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CAS RN: 1066-12-2 | Product Number: D5661
2-trans-Dodecenoyl-Co A
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Purity: >86.0%(HPLC)
Synonyms:
- S-(2E)-2-Dodecenoate Coenzyme A
- S-[2-[3-[(2R)-4-[[[[[[(2R,3S,4R,5R)-5-(6-Amino-9H-purin-9-yl)-4-hydroxy-3-(phosphonooxy)tetrahydrofuran-2-yl]methoxy](hydroxy)phosphoryl]oxy](hydroxy)phosphoryl]oxy]-2-hydroxy-3,3-dimethylbutanamido]propanamido]ethyl] (E)-Dodec-2-enethioate
Product Documents:
| Size | Unit Price | Same Day | 2-3 Business Days | Other Lead Time | Quantity |
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|---|---|---|---|---|---|---|
| 5MG |
S$286.50
|
2 | 0 | Contact Us |
|
|
| 25MG |
S$928.50
|
7 | 0 | It can be shipped in about 2 weeks after ordering |
|
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| Product Number | D5661 |
Purity / Analysis Method 
|
>86.0%(HPLC) |
| Molecular Formula / Molecular Weight | C__3__3H__5__6N__7O__1__7P__3S = 947.82 |
| Physical State (20 deg.C) | Solid |
| Storage Temperature
|
Frozen (-20°C) |
| Store Under Inert Gas | Store under inert gas |
| Condition to Avoid | Light Sensitive,Moisture Sensitive,Heat Sensitive |
| CAS RN | 1066-12-2 |
| Reaxys Registry Number | 22577096 |
| PubChem Substance ID | 468591483 |
Specifications
| Appearance | White to Almost white powder to crystaline |
| Purity(HPLC) | min. 86.0 area% |
| NMR | confirm to structure |
Properties (reference)
GHS
Related Laws:
Transport Information:
| H.S.code* | 2934.99-000 |
Application
The Detection of Mycobacterium tuberculosis
This compound has been reported to be used for the detection of Mycobacterium tuberculosis (measurement of enoyl reductase of Mycobacterium tuberculosis).
References
- High Affinity InhA Inhibitors with Activity against Drug-Resistant Strains of Mycobacterium tuberculosis
- Encoded Library Technology as a Source of Hits for the Discovery and Lead Optimization of a Potent and Selective Class of Bactericidal Direct Inhibitors of Mycobacterium tuberculosis InhA
- Discovery of New and Potent InhA Inhibitors as Antituberculosis Agents: Structure-Based Virtual Screening Validated by Biological Assays and X-ray Crystallography
- Roles of tyrosine 158 and lysine 165 in the catalytic mechanism of InhA, the enoyl-ACP reductase from Mycobacterium tuberculosis
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