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| Product | Description | |
|---|---|---|
| Brefeldin A (Standard) | Brefeldin A (Standard) (BFA (Standard)) is the analytical standard of Rutin. This product is intended for research and analytical applications. Brefeldin A (BFA) is a lactone antibiotic and a specific inhibitor of protein trafficking. Brefeldin A blocks the transport of secreted and membrane proteins from endoplasmic reticulum to Golgi apparatus. Brefeldin A is also an autophagy and mitophagy inhibitor. Brefeldin A inhibits HSV-1 and has anti-cancer activity. Uses: Scientific research. Category: Signaling pathways. Alternative Names: BFA (Standard); Cyanein (Standard); Decumbin (Standard). CAS No. 20350-15-6. Pack Sizes: 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-16592R. |  |
| Brefeldin B | Brefeldin is an antibiotic produced by Penicillum brefeldianum S-464, Pen. cyaneum S-ll, Pen. decumbens, Pen. simplicissimum S-544, etc. Molecular formula: C15H22O4. Mole weight: 266.33. |  |
| Brefeldin C | Brefeldin is an antibiotic produced by Penicillum brefeldianum S-464, Pen. cyaneum S-ll, Pen. decumbens, Pen. simplicissimum S-545, etc. Alternative Names: (1S,2Z,7S,10Z,12R,13R)-12-hydroxy-7-methyl-8-oxabicyclo[11.3.0]hexadeca-2,10-dien-9-one; 4H-Cyclopent(f)oxacyclotridecin-4-one, 1,6,7,8,9,11a,12,13,14,14a-decahydro-1-hydroxy-6-methyl-, (1R-(1R*,2E,6S*,10E,11aS*,14aR*))-. Grades: 95%. CAS No. 73899-78-2. Molecular formula: C16H24O3. Mole weight: 264.36. | |
| Bremelanotide | Bremelanotide (PT-141) is a melanocortin receptor agonist. Bremelanotide can activate MC4R and increases dopamine release. Bremelanotide induces appetitive sexual behaviors, female mounting behavior, and repetitive self-grooming. Bremelanotide can be used for the research of hypoactive sexual desire disorders[1][2][3]. Uses: Scientific research. Category: Signaling pathways. Alternative Names: PT-141. CAS No. 189691-06-3. Pack Sizes: 10 mM * 1 mL in Water; 5 mg; 10 mg; 25 mg. Product ID: HY-18678. | |
| Bremelanotide | Bremelanotide is a peptide melanocortin receptor agonist developed for the treatment of sexual dysfunction, hemorrhagic shock and reperfusion injury. Uses: bremelanotide is a synthetic peptide drug that has generated a lot of interest in the drug development community due to its potential applications in sexual dysfunction and other conditions. this peptide is a synthetic analog of the natural hormone alpha-msh (melanocyte stimulating hormone) and acts as a non-selective agonist of the melanocortin receptors mc3-r and mc4-r. one of the main areas. Alternative Names: (Ac-Nle4, Asp5, D-Phe7, Lys10)-cyclo-α-MSH (4-10); PT 141; PT-141; PT141. CAS No. 189691-06-3. Molecular formula: C50H68N14O10. Mole weight: 1025.16. | |
| Bremelanotide Acetate | Bremelanotide Acetate is a heptapeptide melanocortin agonist. Bremelanotide, formerly known as PT-141, employed in clinical trials for sexual dysfunction including both male erectile dysfunction (ED) and female sexual dysfunction or disorder (FSD), is a f. Alternative Names: PT141 acetate. CAS No. 1607799-13-2. Molecular formula: C52H72N14O12. Mole weight: 1085.22. | |
| Bremelanotide Acetate | Bremelanotide (PT-141) Acetate is a melanocortin receptor agonist. Bremelanotide Acetate can activate MC4R and increases dopamine release. Bremelanotide Acetate induces appetitive sexual behaviors, female mounting behavior, and repetitive self-grooming. Bremelanotide Acetate can be used for the research of hypoactive sexual desire disorders[1][2][3]. Uses: Scientific research. Category: Signaling pathways. Alternative Names: PT-141 Acetate. CAS No. 1607799-13-2. Pack Sizes: 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-18678A. | |
| Bremelanotide Acetate Hydrate | Bremelanotide is a melanocortin receptor agonist shown to improve female sexual function in females suffering from sexual dysfunction. Group: Biochemicals. Grades: Highly Purified. Pack Sizes: 25mg, 100mg. Molecular Formula: C52H74N14O13. US Biological Life Sciences. |  Worldwide |
| Brenetafusp | Brenetafusp is a TCR/anti-CD3 bispecific fusion protein, consisting of a TCR targeting the PRAME peptide and an anti-CD3 scFv effector domain. Brenetafusp redirects CD3+ T cells to kill PRAME+ tumor cells. Brenetafusp can be used in research related to cutaneous melanoma, non-small cell lung cancer, ovarian cancer, endometrial cancer, triple-negative breast cancer, and small cell lung cancer[1]. Uses: Scientific research. Category: Signaling pathways. Alternative Names: IMC-F106C. CAS No. 2736407-54-6. Pack Sizes: 1 mg; 5 mg. Product ID: HY-P990717. | |
| Brenipatide | Brenipatide (LY-3537031) is a dual glucagon-like peptide-1 (GLP-1) and gastric inhibitory polypeptide (GIP) receptor agonist. Brenipatide can be used for the study of metabolic disorders, obesity and diabetes[1]. Uses: Scientific research. Category: Signaling pathways. Alternative Names: LY-3537031. CAS No. 2408921-49-1. Pack Sizes: 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-P11666. | |
| Brensocatib | Brensocatib (AZD7986) is an oral dipeptidyl peptidase 1 (DPP1) inhibitor with pIC50s of 6.85, 7.6, 7.7, 7.8, and 7.8 in human, mouse, rat, dog and rabbit, respectively[1]. Uses: Scientific research. Category: Signaling pathways. Alternative Names: AZD7986; INS 1007. CAS No. 1802148-05-5. Pack Sizes: 10 mM * 1 mL in DMSO; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg; 500 mg; 1 g. Product ID: HY-101056. | |
| Brentuximab | Brentuximab (CAC-10) is a chimeric antibody targeting CD30. Brentuximab is conjugated with Monomethyl auristatin E (MMAE) (HY-15162) to form the antibody-drug conjugate Brentuximab vedotin (HY-P99107A). Brentuximab can be used for the research of cancer, such as lymphoma[1]. Uses: Scientific research. Category: Signaling pathways. Alternative Names: CAC-10. CAS No. 2088770-90-3. Pack Sizes: 1 mg; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-P99151. | |
| Brentuximab vedotin | Brentuximab vedotin is an antibody-drug conjungate (ADC) used for the treatment of relapsed or refractory Hodgkin lymphoma (HL) and systemic anaplastic large cell lymphoma (ALCL). Brentuximab vedotin acts through targeting tumor cells with CD30 antigen expressed in. Uses: The treatment of hodgkin lymphoma and alcl. Alternative Names: SGN-35; previously cAC10-vcMMAE; SGN 35; SGN35. CAS No. 914088-09-8. | |
| Brentuximab vedotin (solution) | Brentuximab vedotin (solution) (cAC10-vcMMAE) is an antibody-drug conjugate (ADC) comprising an anti-CD30 antibody and the cytotoxic agent Monomethyl auristatin E (MMAE). The antibody portion is Brentuximab (HY-P99151), and the drug-linker conjugate for ADC is VcMMAE (HY-15575). Brentuximab vedotin (solution) inhibits CD30-positive cells with an IC50 of 2.5 ng/mL. Brentuximab vedotin (solution) can be used for the research of relapsed and refractory Hodgkin lymphoma[1][2]. Uses: Scientific research. Category: Signaling pathways. CAS No. 914088-09-8. Pack Sizes: 1 mg; 5 mg. Product ID: HY-P99107A. | |
| Brepocitinib | Brepocitinib (PF-06700841) is a potent dual Janus kinase 1 (JAK1) and TYK2 inhibitor with IC50s of 17 nM and 23 nM, respectively. Brepocitinib also inhibits JAK2 and JAK3 with IC50s of 77 nM and 6.49 μM, respectively[1]. Uses: Scientific research. Category: Signaling pathways. Alternative Names: PF-06700841. CAS No. 1883299-62-4. Pack Sizes: 10 mM * 1 mL in DMSO; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg; 250 mg. Product ID: HY-112708. | |
| Brepocitinib P-Tosylate | Brepocitinib (PF-06700841) P-Tosylate is a potent dual Janus kinase 1 (JAK1) and TYK2 inhibitor with IC50s of 17 nM and 23 nM, respectively. Brepocitinib P-Tosylate also inhibits JAK2 and JAK3 with IC50s of 77 nM and 6.49 μM, respectively[1]. Uses: Scientific research. Category: Signaling pathways. Alternative Names: PF-06700841 P-Tosylate. CAS No. 2140301-96-6. Pack Sizes: 10 mM * 1 mL in DMSO; 1 mg; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg; 250 mg. Product ID: HY-112708A. | |
| Brequinar | Brequinar (DUP785) is a potent inhibitor of dihydroorotate dehydrogenase (DHODH) with an IC50 of 5.2 nM for human DHODH. Brequinar has potent activities against a broad spectrum of viruses. Brequinar also has an anti-SARS2 activity. Uses: Scientific research. Category: Signaling pathways. Alternative Names: DUP785; NSC 368390. CAS No. 96187-53-0. Pack Sizes: 10 mM * 1 mL in DMSO; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-108325. | |
| Brequinar sodium | Brequinar sodium is a potent and selective dihydroorotate dehydrogenase (DHODH) inhibitor (IC50 = ~20 nM), which causes the blockade of de novo pyrimidine nucleotide biosynthesis. Uses: Antineoplastic agents. Alternative Names: Dup785; Dup 785; Dup-785; Brequinar Sodium. 6-Fluoro-2-(2'-fluoro[1,1'-biphenyl]-4-yl)-3-methyl-4-quinolinecarboxylic acid sodium; Dup 785. Grades: ≥99% by HPLC. CAS No. 96201-88-6. Molecular formula: C23H14F2NO2Na. Mole weight: 397.35. | |
| Bretazenil | Bretazenil (Ro 16-6028) is a partial agonist at the gamma-aminobutyric acid A (GABAA) receptor-linked benzodiazepine site. Bretazenil is potent benzodiazepine examined, exhibiting an IC50 (concentration at which half-maximal inhibition of specific [35S]TBPS binding occurs) of 6.1 nM. Bretazenil shows an EC50 of 10 nM for recombinant α1β1γ2. Anticonvulsant effects[1][2][3]. Uses: Scientific research. Category: Signaling pathways. Alternative Names: Ro 16-6028. CAS No. 84379-13-5. Pack Sizes: 10 mM * 1 mL in DMSO; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-105056. | |
| Bretazenil | Bretazenil. Group: Biochemicals. Grades: Purified. CAS No. 84379-13-5. Pack Sizes: 10mg. US Biological Life Sciences. | Worldwide |
| Bretisilocin | Bretisilocin (GM-2505) is the agonist for 5-HT2A receptor and a serotonin releaser. Bretisilocin exhibits antidepressant activity and can be used in the study of depression[1][2]. Uses: Scientific research. Category: Signaling pathways. Alternative Names: GM-2505. CAS No. 2698331-35-8. Pack Sizes: 10 mM * 1 mL in DMSO; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-172420. | |
| Bretylium Tosylate | Bretylium tosylate has a biphasic response, initially inducing norepinephrine release followed by sympathetic ganglionic blockade. Bretylium tosylate is a class III antiarrhythmic agent and a competitive inhibitor of acetylcholinesterase. Group: Biochemicals. Alternative Names: 2-Bromo-N-ethyl-N, N-dimethyl Benzene methanaminium 4-Methyl Benzene sulfonate; (o-Bromobenzyl) ethyldimethylammonium p-Toluenesulfonate; (o-Bromobenzyl) ethyldimethylammonium p-Toluenesulfonate; ASL 603; Bretylan; Bretylate; Bretylium p-Toluenesulfonate; Bretylium Tosilate; Bretylol; Darenthin; N-Ethyl-N-(o-bromobenzyl)-N,N-dimethylammonium Tosylate; NSC 62164; Ornid. Grades: Highly Purified. CAS No. 61-75-6. Pack Sizes: 10mg. US Biological Life Sciences. | Worldwide |
| Bretylium Tosylate | Bretylium tosylate is a class III antiarrhythmic agent that also exhibits class II (antiadrenergic) properties, used primarily in emergency settings for the treatment of life-threatening ventricular arrhythmias. It is administered intravenously or intramuscularly and acts by suppressing ventricular fibrillation and ventricular tachycardia. The drug is a quaternary ammonium compound that accumulates in sympathetic ganglia and nerve terminals. Applications: It is indicated for the treatment of ventricular fibrillation and hemodynamically unstable ventricular tachycardia that is unresponsive to other antiarrhythmics, particularly in the setting of acute myocardial infarction. however, its use has declined significantly due to the availability of more effective and safer agents such as amiodarone. it remains available as a second-line agent in advanced cardiac life support protocols. Category: Antiarrhythmic apis. Synonyms: Bretylol; Bretylium tosilate; Darentin; Tosilato de bretilio; Tosilate de bretylium; Bretylii tosilas; ASL-603; Bretilio tosilato. CAS No. 61-75-6. Product ID: API0231559. Molecular formula: C18H24BrNO3S. Mole weight: 414.4. EINECS: 200-516-8. InChIKey: KVWNWTZZBKCOPM-UHFFFAOYSA-M. Appearance: White to off-white crystalline powder. |  |
| Brevetoxin-3 | Brevetoxin-3 (PbTx-3) is a potent allosteric voltage-gated Na+ channel activator and has multiple active centers (A-ring lactone, C-42 of R side chain)[1]. Brevetoxin-3 (PbTx-3) has a high affinity to site 5 of the voltage-sensitive Na+ channels, inhibits the inactivation of Na+ channels and prolongs the mean open time of these channels. Brevetoxin-3 (PbTx-3) repeated exposures can lead to prolonged airway hyperresponsiveness (AHR) and lung inflammation[2]. Uses: Scientific research. Category: Signaling pathways. Alternative Names: PbTx-3. CAS No. 85079-48-7. Pack Sizes: 100 μg. Product ID: HY-12545. | |
| Brevetoxin 6 | Brevetoxin 6 is a polyacyl toxoid produced by Ptychodiscus brevis (Gymnodiniuin bervis). Alternative Names: Brevetoxin PbTx-6. Molecular formula: C50H70O15. Mole weight: 911.08. | |
| Brevetoxin A | Brevetoxin A is a polyacyl toxoid produced by Ptychodiscus brevis (Gymnodiniuin bervis). It has a strong effect of activating cell membrane sodium channels, and Tetrodotoxin can counteract its activity. Uses: Adcs cytotoxin. Alternative Names: Brevetoxin PbTx 1; Ptychodiscus brevis toxin 1. Grades: 98%. CAS No. 98112-41-5. Molecular formula: C49H70O13. Mole weight: 867.06. | |
| Brevetoxin B | Brevetoxin B is a polyacyl toxoid produced by Ptychodiscus brevis (Gymnodiniuin bervis). It has a strong effect of activating cell membrane sodium channels, and Tetrodotoxin can counteract its activity. Alternative Names: PbTx-2. Grades: ≥95%. CAS No. 79580-28-2. Molecular formula: C50H70O14. Mole weight: 895.08. | |
| Brevetoxin PbTx-3 | An activator of voltage-sensitive Na+ channels, a suite of cyclic polyether compounds produced naturally by a species of dinoflagellate known as Karenia brevis. A ciguatoxin comprising a linear sequence of ten trans-fused five-, six-, eight- and nine-membered rings. Alternative Names: Brevetoxin 3; Brevetoxin T17; Dihydrobrevetoxin B; Brevetoxin PbTx 3; GB 3 toxin; T17 toxin; T-17 toxin; PbTx 3; Toxin T-17; Ptychodiscus brevis toxin 3; GB 3; 42-Deoxo-42-hydroxybrevetoxin B; Brevetoxin B, 42-deoxo-42-hydroxy-. Grades: 95 % (HPLC). CAS No. 85079-48-7. Molecular formula: C50H72O14. Mole weight: 897.11. | |
| Brevianamide F | Brevianamide F, belongs to a class of naturally occurring 2,5-diketopiperazines, is produced by the fungi A.fumigates and Aspergillus sp. Alternative Names: Cyclo-L-Trp-L-Pro; L-prolyl-L-tryptophan. Grades: ≥95%. CAS No. 38136-70-8. Molecular formula: C16H17N3O2. Mole weight: 283.33. | |
| brevianamide F prenyltransferase (deoxybrevianamide E-forming) | The enzyme from the fungus Aspergilus sp. MF297-2 is specific for brevianamide F, while the enzyme from Aspergillus versicolor accepts a broad range of trytophan-containing cyclic dipeptides. Involved in the biosynthetic pathways of several indole alkaloids such as paraherquamides and malbrancheamides. Group: Enzymes. Synonyms: NotF; BrePT; brevianamide F reverse prenyltransferase. Enzyme Commission Number: EC 2.5.1.109. 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-2725; brevianamide F prenyltransferase (deoxybrevianamide E-forming); EC 2.5.1.109; NotF; BrePT; brevianamide F reverse prenyltransferase. Cat No: EXWM-2725. |  |
| Brevianamide L | Brevianamide L is an alkaloid metabolite produced by various Streptomyces, Actinomycetes, and Aspergillus strains. CAS No. 1174538-68-1. Molecular formula: C22H23N3O4. Mole weight: 393.44. | |
| Brevicompanine B | Brevicompanine B is a diketopiperazine related metabolite produced by Penicillium and Aspergillus species. Brevicompanine B was found to be active against the malaria parasite Plasmodium falciparum and has been demonstrated to show pronounced plant growth regulatory activity but is devoid of antifungal or antibacterial activity. Group: Biochemicals. Grades: Highly Purified. CAS No. 215121-47-4. Pack Sizes: 1mg. US Biological Life Sciences. | Worldwide |
| Brevicompanine B | A diketopiperazine-related metabolite produced by penicillium brevicompactum and aspergillus species. It has obvious plant growth regulation activity, but is devoid of antifungal or antimicrobial activity. It is active against Plasmodium falciparum. Alternative Names: (3R,5aS,10bR,11aS)-10b-(1,1-dimethyl-2-propen-1-yl)-6,10b,11,11a-tetrahydro-3-(2-methylpropyl)-2H-pyrazino[1',2':1,5]pyrrolo[2,3-b]indole-1,4(3H,5aH)-dione. Grades: >99% by HPLC. CAS No. 215121-47-4. Molecular formula: C22H29N3O2. Mole weight: 367.48. | |
| Brevifolincarboxylic acid | Brevifolincarboxylic acid. Group: Biochemicals. Grades: Plant Grade. CAS No. 18490-95-4. Pack Sizes: 10mg. Molecular Formula: C13H8O8, Molecular Weight: 292.2. US Biological Life Sciences. | Worldwide |
| Brevifolincarboxylic acid | Brevifolincarboxylic acid. Alternative Names: 1,2,3,5-tetrahydro-7,8,9-trihydroxy-3,5-dioxo-cyclopenta[c][2]benzopyran-1-carboxylic acid. CAS No. 18490-95-4. Purity: >95.0%. Product ID: FFC-AR-18490954. Molecular formula: C13H8O8. Mole weight: 292.2. IUPAC Name: 7,8,9-trihydroxy-3,5-dioxo-1,2-dihydrocyclopenta[c]isochromene-1-carboxylic acid. Alfa Chemistry - ISO 9001:32057 Certified. |  |
| Brevifolincarboxylic acid | Brevifolincarboxylic acid is a phenolic compound. Brevifolincarboxylic acid can be isolated from Duchesnea chrysantha. Brevifolincarboxylic acid inhibits α-glucosidase with an IC50 value of 323.46 μM. Brevifolincarboxylic acid has an inhibitory effect on the aryl hydrocarbon receptor (AhR). Brevifolincarbacid scavenges ROS. Brevifolincarbacid restores the glucose uptake activity of myotubes. Brevifolincarboxylic acid has antitumor activity against lung and gastric cancer. Brevifolincarbacid can be used in the study of diabetes and inflammatory diseases[1][2][3][4][5][6]. Uses: Scientific research. Category: Signaling pathways. CAS No. 18490-95-4. Pack Sizes: 1 mg; 5 mg; 10 mg. Product ID: HY-N4095. | |
| Brevilin A | Brevilin A, also called 6-O-Angeloylplenolina, is a natural sesquiterpenoid found in the herbs of Centipeda minima, it exhibits the antigiardial activity (IC50 = 16.1 μM) and is similarly active in vitro against Entamoeba histolytica (IC50 between 4.5 and 9 μM) and against Plasmodium falciparum (IC50 = 9.42 μM). Brevilin A inhibits janus kinase activity and exhibits both strong STAT3 signal inhibition and STAT3 signal dependent cell growth inhibition. Uses: Anti-giardial. Alternative Names: 6-O-Angeloylplenolin. Grades: >91%. CAS No. 16503-32-5. Molecular formula: C20H26O5. Mole weight: 346.4. | |
| Brevilin A | Brevilin A is an orally active STAT3/JAK inhibitor (STAT3 IC50=?10.6 μM). Brevilin A shows anti-tumor activity, anti-proliferative activity to cancer cells, and can induce apoptosis and autophagy[1][2]. Uses: Scientific research. Category: Signaling pathways. CAS No. 16503-32-5. Pack Sizes: 10 mM * 1 mL in DMSO; 1 mg; 5 mg; 10 mg; 25 mg. Product ID: HY-N2959. | |
| Brevinin-1 | The unique antimicrobial peptide named brevinin-1 was isolated from the skin of the frog, Rana brevipoda porsa. The minimum inhibitory concentration of brevinin-1 against the growth of St. aureus and E. coli was determined to be 8 micrograms/ml and 34 micrograms/ml. Alternative Names: Brevinin-1; 145963-49-1; brevinin-1 protein, Rana; Brevinin 1; AMGDYQVEJJSZSQ-IMDMOUBVSA-N; Brevinin-1 (KFHEKHHSHRGY-acid); C121H202N28O26S2; RS-2012; C121-H202-N28-O26-S2. CAS No. 145963-49-1. Molecular formula: C121H202N28O26S2. Mole weight: 2529.2. | |
| Brevinin-1-01 | Brevinin-1-01 was found in Amolops sp. jingdongensis. It has antimicrobial activity. | |
| Brevinin-1-AJ1 antimicrobial peptide precursor | Brevinin-1-AJ1 antimicrobial peptide precursor was found in Amolops jingdongensis. It is against E. coli, B. dysenteriae (MIC=9.38 microg/ml), S. aureus, B. subtilis, and C. albicans. | |
| Brevinin-1-AJ3 antimicrobial peptide precursor | Brevinin-1-AJ3 antimicrobial peptide precursor was found in Amolops sp. jingdongensis. | |
| Brevinin-1AUa | Brevinin-1AUa was found in Rana aurora aurora. Brevinin-1AUa showed potent antimicrobial activity but was strongly hemolytic (HC50 < 10 microM). | |
| Brevinin-1AUb | Brevinin-1AUb was found in Rana aurora aurora. Brevinin-1AUb showed potent antimicrobial activity but was strongly hemolytic (HC50 < 10 microM). Grades:>97% by HPLC. | |
| Brevinin-1AVa | Brevinin-1AVa has antimicrobial activity. Brevinin-1AVb was found in Rana arvalis. | |
| Brevinin-1AVb | Brevinin-1AVb has antimicrobial activity. Brevinin-1AVb was found in Rana arvalis. | |
| Brevinin-1Ba | Brevinin-1Ba was found in Rana berlandieri. It has antibacterial activity against Gram-positive bacterium S.aureus. | |
| Brevinin-1Bb | Brevinin-1Bb was found in Rana berlandieri. It contains one disulfide bond. Brevinin-1Bb has antibacterial activity against Gram-positive bacterium S.aureus and Gram-negative bacterium E.coli. It also has activity against C.albicans. Grades: >98% by HPLC. Molecular formula: C122H196N28O26S3. Mole weight: 2567.22. | |
| Brevinin-1Bc | Brevinin-1Bc was found in Rana berlandieri. It contains one disulfide bond. Brevinin-1Bc has antibacterial activity against Gram-positive bacterium S.aureus. Grades: >95% by HPLC. Molecular formula: C128H200N28O26S2. Mole weight: 2611.25. | |
| Brevinin-1Bd | Brevinin-1Bd was found in Rana berlandieri. It contains one disulfide bond. Brevinin-1Bd has antibacterial activity against Gram-positive bacterium S.aureus and Gram-negative bacterium E.coli. It also has activity against C.albicans. Grades: >97% by HPLC. Molecular formula: C122H196N28O26S2. Mole weight: 2535.16. | |
| Brevinin-1Be | Brevinin-1Be was found in Rana berlandieri. It has antibacterial activity against Gram-positive bacterium S.aureus and Gram-negative bacterium E.coli. | |
| Brevinin-1Bf | Brevinin-1Bf was found in Rana berlandieri. It contains one disulfide bond. Brevinin-1Bf has antibacterial activity against Gram-positive bacterium S.aureus and Gram-negative bacterium E.coli. Molecular formula: C126H194N28O27S3. Mole weight: 2629.25. | |
| Brevinin-1BLa | Brevinin-1BLa is an antimicrobial peptide isolated from Rana blairi. | |
| Brevinin-1BLb | Brevinin-1BLb is an antimicrobial peptide isolated from Rana blairi. | |
| Brevinin-1BLc | Brevinin-1BLc is an antimicrobial peptide isolated from Rana blairi. | |
| Brevinin-1BYb | Brevinin-1BYb is isolated from Rana boylii. Brevinin-1BYb has antibacterial activity against Gram-positive bacterium S.aureus and Gram-negative bacterium E.coli. It also has moderate antifungal activity against C.albicans and strong hemolytic activity. Grades: >97% by HPLC. Molecular formula: C123H206N28O27S2. Mole weight: 2573.24. | |
| Brevinin-1BYc | Brevinin-1BYc is isolated from Rana boylii. Brevinin-1BYc has antibacterial activity against Gram-positive bacterium S.aureus. It has weak antifungal activity against C.albicans. Grades: >97% by HPLC. Molecular formula: C119H205N27O28S2. Mole weight: 2526.19. | |
| Brevinin-1BY precursor | Brevinin-1BY precursor is an antimicrobial peptide isolated from Rana boylii. | |
| Brevinin-1CDYa | Brevinin-1CDYa is isolated from Rana dybowskii. Brevinin-1CDYa has low activity against the Gram-positive bacterium S.aureus (MIC=12.5 μM) and the Gram-negative bacterium E.coli (MIC=25 μM). It has weak hemolytic activity against human erythrocytes. Grades: >98% by HPLC. | |
| Brevinin-1CDYd | Brevinin-1CDYd is an antimicrobial peptide isolated from Rana dybowskii. | |
| Brevinin-1CG1 | Brevinin-1CG1 is an antimicrobial peptide isolated from Amolops chunganensis. It is active against Gram-positive bacteria R.rhodochrous X15 and B.licheniformis X39 and against Gram-negative bacterium E.coli. Brevinin-1CG1 has antifungal activity against a slime mold isolate. It also has weak hemolytic activity against human erythrocytes. Grades: >96% by HPLC. | |
| Brevinin-1CG1 antimicrobial peptide precursor | Brevinin-1CG1 antimicrobial peptide precursor is isolated from Amolops chunganensis. | |
| Brevinin-1CG2 | Brevinin-1CG2 is an antimicrobial peptide isolated from Amolops chunganensis. It is active against a variety of Gram-positive and some Gram-negative bacterial strains. Brevinin-1CG2 has antifungal activity against C.albicans and a slime mold isolate. It also has hemolytic activity against human erythrocytes. | |
| Brevinin-1CG2 antimicrobial peptide precursor | Brevinin-1CG2 antimicrobial peptide precursor is isolated from Amolops chunganensis. | |
| Brevinin-1CG3 | Brevinin-1CG3 is isolated from Amolops chunganensis. Brevinin-1CG3 is primarily active against Gram-positive bacteria. It is also highly active against Gram-negative P. faecalis X29 and S. rubidaea. Grades: >95% by HPLC. | |
| Brevinin-1CG3 antimicrobial peptide precursor | Brevinin-1CG3 antimicrobial peptide precursor is isolated from Amolops chunganensis. | |
| Brevinin-1CG4 | Brevinin-1CG4 is an antimicrobial peptide isolated from Amolops chunganensis. Brevinin-1CG4 is active against a variety of Gram-positive and some Gram-negative bacterial strains. It has antifungal activity against C.albicans and a slime mold isolate. It also has hemolytic activity against human erythrocytes. | |
| Brevinin-1CG5 | Brevinin-1CG5 is an antimicrobial peptide isolated from Amolops chunganensis. It is active against a variety of Gram-positive and Gram-negative bacterial strains. Brevinin-1CG5 has antifungal activity against C.albicans and a slime mold isolate. It also has hemolytic activity against human erythrocytes. | |
| Brevinin-1CG5 antimicrobial peptide precursor | Brevinin-1CG5 antimicrobial peptide precursor has antibacterial and antifungal activity. Brevinin-1CG5 antimicrobial peptide precursor was found in Amolops chunganensis. Grades: >95% by HPLC. | |
| Brevinin-1CHa | Brevinin-1CHa is an antimicrobial peptide isolated from Lithobates chiricahuensis. | |
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