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| Product | Description | |
|---|---|---|
| Clarithromycin Impurity H | Clarithromycin Impurity H. Uses: For analytical and research use. CAS No. 127140-69-6. Mole weight: 761.94. Catalog: AP127140696. |  |
| Clarithromycin Impurity I | Clarithromycin Impurity I. Uses: For analytical and research use. Alternative Names: (3R,4S,5S,6R,7R,9R,11R,12R,13S,14R)-6-(((2S,3R,4S,6R)-4-(dimethylamino)-3-hydroxy-6-methyltetrahydro-2H-pyran-2-yl)oxy)-14-ethyl-4,12,13-trihydroxy-7-methoxy-3,5,7,9,11,13-hexamethyloxacyclotetradecane-2,10-dione. CAS No. 118058-74-5. Molecular formula: C30H55NO10. Mole weight: 589.76. Catalog: APB118058745. | |
| Clarithromycin Impurity J | Clarithromycin Impurity J. Uses: For analytical and research use. Alternative Names: (3R,4S,5S,6R,7R,9R,11S,12R,13S,14R,E)-6-(((2S,3R,4S,6R)-4-(dimethylamino)-3-hydroxy-6-methyltetrahydro-2H-pyran-2-yl)oxy)-14-ethyl-7,12,13-trihydroxy-4-(((2R,4R,5S,6S)-5-hydroxy-4-methoxy-4,6-dimethyltetrahydro-2H-pyran-2-yl)oxy)-10-(hydroxyimino)-3,5,7,9,11,13-hexamethyloxacyclotetradecan-2-one. CAS No. 13127-18-9. Molecular formula: C37H68N2O13. Mole weight: 748.94. Catalog: APB13127189. | |
| Clarithromycin impurity JA | Clarithromycin impurity JA. Uses: For analytical and research use. Molecular formula: C49H96N2O15Si2. Mole weight: 1008.63. Catalog: APB07068. | |
| Clarithromycin impurity JB | Clarithromycin impurity JB. Uses: For analytical and research use. Molecular formula: C48H94N2O14Si2. Mole weight: 979.45. Catalog: APB07071. | |
| Clarithromycin impurity JD | Clarithromycin impurity JD. Uses: For analytical and research use. Molecular formula: C48H94N2O14Si2. Mole weight: 979.45. Catalog: APB07072. | |
| Clarithromycin impurity JE | Clarithromycin impurity JE. Uses: For analytical and research use. Molecular formula: C50H98N2O14Si2. Mole weight: 1006.66. Catalog: APB07073. | |
| Clarithromycin impurity JF | Clarithromycin impurity JF. Uses: For analytical and research use. Molecular formula: C50H98N2O14Si2. Mole weight: 1006.66. Catalog: APB07074. | |
| Clarithromycin impurity JG | Clarithromycin impurity JG. Uses: For analytical and research use. Molecular formula: C45H88N2O13Si2. Mole weight: 920.58. Catalog: APB07075. | |
| Clarithromycin impurity JK | Clarithromycin impurity JK. Uses: For analytical and research use. Molecular formula: C33H59NO8Si. Mole weight: 625.4. Catalog: APB07076. | |
| Clarithromycin impurity JN | Clarithromycin impurity JN. Uses: For analytical and research use. Molecular formula: C49H94N2O13Si2. Mole weight: 974.63. Catalog: APB07077. | |
| Clarithromycin Impurity K | Clarithromycin Impurity K. Uses: For analytical and research use. Alternative Names: (1S,2R,5R,6S,7S,8R,9R,Z)-8-(((2S,3R,4S,6R)-4-(dimethylamino)-3-hydroxy-6-methyltetrahydro-2H-pyran-2-yl)oxy)-2-ethyl-6-hydroxy-9-methoxy-1,5,7,9,11,13-hexamethyl-3,15-dioxabicyclo[10.2.1]pentadeca-11,13-dien-4-one. CAS No. 127157-35-1. Molecular formula: C30H51NO8. Mole weight: 553.73. Catalog: APB127157351. | |
| Clarithromycin Impurity L | Clarithromycin Impurity L. Uses: For analytical and research use. Alternative Names: (3R,4S,5S,6R,7R,9R,11S,12R,13S,14R,Z)-6-(((2S,3R,4S,6R)-4-(dimethylamino)-3-hydroxy-6-methyltetrahydro-2H-pyran-2-yl)oxy)-14-ethyl-12,13-dihydroxy-4-(((2R,4R,5S,6S)-5-hydroxy-4-methoxy-4,6-dimethyltetrahydro-2H-pyran-2-yl)oxy)-10-(hydroxyimino)-7-methoxy-3,5,7,9,11,13-hexamethyloxacyclotetradecan-2-one. CAS No. 127253-05-8. Molecular formula: C38H70N2O13. Mole weight: 762.97. Catalog: APB127253058. | |
| Clarithromycin Impurity L | Clarithromycin (9Z)-Oxime is an impurity of Clarithromycin. Synonyms: Clarithromycin (9Z)-Oxime; 6-O-Methylerythromycin (9Z)-9-Oxime; (3R,4S,5S,6R,7R,9R,11S,12R,13S,14R,Z)-6-(((2S,3R,4S,6R)-4-(Dimethylamino)-3-hydroxy-6-methyltetrahydro-2H-pyran-2-yl)oxy)-14-ethyl-12,13-dihydroxy-4-(((2R,4R,5S,6S)-5-hydroxy-4-methoxy-4,6-di. Grade: >95%. CAS No. 127253-05-8. Molecular formula: C38H70N2O13. Mole weight: 762.97. |  |
| Clarithromycin Impurity M | Clarithromycin Impurity M. Uses: For analytical and research use. Alternative Names: (3R,4S,5S,6R,7R,9R,11S,12R,13S,14R,E)-14-ethyl-12,13-dihydroxy-4-(((2R,4R,5S,6S)-5-hydroxy-4-methoxy-4,6-dimethyltetrahydro-2H-pyran-2-yl)oxy)-6-(((2S,3R,4S,6R)-3-hydroxy-6-methyl-4-(methylamino)tetrahydro-2H-pyran-2-yl)oxy)-10-(hydroxyimino)-7-methoxy-3. CAS No. 127182-43-8. Molecular formula: C37H68N2O13. Mole weight: 748.94. Catalog: APB127182438. | |
| Clarithromycin Impurity N | Clarithromycin Impurity N. Uses: For analytical and research use. Alternative Names: (3R,4S,5S,6R,7R,9R,13S,14R,E)-6-(((2S,3R,4S,6R)-4-(dimethylamino)-3-hydroxy-6-methyltetrahydro-2H-pyran-2-yl)oxy)-14-ethyl-13-hydroxy-4-(((2R,4R,5S,6S)-5-hydroxy-4-methoxy-4,6-dimethyltetrahydro-2H-pyran-2-yl)oxy)-7-methoxy-3,5,7,9,11,13-hexamethyloxacycl. CAS No. 144604-03-5. Molecular formula: C38H67NO12. Mole weight: 729.94. Catalog: APB144604035. | |
| Clarithromycin Impurity N | (10E)-10,11-Didehydro-11-deoxy-6-O-methylerythromycin is the Erythromycin derivative. Synonyms: (10E)-10,11-Didehydro-11-deoxy-6-O-methylerythromycin; Oxacyclotetradecane Erythromycin Derivative. Grade: > 95%. CAS No. 144604-03-5. Molecular formula: C38H67NO12. Mole weight: 729.94. | |
| Clarithromycin Impurity O | Clarithromycin (9Z)-O-Methyloxime is an impurity of Clarithromycin. Synonyms: Clarithromycin (9Z)-O-Methyloxime; 6-O-Methylerythromycin (9Z)-9-O-Methyloxime; Oxacyclotetradecane Erythromycin deriv.; Erythromycin, 6-O-methyl-, 9-O-methyloxime, (9Z)-; (9Z)-6-O-Methylerythromycin 9-(O-methyloxime). Grade: >95%. CAS No. 127252-80-6. Molecular formula: C39H72N2O13. Mole weight: 776.99. | |
| Clarithromycin Impurity O | Clarithromycin Impurity O. Uses: For analytical and research use. Alternative Names: (3R,4S,5S,6R,7R,9R,11S,12R,13S,14R,Z)-6-(((2S,3R,4S,6R)-4-(dimethylamino)-3-hydroxy-6-methyltetrahydro-2H-pyran-2-yl)oxy)-14-ethyl-12,13-dihydroxy-4-(((2R,4R,5S,6S)-5-hydroxy-4-methoxy-4,6-dimethyltetrahydro-2H-pyran-2-yl)oxy)-7-methoxy-10-(methoxyimino)-. CAS No. 127252-80-6. Molecular formula: C39H72N2O13. Mole weight: 776.99. Catalog: APB127252806. | |
| Clarithromycin Impurity Q | Clarithromycin Impurity Q. Uses: For analytical and research use. CAS No. 118074-07-0. Mole weight: 763.95. Catalog: AP118074070. | |
| Clarithromycin Impurity R | Clarithromycin Impurity R. Uses: For analytical and research use. CAS No. 992-62-1. Mole weight: 719.90. Catalog: AP992621-A. | |
| Clarithromycin lactobionate | Clarithromycin, a CYP3A4 inhibitor, is a macrolide antibiotic used to treat pharyngitis, tonsillitis, acute maxillary sinusitis, acute bacterial exacerbation of chronic bronchitis, pneumonia, skin and skin structure infections. Synonyms: Erythromycin, 6-O-methyl-, 4-O-β-D-galactopyranosyl-D-gluconate (salt); D-Gluconic acid, 4-O-β-D-galactopyranosyl-, compd with 6-O-methylerythromycin (1:1); (2R,3R,4R,5R)-2,3,5,6-Tetrahydroxy-4-{[(2S,3R,4S,5R,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)tetrahydro-2H-pyran-2-yl]oxy}hexanoic acid with (3R,4S,5S,6R,7R,9R,11R,12R,13S,14R)-6-{[(2S,3R,4S,6R)-4-(dimethylamino)-3-hydroxy-6-methyltetrahydro-2H-pyran-2-yl]oxy}-14-ethyl-12,13-dihydroxy-4-{[(2R,4R,5S,6S)-5-hydroxy-4-methoxy-4,6-dimethyltetrahydro-2H-pyran-2-yl]oxy}-7-methoxy-3,5,7,9,11,13-hexamethyloxacyclotetradecane-2,10-dione (1:1). Grade: ≥95%. CAS No. 135326-55-5. Molecular formula: C38H69NO13.C12H22O12. Mole weight: 1106.25. | |
| Clarithromycin N-Oxide | Clarithromycin N-oxide is an urinary metabolite of Clarithromycin, a macrolide antibiotic. Synonyms: 6-O-Methylerythromycin N-Oxide; USP Clarithromycin Impurity Q. Grade: > 95%. CAS No. 118074-07-0. Molecular formula: C38H69NO14. Mole weight: 763.95. | |
| Clarithromycin Related Compound A | Clarithromycin Related Compound A. Uses: For analytical and research use. CAS No. 81103-14-2. Mole weight: 761.98. Catalog: AP81103142. | |
| Clarithromycin related compound C | An impurity found in the macrolide antibiotic, Clarithromycin. Synonyms: 6-O-Methylerythromycin 9-Oxime; Clarithromycin Impurity C. Grade: >95% by HPLC. CAS No. 103450-87-9. Molecular formula: C38H70N2O13. Mole weight: 762.97. | |
| Clarithromycin related compound H | N-Demethyl-N-formylclarithromycin is an impurity of the semi-synthetic macrolide antibiotic Clarithromycin. Synonyms: N-Demethyl-N-formyl Clarithromycin; N-Demethyl-N-formyl-6-O-methylerythromycin; 3"-N-Demethyl-3"-N-formylclarithromycin; USP Clarithromycin Impurity H; Clarithromycin impurity H. Grade: >95%. CAS No. 127140-69-6. Molecular formula: C38H67NO14. Mole weight: 761.94. | |
| Clarithromycin related compound I | An impurity found in the macrolide antibiotic, Clarithromycin. Synonyms: De(cladinosyl) Clarithromycin; 3-O-De(2,6-dideoxy-3-C-methyl-3-O-methyl-α-L-ribo-hexopyranosyl)-6-O-methylerythromycin; 5-O-Desosaminyl-6-O-methylerythronolide A; 3-O-Decladinosyl-6-O-methylerythronolide A; Clarithromycin EP Impurity I. Grade: ≥90.0%. CAS No. 118058-74-5. Molecular formula: C30H55NO10. Mole weight: 589.77. | |
| Clarithromycin related compound K | 3-O-De(cladinosyl)-8,9,10,11-tetradehydro-9-deoxo-11,12-dideoxy-9,12-epoxy Clarithromycin is an impurity of Clarithromycin. Synonyms: 3-O-De(cladinosyl)-8,9,10,11-tetradehydro-9-deoxo-11,12-dideoxy-9,12-epoxy Clarithromycin; 3-O-De(2,6-dideoxy-3-C-methyl-3-O-methyl-α-L-ribo-hexopyranosyl)-8,9,10,11-tetradehydro-9-deoxo-11,12-dideoxy-9,12-epoxy-6-O-methylerythromycin; Clarithromycin EP Impurity K. Grade: >95%. CAS No. 127157-35-1. Molecular formula: C30H51NO8. Mole weight: 553.73. | |
| Clarithromycin related compound M | N-Desmethyl-6-O-methylerythromycin (9E)-Oxime is a derivative of Clarithromycin. Synonyms: N-Desmethyl-6-O-methylerythromycin (9E)-Oxime; 3''-N-Demethyl-6-O-methylerythromycin A (E)-9-oxime. Grade: >95%. CAS No. 127182-43-8. Molecular formula: C37H68N2O13. Mole weight: 748.94. | |
| Clarithromycin Trimethylsilyl O-Methyl Trityl Hydrazone | Clarithromycin Trimethylsilyl O-Methyl Trityl Hydrazone is an intermediate in synthesizing 4'',6-Di-O-methylerythromycin, a derivative of O-methylerythromycin and may be used in the treatment of lung diseases requiring antibiotics. Synonyms: (3R,4S,5S,6R,7R,9R,11S,12R,13S,14R,E)-4-(((2R,4R,5S,6S)-4,5-Dimethoxy-4,6-dimethyltetrahydro-2H-pyran-2-yl)oxy)-6-(((2S,3R,4S,6R)-4-(dimethylamino)-6-methyl-3-((trimethylsilyl)oxy)tetrahydro-2H-pyran-2-yl)oxy)-14-ethyl-12,13-dihydroxy-7-methoxy-3,5,7,9,11,13-hexamethyl-10-(2-tritylhydrazono)oxacyclotetradecan-2-one. Molecular formula: C61H95N3O12Si. Mole weight: 1090.51. | |
| Clarithromycin Trimethylsilyl Trityl Hydrazone | Clarithromycin Trimethylsilyl Trityl Hydrazone is an intermediate in synthesizing 4'',6-Di-O-methylerythromycin, a derivative of O-methylerythromycin and may be used in the treatment of lung diseases requiring antibiotics. Synonyms: (3R,4S,5S,6R,7R,9R,11S,12R,13S,14R,E)-6-(((2S,3R,4S,6R)-4-(Dimethylamino)-6-methyl-3-((trimethylsilyl)oxy)tetrahydro-2H-pyran-2-yl)oxy)-14-ethyl-12,13-dihydroxy-4-(((2R,4R,5S,6S)-5-hydroxy-4-methoxy-4,6-dimethyltetrahydro-2H-pyran-2-yl)oxy)-7-methoxy-3,5,7,9,11,13-hexamethyl-10-(2-tritylhydrazono)oxacyclotetradecan-2-one. Molecular formula: C60H93N3O12Si. Mole weight: 1076.48. | |
| Clarithromycin Trityl Hydrazone | Clarithromycin Trityl Hydrazone is an intermediate in synthesizing 4'',6-Di-O-methylerythromycin, a derivative of O-methylerythromycin and may be used in the treatment of lung diseases requiring antibiotics. Synonyms: (9E)-6-O-Methylerythromycin 9-[2-(triphenylmethyl)hydrazone]; Erythromycin, 6-O-methyl-, 9-[2-(triphenylmethyl)hydrazone], (9E)-; (3R,4S,5S,6R,7R,9R,11S,12R,13S,14R,E)-6-(((2S,3R,4S,6R)-4-(Dimethylamino)-3-hydroxy-6-methyltetrahydro-2H-pyran-2-yl)oxy)-14-ethyl-12,13-dihydroxy-4-(((2R,4R,5S,6S)-5-hydroxy-4-methoxy-4,6-dimethyltetrahydro-2H-pyran-2-yl)oxy)-7-methoxy-3,5,7,9,11,13-hexamethyl-10-(2-tritylhydrazono)oxacyclotetradecan-2-one. CAS No. 1030374-65-2. Molecular formula: C57H85N3O12. Mole weight: 1004.30. | |
| Claritone | Claritone ®. CAS No. 74338-72-0. VIGON Item # 502631. Categories: Speciality Ingrdients Suppliers, Fragrances, Perfumers, clary octenone. |  America & Internationally |
| Clary sage oil | Clary sage oil. Alternative Names: Muscatel sage oil salvia sclarea L. CAS No. 8016-63-5. Purity: 0.98. Product ID: CI-EO-0053. Molecular formula: C152H169Cl10N5O20S5. Mole weight: 2900.8 g/mol. Alfa Chemistry - ISO 9001:32057 Certified. |  |
| Clascoterone | Clascoterone (Cortexolone 17 alpha-propionate;Cortexolone 17α-propionate;CB-03-01) is a new topical and peripherally selective androgen antagonist. Uses: Scientific research. Category: Signaling pathways. Alternative Names: Cortexolone 17 alpha-propionate; Cortexolone 17α-propionate; CB-03-01. CAS No. 19608-29-8. Pack Sizes: 10 mM * 1 mL in DMSO; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg; 500 mg. Product ID: HY-13331. |  |
| Claseprubart | Claseprubart (DNTH103) is an inhibitor targeting C1s of the complement system and an inhibitor of the C1 component of the complement cascade. Claseprubart is in phase 2 clinical evaluation. Claseprubart has application potential in research related to multifocal motor neuropathy and generalized myasthenia gravis[1][2][3]. Uses: Scientific research. Category: Signaling pathways. Alternative Names: DNTH103. CAS No. 2922766-89-8. Pack Sizes: 1 mg; 5 mg; 10 mg; 25 mg. Product ID: HY-P991127. | |
| Class A CpG oligonucleotide (Mouse specific) | CpG ODNs are synthetic oligonucleotides that contain unmethylated CpG dinucleotides in specific sequence contexts (CpG motifs). These CpG motifs are present at a 20-fold greater frequency in bacterial DNA than in mammalian DNA. CpG ODNs are recognized by Toll-like receptor 9 (TLR9), which leads to strong immunostimulatory effects.ODN 1585 is a class A CpG ODN specific for mouse TLR9. Class A CpG ODNs are characterized by a central, phosphodiester, CpG-containing palindromic motif and a 3'phosphorothioate poly-G string.They induce high IFN-α production from plasmacytoid dendritic cells (pDCs) but are weak stimulators of TLR9-dependent NF-κB signaling. Group: Others. Synonyms: CpG oligonucleotides; ODNs; ODN 1585; CpG ODNs; CpG. Storage: Upon receipt, store at -20 °C. Form: Lyophilized powder. CpG oligonucleotides; ODNs; ODN 1585; CpG ODNs; CpG. Cat No: LIGC-010. |  |
| classical-complement-pathway C3/C5 convertase | A complex of complement fragments C4b, C2a and C2b. C2a contains the active site, C2b the site for C4b binding. C2a and C2b are formed by cleavage of proenzyme C2 by complement subcomponent C1s. Cleavage of C5 requires complement fragment C3b which binds C5 and renders it susceptible to cleavage by the C4b,2a complex. Includes former EC 3.4.21.44. Complement component C2a is in peptidase family S1 (trypsin family). Group: Enzymes. Synonyms: C3 convertase; C42; C4b,2a; C5 convertase; C423; C4b,2a,3b; C42; C5 convertase; C423; C4b,2a,3b; complement C.hivin.4.hivin2; complement C3 convertase. Enzyme Commission Number: EC 3.4.21.43. CAS No. 56626-15-4. Storage: Store it at +4 ?C for short term. For long term storage, store it at -20 ?C?-80 ?C. Form: Liquid or lyophilized powder. EXWM-4137; classical-complement-pathway C3/C5 convertase; EC 3.4.21.43; 56626-15-4; C3 convertase; C42; C4b,2a; C5 convertase; C423; C4b,2a,3b; C42; C5 convertase; C423; C4b,2a,3b; complement C.hivin.4.hivin2; complement C3 convertase. Cat No: EXWM-4137. | |
| Class II sec-dependent bacteriocin | Class II sec-dependent bacteriocin is from Enterococcus hirae. It has antimicrobial activity. | |
| clasto-Lactacystin β-lactone | Clasto-Lactacystin β-lactone, a natural active metabolite of lactacystin, which is a metabolite of Streptomyces, acts as an irreversible 20S proteasome inhibitor. Uses: Scientific research. Category: Signaling pathways. Alternative Names: Omuralide; β-Clastolactacystin. CAS No. 154226-60-5. Pack Sizes: 50 μg (2.34 mM * 100 μL in Methyl acetate). Product ID: HY-108549. | |
| Clasto-Lactacystin β-lactone | Clasto-Lactacystin β-lactone is a microbial metabolite isolated from Streptomyces that is now widely used as a selective inhibitor of the 20S proteasome. Clasto-lactacystin β-lactone was later identified as the active metabolite of lactacystin, resulting from the elimination of cysteine and the formation of a reactive β-lactone. It is 20-fold more potent than Lactacystin. Synonyms: β-Clastolactacystin; Omuralide. Grade: ≥95%. CAS No. 154226-60-5. Molecular formula: C10H15NO4. Mole weight: 213.23. | |
| Claturafenib | Claturafenib ( PF-07799933) is an orally active inhibitor of pan-mutant BRAF. Claturafenib inhibits pERK in cells (IC50 value of 1.6 nM in HT29 cells). Claturafenib has anticancer activity against BRAFG469A mutant NSCLC and BRAFK601E mutant melanoma[1]. Uses: Scientific research. Category: Signaling pathways. Alternative Names: PF-07799933; ARRY-440. CAS No. 2754408-94-9. Pack Sizes: 10 mM * 1 mL in DMSO; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg; 1 g. Product ID: HY-159795. | |
| C-Laurdan | C-Laurdan is a modified Laurdan (HY-D0080) probe that imaging lipid rafts with environmentally sensitive fluorescence. C-Laurdan can be used in research of lipid arrangement and fluidity in biological membranes or artificial lipid membranes[1]. Uses: Scientific research. Category: Signaling pathways. CAS No. 959839-06-6. Pack Sizes: 10 mM * 1 mL in DMSO; 2 mg; 5 mg. Product ID: HY-D1378. | |
| Clausine Z | Clausine Z comes from the herbs of Clausena excavata. Uses: Inhibitory activity on cdk5. Synonyms: 1,6-Dihydroxy-9H-carbazole-3-carbaldehyde; 3-formyl-1,6-dihydroxycarbazole. Grade: > 95%. CAS No. 866111-14-0. Molecular formula: C13H9NO3. Mole weight: 227.2. | |
| Clavam-2-carboxylate | It is produced by the strain of Strrptomyces clavuligerus. Clavam-2-carboxylate has the activity against part of fungi. Synonyms: SCHEMBL8589184. CAS No. 212268-81-0. Molecular formula: C6H7NO4. Mole weight: 157.12. | |
| Clavam-2-carboxylate Potassium | Clavam-2-carboxylate Potassium is an impurity of Clavulanic Acid, a β-lactamase inhibitor, typically added to amoxicillin to increase its effectiveness. Synonyms: (3R,5S)-7-oxo-1-azabicyclo[3.2.0]heptane-3-carboxylate Potassium. CAS No. 2196185-67-6. Molecular formula: C6H6KNO4. Mole weight: 195.21. | |
| clavaminate synthase | Contains nonheme iron. Catalyses three separate oxidative reactions in the pathway for the biosythesis of the β-lactamase inhibitor clavulanate in Streptomyces clavuligerus. The first step (hydroxylation) is separated from the latter two (oxidative cyclization and desaturation) by the action of EC 3.5.3.22, proclavaminate amidinohydrolase. The three reactions are all catalysed at the same nonheme iron site. Group: Enzymes. Synonyms: clavaminate synthase 2; clavaminic acid synthase. Enzyme Commission Number: EC 1.14.11.21. CAS No. 122799-56-8. Storage: Store it at +4 ?C for short term. For long term storage, store it at -20 ?C?-80 ?C. Form: Liquid or lyophilized powder. EXWM-0638; clavaminate synthase; EC 1.14.11.21; 122799-56-8; clavaminate synthase 2; clavaminic acid synthase. Cat No: EXWM-0638. | |
| Clavamycin A | Clavamycin A is produced by the strain of Streptomyces hygroscopicus NRRL 15846. It has strong anti-candida activity, and its action can be antagonized by dipeptide or tripeptide, but amino acid can not cancel its action. No antibacterial activity and no inhibition of β-lactamase. Synonyms: Serine, 3-(7-oxo-4-oxa-1-azabicyclo(3.2.0)hept-3-yl)-N-(3-(7-oxo-4-oxa-1-azabicyclo(3.2.0)hept-3-yl)seryl)-. CAS No. 103059-93-4. Molecular formula: C16H22N4O9. Mole weight: 414.37. | |
| Clavamycin B | Clavamycin B is produced by the strain of Streptomyces hygroscopicus NRRL 15846. It has strong anti-candida activity, and its action can be antagonized by dipeptide or tripeptide, but amino acid can not cancel its action. No antibacterial activity and no inhibition of β-lactamase. Synonyms: CHEBI:81031. Molecular formula: C13H22N4O8. Mole weight: 362.34. | |
| Clavamycin C | Clavamycin C is produced by the strain of Streptomyces hygroscopicus NRRL 15846. It has strong anti-candida activity, and its action can be antagonized by dipeptide or tripeptide, but amino acid can not cancel its action. No antibacterial activity and no inhibition of β-lactamase. Synonyms: CHEBI:81032. Molecular formula: C13H22N4O8. Mole weight: 362.34. | |
| Clavanin-A | Clavanin A was found in invertebrate Styela clava. It has antibacterial and antifungal activity. Clavanin A was in vitro evaluated against Staphylococcus aureus and Escherichia coli as well as toward L929 mouse fibroblasts and skin primary cells (SPCs). Grade: >96% by HPLC. Molecular formula: C131H184N34O27. Mole weight: 2667.07. | |
| Clavanin-B | Clavanin B is an alpha-helical antimicrobial peptide isolated from Styela clava. Molecular formula: C131H184N36O27. Mole weight: 2695.08. | |
| Clavanin-C | Clavanin-C was found in Styela clava. It has antimicrobial activity against E.coli, L.monocytogenes and C.albicans. | |
| Clavanin-D | Clavanin-D was found in Styela clava. It has antimicrobial activity against E.coli, L.monocytogenes and C.albicans. Molecular formula: C131H191N35O26. Mole weight: 2672.13. | |
| Clavanin-E | Clavanin E has antimicrobial activity. The source of Clavanin E is invertebrate Styela clava. Grade: >97% by HPLC. Molecular formula: C130H193N35O25. Mole weight: 2646.14. | |
| Clavariopsin A | It is produced by the strain of Clavariopsis aquatica AJ117363. Clavariopsin A has anti-candida albicans, Aspergillus fumigata and Aspergillus Niger activity, and has little effect on bacteria. Synonyms: Clarvariopsin A; 2-{(4S,7S,10S,13S,16S,22S,25S,28R)-3,6,9,12,15,18,21,24,30-Nonaaza-13,16-bis((1S)-1-methylpropyl)-25-[(4-methoxyphenyl)methyl]-3,9,12,15,21-pentamethyl-27-oxa-2,5,8,11,14,17,20,23,26,29-decaoxo-4,7,22,28-tetrakis(methylethyl)bicyclo[28.4.0]tetratriacont-10-yl}acetic acid. Molecular formula: C59H95N9O14. Mole weight: 1154.43. | |
| Clavariopsin B | It is produced by the strain of Clavariopsis aquatica AJ117363. Clavariopsin B has anti-candida albicans, Aspergillus fumigata and Aspergillus Niger activity, and has little effect on bacteria. Synonyms: 2-{(4S,7S,10S,13S,16S,22S,25S,28R)-3,6,9,12,15,18,21,24,30-Nonaaza-13,16-bis((1S)-1-methylpropyl)-25-[(4-methoxyphenyl)methyl]-9,12,15,21-tetramethyl-27-oxa-2,5,8,11,14,17,20,23,26,29-decaoxo-4,7,22,28-tetrakis(methylethyl)bicyclo[28.4.0]tetratriacont-10-yl}acetic acid. Molecular formula: C58H93N9O14. Mole weight: 1140.41. | |
| Clavaspirin | Clavaspirin was found in Styela clava. It exhibits broad-spectrum antimicrobial activity against both Gram-positive and Gram-negative bacteria. Clavaspirin also has potent hemolytic activity. | |
| Clavicoronic acid | Clavicoronic acid is produced by the strain of Clavicorona pyxidata. It can inhibit the reverse transcriptase activity of myeloblastocytosis virus (AMV) and Moloney mouse leukemia virus (MMuLV). Synonyms: (6-Formyl-2,2,4-trimethyl-2,3,3a,7a-tetrahydro-1H-inden-5-yl)(oxo)acetic acid; 1H-Indene-5-acetic acid, 6-formyl-2,3,3a,7a-tetrahydro-2,2,4-trimethyl-alpha-oxo-, (3aS-cis)-. CAS No. 139748-98-4. Molecular formula: C15H18O4. Mole weight: 262.30. | |
| Clavilactone A | Clavilactone A is produced by the strain of Clitocybe clavipes. It can inhibit the germination of seeds. Molecular formula: C15H16O5. Mole weight: 276.28. | |
| Clavilactone C | Clavilactone C is produced by the strain of Clitocybe clavipes. It can inhibit the germination of seeds. Molecular formula: C16H16O6. Mole weight: 304.29. | |
| Clavulanate lithium | Clavulanate lithium is a potent β-lactamase inhibitor and acts as an antibiotic[1][2]. Uses: Scientific research. Category: Signaling pathways. CAS No. 61177-44-4. Pack Sizes: 10 mM * 1 mL in DMSO; 5 mg; 10 mg; 25 mg; 50 mg. Product ID: HY-A0256B. | |
| Clavulanate Lithium | A beta-lactamase inhibitor. It can irreversibly inactivate beta-lactamase enzymes of beta-lactam resistant microbes preventing them from breaking down beta-lactam antibiotics. Synonyms: (2R,5R,Z)-3-(2-hydroxyethylidene)-7-oxo-4-oxa-1-azabicyclo[3.2.0]heptane-2-carboxylate Lithium; Clavulanic acid, lithium salt. Grade: ≥98%. CAS No. 61177-44-4. Molecular formula: C8H8LiNO5. Mole weight: 205.09. | |
| Clavulanate Potassium (1:1 mixture with silicon dioxide) | Clavulanate Potassium is a semi-synthetic beta-lactamase inhibitor isolated from streptomyces. It contains a beta-lactam ring and binds strongly to beta-lactamase at or near its active site. It is used in conjunction with beta-lactamase susceptible penicillins to treat infections caused by beta-lactamase producing organisms. It is commonly combined with amoxicillin or ticarcillin to increase its effectiveness. Uses: Beta-lactamase inhibitors. Synonyms: Amonate; MM-14151; MM14151. CAS No. 61177-45-5. Molecular formula: C8H8KNO5. Mole weight: 237.25. | |
| Clavulanate Potassium EP Impurity B Sodium Salt | Clavulanate Potassium EP Impurity B Sodium Salt. Uses: For analytical and research use. Molecular formula: C11H15N2O4·Na. Mole weight: 262.24. Catalog: APB07320. | |
| Clavulanate Potassium Impurity 16 | Clavulanate Potassium Impurity 16. Uses: For analytical and research use. CAS No. 63819-70-5. Molecular formula: C8H18N2O. Mole weight: 158.25. Catalog: APB63819705. | |
| Clavulanate Potassium, Streptomyces sp. | Clavulanic acid is a beta-lactam antibiotic produced by several species of the genus Streptomyces. The free acid degrades and is isolated and maintained as either the sodium or potassium salt. Clavulanate is a weak antibiotic but is a potent inhibitor of beta- lactamases. In combination with penicillin and cephalosporins it shows potent synergistic activity. Clavulanic acid is a suicide inhibitor, covalently binding to a serine residue in the active site of the beta-lactamase. Group: Biochemicals. Alternative Names: Timentin; Ticarcillin; MM 14151; [2R-(2α, 3Z, 5α)]-3-(2-hydroxyethylidene)-7-oxo-4-oxa- 1-azabicyclo[3. 2. 0]heptane-2-carboxylate potassium salt. Grades: Highly Purified. CAS No. 61177-45-5. Pack Sizes: 5mg. US Biological Life Sciences. |  Worldwide |
| Clavulanate-TEG-Biotin | Clavulanate-TEG-Biotin. Synonyms: 13-oxo-17-((3aS,4S,6aR)-2-oxohexahydro-1H-thieno[3,4-d]imidazol-4-yl)-3,6,9,12-tetraoxaheptadecyl (2R,5R,Z)-3-(2-hydroxyethylidene)-7-oxo-4-oxa-1-azabicyclo[3.2.0]heptane-2-carboxylate. Molecular formula: C26H39N3O11S. Mole weight: 601.7. | |
| Clavulanic acid | It is produced by the strain of Streptomyces clavuligerus. Clavulanic acid has a strong inhibition of β-lactamase activity, almost no antibacterial effect. Synonyms: Acido clavulanico; Acide clavulanique; acidum clavulanicum; Clavulansaeure. Grade: 95%. CAS No. 58001-44-8. Molecular formula: C8H9NO5. Mole weight: 199.16. | |
| Clavulanic acid | Clavulanic acid is a naturally occurring powerful bacterial β-lactamases inhibitor for research of infections caused by bacteria, including infections of the ears. Clavulanic acid is active against a wide spectrum of gram-positive and gram-negative bacterias[1]. Uses: Scientific research. Category: Signaling pathways. CAS No. 58001-44-8. Pack Sizes: 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-A0256. | |
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