CAS 6834-98-6

Fungichromin

Description:

Fungichromin, with the CAS number 6834-98-6, is a chemical compound known for its antifungal properties. It is classified as a natural product, specifically a type of antibiotic derived from certain microbial sources. Fungichromin exhibits a complex structure that contributes to its biological activity, making it effective against various fungal pathogens. Its mechanism of action typically involves disrupting fungal cell membrane integrity or inhibiting essential metabolic processes, which can lead to cell death. The compound is of interest in pharmaceutical and agricultural applications, particularly in developing treatments for fungal infections and as a potential biopesticide. Additionally, research into its properties may reveal insights into its efficacy, safety, and potential resistance mechanisms in target organisms. As with many bioactive compounds, the study of Fungichromin encompasses aspects of chemistry, microbiology, and pharmacology, highlighting its significance in both medical and environmental contexts.

Formula: C₃₅H₅₈O₁₂

InChI: InChI=1/C35H58O12/c1-4-5-11-16-29(41)32-30(42)20-26(38)18-24(36)17-25(37)19-27(39)21-31(43)34(45)33(44)22(2)14-12-9-7-6-8-10-13-15-28(40)23(3)47-35(32)46/h6-10,12-15,23-34,36-45H,4-5,11,16-21H2,1-3H3/b7-6+,10-8+,12-9+,15-13+,22-14+/t23-,24+,25-,26+,27-,28+,29-,30+,31-,32-,33-,34-/m1/s1

InChI key: InChIKey=AGJUUQSLGVCRQA-SWOUQTJZSA-N

SMILES: [C@H](CCCCC)(O)[C@@]1([C@@H](O)C[C@@H](O)C[C@@H](O)C[C@@H](O)C[C@@H](O)C[C@@H](O)[C@@H](O)[C@H](O)\C(\C)=C\C=C\C=C\C=C\C=C\[C@H](O)[C@@H](C)OC1=O)[H]

Synonyms:

• (3R,4S,6S,8S,10R,12R,14R,15R,16R,17E,19E,21E,23E,25E,27S,28R)-4,6,8,10,12,14,15,16,27-Nonahydroxy-3-[(1R)-1-hydroxyhexyl]-17,28-dimethyloxacyclooctacosa-17,19,21,23,25-pentaen-2-one
• Pentamycin
• S 232
• Lagosin
• Oxacyclooctacosa-17,19,21,23,25-pentaen-2-one, 4,6,8,10,12,14,15,16,27-nonahydroxy-3-(1-hydroxyhexyl)-17,28-dimethyl-, [3R-[3R*(R*),4S*,6S*,8S*,10R*,12R*,14R*,15R*,16R*,17E,19E,21E,23E,25E,27S*,28R*]]-
• Lagosin (antibiotic)
• NSC 105388
• Oxacyclooctacosa-17,19,21,23,25-pentaen-2-one, 4,6,8,10,12,14,15,16,27-nonahydroxy-3-[(1R)-1-hydroxyhexyl]-17,28-dimethyl-, (3R,4S,6S,8S,10R,12R,14R,15R,16R,17E,19E,21E,23E,25E,27S,28R)-
• 14-Hydroxyfilipin
• Cogomycin
• (3R,4S,6S,8S,10R,12R,14R,15R,16R,17E,19E,21E,23E,25E,27S,28R)-4,6,8,10,12,14,15,16,27-nonahydroxy-3-[(1R)-1-hydroxyhexyl]-17,28-dimethyloxacyclooctacosa-17,19,21,23,25-pentaen-2-one (non-preferred name)
• (17E,19E,21E,23E,25E)-4,6,8,10,12,14,15,16,27-nonahydroxy-3-(1-hydroxyhexyl)-17,28-dimethyloxacyclooctacosa-17,19,21,23,25-pentaen-2-one (non-preferred name)
• Fungichromin
• Antibiotic A-246
• Oxacyclooctacosane, fungichromin deriv.
• NSC 276732
• S-232

Lagosin

CAS: 6834-98-6

Lagosin is a polyene antibiotic that has been shown to have antimicrobial activity against Gram-positive and Gram-negative bacteria. This drug has been used in the treatment of infectious diseases, such as septicemia or meningitis caused by bacterial infections. Lagosin is active against bacteria that are resistant to other antibiotics because it interacts with the cell wall and causes cell lysis. The mechanism of action for Lagosin is similar to that of amphotericin B and nystatin, which are also polyene antibiotics. The antibacterial activity of this drug may be due to its ability to interact with cells and cause cell lysis. Lagosin has also been shown to have anti-inflammatory properties, which may be due to its ability to inhibit prostaglandin synthesis.

Formula: C₃₅H₅₈O₁₂

Purity: Min. 95%

Molecular weight: 670.8 g/mol

Ref: 3D-GAA83498