ACV trifluoroacetate salt
Modify Date: 2025-08-20 19:14:40
ACV trifluoroacetate salt structure
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Common Name | ACV trifluoroacetate salt | ||
|---|---|---|---|---|
| CAS Number | 32467-88-2 | Molecular Weight | 363.430 | |
| Density | 1.3±0.1 g/cm3 | Boiling Point | 718.1±60.0 °C at 760 mmHg | |
| Molecular Formula | C14H25N3O6S | Melting Point | N/A | |
| MSDS | N/A | Flash Point | 388.1±32.9 °C | |
Use of ACV trifluoroacetate saltACV Tripeptide is a key biosynthetic precursor of penicillin and cephalosporins and is found in Penicillium chrysogenum and Acremonium chrysogenum. ACV Tripeptide is synthesized by a large non-ribosomal peptide synthase called ACV synthase, which is encoded by the 11 kb The pchAB gene encodes this enzyme[1]. |
| Name | (2S)-2-amino-6-[[(2R)-1-[[(1R)-1-carboxy-2-methylpropyl]amino]-1-oxo-3-sulfanylpropan-2-yl]amino]-6-oxohexanoic acid |
|---|---|
| Synonym | More Synonyms |
| Description | ACV Tripeptide is a key biosynthetic precursor of penicillin and cephalosporins and is found in Penicillium chrysogenum and Acremonium chrysogenum. ACV Tripeptide is synthesized by a large non-ribosomal peptide synthase called ACV synthase, which is encoded by the 11 kb The pchAB gene encodes this enzyme[1]. |
|---|---|
| Related Catalog |
| Density | 1.3±0.1 g/cm3 |
|---|---|
| Boiling Point | 718.1±60.0 °C at 760 mmHg |
| Molecular Formula | C14H25N3O6S |
| Molecular Weight | 363.430 |
| Flash Point | 388.1±32.9 °C |
| Exact Mass | 363.146393 |
| PSA | 204.60000 |
| LogP | 0.56 |
| Vapour Pressure | 0.0±5.0 mmHg at 25°C |
| Index of Refraction | 1.545 |
| InChIKey | BYEIJZFKOAXBBV-ATZCPNFKSA-N |
| SMILES | CC(C)C(NC(=O)C(CS)NC(=O)CCCC(N)C(=O)O)C(=O)O |
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Name: Beta-lactamase induction in Bacillus licheniformis
Source: ChEMBL
Target: Regulatory protein BlaR1
External Id: CHEMBL820826
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Name: Antibiotic activity against Micrococcus luteus (ATCC 9341 strain)
Source: ChEMBL
Target: NON-PROTEIN TARGET
External Id: CHEMBL731810
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Name: Anti-micrococcus luteus activity was tested for inhibition of isopenicillin N synthet...
Source: ChEMBL
Target: Isopenicillin N synthase
External Id: CHEMBL697571
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Name: Cytotoxicity on human P3HR1 derived H1 cells
Source: ChEMBL
Target: N/A
External Id: CHEMBL687761
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Name: Effective concentration of compound against Epstein Barr virus was determined
Source: ChEMBL
Target: Human gammaherpesvirus 4
External Id: CHEMBL678772
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| N-[(5S)-5-Amino-5-carboxypentanoyl]-L-cysteinyl-D-valine |
| ACV |
| N-[N-(L-5-Amino-5-carboxyvaleryl)-L-cysteinyl]-D-valine |
| AADCV |
| Acv tripeptide |
| D-Valine,N-((5S)-5-amino-5-carboxy-1-oxopentyl)-L-cysteinyl |
| d-(L-a-Aminoadipyl)-L-cysteinyl-D-valine |
| l-d-(a-aminoadipoyl)-l-cysteinyl-d-valine |
| 5-(2-Aminoad)-cys-val |