Email:
 Phone:
Get A Quote

CJ-14877

* Please be kindly noted products are not for therapeutic use. We do not sell to patients.

CJ-14877
Category Antibiotics
Catalog number BBF-02770
CAS
Molecular Weight 211.21
Molecular Formula C10H13NO4

Online Inquiry

Capabilities & Facilities

Fermentation Lab

4 R&D and scale-up labs

2 Preparative purification labs

Fermentation Plant

Semi pilot, pilot and industrial plant 4 Manufacturing sites 7 Production lines at pilot scale 100+ Reactors of 30-4000 L; 170+ reactors of 20 KL-30 KL; 24+ reactors of >100 KL 2 Hydrogenation reactors (200 L, 4Mpa and 1000L, 4Mpa)

Product Description

It is originally isolated from Marasmiellus sp. CL21624. CJ-14877 inhibited human blood interleukin-1β (IL-1β) production induced by lipoglycan (LPS) with an IC50 of 0.1 μmol/L.

  • Specification
  • Properties
  • Reference Reading
  • Price Product List
Synonyms 2-Pyridinecarboxylic acid, 5-[(1S,2S)-1,2-dihydroxypropyl]-, methyl ester
IUPAC Name methyl 5-[(1S,2S)-1,2-dihydroxypropyl]pyridine-2-carboxylate
Canonical SMILES CC(C(C1=CN=C(C=C1)C(=O)OC)O)O
InChI InChI=1S/C10H13NO4/c1-6(12)9(13)7-3-4-8(11-5-7)10(14)15-2/h3-6,9,12-13H,1-2H3/t6-,9+/m0/s1
InChI Key XZXCYBBAXJQLFQ-IMTBSYHQSA-N
Appearance White Powder
Antibiotic Activity Spectrum neoplastics (Tumor)
Boiling Point 399.9±37.0°C at 760 mmHg
Density 1.3±0.1 g/cm3
1. Novel cytokine production inhibitors produced by a basidiomycete, Marasmiellus sp
K Ichikawa, H Hirai, M Ishiguro, T Kambara, Y Kato, Y J Kim, Y Kojima, Y Matsunaga, H Nishida, Y Shiomi, N Yoshikawa, N Kojima J Antibiot (Tokyo). 2001 Sep;54(9):703-9. doi: 10.7164/antibiotics.54.703.
New cytokine production inhibitors, CJ-14,877 (I) and CJ-14,897 (II), were isolated from the fermentation broth of a basidiomycete, Marasmiellus sp. CL21624. Their structures were determined to be methyl-(7S,8S)-5-(7,8-dihydroxypropyl)pyridine-2-carboxylate and methyl-(7S,8S)-5-(8-acetoxy-7-hydroxypropyl)pyridine-2-carboxylate [corrected], respectively, by spectroscopic analyses. These compounds showed inhibitory activities for lipopolysaccharide-induced production of interleukin-1beta and tumor necrosis factor-alpha in human whole blood with IC50 values of the range from 0.059 to 2.6 microM.
2. First asymmetric synthesis of CJ-14877 and its enantiomer and their interleukin-1beta inhibitory activities
Yutaka Aoyagi, Yoshiyuki Adachi, Shunta Akagi, Naohito Ohno, Koichi Takeya Bioorg Med Chem Lett. 2009 Apr 1;19(7):1876-8. doi: 10.1016/j.bmcl.2009.02.064. Epub 2009 Feb 21.
A potent antiinflammatory methyl picolinate alkaloid CJ-14877 [(+)-1] and its enantiomer (-)-1 were synthesized in two steps starting from commercially available methyl 5-bromopicolinate. The synthesis includes microwave-assisted Suzuki coupling reaction and Sharpless asymmetric dihydroxylation.

Bio Calculators

  • Solution Dilution Calculator
  • Molecular Weight Calculator
  • Molarity Calculator
Stock concentration: *
Desired final volume: *
Desired concentration: *

L

* Our calculator is based on the following equation:
Concentration (start) x Volume (start) = Concentration (final) x Volume (final)
It is commonly abbreviated as: C1V1 = C2V2

Calculate
* Total Molecular Weight:
g/mol
Tip: Chemical formula is case sensitive. C22H30N4O √ c22h30n40 ╳
g/mol
g

Recently viewed products

Linezolid | Acoradiene, (-)-beta- | Nemadectin | CJ 14258 | Tylopeptin A | CJ-12954 | Leucomycin A4 | CJ-17665 | CJ-14877

Online Inquiry

USA

  • International : 
    US & Canada (Toll free):
  • Fax:
  • Email:

UK

  • Tel:
  • Email:

Copyright © 2025 BOC Sciences. All rights reserved.

cartIcon
Inquiry Basket
Loading ......
Delete selectedGo to checkout