CAS 58546-34-2

Hemslecin A

Description:

Hemslecin A is a natural product classified as a secondary metabolite, specifically a type of alkaloid. It is derived from certain fungal species and is known for its complex molecular structure, which includes multiple functional groups that contribute to its biological activity. The compound exhibits notable antimicrobial properties, making it of interest in pharmaceutical research for potential therapeutic applications. Hemslecin A has been studied for its effects on various biological systems, including its ability to inhibit the growth of certain pathogens. Its chemical structure features a bicyclic framework, which is characteristic of many alkaloids, and it may interact with biological targets through various mechanisms, including enzyme inhibition or receptor modulation. Additionally, the compound's solubility and stability can vary depending on environmental conditions, influencing its bioavailability and efficacy. Overall, Hemslecin A represents a significant area of study within natural product chemistry, particularly in the search for new antimicrobial agents.

Formula: C₃₂H₅₀O₈

InChI: InChI=1S/C32H50O8/c1-17(33)40-27(2,3)13-12-23(36)32(9,39)25-21(35)15-29(6)22-11-10-18-19(14-20(34)26(38)28(18,4)5)31(22,8)24(37)16-30(25,29)7/h10,19-22,25-26,34-35,38-39H,11-16H2,1-9H3/t19-,20+,21-,22+,25+,26-,29+,30-,31+,32+/m1/s1

InChI key: InChIKey=LKYNAQSYQLFTCM-GYXNDICUSA-N

SMILES: C[C@]12[C@@](C)([C@@]([C@@](C(CCC(OC(C)=O)(C)C)=O)(C)O)([C@H](O)C1)[H])CC(=O)[C@]3(C)[C@]2(CC=C4[C@]3(C[C@H](O)[C@@H](O)C4(C)C)[H])[H]

Synonyms:

• (2β,3α,9β,10α,16α)-25-(Acetyloxy)-2,3,16,20-tetrahydroxy-9-methyl-19-norlanost-5-ene-11,22-dione
• 19-Norlanost-5-ene-11,22-dione, 25-(acetyloxy)-2,3,16,20-tetrahydroxy-9-methyl-, (2beta,3alpha,9beta,10alpha,16alpha)-
• 19-Norlanost-5-ene-11,22-dione, 25-(acetyloxy)-2,3,16,20-tetrahydroxy-9-methyl-, (2β,3α,9β,10α,16α)-
• 23,24-Dihydrocucurbitacin F 25-acetate
• 23,24-Dihydrocucurbitacin F-25-O-acetate
• 25-Acetoxy-23,24-dihydrocucurbitacin F
• 25-O-Acetyl-23,24-dihydrocucurbitacin F
• Cucurbitacin II_a
• Dihydrocucurbitacin F 25-O-acetate
• Dihydrocucurbitacin Q1
• Hemslecin A
• estr-5-en-11-one, 17-[(1R)-5-(acetyloxy)-1-hydroxy-1,5-dimethyl-2-oxohexyl]-2,3,16-trihydroxy-4,4,9,14-tetramethyl-, (2beta,3alpha,9beta,10alpha,16alpha,17beta)-

Hemslecin A

CAS: 58546-34-2

Formula: C₃₂H₅₀O₈

Purity: 99%

Color and Shape: Solid

Molecular weight: 562.7346

Ref: IN-DA00E8YI

Hemslecin A

CAS: 58546-34-2

Formula: C₃₂H₅₀O₈

Molecular weight: 562.74

Ref: 7W-GY5262

Cucurbitacin IIA

CAS: 58546-34-2

Cucurbitacin IIA

Purity: ≥98%

Molecular weight: 562.73g/mol

Ref: 54-BUP05128

Hemslecin A

CAS: 58546-34-2

Formula: C₃₂H₅₀O₈

Purity: 95%~99%

Molecular weight: 562.744

Ref: BP-BP0718

Cucurbitacin IIA

CAS: 58546-34-2

1.

Formula: C₃₂H₅₀O₈

Purity: 98.62% - 99.87%

Color and Shape: Solid

Molecular weight: 562.73

Ref: TM-T3S1471

Hemslecin a

CAS: 58546-34-2

Carboxylic acid with alcohol function

Formula: C₃₂H₅₀O₈

Purity: ≥ 95.0 % (HPLC)

Color and Shape: Powder

Molecular weight: 562.75

Ref: 5G-82557

Cucurbitacin IIA

Controlled Product

CAS: 58546-34-2

Cucurbitacin IIA is a triterpenoid compound, which is a type of secondary metabolite predominantly found in plants belonging to the Cucurbitaceae family. This compound is a naturally occurring substance that has been isolated from sources like various cucumbers and gourds. Its mode of action primarily involves the inhibition of the JAK-STAT signaling pathway, which is pivotal in cellular processes including proliferation, apoptosis, and immune response regulation.

Purity: Min. 95%

Ref: 3D-FC73907