ORITAVANCIN

Oritavancin is a longacting lipoglycopeptide antibiotic inhibiting cellwall synthesis in grampositive bacteria. Benefits include singledose therapy for skin infections. Side effects include headache, nausea, infusion reactions, and coagulation test interference. Only GMP materials will be supplied, logistics all according to GDP.

SKU: 93b0602c52ed Category: Tag:

Product Description


Mechanism of Action

ORITAVANCIN shows a complex, multipathway biochemical interaction profile involving modulation of enzymeregulated catalytic cycles, receptorlevel signalling networks, intracellular ion dynamics, mitochondrial respiratory control, redoxbalance adaptation, cytoskeletal organisation and transcriptionfactor regulatory behaviour. Its physicochemical structure supports direct or indirect interaction with catalytic residues, allosteric pockets, membranespanning receptors, signalling intermediates and structural proteins, enabling influence over secondmessenger pathways (Ca²⁺, cAMP, IP, DAG), phosphorylation kinetics, ROS generation and mitochondrial ATPsynthesis efficiency.

Depending on concentration, exposure duration and biological substrate, ORITAVANCIN may shift metabolic routing, alter vesicular transport, influence chromatin accessibility, modify transcriptional clusters, or recalibrate mitochondrial stressresponse thresholds across diverse experimental models.

Benefits and Advantages

Common applications in research environments include:

  • Highresolution receptorligand interaction analysis and molecular docking validation
  • Enzymekinetic dissection and catalyticpathway reconstruction
  • Mitochondrialperformance assays, redoxstress modelling and ATPflux quantification
  • Multiomics integration: transcriptomics, metabolomics, proteomics, phosphoproteomics
  • Cytoskeletaldynamics studies involving actin, tubulin and membranetension regulation
  • Apoptosis, autophagy, necroptosis, ferroptosis and stressresponse pathway mapping
  • SAR (structureactivity relationship) investigation and molecularoptimisation workflows
  • Preclinical pharmacodynamic modelling and mechanistic doseresponse assays

Side Effects and Risks

Potential laboratoryobserved risks include:

  • ROS accumulation and oxidativestress imbalance
  • Mitochondrial hyperactivation or respiratorychain suppression
  • Disruption of Ca²⁺/Na⁺/K⁺ ionic homeostasis and ionchannel behaviour
  • Unintended receptor crossactivation or inhibitory interference
  • Cytoarchitectural destabilisation, membrane fragility or impaired trafficking
  • Dosedependent cytotoxicity and activation of apoptosis/autophagy signalling
  • Transcriptional and epigenetic instability under prolonged exposure
  • Inflammatory pathway activation (NF-κB, MAPK, JNK)

Use exclusively under controlled laboratory conditions, following strict biosafety and handling protocols.

Only GMP materials will be supplied, logistics all according to GDP.

Datasheet


Molecular Formula

C86H97Cl3N10O26

Molecular Weight

1793.1 g/mol

CAS Number

171099-57-3

Storage Condition

Store in a cool, dry place. Keep container tightly closed. Protect from moisture and light.

Solubility

Solubility depends on solvent and conditions (e.g., pH). Please contact us for solvent-specific guidance.

Purity

Purity information is available upon request (COA).

Synonym

Oritavancin; 171099-57-3; LY333328; Chlorobiphenyl-chloroeremomycin; LY-333328

IUPAC/Chemical Name

(1S,2R,18R,19R,22S,25R,28R,40S)-2-[(2R,4S,5R,6S)-4-amino-5-hydroxy-4,6-dimethyloxan-2-yl]oxy-22-(2-amino-2-oxoethyl)-5,15-dichloro-48-[(2S,3R,4S,5S,6R)-3-[(2S,4S,5R,6S)-4-[[4-(4-chlorophenyl)phenyl]methylamino]-5-hydroxy-4,6-dimethyloxan-2-yl]oxy-4,5-dihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-18,32,35,37-tetrahydroxy-19-[[(2R)-4-methyl-2-(methylamino)pentanoyl]amino]-20,23,26,42,44-pentaoxo-7,13-dioxa-21,24,27,41,43-pentazaoctacyclo[26.14.2.23,6.214,17.18,12.129,33.010,25.034,39]pentaconta-3,5,8,10,12(48),14,16,29(45),30,32,34(39),35,37,46,49-pentadecaene-40-carboxylic acid

InChl Key

VHFGEBVPHAGQPI-LXKZPTCJSA-N

InChl Code

InChI=1S/C86H97Cl3N10O26/c1-35(2)22-51(92-7)77(110)98-67-69(105)42-15-20-55(49(88)24-42)120-57-26-44-27-58(73(57)125-84-74(71(107)70(106)59(34-100)122-84)124-62-32-86(6,76(109)37(4)119-62)93-33-38-8-10-39(11-9-38)40-12-17-45(87)18-13-40)121-56-21-16-43(25-50(56)89)72(123-61-31-85(5,91)75(108)36(3)118-61)68-82(115)97-66(83(116)117)48-28-46(101)29-54(103)63(48)47-23-41(14-19-53(47)102)64(79(112)99-68)96-80(113)65(44)95-78(111)52(30-60(90)104)94-81(67)114/h8-21,23-29,35-37,51-52,59,61-62,64-72,74-76,84,92-93,100-103,105-109H,22,30-34,91H2,1-7H3,(H2,90,104)(H,94,114)(H,95,111)(H,96,113)(H,97,115)(H,98,110)(H,99,112)(H,116,117)/t36-,37-,51+,52-,59+,61-,62-,64+,65+,66-,67+,68-,69+,70+,71-,72+,74+,75-,76-,84-,85-,86-/m0/s1

References

https://pubchem.ncbi.nlm.nih.gov/compound/16136912;

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