structure of Galbacin

Galbacin

CAS No.: 178740-32-4
M. Wt: 340.370
M. Fa: C20H20O5
InChI Key: QFUXQRHAJWXPGP-UHFFFAOYSA-N

Names and Identifiers of Galbacin

CAS Number

178740-32-4

IUPAC Name

5-[5-(1,3-benzodioxol-5-yl)-3,4-dimethyloxolan-2-yl]-1,3-benzodioxole

InChI

InChI=1S/C20H20O5/c1-11-12(2)20(14-4-6-16-18(8-14)24-10-22-16)25-19(11)13-3-5-15-17(7-13)23-9-21-15/h3-8,11-12,19-20H,9-10H2,1-2H3

InChIKey

QFUXQRHAJWXPGP-UHFFFAOYSA-N

Canonical SMILES

CC1C(C(OC1C2=CC3=C(C=C2)OCO3)C4=CC5=C(C=C4)OCO5)C

Physical and chemical properties of Galbacin

Boiling Point

460.6±45.0 °C at 760 mmHg

Density

1.3±0.1 g/cm3

Exact Mass

340.131073

Flash Point

190.1±28.6 °C

Index of Refraction

1.585

LogP

4.77

Molecular Formula

C20H20O5

Molecular Weight

340.370

Storage condition

-20℃

Vapour Pressure

0.0±1.1 mmHg at 25°C

Applications of Galbacin

(-)-Galbacin has diverse applications across various fields:

  • Chemistry: It serves as a chiral building block in synthesizing complex molecules.
  • Biology: Investigated for its potential therapeutic effects, particularly in drug discovery.
  • Industry: Utilized in producing fine chemicals and pharmaceuticals due to its unique properties and reactivity.

Interaction Studies of Galbacin

Studies exploring the interactions of (-)-Galbacin with biological targets have revealed its potential to modulate enzyme activity and influence cellular pathways. These interactions are crucial for understanding its biological effects and therapeutic potential. For instance, research has demonstrated its ability to inhibit specific enzymes linked to cancer cell proliferation, suggesting a pathway for developing anticancer drugs.

Biological Activity of Galbacin

Research indicates that (-)-Galbacin exhibits significant biological activities, particularly in the realms of antimicrobial and anticancer properties. Its mechanism of action may involve interactions with specific enzymes or receptors, modulating biochemical pathways that affect cell proliferation and survival. Studies have shown that it can inhibit certain enzymes linked to cancer progression, making it a candidate for further therapeutic exploration.

Retrosynthesis analysis of Galbacin

  • Route#1

    Cas:274-09-9
    Cas:178740-32-4