Page last updated: 2024-11-13

albicidin

Description Research Excerpts Clinical Trials Roles Classes Pathways Study Profile Bioassays Related Drugs Related Conditions Protein Interactions Research Growth Market Indicators

Description

albicidin: partially characterized as a 38 carbon compound with several aromatic rings; from Xanthomonas albilineans; Albicidin blocked DNA synthesis in intact cells of a PolA- EndA- Escherichia coli strain; albicidin resistance gene (albB) from Alcaligenes denitrificans encodes a 23 kDa protein capable of detoxifying albicidin by reversible binding [Medical Subject Headings (MeSH), National Library of Medicine, extracted Dec-2023]

Cross-References

ID SourceID
PubMed CID78322514
SCHEMBL ID15956023
SCHEMBL ID15956026
MeSH IDM0133868

Synonyms (7)

Synonym
albicidin
SCHEMBL15956023
SCHEMBL15956026
(s,e)-4-(4-(4-(3-cyano-2-(4-(3-(4-hydroxyphenyl)-2-methylacrylamido)benzamido) propanamido)benzamido)-2-hydroxy-3-methoxybenzamido)-2-hydroxy-3-methoxybenzoic acid
NZSWNNDHPOTJNH-VEJILBAHSA-N
BWH ,
AKOS040747787

Research Excerpts

Overview

Albicidin is a highly potent antibacterial compound synthesized by the plant-pathogenic bacterium Xanthomonas albilineans. Albicidins are a family of phytotoxins and antibiotics which play an important role in the pathogenesis of sugarcane leaf scald disease.

ExcerptReferenceRelevance
"Albicidin is a potent antibacterial oligoaromatic peptide that is susceptible to the protease AlbD, a resistance factor. "( Overcoming AlbD Protease Resistance and Improving Potency: Synthesis and Bioactivity of Antibacterial Albicidin Analogues with Amide Bond Isosteres.
Hommernick, K; Kleebauer, L; Seidel, M; Süssmuth, RD; Weston, JB; Zborovsky, L, 2021
)
2.28
"Albicidin is a highly potent antibacterial compound synthesized by the plant-pathogenic bacterium Xanthomonas albilineans."( Molecular insights into antibiotic resistance - how a binding protein traps albicidin.
Alings, C; Driller, R; Friedrich, T; Grätz, S; Kerwat, D; Kunert, M; Loll, B; Mainz, A; Petras, D; Rostock, L; Schmitt, FJ; Süssmuth, RD; von Eckardstein, L; Wahl, MC, 2018
)
1.43
"Albicidin is a potent DNA gyrase inhibitor produced by the sugarcane pathogenic bacterium Xanthomonas albilineans. "( The gyrase inhibitor albicidin consists of p-aminobenzoic acids and cyanoalanine.
Cociancich, S; Duplan, S; Hügelland, M; Kemper, S; Kretz, J; Mainz, A; Marguerettaz, M; Noëll, J; Pesic, A; Petras, D; Pieretti, I; Rott, P; Royer, M; Schubert, V; Süssmuth, RD; Uhlmann, S; Vieweg, L, 2015
)
2.18
"Albicidin is a nanomolar inhibitor of the bacterial DNA gyrase with a strong activity against various Gram-negative bacteria."( The Albicidin Resistance Factor AlbD Is a Serine Endopeptidase That Hydrolyzes Unusual Oligoaromatic-Type Peptides.
Cociancich, S; Grätz, S; Kerwat, D; Kretz, J; Mainz, A; Pesic, A; Royer, M; Süssmuth, RD; Vieweg, L, 2015
)
1.7
"Albicidin is a potent antibiotic and phytotoxin produced by Xanthomonas albilineans which targets the plant and bacterial DNA gyrase. "( The O-Carbamoyl-Transferase Alb15 Is Responsible for the Modification of Albicidin.
Arasté, J; Cociancich, S; Hempel, BF; Kerwat, D; Marguerettaz, M; Pesic, A; Petras, D; Royer, M; Semsary, S; Süssmuth, RD; von Eckardstein, L, 2016
)
2.11
"Albicidin is a pathotoxin produced by Xanthomonas albilineans, a xylem-invading pathogen that causes leaf scald disease of sugarcane. "( Substrate specificity-conferring regions of the nonribosomal peptide synthetase adenylation domains involved in albicidin pathotoxin biosynthesis are highly conserved within the species Xanthomonas albilineans.
Cociancich, S; Letourmy, P; Perrier, X; Renier, A; Rott, PC; Royer, M; Vivien, E, 2007
)
1.99
"Albicidins are a family of phytotoxins and antibiotics which play an important role in the pathogenesis of sugarcane leaf scald disease. "( High affinity binding of albicidin phytotoxins by the AlbA protein from Klebsiella oxytoca.
Birch, RG; Xu, J; Zhang, L, 1998
)
2.05

Treatment

ExcerptReferenceRelevance
"Pretreatment with albicidin protected AlbA against modification by DEPC, with a 1 : 1 molar ratio of albicidin to the protected histidine residues."( Identification of the essential histidine residue for high-affinity binding of AlbA protein to albicidin antibiotics.
Birch, RG; Li, Q; Weng, LX; Xu, JL; Zhang, LH, 2003
)
0.86
[information is derived through text-mining from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Research

Studies (45)

TimeframeStudies, This Drug (%)All Drugs %
pre-19902 (4.44)18.7374
1990's10 (22.22)18.2507
2000's13 (28.89)29.6817
2010's14 (31.11)24.3611
2020's6 (13.33)2.80
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Market Indicators

Research Demand Index: 31.09

According to the monthly volume, diversity, and competition of internet searches for this compound, as well the volume and growth of publications, there is estimated to be moderate demand-to-supply ratio for research on this compound.

MetricThis Compound (vs All)
Research Demand Index31.09 (24.57)
Research Supply Index3.83 (2.92)
Research Growth Index5.25 (4.65)
Search Engine Demand Index39.34 (26.88)
Search Engine Supply Index2.00 (0.95)

This Compound (31.09)

All Compounds (24.57)

Study Types

Publication TypeThis drug (%)All Drugs (%)
Trials0 (0.00%)5.53%
Reviews1 (2.22%)6.00%
Case Studies0 (0.00%)4.05%
Observational0 (0.00%)0.25%
Other44 (97.78%)84.16%
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]