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| Product | Description | |
|---|---|---|
| Bacteriocin L-1077 | Bacteriocin L-1077 is an antimicrobial peptide produced by Lactobacillus salivarius 1077 (NRRL B-50053). It has antibacterial activity against Gram-negative bacteria and Gram-positive bacteria. Synonyms: Thr-Asn-Tyr-Gly-Asn-Gly-Val-Gly-Val-Pro-Asp-Ala-Ile-Met-Ala-Gly-Ile-Ile-Lys-Leu-Ile-Phe-Ile-Phe-Asn-Ile-Arg-Gln-Gly-Tyr-Asn-Phe-Gly-Lys-Lys-Ala-Thr. Grade: >98%. Molecular formula: C185H290N48O49S. Mole weight: 4002.69. |  |
| Bacteriocin lactocin-705 | Bacteriocin lactocin-705 is an antimicrobial peptide produced by Lactobacillus paracasei. It has antibacterial activity against several lactic acid bacteria, Listeria, Streptococci, etc. Synonyms: Gly-Met-Ser-Gly-Tyr-Ile-Gln-Gly-Ile-Pro-Asp-Phe-Leu-Lys-Gly-Tyr-Leu-His-Gly-Ile-Ser-Ala-Ala-Asn-Lys-His-Lys-Lys-Gly-Arg-Leu; Lactocin-705 (Bacteriocin). Grade: 98%. Molecular formula: C152H242N44O40S. Mole weight: 3357.92. | |
| Bacteriocin lactocin-S | Bacteriocin lactocin-S is an antimicrobial peptide produced by Lactobacillus sakei L45. It has antibacterial activity and inhibits the growth of selected species of the genera Lactobacillus, Pedicoccus, and Leuconostoc. It contains at least two lanthionines, which are probably formed between the serine in position 23 and the cysteine in position 28, and between the serine in position 32 and the cysteine in position 37. Synonyms: Ser-Thr-Pro-Val-Leu-Ala-Ser-Val-Ala-Val-Ser-Met-Glu-Leu-Leu-Pro-Thr-Ala-Ser-Val-Leu-Tyr-Ser-Asp-Val-Ala-Gly-Cys-Phe-Lys-Tyr-Ser-Ala-Lys-His-His-Cys; lasA; Lactocin S (Bacteriocin). Grade: >85%. CAS No. 125387-34-0. | |
| Bacteriocin lactococcin MMFII | Bacteriocin lactococcin MMFII is a novel class IIa bacteriocin produced by Lactococcus lactis MMFII, isolated from a Tunisian dairy product. It has antibacterial activity against Listeria monocytogenes and Lactococcus cremoris. Synonyms: Thr-Ser-Tyr-Gly-Asn-Gly-Val-His-Cys-Asn-Lys-Ser-Lys-Cys-Trp-Ile-Asp-Val-Ser-Glu-Leu-Glu-Thr-Tyr-Lys-Ala-Gly-Thr-Val-Ser-Asn-Pro-Lys-Asp-Ile-Leu-Trp (Disulfide bridge: Cys9-Cys14); Lactococcin MMFII. Grade: ≥95%. Molecular formula: C183H278N48O58S2. Mole weight: 4142.64. | |
| Bacteriocin leucocin-A | Bacteriocin leucocin-A is an antimicrobial peptide produced by Leuconostoc gelidum UAL187. It has antibacterial activity against Gram-positive bacteria: Lactic acid bacteria, Listeria monocytogenes. Synonyms: lcnA; Leucocin A-UAL 187; Leu A; Leucocin-A; Leucocin A-TA33a; Leucocin A-QU15; Lys-Tyr-Tyr-Gly-Asn-Gly-Val-His-Cys-Thr-Lys-Ser-Gly-Cys-Ser-Val-Asn-Trp-Gly-Glu-Ala-Phe-Ser-Ala-Gly-Val-His-Arg-Leu-Ala-Asn-Gly-Gly-Asn-Gly-Phe-Trp (Disulfide bridge: Cys9-Cys14). Grade: >85%. CAS No. 139069-78-6. Molecular formula: C174H246N52O50S2. Mole weight: 3930.32. | |
| Bacteriocin leucocin-B | Bacteriocin leucocin-B is an antimicrobial peptide produced by Leuconostoc mesenteroides. It has antibacterial activity against a wide spectrum of lactic acid bacteria. Synonyms: Leu B; Leucocin B-TA33a; Leucocin-B; Lys-Gly-Lys-Gly-Phe-Trp-Ser-Trp-Ala-Ser-Lys-Ala-Thr-Ser-Trp-Leu-Thr-Gly-Pro-Gln-Gln-Pro-Gly-Ser-Pro-Leu-Leu-Lys-Lys-His-Arg. Grade: >95%. Molecular formula: C161H246N46O40. Mole weight: 3466.01. | |
| Bacteriocin leucocin C | Bacteriocin leucocin C is an antimicrobial peptide produced by Leuconostoc mesenteroides. It has antibacterial activity against a wide spectrum of lactic acid bacteria. Synonyms: Leucocin C; Leu C; Lys-Asn-Tyr-Gly-Asn-Gly-Val-His-Cys-Thr-Lys-Lys-Gly-Cys-Ser-Val-Asp-Trp-Gly-Tyr-Ala-Trp-Thr-Asn-Ile-Ala-Asn-Asn-Ser-Val-Met-Asn-Gly-Leu-Thr-Gly-Gly-Asn-Ala-Gly-Trp-His-Asn. Grade: >85%. CAS No. 386254-62-2. Molecular formula: C198H291N61O61S3. Mole weight: 4598.04. | |
| Bacteriocin LS2 | Bacteriocin LS2 is an antimicrobial peptide produced by Lactobacillus salivarius BGHO1. It has antimicrobial activity. Synonyms: bacls2; Thr-Asn-Trp-Lys-Lys-Ile-Gly-Lys-Cys-Tyr-Ala-Gly-Thr-Leu-Gly-Ser-Ala-Val-Leu-Gly-Phe-Gly-Ala-Met-Gly-Pro-Val-Gly-Tyr-Trp-Ala-Gly-Ala-Gly-Val-Gly-Tyr-Ala-Ser-Phe-Cys. Grade: >98%. Molecular formula: C190H279N47O50S3. Mole weight: 4117.77. | |
| Bacteriocin mesentericin Y105 | Bacteriocin mesentericin Y105 is an antimicrobial peptide produced by Leuconostoc mesenteroides. It has antibacterial activity against Listeria monocytogenes. Synonyms: MesY105; Lys-Tyr-Tyr-Gly-Asn-Gly-Val-His-Cys-Thr-Lys-Ser-Gly-Cys-Ser-Val-Asn-Trp-Gly-Glu-Ala-Ala-Ser-Ala-Gly-Ile-His-Arg-Leu-Ala-Asn-Gly-Gly-Asn-Gly-Phe-Trp (Disulfide bridge: Cys9-Cys14); mesY. Grade: ≥95%. Molecular formula: C169H244N52O50S2. Mole weight: 3868.25. | |
| Bacteriocin microcin B17 | Bacteriocin microcin B17 is an antimicrobial peptide produced by Escherichia coli. It has antimicrobial activity. MccB17 was the first compound discovered from the Thiazole/Oxazole-Modified Microcins (TOMMs) family and the Linear Azole-containing peptides (LAPs). These ribosomal peptides are post-translationally modified to convert serine and cysteine residues into oxazole and thiazole rings. Synonyms: mcbA; MccB17. Grade: >98%. | |
| Bacteriocin OR-7 | Bacteriocin OR-7 is an antimicrobial peptide produced by Lactobacillus salivarius strain NRRL B-30514. It has antibacterial activity against Gram-negative bacteria. Synonyms: Lys-Thr-Tyr-Tyr-Gly-Thr-Asn-Gly-Val-His-Cys-Thr-Lys-Asn-Ser-Leu-Trp-Gly-Lys-Val-Arg-Leu-Lys-Asn-Met-Lys-Tyr-Asp-Gln-Asn-Thr-Thr-Tyr-Met-Gly-Arg-Leu-Gln-Asp-Ile-Leu-Leu-Gly-Trp-Ala-Thr-Gly-Ala-Phe-Gly-Lys-Thr-Phe-His; Bacteriocin OR-7 (Bacteriocin). Grade: >98%. | |
| Bacteriocin piscicolin-126 | Bacteriocin piscicolin-126 is an antimicrobial peptide produced by Carnobacterium piscicola JG126. It has antibacterial activity against Gram-positive bacteria. Synonyms: pisA; Pisc126; Lys-Tyr-Tyr-Gly-Asn-Gly-Val-Ser-Cys-Asn-Lys-Asn-Gly-Cys-Thr-Val-Asp-Trp-Ser-Lys-Ala-Ile-Gly-Ile-Ile-Gly-Asn-Asn-Ala-Ala-Ala-Asn-Leu-Thr-Thr-Gly-Gly-Ala-Ala-Gly-Trp-Asn-Lys-Gly (Disulfide bridge: Cys9-Cys14). Grade: >85%. Molecular formula: C190H293N57O61S2. Mole weight: 4415.89. | |
| Bacteriocin plantaricin ASM1 | Bacteriocin plantarican ASM1 is an antimicrobial peptide produced by Lactobacillus plantarum A-1. It has antibacterial activity against Gram-positive bacteria. It contains two intramolecular disulfide bonds. Synonyms: PASM1; bactA1; Lys-Pro-Ala-Trp-Cys-Trp-Tyr-Thr-Leu-Ala-Met-Cys-Gly-Ala-Gly-Tyr-Asp-Ser-Gly-Thr-Cys-Asp-Tyr-Met-Tyr-Ser-His-Cys-Phe-Gly-Val-Lys-His-Ser-Ser-Gly-Gly-Gly-Gly-Ser-Tyr-His-Cys. Grade: >85%. Molecular formula: C203H275N53O60S7. Mole weight: 4642.17. | |
| Bacteriocin rhamnosin A | Bacteriocin rhamnosin A is an antimicrobial peptide produced by Lactobacillus rhamnosus strain 68. It has antibacterial activity against Gram-positive bacteria. Synonyms: Rhamnosin A (Bacteriocin); Ala-Val-Pro-Ala-Val-Arg-Lys-Thr-Asn-Glu-Thr-Leu-Asp. Grade: ≥97%. Molecular formula: C60H104N18O21. Mole weight: 1413.59. | |
| Bacteriocin SRCAM 1580 | Bacteriocin SRCAM 1580 is an antimicrobial peptide produced by Paenibacillus polymyxa (Bacillus circulans). It has antibacterial activity against Gram-positive bacteria: Clostridium jejuni. Synonyms: Val-Asn-Tyr-Gly-Asn-Gly-Val-Ser-Cys-Ser-Lys-Thr-Lys-Cys-Ser-Val-Asn-Trp-Gly-Ile-Ile-Thr-His-Gln-Ala-Phe-Arg-Val-Thr-Ser-Gly-Val-Ala-Ser-Gly (Disulfide bridge: Cys9-Cys14). Grade: ≥96%. Molecular formula: C156H245N47O49S2. Mole weight: 3627.07. | |
| Bacteriocin SRCAM 37 | Bacteriocin SRCAM 37 is an antimicrobial peptide produced by Paenibacillus polymyxa (Bacillus polymyxa). It has antibacterial activity against Gram-positive bacteria: Clostridium jejuni. Synonyms: Phe-Val-Tyr-Gly-Asn-Gly-Val-Thr-Ser-Ile-Leu-Val-Gln-Ala-Gln-Phe-Leu-Val-Asn-Gly-Gln-Arg-Arg-Phe-Phe-Tyr-Thr-Pro-Asp-Lys. Grade: >97%. Molecular formula: C162H242N42O43. Mole weight: 3465.96. | |
| Bacteriocin SRCAM 602 | Bacteriocin SRCAM 602 is an antimicrobial peptide produced by Paenibacillus polymyxa (Bacillus polymyxa). It has antibacterial activity against Gram-positive bacteria: Clostridium jejuni. Synonyms: Ala-Thr-Tyr-Tyr-Gly-Asn-Gly-Leu-Tyr-Cys-Asn-Lys-Gln-Lys-His-Tyr-Thr-Trp-Val-Asp-Trp-Asn-Lys-Ala-Ser-Arg-Glu-Ile-Gly-Lys-Ile-Thr-Val-Asn-Gly-Trp-Val-Gln-His. Grade: ≥96%. Molecular formula: C211H307N59O58S. Mole weight: 4630.19. | |
| Bacteriocin sublancin-168 | Bacteriocin sublancin-168 is an antimicrobial peptide produced by Bacillus phage SPbeta (Bacillus phage SPBc2, Bacteriophage SP-beta). It has antibacterial activity against Gram-positive bacteria. It is an unusual S-linked glycopeptide with a glucose (Glc) moiety β-linked to cysteine-22 (Cys-22). Synonyms: Sublancin-168 (Bacteriocin); Gly-Leu-Gly-Lys-Ala-Gln-Cys-Ala-Ala-Leu-Trp-Leu-Gln-Cys-Ala-Ser-Gly-Gly-Thr-Ile-Gly-Cys(Glc)-Gly-Gly-Gly-Ala-Val-Ala-Cys-Gln-Asn-Tyr-Arg-Gln-Phe-Cys-Arg (Disulfide bridge: Cys7-Cys36, Cys14-Cys29). Grade: >85%. | |
| Bacteriocin thuricin-S | Bacteriocin thuricin-S is an antimicrobial peptide produced by Bacillus thuringiensis subsp. entomocidus. It has antibacterial activity against Gram-positive bacteria L.monocytogenes, B.subtilis and other Bacillus, E.cloacae, L.acidophilus, L.lactis, P.acidilactici, S.thermophilus, and several Gram-negative bacteria including S.cholerae, S.flexneri and P.aeruginosa. Synonyms: Thuricin-S (Bacteriocin); DWTAWSALVAAACSVELL. Grade: >85%. | |
| Bacteriological agar | for molecular biology. Group: Fluorescence/luminescence spectroscopy. |  |
| Bacteriological Peptone | 100g Pack Size. Group: Amino Acids, Analytical Reagents, Biochemicals, Diagnostic Raw Materials. Formula: N/A. CAS No. 73049-73-7. Prepack ID 90018563-100g. See USA prepack pricing. |  |
| Bacteriopheophytin | Bacteriopheophytin, also known as Bacteriopheophytin a, is a Pigment which is the degradation product of bacteriochlorophyll. Uses: Designed for use in research and industrial production. Additional or Alternative Names: Bacteriopheophytin; Bacteriopheophytin A. Product Category: Others. Appearance: To be determined. CAS No. 17453-58-6. Molecular formula: C55H76N4O6. Mole weight: 889.24. Purity: >98%. IUPACName: methyl (3R,11R,12R,21S,22S)-16-acetyl-11-ethyl-12,17,21,26-tetramethyl-4-oxo-22-[3-oxo-3-[(E,7R,11R)-3,7,11,15-tetramethylhexadec-2-enoxy]propyl]-7,23,24,25-tetrazahexacyclo[18.2.1.15,8.110,13.115,18.02,6]hexacosa-1(23),2(6),5(26),8,10(25),13,15,17,19-nonaene-3-carboxylate. Canonical SMILES: O=C([C@@H](C1=O)C2=C(N/3)C1=C(C)C3=C\C([C@H](CC)[C@H]/4C)=NC4=C/C5=C(C(C)=O)C(C)=C(N5)/C=C6[C@@H](C)[C@H](CCC(OC/C=C(C)/CCC[C@H](C)CCC[C@H](C)CCCC(C)C)=O)C2=N/6)OC. Product ID: ACM17453586. Alfa Chemistry ISO 9001:2015 Certified. Categories: Bacteriophaeophytin. |  |
| Bacteriorhodopsin from Halobacterium salinarum | native sequence, lyophilized powder. Group: Fluorescence/luminescence spectroscopy. | |
| Bactobolin | Bactobolin is produced by the strain of Pseudomonas yoshitomensis. It has the activity of anti-gram-positive bacteria and negative bacteria, and can be used to inhibit experimental tumor. Synonyms: (-)-Bactobolin; Antibiotic BN 183B; Propanamide, 2-amino-N-(3-(dichloromethyl)-3,4,4a,5,6,7-hexahydro-5,6,8-trihydroxy-3-methyl-1-oxo-1H-2-benzopyran-4-yl)-, (3S-(3alpha,4alpha(R*),4abeta,5beta,6alpha))-. CAS No. 72615-20-4. Molecular formula: C14H20Cl2N2O6. Mole weight: 383.22. | |
| Bactofencin A | Bactofencin A is an antimicrobial peptide produced by Lactobacillus salivarius DPC6502. It has antibacterial activity against Listeria monocytogenes and Staphylococcus aureus. Synonyms: Lys-Arg-Lys-Lys-His-Arg-Cys-Arg-Val-Tyr-Asn-Asn-Gly-Met-Pro-Thr-Gly-Met-Tyr-Arg-Trp-Cys (Disulfide bridge: Cys7-Cys22). Grade: >98%. Molecular formula: C119H188N42O28S4. Mole weight: 2783.32. | |
| Bactrocerin-1 | Bactrocerin-1 is an antimicrobial peptide produced by Bactrocera dorsalis. It has a very broad spectrum of anti-microbial activity against Gram-positive bacteria, Gram-negative bacteria, and fungi. Synonyms: Val-Gly-Lys-Thr-Trp-Ile-Lys-Val-Ile-Arg-Gly-Ile-Gly-Lys-Ser-Lys-Ile-Lys-Trp-Gln; L-valylglycyl-L-lysyl-L-threonyl-L-tryptophyl-L-isoleucyl-L-lysyl-L-valyl-L-isoleucyl-L-arginylglycyl-L-isoleucylglycyl-L-lysyl-L-seryl-L-lysyl-L-isoleucyl-L-lysyl-L-tryptophyl-L-glutamine. Grade: 96%. CAS No. 1100646-39-6. Molecular formula: C110H185N31O24. Mole weight: 2325.87. | |
| Baculoviral IAP repeat-containing protein 5 (95-104) | Baculoviral IAP repeat-containing protein 5 (95-104) is a truncated fragment of Baculoviral IAP repeat-containing protein 5. Baculoviral IAP repeat-containing protein 5 is a multitasking protein that has dual roles in promoting cell proliferation and preventing apoptosis. Synonyms: Apoptosis inhibitor 4 (95-104); Apoptosis inhibitor survivin (95-104). | |
| Baculoviral IAP repeat-containing protein 5 (97-111) | Baculoviral IAP repeat-containing protein 5 (97-111) is a truncated fragment of Baculoviral IAP repeat-containing protein 5. Baculoviral IAP repeat-containing protein 5 is a multitasking protein that has dual roles in promoting cell proliferation and preventing apoptosis. Synonyms: Apoptosis inhibitor 4 (97-111); Apoptosis inhibitor survivin (97-111). | |
| Baculoviral IAP repeat-containing protein 7 (280-289) | Baculoviral IAP repeat-containing protein 7 (280-289) is amino acids 280 to 289 fragment of Baculoviral IAP repeat-containing protein 7. Baculoviral IAP repeat-containing protein 7 is a multi-functional protein which regulates not only caspases and apoptosis, but also modulates inflammatory signaling and immunity, mitogenic kinase signaling and cell proliferation, as well as cell invasion and metastasis. It is beneficial to research in the treatment of melanoma. Synonyms: Apoptosis inhibitor 2 (280-289); Cellular inhibitor of apoptosis 2 (280-289); Inhibitor of apoptosis protein 1 (280-289); RING finger protein 49 (280-289); RING-type E3 ubiquitin transferase BIRC3 (280-289). | |
| BADGE | BADGE. Group: Biochemicals. Grades: Purified. CAS No. 1675-54-3. Pack Sizes: 10mg, 50mg. US Biological Life Sciences. |  Worldwide |
| BAD, GST tagged human | recombinant, expressed in baculovirus infected Sf9 cells, ?70% (SDS-PAGE), buffered aqueous glycerol solution. Group: Fluorescence/luminescence spectroscopy. | |
| Badione A | It is produced by the strain of Xerocomus badius. Badione A can form a stable salt with potassium ions. Molecular formula: C36H18O17. Mole weight: 722.52. | |
| Badione B | It is produced by the strain of Xerocomus badius. Badione B can form a stable salt with potassium ions. Molecular formula: C36H18O18. Mole weight: 738.52. | |
| b-Aescin | b-Aescin, a natural compound extracted from the seeds of the horse chestnut tree, serves as a prominent treatment option in the biomedical industry for chronic venous insufficiency, presenting benefits such as symptom alleviation of edema and pain. This versatile compound also exhibits anti-inflammatory properties and promising indications of inhibiting tumor growth in specified cancer cell lines, making it an invaluable asset in the medical community. Uses: Cardiovascular agents. Synonyms: b-Escin; β-Escin; Flogencyl; β-Aescin. CAS No. 11072-93-8. Molecular formula: C55H86O24. Mole weight: 1131.26. | |
| Bafetinib | Bafetinib, also known as INNO-406, is an orally bioavailable 2-phenylaminopyrimidine derivative with potential antineoplastic activity. Bafetinib specifically binds to and inhibits the Bcr/Abl fusion protein tyrosine kinase, an abnormal enzyme produced by Philadelphia chromosomal translocation associated with chronic myeloid leukemia (CML). Synonyms: INNO406; INNO-406; INNO 406; NS187; NS-187; NS 187; Bafetinib. Grade: 0.98. CAS No. 859212-16-1. Molecular formula: C30H31F3N8O. Mole weight: 576.61. | |
| Bafetinib | Bafetinib is an orally active Lyn/Bcr-Abl tyrosine kinase inhibitor. Bafetinib enhances the activity of several pro-apoptotic Bcl-2 homology (BH) 3-pure proteins (Bim, Bad, Bmf, and Bik) through intrinsic apoptotic pathways regulated by the Bcl-2 family, and induces apoptosis of Ph+ leukemia cells. Bafetinib has antitumor activity[1][2][3]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: INNO-406; NS-187. CAS No. 859212-16-1. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 50 mg; 100 mg. Product ID: HY-50868. |  |
| Bafetinib | A substituted benzamide derivative structurally related to STI-571 (Imatinib Mesylate). It was identified as highly potent Bcr-Abl kinase inhibitor. Group: Biochemicals. Alternative Names: N-[3- ([4, 5'-Bipyrimidin]-2-ylamino) -4-methylphenyl]-4-[[ (3S) -3- (dimethylamino) -1-pyrrolidinyl]methyl]-3- (trifluoromethyl) benzamide; INNO 406; NS 187. Grades: Highly Purified. CAS No. 859212-16-1. Pack Sizes: 1mg. US Biological Life Sciences. | Worldwide |
| BAFF from rat | recombinant, expressed in E. coli, ?95% (SDS-PAGE), ?95% (HPLC). Group: Fluorescence/luminescence spectroscopy. | |
| BAFF human | Animal-component free, recombinant, expressed in E. coli, ?98% (SDS-PAGE), ?98% (HPLC). Group: Fluorescence/luminescence spectroscopy. | |
| BAFF Receptor human | recombinant, expressed in E. coli, ?95% (SDS-PAGE), ?95% (HPLC), suitable for cell culture. Group: Fluorescence/luminescence spectroscopy. | |
| BAFF, soluble human | >95% (SDS-PAGE), recombinant, expressed in E. coli, lyophilized powder. Group: Fluorescence/luminescence spectroscopy. | |
| Bafilomycin | Bafilomycins are a family of macrolide antibiotics isolated from Streptomycetes sp. They exhibits antitumor, antiparasitic, immunosuppressant and antifungal activity. CAS No. 151499-39-7. | |
| Bafilomycin a1 | Bafilomycin A1 (BafA1) is a specific and reversible inhibitor of vacuolar H+-ATPase (V-ATPase) with IC50 values of 4-400 nmol/mg. Bafilomycin A1, a macrolide antibiotic, is also used as an autophagy inhibitor at the late stage. Bafilomycin A1 blocks autophagosome-lysosome fusion and inhibits acidification and protein degradation in lysosomes of cultured cells. Bafilomycin A1 induces apoptosis. Uses: Designed for use in research and industrial production. Product Category: Inhibitors. CAS No. 88899-55-2. Molecular formula: C35H58O9. Mole weight: 622.83. Purity: >98 %. Product ID: ACM88899552. Alfa Chemistry ISO 9001:2015 Certified. | |
| Bafilomycin A1 | Bafilomycin A1 (BafA1) is a specific and reversible inhibitor of vacuolar H + -ATPase ( V-ATPase ) with IC 50 values of 4-400 nmol/mg. Bafilomycin A1, a macrolide antibiotic, is also used as an autophagy inhibitor at the late stage. Bafilomycin A1 blocks autophagosome-lysosome fusion and inhibits acidification and protein degradation in lysosomes of cultured cells. Bafilomycin A1 induces apoptosis [1] [2] [3]. Uses: Scientific research. Group: Natural products. Alternative Names: BafA1. CAS No. 88899-55-2. Pack Sizes: 100 μg; 500 μg; 1 mg; 5 mg; 10 mg. Product ID: HY-100558. | |
| Bafilomycin A1 | It is produced by the strain of Streptomyces griseus ssp. sulphurus TU 1022 and Str. griseus TU 2437. Bafilomycin A1 is a vacuolar H+-ATPase inhibitor with IC50 of 0.44 nM. It can inhibit the growth of gram-positive bacteria, negative bacteria, fungi, yeast and protozoa, and has the effects of insect killing, nematode killing and immunosuppression. Synonyms: NSC 381866; NSC-381866; NSC381866; Oxacyclohexadeca-3,5,11,13-tetraen-2-one, 8-hydroxy-16-[(1S,2R,3S)-2-hydroxy-1-methyl-3-[(2R,4R,5S,6R)-tetrahydro-2,4-dihydroxy-5-methyl-6-(1-methylethyl)-2H-pyran-2-yl]butyl]-3,15-dimethoxy-5,7,9,11-tetramethyl-, (3Z,5E,7R,8S,9S,11E,13E,15S,16R)-; (3Z,5E,7R,8S,9S,11E,13E,15S,16R)-8-Hydroxy-16-[(1S,2R,3S)-2-hydroxy-1-methyl-3-[(2R,4R,5S,6R)-tetrahydro-2,4-dihydroxy-5-methyl-6-(1-methylethyl)-2H-pyran-2-yl]butyl]-3,15-dimethoxy-5,7,9,11-tetramethyloxacyclohexadeca-3,5,11,13-tetraen-2-one; Hygrolidin, 21-O-de(3-carboxy-1-oxo-2-propenyl)-2-demethyl-2-methoxy-24-methyl-; (-)-Bafilomycin A1; Oxacyclohexadeca-3,5,11,13-tetraen-2-one, 8-hydroxy-16-[2-hydroxy-1-methyl-3-[tetrahydro-2,4-dihydroxy-5-methyl-6-(1-methylethyl)-2H-pyran-2-yl]butyl]-3,15-dimethoxy-5,7,9,11-tetramethyl-, [7R-[3Z,5E,7R*,8S*,9S*,11E,13E,15S*,16R*[1S*,2R*,3S*(2R*,4R*,5S*,6R*)]]]-. Grade: ≥95% by HPLC. CAS No. 88899-55-2. Molecular formula: C35H58O9. Mole weight: 622.83. | |
| Bafilomycin A1 | Bafilomycin A1 Inhibitor. Uses: Scientific use. Product Category: T6740. CAS No. 88899-55-2. |  |
| Bafilomycin A1 from Streptomyces griseus | ?90% (HPLC). Group: Fluorescence/luminescence spectroscopy. | |
| Bafilomycin A1 (NSC381866) | Bafilomycin A1 is a member of a potent family of macrocyclic lactones with a broad spectrum of biological activity including activity against bacteria, yeast, fungi, nematodes, insects and antitumor cell lines. Bafilomycin A1 is an inhibitor of vacuolar-type ATPase. Related to: Bafilomycin B1, Bafilomycin C1, Concanamycin A.Source:Streptomyces griseus. Group: Biochemicals. Alternative Names: 21-O-De(3-carboxy-1-oxo-2-propenyl)-2-demethyl-2-methoxy-24-methyl-hygrolidin Oxacyclohexadecane, hygrolidin deriv.; (-)-Bafilomycin A1; NSC 381866; [7R-[3Z, 5E, 7R*, 8S*, 9S*, 11E, 13E, 15S*, 16R*[1S*, 2R*, 3S*(2R*, 4R*, 5S*, 6R*)]]]-8-Hydroxy-16-[2-hydroxy-1-methyl-3-[tetrahydro-2, 4-dihydroxy-5-methyl-6-(1-methylethyl)-2H-pyran-2-yl]butyl]-3, 15-dimethoxy-5, 7, 9, 11-tetramethyl-oxacyclohexadeca-3, 5, 11, 13-tetraen-2-one. Grades: Highly Purified. CAS No. 88899-55-2. Pack Sizes: 100ug, 1mg. Molecular Formula: C35H58O9, Molecular Weight: 622.8. US Biological Life Sciences. | Worldwide |
| Bafilomycin A1 Ready Made Solution | 0.16 mM in DMSO, from Streptomyces griseus. Group: Fluorescence/luminescence spectroscopy. | |
| Bafilomycin b1 | Bafilomycin B1 is a macrolide antibiotic isolated from Streptomyces sp, inhibits Gram-positive bacteria and fungi, and acts as an inhibitor of K+-dependent ATPase of E. coli. Uses: Designed for use in research and industrial production. Product Category: Inhibitors. CAS No. 88899-56-3. Molecular formula: C44H65NO13. Mole weight: 815.99. Purity: 0.9822. Product ID: ACM88899563. Alfa Chemistry ISO 9001:2015 Certified. Categories: Bafilomycin-A1. | |
| Bafilomycin B1 | Bafilomycin B1 is produced by the strain of Streptomyces griseus ssp. sulphurus TU 1022 and Str. griseus TU 2437. A member of a potent family of macrocyclic lactones; broadly active against bacteria, fungi, insects, nematodes and protozoans; a potential agent for treating osteoporosis. It can inhibit the growth of gram-positive bacteria, negative bacteria, fungi, yeast and protozoa, and has the effects of insect killing, nematode killing and immunosuppression. Synonyms: Setamycin. Grade: >95% by HPLC. CAS No. 88899-56-3. Molecular formula: C44H65NO13. Mole weight: 815.98. | |
| Bafilomycin B1 (Setamycin) | Bafilomycin B1 shares the same mode of action and activity as its more accessible A1 analogue Bafilomycin B1 is broadly active against bacteria, fungi, insects, nematodes and protozoans. Bafilomycin B1 has attracted interest as a potential antiosteoporotic agent in treating bone lytic diseases. Group: Biochemicals. Alternative Names: Setamycin. Grades: Highly Purified. CAS No. 88899-56-3. Pack Sizes: 1mg. US Biological Life Sciences. | Worldwide |
| Bafilomycin B1 (Setamycin, BRN4640118) | Macrolide antibiotic. Specific vacuolar-type H+-ATPase inhibitor. Group: Biochemicals. Grades: Highly Purified. CAS No. 88899-56-3. Pack Sizes: 100ug, 1mg, 5mg. US Biological Life Sciences. | Worldwide |
| Bafilomycin b2 | Bafilomycin b2. Uses: Designed for use in research and industrial production. Additional or Alternative Names: BAFILOMYCIN B2. Product Category: Heterocyclic Organic Compound. CAS No. 88907-48-6. Molecular formula: C45H67NO13. Mole weight: 830.01. Purity: 0.96. IUPACName: [(2R,4R,5R,6R)-2-[(2S,3R,4S)-3-hydroxy-4-[(2R,3S,4E,6E,9S,10S,11R,12E,14E)-10-hydroxy-3,15-dimethoxy-7,9,11,13-tetramethyl-16-oxo-1-oxacyclohexadeca-4,6,12,14-tetraen-2-yl]pentan-2-yl]-2-methoxy-5-methyl-6-propan-2-yloxan-4-yl] (E)-4-[(2-hydroxy-5-oxocycl. Canonical SMILES: CC1CC(=CC=CC(C(OC(=O)C(=CC(=CC(C1O)C)C)OC)C(C)C(C(C)C2(CC(C(C(O2)C(C)C)C)OC(=O)C=CC(=O)NC3=C(CCC3=O)O)OC)O)OC)C. Product ID: ACM88907486. Alfa Chemistry ISO 9001:2015 Certified. Categories: Bafilomycin (BAF). | |
| Bafilomycin c1 | Bafilomycin C1 is a macrolide antibiotic isolated from Streptomyces sp. Bafilomycin C1 is a potent, specific and reversible inhibitor of vacuolar-type H+-ATPases (V-ATPases). Bafilomycin C1 inhibits growth of gram-positive bacteria and fungi. Bafilomycin C1 induces cell apoptosis and can be used for the study of hepatocellular carcinoma (HCC). Uses: Designed for use in research and industrial production. Additional or Alternative Names: BAFILOMYCIN C1;2-Demethyl-2-methoxy-24-methylhygrolidin;Antibiotic L-681110A1;L-681110A1. Product Category: Inhibitors. Appearance: Light tan solid. CAS No. 88979-61-7. Molecular formula: C39H60O12. Mole weight: 720.8865. Purity: 0.96. IUPACName: 4-[2-hydroxy-2-[3-hydroxy-4-(10-hydroxy-3,15-dimethoxy-7,9,11,13-tetramethyl-16-oxo-1-oxacyclohexadeca-4,6,12,14-tetraen-2-yl)pentan-2-yl]-5-methyl-6-propan-2-yloxan-4-yl]oxy-4-oxobut-2-enoic acid. Canonical SMILES: CC1CC(=CC=CC(C(OC(=O)C(=CC(=CC(C1O)C)C)OC)C(C)C(C(C)C2(CC(C(C(O2)C(C)C)C)OC(=O)C=CC(=O)O)O)O)OC)C. Density: 1.18 g/cm³. Product ID: ACM88979617. Alfa Chemistry ISO 9001:2015 Certified. Categories: Bafilomycin-A1. | |
| Bafilomycin C1 | Bafilomycin C1 is a macrolide compound found in Streptomyces and an inhibitor of V-ATPase protein. It has a wide range of activities against bacteria, fungi, insects, and nematodes. It is a potential drug for the treatment of osteoporosis. Synonyms: L-681,110A1. Grade: >95% by HPLC. CAS No. 88979-61-7. Molecular formula: C39H60O12. Mole weight: 720.88. | |
| Bafilomycin C1 (Antibiotic L-681,110A1) | Bafilomycin C1 shares the same mode of action and activity as its more accessible A1 analogue Bafilomycin C1 is broadly active against bacteria, fungi, insects, nematodes and cestodes. Bafilomycin C1 has attracted interest as a potential antiosteoporotic agent in treating bone lytic diseases.The presence of the fumarate group has provided an ideal ligand for affinity chromatography of V-ATPase. Group: Biochemicals. Alternative Names: Antibiotic L-681,110A1. Grades: Highly Purified. CAS No. 88979-61-7. Pack Sizes: 1mg. US Biological Life Sciences. | Worldwide |
| Bafilomycin C1 (L-681,110A1, 2-Demethyl-2-methoxy-24-methyl-hygrolidin) | Antibiotic. Specific vacuolar-type H+-ATPase inhibitor. Inhibitor of autophagic degradation by rising lysosomal pH and thus inactivating the lysosomal acid hydrolases. Antibacterial, antifungal, insecticidal and antihelmintic. Potential anti-osteoporotic agent in treating bone lytic diseases. Neuroprotection inducer. Group: Biochemicals. Grades: Highly Purified. CAS No. 88979-61-7. Pack Sizes: 1mg. US Biological Life Sciences. | Worldwide |
| Bafilomycin D | Bafilomycin D is a specific inhibitor of vacuolar-type ATPase ( V-ATPase ). Bafilomycin D has antimicrobial, insecticidal, herbicidal and cytotoxic activity [1]. Uses: Scientific research. Group: Natural products. CAS No. 98813-13-9. Pack Sizes: 1 mg. Product ID: HY-108970. | |
| Bafilomycin D | Bafilomycin D is a macrolide antibiotic produced by Streptomyces. Bafilomycin D is an inhibitor that is more selective than Balifomycin A. Synonyms: Tubaymycin, 3D5. Grade: >99% by HPLC. CAS No. 98813-13-9. Molecular formula: C35H56O8. Mole weight: 604.81. | |
| Bafilomycin D (Tubaymycin, Antibiotic 3D5) | Bafilomycin D shares the same mode of action as bafilomycin A1 which has been the analog of choice in cell biology studies of the role of ATPase. Bafilomycin D contains the ring opened side chain and is a much more stable analog of bafilomycin A1. In-house data demonstrate that bafilomycin D is also a much more selective inhibitor of mammalian cells than bafilomycin A which exhibits a broad profile against tumor cells, fungi and nematodes. Limited availability has restricted a more in depth investigation of this metabolite. Group: Biochemicals. Alternative Names: Tubaymycin, Antibiotic 3D5. Grades: Highly Purified. CAS No. 98813-13-9. Pack Sizes: 1mg. US Biological Life Sciences. | Worldwide |
| Bafisontamab | Bafisontamab (EMB-01) is a bispecific antibody targeting EGFR and cMET with antitumor activity[1]. Uses: Scientific research. Group: Inhibitory antibodies. Alternative Names: EMB-01. CAS No. 2437210-79-0. Pack Sizes: 1 mg; 5 mg. Product ID: HY-P99455. | |
| Bag-1 | Bag-1 is a novel potent, non-peptidic bombesin receptor subtype-3 (BRS-3) agonist. Grade: 98%. CAS No. 1021937-07-4. Molecular formula: C22H27N3. Mole weight: 333.5. | |
| BAG1 (72-end), GST tagged human | recombinant, expressed in E. coli, ?70% (SDS-PAGE), buffered aqueous glycerol solution. Group: Fluorescence/luminescence spectroscopy. | |
| Bag-2 | Bag-2 is a new powerful non-peptide bombesin receptor subtype 3 (BRS-3) agonist. Synonyms: Bag-2; 1021936-34-4; CHEMBL1084942; 2-[4-[2-[5-(cyclopentylmethyl)-1H-imidazol-2-yl]ethyl]phenyl]benzoic acid[3H]bag-2. Grade: 98%. CAS No. 1021936-34-4. Molecular formula: C24H26N2O2. Mole weight: 374.5. | |
| BAG 956 | BAG 956. Group: Biochemicals. Grades: Purified. CAS No. 853910-02-8. Pack Sizes: 10mg, 50mg. US Biological Life Sciences. | Worldwide |
| Bagougeramine A | Bagougeramine A is produced by the strain of Bacillus circulans TB-2125. Both of A and B have activities against gram-positive bacteria and negative bacteria, and B has higher activity than A, except for Pseudomonas aeruginosa A3. Synonyms: beta-D-Glucopyranuronamide, 4-((3-((aminoiminomethyl)amino)-N-(N-methylglycyl)-D-alanyl)amino)-1-(4-amino-2-oxo-1(2H)-pyrimidinyl)-1,4-dideoxy-. CAS No. 104840-35-9. Molecular formula: C17H28N10O7. Mole weight: 484.47. | |
| Bagougeramine B | Bagougeramine B is produced by the strain of Bacillus circulans TB-2125. Both of A and B have activities against gram-positive bacteria and negative bacteria, and B has higher activity than A, except for Pseudomonas aeruginosa A3. Synonyms: beta-D-Glucopyranuronamide, N-(3-((4-aminobutyl)amino)propyl)-4-((3-((aminoiminomethyl)amino)-N-(N-methylglycyl)-D-alanyl)amino)-1-(4-amino-2-oxo-1(2H)-pyrimidinyl)-1,4-dideoxy-. CAS No. 104840-34-8. Molecular formula: C24H44N12O7. Mole weight: 612.68. | |
| Bagremycin A | It is produced by the strain of Streptomyces sp. Tu 4128. Bagremycin A has weak activity against gram-positive bacteria, Saccharomyces cerevisiae and Candida albicans. Synonyms: CHEMBL4125959. Molecular formula: C15H13NO3. Mole weight: 255.27. | |
| Bagremycin B | It is produced by the strain of Streptomyces sp. Tu 4128. Bagremycin B has weaker activity against gram-positive bacteria, Saccharomyces cerevisiae and Candida albicans than A. Synonyms: CHEMBL4129272. Molecular formula: C17H15NO4. Mole weight: 297.30. | |
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