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BOC Sciences
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info@bocsci.com |
| Products Intro: |
Product Name:Tyrocidine A
CAS:1481-70-5
Remarks:Tyrocidine A is a peptide antibiotic originally isolated from Bac. brevis. It is resistant to gram-p
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| Company Name: |
Wuxi Zhongkun Biochemical Technology Co., Ltd.
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sales@reading-chemicals.com |
| Products Intro: |
Product Name:Cyclo(D-Phe-Pro-Phe-D-Phe-Asn-Gln-Tyr-Val-Orn-Leu-)
CAS:1481-70-5
Purity:95%+ Package:根据客户需求包装
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| Company Name: |
Hangzhou Peptidego Biotech Co.,Ltd.
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| Tel: |
0571-87213919 |
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eric@peptidego.com |
| Products Intro: |
Product Name:Cyclo(D-Phe-Pro-Phe-D-Phe-Asn-Gln-Tyr-Val-Orn-Leu-)
CAS:1481-70-5
Purity:95% or 98% Package:1mg；5mg；10mg；50mg；100mg,1g or according to customer's detail requirement.
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| | Cyclo(D-Phe-Pro-Phe-D-Phe-Asn-Gln-Tyr-Val-Orn-Leu-) Basic information |
| Product Name: | Cyclo(D-Phe-Pro-Phe-D-Phe-Asn-Gln-Tyr-Val-Orn-Leu-) | | Synonyms: | Cyclo(D-Phe-Pro-Phe-D-Phe-Asn-Gln-Tyr-Val-Orn-Leu-);Cyclo[L-Asn-L-Gln-L-Tyr-L-Val-L-Orn-L-Leu-D-Phe-L-Pro-L-Phe-D-Phe-];Tyrocidine A;Cyclo(L-asparaginyl-L-glutaminyl-L-tyrosyl-L-valyl-L-ornithyl-L-leucyl-D-phenylalanyl-L-prolyl-L-phenylalanyl-D-phenylalanyl) | | CAS: | 1481-70-5 | | MF: | C66H87N13O13 | | MW: | 1270.5 | | EINECS: | | | Product Categories: | | | Mol File: | 1481-70-5.mol |  |
| | Cyclo(D-Phe-Pro-Phe-D-Phe-Asn-Gln-Tyr-Val-Orn-Leu-) Chemical Properties |
| Melting point | 240-242 °C | | Boiling point | 1630.6±65.0 °C(Predicted) | | density | 1.33±0.1 g/cm3(Predicted) | | pka | 9.89±0.15(Predicted) |
| | Cyclo(D-Phe-Pro-Phe-D-Phe-Asn-Gln-Tyr-Val-Orn-Leu-) Usage And Synthesis |
| Definition | ChEBI: Tyrocidine A is a homodetic cyclic decapeptide consisting of D-Phe, L-Pro, L-Phe, D-Phe, L-Asn, L-Gln, L-Tyr, L-Val, L-Orn, and L-Leu residues coupled in sequence and cyclised head-to-tail. It has a role as an antibacterial agent and a bacterial metabolite. It is a homodetic cyclic peptide, a peptide antibiotic and a macrocycle. | | Purification Methods | Crystallise tyrocidine A as the hydrochloride from MeOH or EtOH/HCl. [Paladin & Craig J Am Chem Soc 76 688 1954, King & Craig J Am Chem Soc 77 6624 1955, Okamoto et al. Bull Chem Soc Jpn 50 231 1977, Beilstein 26 III/IV 4280.] |
| | Cyclo(D-Phe-Pro-Phe-D-Phe-Asn-Gln-Tyr-Val-Orn-Leu-) Preparation Products And Raw materials |
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