ChemicalBook > Product Catalog >Biochemical Engineering >Biochemical Reagents >Agonist Inhibitors >Pretomanid

Pretomanid

Pretomanid Suppliers list
Company Name: Rayge(SuZhou)New Materials Co.,Ltd  Gold
Tel: 0512-87813132-801 13913535368
Email: 3043369320@qq.com
Company Name: Anhui Shuoyuan Pharmaceutical Technology R&D Co.,Ltd  Gold
Tel: 05558228005 18151793555
Email: 413315120@qq.com
Company Name: Yaopu(Shanghai) Pharmaceutical Technology Co., Ltd  Gold
Tel: 50929289 18616309303
Email: sales@ypptech.com.cn
Company Name: Hubei wei shi reagent group ltd., company  Gold
Tel: 17771898297 13125137661
Email: 2853877621@qq.com
Company Name: Shanghai Yatan Pharmaceutical Research and Development Co. LTD  Gold
Tel: 15512780135
Email: songqw@neutanpharma.com

Pretomanid manufacturers

  • Pretomanid
  • Pretomanid pictures
  • 2026-09-17
  • CAS:187235-37-6
  • Min. Order: 1g
  • Purity: More Than 99%
  • Supply Ability: 100kg/Month
  • Pretomanid.
  • Pretomanid. pictures
  • 2026-09-17
  • CAS:187235-37-6
  • Min. Order: 1g
  • Purity: More Than 99%
  • Supply Ability: 100kg/Month
  • Pretomanid
  • Pretomanid pictures
  • 2026-05-18
  • CAS:187235-37-6
  • Min. Order: 1kg
  • Purity: 98%

Related articles

Pretomanid Basic information
Product Name:Pretomanid
Synonyms:PA 824;(S)-PA 824;(6S)-6,7-Dihydro-2-nitro-6-[[4-(trifluoromethoxy)phenyl]methoxy]-5H-imidazo[2,1-b][1,3]oxazine;(S)-6,7-Dihydro-2-nitro-6-[[4-(trifluoromethoxy)phenyl]methoxy]-5H-imidazo[2,1-b][1,3]oxazine;5H-IMidazo[2,1-b][1,3]oxazine, 6,7-dihydro-2-nitro-6-[[4-(trifluoroMethoxy)phenyl]Methoxy]-, (6S)-;(S)-6-(4-(trifluoromethoxy)benzyloxy)-2-nitro-6,7-dihydro-5H-imidazo[2,1-b][1,3]oxazine;(6S)-6,7-Dihydro-2-nitro-6-[[4-(trifluoromethoxy)phenyl]methoxy]-5H-imidazo[2,1-b][1,3]oxazine PA-824;EOS-60675
CAS:187235-37-6
MF:C14H12F3N3O5
MW:359.26
EINECS:1533716-785-6
Product Categories:Aromatics;Heterocycles;Intermediates & Fine Chemicals;Pharmaceuticals;Inhibitors
Mol File:187235-37-6.mol
Pretomanid Structure
Pretomanid Chemical Properties
Melting point 149-150℃
Boiling point 462.3±55.0 °C(Predicted)
density 1.58
storage temp. -20°C
solubility DMSO (Slightly), Methanol (Slightly)
pka-0.67±0.40(Predicted)
form powder
color white to brown
Optical Rotation[α]/D -40 to -48°, c = 1 in methanol
InChIInChI=1S/C14H12F3N3O5/c15-14(16,17)25-10-3-1-9(2-4-10)7-23-11-5-19-6-12(20(21)22)18-13(19)24-8-11/h1-4,6,11H,5,7-8H2/t11-/m0/s1
InChIKeyZLHZLMOSPGACSZ-NSHDSACASA-N
SMILESO1C[C@@H](OCC2=CC=C(OC(F)(F)F)C=C2)CN2C=C([N+]([O-])=O)N=C12
Safety Information
WGK Germany WGK 3
HS Code 2933992000
Storage Class11 - Combustible Solids
Hazard ClassificationsEye Irrit. 2
Skin Irrit. 2
STOT SE 3
MSDS Information
Pretomanid Usage And Synthesis
UsesA novel anti-tuberculosis drug.
Biological Activitypa-824, a bicyclic nitroimidazoles, is an anti-tuberculosis (tb) agent that exerts potent in vitro activity against mycobacterium tuberculosis with the minimal inhibition concentration (mic) ranging from 0.015 μg/ml to 0.25 μg/ml and remains actively against a wide range of isolates that are resistant to commonly used anti-tb agents leading to its successful application in the treatment of tb [1].pa-824 has been found to exhibit bactericidal activity against replicating bacilli and non-replicating bacilli under hypoxic or prolonged culture conditions in a dose dependent fashion through two possible mechanisms, which include pa-824 induced inhibition of ketomycolate synthesis and pa-824 mediated donation of nitric oxide during enzymatic nitro-reduction [1].
Biochem/physiol ActionsPA-824 is an anti-tuberculosis drug.
SynthesisPretomanid can be produced as follow
Pretomanid synthesis
references[1] ahmad z, peloquin ca, singh rp, derendorf h, tyagi s, ginsberg a, grosset jh, nuermberger el. pa-824 exhibits time-dependent activity in a murine model of tuberculosis. antimicrob agents chemother. 2011 jan;55(1):239-45. doi: 10.1128/aac.00849-10. epub 2010 oct 11.
Pretomanid Preparation Products And Raw materials
Tag:Pretomanid(187235-37-6) Related Product Information
Sulfanilamide DEMETON S lygtf Sorafenib Gefitinib CZC24832 Ribociclib Erlotinib hydrochloride Olaparib