
Macrolactams
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Rifabutin, 98%, Thermo Scientific Chemicals
CAS: 72559-06-9 Molecular Formula: C46H62N4O11 Molecular Weight (g/mol): 847.02 MDL Number: MFCD00866816 InChI Key: ATEBXHFBFRCZMA-VXTBVIBXSA-N Synonym: rifabutin,ansamycin,rifabutine,mycobutin,ansatipine,ansatipin,alfacid,rifabutina,rifabutinum,antibiotic lm 427 PubChem CID: 57448257 IUPAC Name: (7S,9E,11S,12R,13S,14R,15R,16R,17S,18S,19E,21Z)-2,15,17-trihydroxy-11-methoxy-3,7,12,14,16,18,22-heptamethyl-1'-(2-methylpropyl)-6,23,32-trioxo-8,33-dioxa-24,27,29-triazaspiro[pentacyclo[23.6.1.1⁴,⁷.0⁵,³¹.0²⁶,³⁰]tritriacontane-28,4'-piperidin]-1,3,5(31),9,19,21,25,29-octaen-13-yl acetate SMILES: CO[C@H]1\C=C\O[C@@]2(C)OC3=C(C)C(O)=C4C(=O)C(NC(=O)\C(C)=C/C=C/[C@H](C)[C@H](O)[C@@H](C)[C@@H](O)[C@@H](C)[C@H](OC(C)=O)[C@@H]1C)=C1NC5(CCN(CC(C)C)CC5)N=C1C4=C3C2=O
PubChem CID | 57448257 |
---|---|
CAS | 72559-06-9 |
Molecular Weight (g/mol) | 847.02 |
MDL Number | MFCD00866816 |
SMILES | CO[C@H]1\C=C\O[C@@]2(C)OC3=C(C)C(O)=C4C(=O)C(NC(=O)\C(C)=C/C=C/[C@H](C)[C@H](O)[C@@H](C)[C@@H](O)[C@@H](C)[C@H](OC(C)=O)[C@@H]1C)=C1NC5(CCN(CC(C)C)CC5)N=C1C4=C3C2=O |
Synonym | rifabutin,ansamycin,rifabutine,mycobutin,ansatipine,ansatipin,alfacid,rifabutina,rifabutinum,antibiotic lm 427 |
IUPAC Name | (7S,9E,11S,12R,13S,14R,15R,16R,17S,18S,19E,21Z)-2,15,17-trihydroxy-11-methoxy-3,7,12,14,16,18,22-heptamethyl-1'-(2-methylpropyl)-6,23,32-trioxo-8,33-dioxa-24,27,29-triazaspiro[pentacyclo[23.6.1.1⁴,⁷.0⁵,³¹.0²⁶,³⁰]tritriacontane-28,4'-piperidin]-1,3,5(31),9,19,21,25,29-octaen-13-yl acetate |
InChI Key | ATEBXHFBFRCZMA-VXTBVIBXSA-N |
Molecular Formula | C46H62N4O11 |
omega-Laurinlactam 99.0+%, TCI America™
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CAS: 947-04-6 Molecular Formula: C12H23NO Molecular Weight (g/mol): 197.32 MDL Number: MFCD00005104 InChI Key: JHWNWJKBPDFINM-UHFFFAOYSA-N Synonym: Cyclododecanone Isooxime PubChem CID: 13690 IUPAC Name: 1-azacyclotridecan-2-one SMILES: O=C1CCCCCCCCCCCN1
PubChem CID | 13690 |
---|---|
CAS | 947-04-6 |
Molecular Weight (g/mol) | 197.32 |
MDL Number | MFCD00005104 |
SMILES | O=C1CCCCCCCCCCCN1 |
Synonym | Cyclododecanone Isooxime |
IUPAC Name | 1-azacyclotridecan-2-one |
InChI Key | JHWNWJKBPDFINM-UHFFFAOYSA-N |
Molecular Formula | C12H23NO |
Apexbio Technology LLC Rifabutin 100mg
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Rifabutin is an antimycobacterial agent derived from rifamycin S belonging to the ansamycin antibiotic class It acts by binding to bacterial RNA polymerase inhibiting RNA synthesis and thus suppressing mycobacterial replication Rifabutin exhibits inhibitory activity against Mycobacterium tuberculosis strains with reported minimum inhibitory concentrations (MICs) typically ranging between 0 125 and 0 25 g/ml Due to its bacterial membrane affinity mediated through electrostatic interactions with phospholipid headgroups Rifabutin has attracted research interest in tuberculosis treatment models Experimentally its administration in murine tuberculosis infection models reduced bacterial load in lung liver and spleen tissues It is additionally investigated in clinical contexts particularly to manage tuberculosis infections in immunocompromised hosts including organ transplant recipients

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Selleck Chemical LLC Rifabutin (LM427) S1741-25mg
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Rifabutin (LM427 Ansamycin) is a semisynthetic ansamycin antibiotic used in the treatment of Mycobacterium avium intracellulare (MAI) and tuberculosis

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Apexbio Technology LLC Rifabutin 1mL DMSO
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Rifabutin is an antimycobacterial agent derived from rifamycin S belonging to the ansamycin antibiotic class It acts by binding to bacterial RNA polymerase inhibiting RNA synthesis and thus suppressing mycobacterial replication Rifabutin exhibits inhibitory activity against Mycobacterium tuberculosis strains with reported minimum inhibitory concentrations (MICs) typically ranging between 0 125 and 0 25 g/ml Due to its bacterial membrane affinity mediated through electrostatic interactions with phospholipid headgroups Rifabutin has attracted research interest in tuberculosis treatment models Experimentally its administration in murine tuberculosis infection models reduced bacterial load in lung liver and spleen tissues It is additionally investigated in clinical contexts particularly to manage tuberculosis infections in immunocompromised hosts including organ transplant recipients

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Apexbio Technology LLC Rifabutin 500mg
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Rifabutin is an antimycobacterial agent derived from rifamycin S belonging to the ansamycin antibiotic class It acts by binding to bacterial RNA polymerase inhibiting RNA synthesis and thus suppressing mycobacterial replication Rifabutin exhibits inhibitory activity against Mycobacterium tuberculosis strains with reported minimum inhibitory concentrations (MICs) typically ranging between 0 125 and 0 25 g/ml Due to its bacterial membrane affinity mediated through electrostatic interactions with phospholipid headgroups Rifabutin has attracted research interest in tuberculosis treatment models Experimentally its administration in murine tuberculosis infection models reduced bacterial load in lung liver and spleen tissues It is additionally investigated in clinical contexts particularly to manage tuberculosis infections in immunocompromised hosts including organ transplant recipients

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Apexbio Technology LLC LY 333531 HYDROCHLORIDE 5MG
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LY 333531 HYDROCHLORIDE 5MG APEXBIO TECHNOLOGIES

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eMolecules Medchem Express / Rifabutin / 50mg / 446268153 / HY-17025 / / 72559-06-9 / [null] / 847.019 / C46H62N4O11
Medchem Express / Rifabutin / 50mg / 446268153 / HY-17025 / / 72559-06-9 / [null] / 847.019 / C46H62N4O11

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TARGETMOL CHEMICALS INC Rifabutin 200MG
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Also available in 1 mL, 25 mg, 50 mg, 100 mg, 500 mg and bulk. Please contact Fisher for quotes. Rifabutin (LM-427) inhibits bacterial DNA-dependent RNA polymerase, thereby suppressing the initiation of RNA formation and leading to inhibition of RNA synthesis and transcription. Rifabutin is a semisynthetic ansamycin antibiotic with potent antimycobacterial properties. Purity 99.27%

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Sigma Organic Chemistry 12-Aminododecanolactam | 250G | 947-04-6 | MFCD00005104
12-Aminododecanolactam , 250G
About this item:
CAS #: 947-04-6
MDL #: MFCD00005104
Purity: ≥98
Molecular Weight: 197.32
UNSPSC Code: 12352100

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