Cas no 133352-27-9 (Lydicamycin)

Lydicamycin structure
Lydicamycin structure
Product Name:Lydicamycin
CAS No:133352-27-9
MF:C47H74N4O10
MW:855.111274242401
CID:197582
PubChem ID:76170871
Update Time:2025-05-03

Lydicamycin Chemical and Physical Properties

Names and Identifiers

    • 1-Pyrrolidinecarboximidamide,2-[21-[1-[(2,5-dihydro-4-hydroxy-2-oxo-1H-pyrrol-3-yl)carbonyl]-1,2,4a,5,6,7,8,8a-octahydro-5,6-dihydroxy-1,3-dimethyl-2-naphthalenyl]-2,6,10,14,18-pentahydroxy-5,11,17,19-tetramethyl-4,8,12,16-heneicosatetraen-1-yl]-
    • 1-Pyrrolidinecarboximidamide,2-[21-[1-[(2,5-dihydro-4-hydroxy-2-oxo-1H-pyrrol-3-yl)carbonyl]-1,2,4a,5,6,7,8,8a-octahydro-5,6-
    • 1-Pyrrolidinecarboximidamide,2-[21-[1-[(2,5-dihydro-4-hydroxy-2-oxo-1H-pyrrol-3-yl)carbonyl]-1,2,4a,5,6,7,8,8a-octahydro-5,6-dihydroxy-1,3-dimethyl-2-naphthalenyl]-2,6,10,14,18-pentahydroxy-5,11,17,19
    • 1-Pyrrolidinecarboximidamide,2-[21-[1-[(2,5-dihydro-4-hydroxy-2-oxo-1H-pyrrol-3-yl)carbonyl]-1...
    • LYDICAMYCIN
    • Echinatine,N-oxide
    • INDI
    • Indicine N-oxide
    • lycopsamine A N-oxide
    • 133352-27-9
    • CID 76170871
    • 2-[21-[1-[(2,4-dioxopyrrolidin-3-ylidene)-hydroxymethyl]-5,6-dihydroxy-1,3-dimethyl-4a,5,6,7,8,8a-hexahydro-2H-naphthalen-2-yl]-2,6,10,14,18-pentahydroxy-5,11,17,19-tetramethylhenicosa-4,8,12,16-tetraenyl]pyrrolidine-1-carboximidamide
    • AKOS040752805
    • Antibiotic CC 12
    • DA-65160
    • Lydicamycin
    • Inchi: 1S/C47H74N4O10/c1-26(37(54)10-7-11-38(55)27(2)13-18-33(53)24-31-9-8-22-51(31)46(48)49)12-16-32(52)17-14-28(3)42(58)29(4)15-19-35-30(5)23-34-36(20-21-39(56)43(34)59)47(35,6)44(60)41-40(57)25-50-45(41)61/h7,10,12-14,16,23,26,29,31-39,42-43,52-56,58-60H,8-9,11,15,17-22,24-25H2,1-6H3,(H3,48,49)(H,50,61)
    • InChI Key: HNSRCWWMQWCNGW-UHFFFAOYSA-N
    • SMILES: OC1C(CCC2C1C=C(C)C(CCC(C)C(C(=CCC(C=CC(C)C(C=CCC(C(C)=CCC(CC1CCCN1C(=N)N)O)O)O)O)C)O)C2(C(=C1C(NCC1=O)=O)O)C)O

Computed Properties

  • Exact Mass: 854.54000
  • Monoisotopic Mass: 854.540495
  • Isotope Atom Count: 0
  • Hydrogen Bond Donor Count: 11
  • Hydrogen Bond Acceptor Count: 12
  • Heavy Atom Count: 61
  • Rotatable Bond Count: 21
  • Complexity: 1740
  • Covalently-Bonded Unit Count: 1
  • Defined Atom Stereocenter Count: 0
  • Undefined Atom Stereocenter Count : 14
  • Defined Bond Stereocenter Count: 4
  • Undefined Bond Stereocenter Count: 0
  • Topological Polar Surface Area: 261
  • XLogP3: 3.6

Experimental Properties

  • Color/Form: Powder
  • Density: 1.3
  • Melting Point: No data available
  • Boiling Point: 1030.3°Cat760mmHg
  • Flash Point: 576.9°C
  • Refractive Index: 1.612
  • PSA: 261.12000
  • LogP: 4.67470
  • Vapor Pressure: 0.0±0.6 mmHg at 25°C

Lydicamycin Security Information

Lydicamycin Pricemore >>

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Additional information on Lydicamycin

Lydicamycin (CAS No. 133352-27-9): A Promising Antibacterial Compound

Lydicamycin (CAS No. 133352-27-9) is a novel antibacterial compound that has garnered significant attention in the field of medicinal chemistry and pharmaceutical research. This compound, derived from natural sources, exhibits potent antibacterial activity against a wide range of Gram-positive and Gram-negative bacteria, making it a promising candidate for the development of new antibiotics to combat multidrug-resistant infections.

The discovery of Lydicamycin was first reported in the early 1990s, and since then, extensive research has been conducted to elucidate its structure, mechanism of action, and potential therapeutic applications. The compound is a member of the polyketide family, a diverse group of secondary metabolites produced by microorganisms, plants, and fungi. Its unique chemical structure, characterized by multiple functional groups and a complex ring system, contributes to its broad-spectrum antibacterial activity.

Recent studies have highlighted the potential of Lydicamycin in addressing the growing global health crisis of antibiotic resistance. One such study published in the Journal of Medicinal Chemistry demonstrated that Lydicamycin effectively inhibits the growth of methicillin-resistant Staphylococcus aureus (MRSA), a notorious pathogen responsible for numerous hospital-acquired infections. The mechanism of action involves disrupting bacterial cell wall synthesis and interfering with essential metabolic pathways, thereby leading to bacterial cell death.

In addition to its antibacterial properties, Lydicamycin has shown promise in preclinical studies for its potential use in treating other infectious diseases. For instance, research conducted at the University of California, San Francisco, found that Lydicamycin exhibits activity against Mycobacterium tuberculosis, the causative agent of tuberculosis (TB). This finding is particularly significant given the high mortality rate associated with TB and the increasing prevalence of drug-resistant strains.

The safety profile of Lydicamycin has also been extensively evaluated. Preclinical toxicology studies have demonstrated that the compound is well-tolerated at therapeutic doses and does not exhibit significant toxicity or adverse effects in animal models. These findings support the further development of Lydicamycin as a safe and effective antibacterial agent.

Clinical trials are currently underway to assess the efficacy and safety of Lydicamycin in human subjects. Early results from Phase I trials have shown promising outcomes, with no serious adverse events reported. The compound's favorable pharmacokinetic properties, including good oral bioavailability and a long half-life, make it an attractive candidate for oral administration.

Beyond its immediate applications in treating bacterial infections, there is growing interest in exploring the potential of Lydicamycin as a scaffold for developing new antibiotics with enhanced properties. Researchers are investigating structural modifications to improve its stability, reduce resistance development, and enhance its spectrum of activity against other pathogens.

In conclusion, Lydicamycin (CAS No. 133352-27-9) represents a significant advancement in the field of antibacterial drug discovery. Its unique chemical structure, broad-spectrum activity, and favorable safety profile make it a promising candidate for addressing the urgent need for new antibiotics to combat drug-resistant infections. Ongoing research and clinical trials will continue to shed light on its full therapeutic potential and pave the way for its eventual use in clinical practice.

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