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| Product | Description | |
|---|---|---|
| Mavacoxib | Mavacoxib. Group: Biochemicals. Alternative Names: 4-[5-(4-Fluorophenyl)-3-(trifluoromethyl)-1H-pyrazol-1-yl]benzenesulfonamide; 4-[5-(4-Fluorophenyl)-3-trifluoromethyl-1H-pyrazol-1-yl]benzenesulfonamide; Mavacoxib; PHA 739521; Trocoxil. Grades: Highly Purified. CAS No. 170569-88-7. Pack Sizes: 100mg. Molecular Formula: C16H11F4N3O2S, Molecular Weight: 385.34. US Biological Life Sciences. |  Worldwide |
| Mavacoxib | Mavacoxib is a selective, oral long-acting cyclooxygenase-2 (COX-2) inhibitor and a long-acting non-steroidal anti-inflammatory drug (NSAID). Mavacoxib is used to treat pain and inflammation associated with degenerative joint disease in dogs [1]. Uses: Scientific research. Group: Signaling pathways. CAS No. 170569-88-7. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg; 50 mg. Product ID: HY-119447. |  |
| Mavacoxib-d4 | Mavacoxib-d4. Group: Biochemicals. Alternative Names: 4-[5-(4-Fluorophenyl)-3-(trifluoromethyl)-1H-pyrazol-1-yl]benzenesulfonamide-d4; 4-[5-(4-Fluorophenyl)-3-trifluoromethyl-1H-pyrazol-1-yl]benzenesulfonamide-d4; Mavacoxib-d4; PHA 739521-d4; Trocoxil-d4. Grades: Highly Purified. Pack Sizes: 1mg. Molecular Formula: C16H7D4F4N3O2S, Molecular Weight: 389.36. US Biological Life Sciences. | Worldwide |
| Mavatrep | Mavatrep (JNJ-39439335) is an orally active, selective and potent TRPV1 antagonist with high affinity for hTRPV1 channels (Ki=6.5 nM). Mavatrep antagonizes capsaicin-induced Ca2+ influx with an IC50 value of 4.6 nM. Mavatrep can be used in some studies of neuropathic pain[1]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: JNJ-39439335. CAS No. 956274-94-5. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-16935. | |
| Mavatrep | Mavatrep is an orally bioavailable, potent and selective TRPV1 antagonist with Ki value of 6.5 nM, which exhibits minimal effect on the enzymatic activity of CYP isoforms 3A4, 1A2, and 2D6. It antagonizes capsaicin-induced Ca2+ influx, with an IC50 value of 4.6 nM in a TRPV1 functional assay, using cells expressing recombinant human TRPV1 channels. It blocks the activation of hTRPV1 channels by Capsaicin and pH in a concentration-dependent fashion, with IC50 values of 23 and 6.8 nM respectively. It exhibits superior pharmacodynamic properties in the CFA model of inflammatory pain in vivo. It was selected for clinical development for the treatment of pain. It was developed by Johnson & Johnson and now in clinic phase 1 with no progress. Uses: Mavatrep was selected for clinical development for the treatment of pain. Synonyms: JNJ-39439335; JNJ 39439335; JNJ39439335; 2-[2-[2-[(E)-2-[4-(trifluoromethyl)phenyl]ethenyl]-3H-benzimidazol-5-yl]phenyl]propan-2-ol. Grades: >98 %. CAS No. 956274-94-5. Molecular formula: C25H21F3N2O. Mole weight: 422.44. |  |
| Mavelertinib | Mavelertinib is a selective, orally available and irreversible EGFR tyrosine kinase inhibitor (EGFR TKI), with IC50s of 5, 4, 12 and 3 nM for Del, L858R, and double mutants T790M/L858R and T790M/Del, respectively. Mavelertinib can be used for the research of non-small-cell lung cancer (NSCLC)[1][2][3][4]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: PF-06747775. CAS No. 1776112-90-3. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-12972. | |
| Mavoglurant | Mavoglurant is a structurally novel, non-competitive mGlu5 receptor antagonist (IC50=30 nM), as a selective non-competitive antagonist. Synonyms: AFQ056; AFQ-056; AFQ 056; (3aR,4S,7aR)-Octahydro-4-hydroxy-4-[2-(3-methylphenyl)ethynyl]-1H-indole-1-carboxylic acid methyl ester; methyl (3aR,4S,7aR)-4-hydroxy-4-[2-(3-methylphenyl)ethynyl]-3,3a,5,6,7,7a-hexahydro-2H-indole-1-carboxylate. Grades: ≥95%. CAS No. 543906-09-8. Molecular formula: C19H23NO3. Mole weight: 313.39. | |
| Mavoglurant | Mavoglurant (AFQ056) is a potent, selective, non-competitive and orally active mGluR5 antagonist, with an IC 50 of 30 nM. Mavoglurant shows a >300 fold selectivity for the mGluR5 over all targets (238) tested. Mavoglurant can be used for the research of Fragile X syndrome (FXS), and L-dopa induced dyskinesias in Parkinson's disease [1] [1] [2]. Mavoglurant is a click chemistry reagent, it contains an Alkyne group and can undergo copper-catalyzed azide-alkyne cycloaddition (CuAAc) with molecules containing Azide groups. Uses: Scientific research. Group: Signaling pathways. Alternative Names: AFQ056. CAS No. 543906-09-8. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-15257. | |
| Mavoglurant racemate | Mavoglurant racemate (AFQ-056 racemate) is the racemate of Mavoglurant. Mavoglurant is a novel, non-competitive mGlu5 receptor antagonist [1]. Mavoglurant (racemate) is a click chemistry reagent, it contains an Alkyne group and can undergo copper-catalyzed azide-alkyne cycloaddition (CuAAc) with molecules containing Azide groups. Uses: Scientific research. Group: Signaling pathways. Alternative Names: AFQ-056 racemate. CAS No. 1636881-61-2. Pack Sizes: 2 mg; 5 mg. Product ID: HY-15257A. | |
| Mavorixafor free base | Mavorixafor, also known as AMD11070, AMD070, X4P-001, is an orally bioavailable and potent CXCR4 inhibitor. AMD11070 is an antagonist of SDF-1α ligand binding (IC50 = 12.5 ± 1.3 nM), inhibits SDF-1 mediated calcium flux (IC50 = 9.0 ± 2.0 nM) and SDF-1α mediated activation of the CXCR4 receptor as measured by a Eu-GTP binding assay (IC50 =39.8 ± 2.5 nM) or a [(35)S]-GTPγS binding assay (IC50 =19.0 ± 4.1 nM), and inhibits SDF-1α stimulated chemotaxis (IC50 =19.0 ± 4.0 nM). AMD11070 abrogates melanoma cell migration and is significantly more effective than AMD3100. AMD11070 represents a novel therapeutic strategy for both B-RAF wild-type and mutated melanomas. Uses: Designed for use in research and industrial production. Additional or Alternative Names: AMD11070, AMD 11070, AMD-11070, AMD070, AMD 070, AMD-070, X4P-001, X49001, X4P 001, Mavorixafor. Product Category: Antagonists. Appearance: Solid powder. CAS No. 558447-26-0. Molecular formula: C21H27N5. Mole weight: 349.48. Purity: >95%. IUPACName: (S)-N1-((1H-benzo[d]imidazol-2-yl)methyl)-N1-(5,6,7,8-tetrahydroquinolin-8-yl)butane-1,4-diamine. Canonical SMILES: NCCCCN([C@@H]1C2=NC=CC=C2CCC1)CC3=NC4=C(N3)C=CC=C4. Product ID: ACM558447260. Alfa Chemistry ISO 9001:2015 Certified. |  |
| Mavorixafor hydrochloride | Mavorixafor (AMD-070) hydrochloride is a potent, selective and orally available CXCR4 antagonist, with an IC 50 value of 13 nM against CXCR4 125 I-SDF binding. Mavorixafor hydrochloride also inhibits the replication of T-tropic HIV-1 (NL4.3 strain) in MT-4 cells and PBMCs with an IC 50 of 1 nM and 9 nM, respectively. Mavorixafor hydrochloride can be used for the study of WHIM syndrome [1]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: AMD-070 hydrochloride; AMD-11070 hydrochloride. CAS No. 880549-30-4. Pack Sizes: 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-50101C. | |
| Mavorixafor trihydrochloride | Mavorixafor trihydrochloride (AMD-070 trihydrochloride) is a potent, selective and orally available CXCR4 antagonist, with an IC50 value of 13 nM against CXCR4 125I-SDF binding, and also inhibits the replication of T-tropic HIV-1 (NL4.3 strain) in MT-4 cells and PBMCs with an IC50 of 1 and 9 nM, respectively.Mavorixafor trihydrochloride can be used for the study of WHIM syndrome[1]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: AMD-070 trihydrochloride; AMD-11070 trihydrochloride. CAS No. 2309699-17-8. Pack Sizes: 10 mM * 1 mL; 2 mg; 5 mg; 10 mg; 50 mg; 100 mg. Product ID: HY-50101A. | |
| Mavrilimumab | Mavrilimumab is a humanized monoclonal antibody targeting granulocyte macrophage colony-stimulating factor receptor (GM-CSF-R). Mavrilimumab has been investigated for the treatment of rheumatoid arthritis. Synonyms: CAM 3001; CAM-3001; CAM3001. CAS No. 1085337-57-0. | |
| Mavrilimumab | Mavrilimumab (CAM 3001) is a monoclonal antibody that binds to the α subunit of the granulocyte-macrophage colony stimulating factor ( GM-CSF ) receptor and blocks intracellular signalling downstream of GM-CSF. GM-CSF might be a mediator of the hyperactive inflammatory response associated with respiratory failure and death [1]. Uses: Scientific research. Group: Inhibitory antibodies. Alternative Names: CAM 3001. CAS No. 1085337-57-0. Pack Sizes: 1 mg; 5 mg; 10 mg. Product ID: HY-P99031. | |
| MAVT | MAVT. Uses: Designed for use in research and industrial production. Additional or Alternative Names: 106241-72-9, 2-Propenoic acid,2-methyl-, 2-(4,6-diamino-1,3,5-triazin-2-yl)ethyl ester, ACMC-1BUX5, AGN-PC-01XBBN, SureCN383376, CTK4A4445, AG-D-20531, 2,4-DIAMINO-6-(METHACRYLOYLOXY)ETHYL-1,3,5-TRIAZINE, 2-(4,6-diamino-1,3,5-triazin-2-yl)ethyl 2-methylprop-2-enoate, 2,4-Diamino-6-[(methacryloyloxy)ethyl]-1,3,5-triazine;2,4-Diamino-6-methacryloyloxyethyl-s-triazine; Curezol MAVT. Product Category: Heterocyclic Organic Compound. CAS No. 106241-72-9. Molecular formula: C9H13N5O2. Mole weight: 223.231820 [g/mol]. Purity: 0.88. IUPACName: 2-(4,6-diamino-1,3,5-triazin-2-yl)ethyl 2-methylprop-2-enoate. Product ID: ACM106241729. Alfa Chemistry ISO 9001:2015 Certified. Categories: MavTV. | |
| MAX-40279 | MAX-40279 is a dual and potent inhibitor of FLT3 kinase and FGFR kinase. MAX-40279 has the potential for the research of acute myelogenous leukemia (AML) (extracted from patent WO2021180032) [1]. Uses: Scientific research. Group: Signaling pathways. CAS No. 2070931-57-4. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-145723. | |
| Maxacalcitol | Maxacalcitol is non-calcemic vitamin D3 analog and ligand of VDR-like receptors. Uses: Dermatologic agents. Synonyms: 22-Oxacalcitriol. Grades: >98%. CAS No. 103909-75-7. Molecular formula: C26H42O4. Mole weight: 418.61. | |
| Maxacalcitol | Maxacalcitol (22-Oxacalcitriol), a vitamin D3 (HY-15398) analog, is an orally active VDR agonist. Maxacalcitol has a limited calcemic effect. Maxacalcitol has the potential for psoriasis and hyperparathyroidism research [1] [2] [3]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: 22-Oxacalcitriol. CAS No. 103909-75-7. Pack Sizes: 1 mg; 5 mg; 10 mg; 25 mg; 50 mg. Product ID: HY-32339. | |
| Maxacalcitol 9-Hydroxy Iso Form | Grades: > 95%. Molecular formula: C26H42O4. Mole weight: 418.6. | |
| Maxacalcitol Impurity B | Synonyms: MC 1292. Grades: > 95%. CAS No. 132071-85-3. Molecular formula: C26H42O4. Mole weight: 418.6. | |
| Maxacalcitol Intermediate | An intermediate of maxacalcitol, which is a derivative of vitamin D3. Maxacalcitol is a potential treatment of secondary hyperparathyroidism. Molecular formula: C38H68O5Si2. Mole weight: 661.127. | |
| Maxacalcitol Preform | Grades: > 95%. Molecular formula: C26H42O4. Mole weight: 418.6. | |
| Maxadilan | Maxadilan, a potent vasodilator isolated from the salivary glands of the sand fly Lutzomyia longipalpis, specifically and effectively activates the mammalian PAC1 receptor, one of the three receptors of PACAP. Synonyms: H-Cys-Asp-Ala-Thr-Cys-Gln-Phe-Arg-Lys-Ala-Ile-Asp-Asp-Cys-Gln-Lys-Gln-Ala-His-His-Ser-Asn-Val-Leu-Gln-Thr-Ser-Val-Gln-Thr-Thr-Ala-Thr-Phe-Thr-Ser-Met-Asp-Thr-Ser-Gln-Leu-Pro-Gly-Asn-Ser-Val-Phe-Lys-Glu-Cys-Met-Lys-Gln-Lys-Lys-Lys-Glu-Phe-Lys-Ala-NH2 (Disulfide bridge: Cys1-Cys5, Cys14-Cys51); Maxadilan (Lutzomyialongipalpis); L-cysteinyl-L-alpha-aspartyl-L-alanyl-L-threonyl-L-cysteinyl-L-glutaminyl-L-phenylalanyl-L-arginyl-L-lysyl-L-alanyl-L-isoleucyl-L-alpha-aspartyl-L-alpha-aspartyl-L-cysteinyl-L-glutaminyl-L-lysyl-L-glutaminyl-L-alanyl-L-histidyl-L-histidyl-L-seryl-L-asparagyl-L-valyl-L-leucyl-L-glutaminyl-L-threonyl-L-seryl-L-valyl-L-glutaminyl-L-threonyl-L-threonyl-L-alanyl-L-threonyl-L-phenylalanyl-L-threonyl-L-seryl-L-methionyl-L-alpha-aspartyl-L-threonyl-L-seryl-L-glutaminyl-L-leucyl-L-prolyl-glycyl-L-asparagyl-L-seryl-L-valyl-L-phenylalanyl-L-lysyl-L-alpha-glutamyl-L-cysteinyl-L-methionyl-L-lysyl-L-glutaminyl-L-lysyl-L-lysyl-L-lysyl-L-alpha-glutamyl-L-phenylalanyl-L-lysyl-L-alaninamide (1->5),(14->51)-bis(disulfide). Grades: 95%. CAS No. 135374-80-0. Molecular formula: C291H466N86O94S6. Mole weight: 6865.82. | |
| MAX dimerization protein 1 (MAD) human | recombinant, expressed in E. coli, ?80% (SDS-PAGE). Group: Fluorescence/luminescence spectroscopy. |  |
| Maximin 1 | Maximin 1 has antibacterial, antifungal, antiviral activity. The source of Maximin 1 is Chinese red belly toad, Bombina maxima, Yunnan, China, Asia. It is active against E. coli ATCC25922, S. aureus ATCC2592, B. pyocyaneus CMCCB10104, B. megatherium, B. dysenterium, K. pneumoniae, and C. albicans ATCC2002 (MIC 3-20 μM). It also has spermicidal effect. Grades: >95% by HPLC. Molecular formula: C120H209N33O35. Mole weight: 2674.14. | |
| Maximin-11 | Maximin-11 is from Bombina maxima and it shows antimicrobial activity against bacteria and against the fungus C.albicans. It has little hemolytic activity. Synonyms: Maximin-11 antimicrobial peptide. | |
| Maximin 15 | Maximin 15 has antibacterial and antifungal activities. The source of Maximin 15 is Bombina maxima [Giant fire-bellied toad]. | |
| Maximin 2 | Maximin 2 has antibacterial and antifungal activities. The source of Maximin 2 is Bombina maxima [Giant fire-bellied toad]. | |
| Maximin 28 | Maximin 28 has antibacterial and antifungal activities. The source of Maximin 28 is Bombina maxima [Giant fire-bellied toad]. | |
| Maximin 3 | Maximin 3 shows antibacterial activity against both Gram-positive and Gram-negative bacteria. It also shows antimicrobial activity against the fungus C.albicans, but not against A.flavus nor P.uticale. It has little hemolytic activity. Maximin 3 possesses a significant cytotoxicity against tumor cell lines and possesses a significant anti-HIV activity. It also shows high spermicidal activity. | |
| Maximin 31 | Maximin 31 has antibacterial and antifungal activities. The source of Maximin 31 is Bombina maxima [Giant fire-bellied toad]. | |
| Maximin 32 | Maximin 32 has antibacterial and antifungal activities. The source of Maximin 32 is Bombina maxima [Giant fire-bellied toad]. | |
| Maximin 39 | Maximin 39 has antibacterial and antifungal activities. The source of Maximin 39 is Bombina maxima [Giant fire-bellied toad]. | |
| Maximin 4 | Maximin 4 has antibacterial, antifungal and antiviral activities. The source of Maximin 4 is Chinese red belly toad, Bombina maxima, Yunnan, China, Asia. It is active against E. coli ATCC25922, S. aureus ATCC2592, B. pyocyaneus CMCCB10104, B. megatherium, B. dysenterium, K. pneumoniae, and C. albicans ATCC2002 (MIC 1.5-15 μM). Synonyms: H-Gly-Ile-Gly-Gly-Val-Leu-Leu-Ser-Ala-Gly-Lys-Ala-Ala-Leu-Lys-Gly-Leu-Ala-Lys-Val-Leu-Ala-Glu-Lys-Tyr-Ala-Asn-OH. Grades: >96% by HPLC. Molecular formula: C119H206N32O33. Mole weight: 2613.09. | |
| Maximin 41 | Maximin 41 has antibacterial and antifungal activities. The source of Maximin 41 is Bombina maxima [Giant fire-bellied toad]. | |
| Maximin 42 | Maximin 42 has antibacterial and antifungal activities. The source of Maximin 42 is Bombina maxima [Giant fire-bellied toad]. Grades: >95% by HPLC. | |
| Maximin 45 | Maximin 45 has antibacterial and antifungal activities. The source of Maximin 45 is Bombina maxima [Giant fire-bellied toad]. | |
| Maximin 49 | Maximin 49 has Antibacterial, Antifungal activity. Maximin 49 was found in brain, Bombina maxima, China, Asia. | |
| Maximin 5 | Maximin 5 shows antibacterial activity against both Gram-positive and Gram-negative bacteria. The only exception is the resistance of E.coli. It also shows antimicrobial activity against fungi C.albicans, A.flavus and P.uticale. It has little hemolytic activity. | |
| Maximin 63 | Maximin 63 has antibacterial and antifungal activities. The source of Maximin 63 is Bombina maxima [Giant fire-bellied toad]. | |
| Maximin 68 | Maximin 68 has antibacterial and antifungal activities. The source of Maximin 68 is Bombina maxima [Giant fire-bellied toad]. | |
| Maximin-7 | The source of Maximin 7 is Chinese red belly toad, Bombina maxima, Yunnan, China, Asia. Maximin 7 shows antimicrobial activity against bacteria and against the fungus C.albicans. It has little hemolytic activity. Molecular formula: C89H155N23O25. Mole weight: 1947.32. | |
| Maximin 77 | Maximin 77 has antibacterial and antifungal activities. The source of Maximin 77 is Bombina maxima [Giant fire-bellied toad]. | |
| Maximin 78 | Maximin 78 has antibacterial and antifungal activities. The source of Maximin 78 is Bombina maxima [Giant fire-bellied toad]. Grades: >97% by HPLC. | |
| Maximin-8 | Maximin-8 has antibacterial and antifungal activities. The source of Maximin-8 is Bombina maxima. | |
| Maximin-9 | Maximin 9 is a novel free thiol containing antimicrobial peptide with antimycoplasma activity from frog Bombina maxima. | |
| Maximin H1 | Maximin H1 shows antibacterial activity against both Gram-positive and Gram-negative bacteria. It also shows antimicrobial activity against the fungus C.albicans. Maximin H1 has strong hemolytic activity. | |
| Maximin-H10 | Maximin-H10 was found in Bombina maxima. Maximin-H10 shows antimicrobial activity against bacteria and against the fungus C.albicans. It also shows strong hemolytic activity. | |
| Maximin-H11 | The source of Maximin-H11 is Bombina maxima. Maximin-H11 shows antimicrobial activity against bacteria and against the fungus C.albicans. It also shows strong hemolytic activity. | |
| Maximin H12 | Maximin H12 has antibacterial and antifungal activities. The source of Maximin H12 is Bombina maxima [Giant fire-bellied toad]. | |
| Maximin-H13 | The source of Maximin-H13 is Bombina maxima. Maximin-H13 shows antimicrobial activity against bacteria and against the fungus C.albicans. It also shows strong hemolytic activity. | |
| Maximin-H14 | The source of Maximin-H14 is Bombina maxima. Maximin-H14 shows antimicrobial activity against bacteria and against the fungus C.albicans. It also shows strong hemolytic activity. | |
| Maximin-H15 | The source of Maximin-H15 is Bombina maxima. Maximin-H15 shows antimicrobial activity against bacteria and against the fungus C.albicans. It also shows strong hemolytic activity. | |
| Maximin-H16 | The source of Maximin-H16 is Bombina maxima. Maximin-H16 shows antimicrobial activity against bacteria and against the fungus C.albicans. It also shows strong hemolytic activity. | |
| Maximin H2 | Maximin H2 has antibacterial and antifungal activities. The source of Maximin H2 is Bombina maxima [Giant fire-bellied toad]. It is highly homologous with bombinin H peptides. Grades: >97% by HPLC. Molecular formula: C91H164N22O23S. Mole weight: 1966.47. | |
| Maximin H3 | Maximin H3 shows antibacterial activity against both Gram-positive and Gram-negative bacteria. It also shows antimicrobial activity against the fungus C.albicans. Maximin H3 has strong hemolytic activity. | |
| Maximin H39 | Maximin H39 has antibacterial and antifungal activities. The source of Maximin H39 is Bombina maxima [Giant fire-bellied toad]. | |
| Maximin H4 | Maximin H4 has antibacterial and antifungal activities. The source of Maximin H4 is Bombina maxima [Giant fire-bellied toad]. It is highly homologous with bombinin H peptides. Grades: >98% by HPLC. Molecular formula: C92H166N24O22. Mole weight: 1960.44. | |
| Maximin-H5 | Maximin H5 is a C-terminally amidated, anionic host defence peptide (MH5N) from toads of the Bombina genus, which was shown to possess activity against the glioma cell line, T98G (EC50 = 125 μM). | |
| Maximin-H6 | The source of Maximin-H6 is Bombina maxima. Maximin-H6 shows antimicrobial activity against bacteria and against the fungus C.albicans. It also shows strong hemolytic activity. | |
| Maximin-H7 | The source of Maximin-H7 is Bombina maxima. Maximin-H7 shows antimicrobial activity against bacteria and against the fungus C.albicans. It also shows strong hemolytic activity. | |
| Maximin-H8 | The source of Maximin-H8 is Bombina maxima. Maximin-H8 shows antimicrobial activity against bacteria and against the fungus C.albicans. It also shows strong hemolytic activity. | |
| Maximin-H9 | The source of Maximin-H9 is Bombina maxima. Maximin-H9 shows antimicrobial activity against bacteria and against the fungus C.albicans. It also shows strong hemolytic activity. | |
| Maximin-Ht | Maximin-Ht is isolated from Bombina maxima and has antimicrobial activity. Grades: >85% (SDS-PAGE). | |
| Maximin-Hu | Maximin-Hu is isolated from Bombina maxima and has antimicrobial activity. Grades: >85% (SDS-PAGE). | |
| Maximin-Hv | The source of Maximin-Hv is Bombina maxima. Maximin-Hv shows antimicrobial activity against bacteria and against the fungus C.albicans. It also shows strong hemolytic activity. | |
| Maximin-Hw | The source of Maximin-Hw is Bombina maxima. Maximin-Hw shows antimicrobial activity against bacteria and against the fungus C.albicans. It also shows strong hemolytic activity. | |
| Maximin S2 | Maximin S2 has an activity against mycoplasma but has no activity against common Gram-positive and Gram-negative bacteria nor fungi. It has no hemolytic activity. | |
| Maximin S3 | Maximin S3 has an activity against mycoplasma but has no activity against common Gram-positive and Gram-negative bacteria nor fungi. It has no hemolytic activity. Grades: >95% by HPLC. Molecular formula: C84H131N23O27S2. Mole weight: 1959.20. | |
| Maximin S4 | Maximin S4 showed no activity against commonly met Gram-positive or negative bacteria but is active against mycoplasma, a cell wall-free bacteria. Grades: >95% by HPLC. Molecular formula: C91H148N26O26S2. Mole weight: 2086.43. | |
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