on the carbon adjacent to the oxygen atom.
• External Descriptors: Not available

Data sources

1. Djoumbou Feunang Y, Eisner R, Knox C, Chepelev L, Hastings J, Owen G, Fahy E, Steinbeck C, Subramanian S, Bolton E, Greiner R, and Wishart DS. ClassyFire: Automated Chemical Classification With A Comprehensive, Computable Taxonomy. Journal of Cheminformatics, 2016, 8:61.

DOI: 10.1186/s13321-016-0174-y

Associated Targets(Human)

KAT2B Tchem Histone acetyltransferase KAT2B (0 Activities)

Discover Target: KAT2B

Activity Type	Activity Value -log(M)	Mechanism of Action	Activity Reference	Publications (PubMed IDs)