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| Product | Description | |
|---|---|---|
| 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 |
| Clascoterone | Clascoterone (Cortexolone 17 alpha-propionate;Cortexolone 17α-propionate;CB-03-01) is a new topical and peripherally selective androgen antagonist. Uses: Scientific research. Group: 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; 100 mg; 500 mg. Product ID: HY-13331. |  |
| 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 (beta-Clastolactacystin, Clasto-lactacystin b-Lactone, Omuralide) | Cell-permeable. A highly specific, potent and irreversible proteasome inhibitor. Lactacystin acts as a precursor for clasto-lactacystin beta-lactone and the latter compound is at least 10 times more active than the parent Lactacystin. Group: Biochemicals. Grades: Highly Purified. CAS No. 154226-60-5. Pack Sizes: 100ug. US Biological Life Sciences. |  Worldwide |
| 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. Group: Natural products. 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. | |
| Clasto-Lactacystin beta-lactone (Omuralide) | In vitro lactacystin does not react with the proteasome. It rather undergoes a spontaneous conversion (lactonization) to the active metabolite clasto-lactacystin beta-lactone. Potent and selective irreversible and cell permeable proteasome inhibitor. Inhibits the chymotrypsin-like, trypsin-like and caspase-like peptidase activity of the proteasome. The active metabolite of lactacystin with higher potency since it does not require hydrolysis in order to become cell permeable. Calpain and cathepsin inhibitor. Apoptosis inducer. Anticancer compound. Induces differentiation and inhibits cell cycle progression in several tumor cell lines. Induces neuritogenesis. Autophagy inducer. Group: Biochemicals. Grades: Highly Purified. CAS No. 154226-60-5. Pack Sizes: 100ug. Molecular Formula: C10H15NO4, Molecular Weight: 213.2. US Biological Life Sciences. | Worldwide |
| Clasto-lactacystin (Clasto-lactacystin b-Lactone, Omuralide) | A cell permeable, irreversible proteasome inhibitor. It is 20-fold more p. Group: Biochemicals. Alternative Names: Clasto-lactacystin b-Lactone, Omuralide. Grades: Highly Purified. Pack Sizes: 100ug. US Biological Life Sciences. | Worldwide |
| clasto-Lactacystin ?-Lactone - CAS 154226-60-5 | A highly specific, cell-permeable, and irreversible 20S proteasome inhibitor. Group: Fluorescence/luminescence spectroscopy. |  |
| Clasto-lactacystin(omuralide) | Clasto-lactacystin (omuralide). Group: Biochemicals. Alternative Names: (1R, 4R, 5S)-1-[(1S)-1-Hydroxy-2-methylpropyl]-4-methyl-6-oxa-2-azabicyclo[3. 2. 0]heptane-3, 7-dione; Clasto-lactacystin b-lactone; Omuralide. Grades: Highly Purified. CAS No. 154226-60-5. Pack Sizes: 1mg. Molecular Formula: C10H15NO4. US Biological Life Sciences. | Worldwide |
| Clathrin-IN-4 | Clathrin-IN-4 (compound 8b), a Wiskostatin (HY-12534) analogue, is a potent inhibitor of clathrin mediated endocytosis with an IC 50 of 2.1 μM. Clathrin-IN-4 is a dynamin I GTPase activity inhibitor with an IC 50 of 9.1 μM [1]. Uses: Scientific research. Group: Signaling pathways. CAS No. 762242-59-1. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-152218. | |
| Claturafenib | Claturafenib ( PF-07799933) is an inhibitor of pan-mutant BRAF. Claturafenib inhibits pERK in HT29 cells with an IC50 value of 1.6 nM[1]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: PF-07799933; ARRY-440. CAS No. 2754408-94-9. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-159795. | |
| 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 | United States Pharmacopeia (USP) Reference Standard. Group: Pharmacopeia & metrological institutes standards. | |
| 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. Group: Signaling pathways. CAS No. 61177-44-4. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg; 50 mg. Product ID: HY-A0256B. | |
| Clavulanate Lithium | United States Pharmacopeia (USP) Reference Standard. Group: Pharmacopeia & metrological institutes standards. | |
| 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 | Clavulanate potassium is a potent β-lactamase inhibitor and acts as an antibiotic [1] [2]. Uses: Scientific research. Group: Signaling pathways. CAS No. 61177-45-5. Pack Sizes: 5 mg; 10 mg. Product ID: HY-A0256A. | |
| 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, 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. Group: Signaling pathways. CAS No. 58001-44-8. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-A0256. | |
| Clavulanic acid dimer impurity | Clavulanic acid dimer impurity. Uses: Designed for use in research and industrial production. Additional or Alternative Names: Clavulanic Acid DiMer IMpurity;(2R,4R,5Z)-4-Carboxy-5-(2-hydroxyethylidene)-3-[[(2R,3Z,5R)-3-(2-hydroxyethylidene)-7-oxo-4-oxa-1-azabicyclo[3.2.0]hept-2-yl]carbonyl]-2-oxazolidineacetic Acid;PotassiuM Clavunate IMpurity E. Product Category: Heterocyclic Organic Compound. CAS No. 1260617-10-4. Molecular formula: C16H18N2O10. Mole weight: 398.32152. Product ID: ACM1260617104. Alfa Chemistry ISO 9001:2015 Certified. |  |
| Clavulanic Acid Methyl Ester | Clavulanic Acid Methyl Ester is a substituted Clavulanic acid as β-lactamase inhibitor. Group: Biochemicals. Alternative Names: (2R, 3Z, 5R)-3-(2-Hydroxyethylidene)-7-oxo-4-oxa-1-azabicyclo[3. 2. 0]heptane-2-carboxylic Acid Methyl Ester; [2R-(2α, 3Z, 5α)]- 3-(2-Hydroxyethylidene)-7-oxo-4-oxa-1-azabicyclo[3. 2. 0]heptane-2-carboxylic Acid Methyl Ester; Methyl Clavulanate. Grades: Highly Purified. CAS No. 57943-82-5. Pack Sizes: 5mg. US Biological Life Sciences. | Worldwide |
| Clavulanic acid methyl ester-d3 | Clavulanic acid methyl ester-d3. Group: Biochemicals. Grades: Highly Purified. Pack Sizes: 2mg, 5mg, 10mg, 25mg, 50mg. US Biological Life Sciences. | Worldwide |
| Clavulanic Acid Potassium Salt in Cellulose (1:1 mixture) | Clavulanic Acid is a β-lactamase inhibitor, typically added to amoxicillin to increase its effectiveness. Group: Biochemicals. Alternative Names: Potassium Clavulanate in Cellulose. Grades: Highly Purified. Pack Sizes: 10g. US Biological Life Sciences. | Worldwide |
| Clavulanic Acid, Potassium Salt (MM 14151, Potassium Clavulanate) | 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: 10mg, 50mg, 100mg, 1g. US Biological Life Sciences. | Worldwide |
| Clavulanic acid potassium salt (Potassium Clavulanate)/Avicel (1:1) | 1g Pack Size. Group: Antibiotics, Bioactive Small Molecules. Formula: C8H8KNO5. CAS No. 61177-45-5. Prepack ID 87644048-1g. Molecular Weight 237.25. See USA prepack pricing. |  |
| Clay | Clay. Uses: For analytical and research use. Group: Process materials, geological, cement & soils. Pack Sizes: 50G. Catalog: APS001262. Shipping: Room Temperature. | |
| Clay-Bentonitic forming | Clay-Bentonitic forming. Uses: For analytical and research use. Group: Process materials, geological, cement & soils. Catalog: APS006799. Shipping: Room Temperature. | |
| Claycomb Medium | without L-glutamine, liquid, sterile-filtered, suitable for cell culture. Group: Fluorescence/luminescence spectroscopy. | |
| Clay Nanoparticles | Clay Nanoparticles. Group: Clay nanopowders. CAS No. 1332-58-7. Molecular formula: 540.46 g/mol. >99%. |  |
| Clay Nanopowder | Clay Nanopowder. Group: Clay nanopowders. CAS No. 1332-58-7. Molecular formula: 540.46 g/mol. >99%. | |
| Clay Nanopowder Montmorillonite | Clay Nanopowder Montmorillonite. Group: Clay nanopowders. 99%. | |
| Clay stable agent | Clay stable agent. Group: Polymers. | |
| Clazakizumab | Clazakizumab is a monoclonal antibody directed against interleukin-6. Clazakizumab has been undergoing a clinical trial for the treatment of CABMR in recipients of a kidney transplant. Synonyms: ALD518; BMS-945429. CAS No. 1236278-28-6. | |
| Clazamycin A | It is produced by the strain of Streptomyces No. NF990-BF4. Clazamycin A has weak activity against gram-positive bacteria, gram-negative bacteria and L1210 cell. Synonyms: (2S-trans)-2-Chloro-5-inino-2,3-dihydro-1H-pyrrolizin-7alpha(5H)-ol. CAS No. 71806-55-8. Molecular formula: C7H9ClN2O. Mole weight: 172.61. | |
| Clazamycin B | It is produced by the strain of Streptomyces No. NF990-BF4. Clazamycin A has weak activity against gram-positive bacteria, gram-negative bacteria and L1210 cell. Synonyms: Antibiotic 354; (2S-cis)-2-Chloro-5-imino-2,3-dihydro-1H-pyrrolizin-7a(5H)-ol. CAS No. 71774-49-7. Molecular formula: C7H9ClN2O. Mole weight: 172.61. | |
| Clazosentan | Clazosentan (Ro 61-1790) is a selective endothelin A (ET A ) receptor antagonist. Clazosentan inhibits ET-1-mediated vasoconstriction. Clazosentan prevents cerebral vasospasm, vasospasm-related cerebral infarction [1] [5]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: Ro 61-1790; VML 588; AXV-034343. CAS No. 180384-56-9. Pack Sizes: 10 mM * 1 mL; 1 mg; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-17352. | |
| Clazosentan | Clazosentan, also called as AXV 034, Ro 61-1790 or VML 588, a novel endothelin A antagonist, improves cerebral blood flow and behavior after traumatic brain injury. In 2016 Actelion plans two phase III trials of Clazosentan for Cerebral vasospasm (in patients with aneurysmal subarachnoid haemorrhage) in Japan. Synonyms: N-[6-(2-hydroxyethoxy)-5-(2-methoxyphenoxy)-2-[2-(2H-tetrazol-5-yl)pyridin-4-yl]pyrimidin-4-yl]-5-methylpyridine-2-sulfonamideAXV034; AXV-034; AXV 034; AXV 034343; AXV-034343; AXV-343434; Ro 61-1790; Ro-61-1790; VML 588; VML-588; VML 588; Clazosentan. Grade: 95%. CAS No. 180384-56-9. Molecular formula: C25H23N9O6S. Mole weight: 577.57. | |
| Clazuril | Clazuril is a synthetic coccidiostat drug administered to animals especially in poultry, to cure coccidiosis. Clazuril has a coccidiocidal effect on the asexual and sexual developmental stages of both Eimeria species, resulting in a complete interruption of the life cycle. Synonyms: R-62690; R62,690; Clazurilum; Clazurilo; (2-Chloro-4-(4,5-dihydro-3,5-dioxo-as-triazin-2(3H)-yl)phenyl)(p-chlorophenyl)acetonitrile. Grade: 95%. CAS No. 101831-36-1. Molecular formula: C17H10Cl2N4O2. Mole weight: 373.19. | |
| CLC TU 055 | CLC TU 055. Group: Polymers. | |
| Cleaning Chemicals |  | |
| Clean Sediment #2 | pkg of 100 g. Group: Certified reference materials (crms). | |
| Clear Flint Glass Marlow Bottle | Clear Flint Glass Marlow Bottle. Product ID: PM-006. Product Keywords: Packaging Materials; Glass Packaging; PM-006; Clear Flint Glass Marlow Bottle. Color: Clear. |  |
| Clear Glass Marlow Bottle | Clear Glass Marlow Bottle. Product ID: PM-002. Product Keywords: Packaging Materials; Glass Packaging; PM-002; Clear Glass Marlow Bottle. Color: Clear. | |
| Clear Glass Ointment Jars Pre-capped with Black Urea Lids | Clear Glass Ointment Jars Pre-capped with Black Urea Lids. Product ID: PM-024. Product Keywords: Packaging Materials; Glass Packaging; PM-024; Clear Glass Ointment Jars Pre-capped with Black Urea Lids. Color: Clear. | |
| Clear Glass Reagent Bottle & Ground Stopper | Clear Glass Reagent Bottle & Ground Stopper. Product ID: PM-003. Product Keywords: Packaging Materials; Glass Packaging; PM-003; Clear Glass Reagent Bottle & Ground Stopper. Color: Clear. | |
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