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| Product | Description | |
|---|---|---|
| Suberoyl Chloride | Suberoyl Chloride. Alternative Names: Octanedioic acid dichloride, Suberic acid dichloride. CAS No. 10027-07-3. Molecular formula: ClCO(CH2)6COCl. Mole weight: 211.09. IUPAC Name: octanedioyl dichloride. SMILES: ClC(=O)CCCCCCC(Cl)=O. InChI: 1S/C8H12Cl2O2/c9-7(11)5-3-1-2-4-6-8(10)12/h1-6H2. |  |
| Suberylglycine | Suberylglycine is an acyl glycine, which is a normally minor metabolite of fatty acid. Uses: Scientific research. Category: Signaling pathways. CAS No. 60317-54-6. Pack Sizes: 10 mM * 1 mL in DMSO; 5 mg; 10 mg; 25 mg; 50 mg. Product ID: HY-113367. |  |
| Sublimated Salicylic Acid | A white to slightly pink crystalline powder or block, obtained by sublimation. It is odorless with a sweetish then pungent taste. Grades: Pharmaceutical grade. Product ID: PAP-0139. |  |
| Sublimed Fullerenes | Sublimed Fullerenes. | |
| Sublobaric acid | Sublobaric acid is isolated from the lichen Anzia hypoleucoides. Alternative Names: 8-Hydroxy-3-methoxy-11-oxo-1-(1-oxopropyl)-6-pentyl-11H-dibenzo[b,e][1,4]dioxepin-7-carboxylic acid; 11H-Dibenzo[b,e][1,4]dioxepin-7-carboxylic acid, 8-hydroxy-3-methoxy-11-oxo-1-(1-oxopropyl)-6-pentyl-. CAS No. 197009-25-9. Molecular formula: C23H24O8. Mole weight: 428.43. |  |
| Submandibular mucin | Submandibular mucin is a high molecular weight glycoprotein that is used as a substrate for the viral enzyme neuraminidase[1]. Uses: Scientific research. Category: Signaling pathways. CAS No. 84195-52-8. Pack Sizes: 50 mg; 100 mg; 500 mg. Product ID: HY-P3008. | |
| Submerochlorophaeic acid | Submerochlorophaeic acid is a substance from the Cladonia chlorophaea. CAS No. 103538-07-4. Molecular formula: C22H26O8. Mole weight: 418.44. | |
| Subpaludosic acid | Subpaludosic acid. CAS No. 103538-08-5. Molecular formula: C21H24O8. Mole weight: 404.41. | |
| SubPC | SubPC. Alternative Names: BORON SUBPHTHALOCYANINE CHLORIDE;Boron subphthalocyanine chloride Dye content ~85 %. CAS No. 36530-06-0. Molecular formula: C24H12BClN6. Mole weight: 430.7g/mol. IUPAC Name: 12-chloro-2,11,13,22,30,31-hexaza-12-boraoctacyclo[21.6.1.110,14.03,11.04,9.013,21.015,20.024,29]hentriaconta-1,3,5,7,9,14(31),15,17,19,21,23(30),24,26,28-tetradecaene. SMILES: B1(N2C3=C4C=CC=CC4=C2N=C5N1C(=NC6=NC(=N3)C7=CC=CC=C76)C8=CC=CC=C85)Cl. InChI: InChI=1S/C24H12BClN6/c26-25-31-21-15-9-3-5-11-17(15)23(31)30-24-18-12-6-4-10-16(18)22(32(24)25)29-20-14-8-2-1-7-13(14)19(27-20)28-21/h1-12H. | |
| Subpeptin JM4-A | Subpeptin JM4-A is an antibacterial peptide produced by Bacillus subtil is JM4. It has an antibacterial activity against Gram-positive and Gram-negative bacteria including Salmonella, B.cereus, B.megaterium, L.casei, L.viridescens, M.flavus, C.glutamicum, C.crenatum, L.mesenteroides, E.faecalis, S.flexneri, S.aureus and B.thuringiensis. Grades: >85% (SDS-PAGE). | |
| Subpeptin JM4-B | Subpeptin JM4-B is an antibacterial peptide produced by Bacillus subtil is JM4. It has an antibacterial activity against Gram-positive and Gram-negative bacteria including Salmonella, B.cereus, B.megaterium, L.casei, L.viridescens, M.flavus, C.glutamicum, C.crenatum, L.mesenteroides, E.faecalis, S.flexneri, S.aureus and B.thuringiensis. Grades: >85% (SDS-PAGE). | |
| Subsekikaic acid | Subsekikaic acid. Alternative Names: Benzoic acid, 2-hydroxy-3-[(2-hydroxy-4-methoxy-6-methylbenzoyl)oxy]-4-methoxy-6-propyl-. CAS No. 132396-94-2. Molecular formula: C20H22O8. Mole weight: 390.38. | |
| Subsphaeric acid | Subsphaeric acid is a depside from dimelaena lichens. CAS No. 120091-90-9. Molecular formula: C21H24O7. Mole weight: 388.41. | |
| Substance P | Substance P, a neuropeptide, is a sensory neuropeptide and inflammatory mediator. The endogenous receptor for substance P is neurokinin 1 receptor (NK1-receptor,NK1R). Alternative Names: Substance P Acetate. CAS No. 33507-63-0. Molecular formula: C63H98N18O13S. Mole weight: 1347.63. | |
| Substance P | Substance P (Neurokinin P) is a CNS-penetrant neuropeptide, acting as a neurotransmitter and as a neuromodulator in the CNS. The endogenous receptor for substance P is neurokinin 1 receptor (NK1-receptor, NK1R). Uses: Scientific research. Category: Signaling pathways. Alternative Names: Neurokinin P. CAS No. 33507-63-0. Pack Sizes: 1 mg; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-P0201. | |
| Substance P (1-7) | Substance P (1-7) is a fragment of Substance P (SP), and Substance P (SP) is an endogenous tachykinin neuropeptide. Alternative Names: Substance P Fragment 1-7. Grades: ≥97% by HPLC. CAS No. 68060-49-1. Molecular formula: C41H65N13O10. Mole weight: 900.04. | |
| Substance P (1-7) 2TFA | Substance P (1-7) 2TFA is the main bioactive metabolite formed after the proteolytic degradation of tachykinin substance P (SP), which has anti-inflammatory, anti-nociceptive, and anti-hyperalgesic effects. Alternative Names: H-Arg-Pro-Lys-Pro-Gln-Gln-Phe-OH.2TFA; L-arginyl-L-prolyl-L-lysyl-L-prolyl-L-glutaminyl-L-glutaminyl-L-phenylalanine trifluoroacetic acid; 1-7-Substance P, 2,2,2-trifluoroacetate (1:2). Grades: ≥95%. Molecular formula: C41H65N13O10.2C2HF3O2. Mole weight: 1128.08. | |
| Substance P (1-7) (TFA) | Substance P (1-7) (TFA) is a fragment of the neuropeptide, substance P (SP). Substance P is a small peptide produced by macrophages, lymphocytes, eosinophils, dendritic cells and nerves. Substance P (1-7)(TFA) gives depressor and bradycardic effects when applied to the nucleus tractus solitarius. Alternative Names: Substance P (1-7) Trifluoroacetate; H-Arg-Pro-Lys-Pro-Gln-Gln-Phe-OH.TFA; L-arginyl-L-prolyl-L-lysyl-L-prolyl-L-glutaminyl-L-glutaminyl-L-phenylalanine trifluoroacetic acid; 1-7-Substance P, 2,2,2-trifluoroacetate (1:1); Substance P (1-7) TFA. Grades: ≥95%. CAS No. 2828433-22-1. Molecular formula: C43H66F3N13O12. Mole weight: 1014.06. | |
| Substance P(1-7) TFA | Substance P(1-7) TFA is a fragment of the neuropeptide, substance P (SP). Substance P(1-7) TFA gives depressor and bradycardic effects when applied to the nucleus tractus solitarius[1]. Uses: Scientific research. Category: Signaling pathways. CAS No. 2828433-22-1. Pack Sizes: 5 mg; 10 mg; 25 mg. Product ID: HY-P1485A. | |
| Substance P (1-9) | Substance P (1-9) is nonapeptide, which decreases the inactivation of substance P by the guinea-pig ileum and urinary bladder. Uses: Scientific research. Category: Signaling pathways. CAS No. 57468-17-4. Pack Sizes: 5 mg; 10 mg. Product ID: HY-P1494. | |
| Substance P (1-9) | Substance P(1-9) is a fragment of Subtance P, which decreases the inactivation of substance P by the guinea-pig ileum and urinary bladder. Alternative Names: H-ARG-PRO-LYS-PRO-GLN-GLN-PHE-PHE-GLY-OH; ARG-PRO-LYS-PRO-GLN-GLN-PHE-PHE-GLY; substance P fragment 1-9. CAS No. 57468-17-4. Molecular formula: C52H77N15O12. Mole weight: 1104.26. | |
| Substance P (5-11) | Substance P (5-11) is a peptide fragment derived from Substance P is a neuropeptide involved in pain transmission and inflammatory responses. Substance P (5-11) is primarily used in biomedical research to study the effects and interactions of Substance P in various diseases, including pain disorders, inflammation and neurodegenerative conditions. Alternative Names: Hepta-Substance P; H-Gln-Gln-Phe-Phe-Gly-Leu-Met-NH2; L-glutaminyl-L-glutaminyl-L-phenylalanyl-L-phenylalanyl-glycyl-L-leucyl-L-methioninamide; 1-Dearginyl-2,4-deprolyl-3-delysine-substance P; 1-Des-arg-2,4-des-pro-3-des-lys-substance P; Substance P, 1-de-L-arginine-2-de-L-proline-3-de-L-lysine-4-de-L-proline-. Grades: ≥95% by HPLC. CAS No. 51165-09-4. Molecular formula: C41H60N10O9S. Mole weight: 869.04. | |
| Substance P (7-11) | Substance P fragment. Increases PGE2 and collagenase production. Involved in pain signal transmission. Anti-inflammatory and immunomodulatory agent. Active in vitro and in vivo. Alternative Names: H-Phe-Phe-Gly-Leu-Met-NH2; SP(7-11); Phe1-Phe2-Gly3-Leu4-Met5-NH2. Grades: >95%. CAS No. 51165-05-0. Molecular formula: C31H44N6O5S. Mole weight: 612.78. | |
| Substance P (9-11) | Substance P (9-11). Group: Biochemicals. Alternative Names: H-Gly-Leu-Met-NH2·HCl. Grades: Highly Purified. CAS No. 40297-96-9. Pack Sizes: 50mg, 100mg, 250mg. US Biological Life Sciences. |  Worldwide |
| Substance P, Free Acid | Substance P, free acid is a natural analogue of substance P, but does not exhibit the biological activity of substance P. Alternative Names: Arg-Pro-Lys-Pro-Gln-Gln-Phe-Phe-Gly-Leu-Met; [Met-OH11]-Substance P; Substance P, 11-L-methionine-; L-arginyl-L-prolyl-L-lysyl-L-prolyl-L-glutaminyl-L-glutaminyl-L-phenylalanyl-L-phenylalanyl-glycyl-L-leucyl-L-methionine. Grades: ≥95%. CAS No. 71977-09-8. Molecular formula: C63H97N17O14S. Mole weight: 1348.61. | |
| Substance P-methyl ester | Substance P-methyl ester. Group: Biochemicals. Grades: Reagent Grade. Pack Sizes: 1mg, 5mg, 25mg. US Biological Life Sciences. | Worldwide |
| subtilisin | Subtilisin is a serine endopeptidase, type example of peptidase family S8. It contains no cysteine residues (although these are found in homologous enzymes). Species variants include subtilisin BPN' (also subtilisin B, subtilopeptidase B, subtilopeptidase C, Nagarse, Nagarse proteinase, subtilisin Novo, bacterial proteinase Novo) and subtilisin Carlsberg (subtilisin A, subtilopeptidase A, alcalase Novo). Similar enzymes are produced by various Bacillus subtilis strains and other Bacillus species. Group: Enzymes. Synonyms: alcalase; alcala. Enzyme Commission Number: EC 3.4.21.62. CAS No. 9014-1-1. Protease. 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-4153; subtilisin; EC 3.4.21.62; 9014-01-1; alcalase; alcalase 0.6L; alcalase 2.5L; ALK-enzyme; bacillopeptidase A; bacillopeptidase B; Bacillus subtilis alkaline proteinase bioprase; bioprase AL 15; bioprase APL 30; colistinase; (see also comments); subtilisin J; subtilisin S41; subtilisin Sendai; subtilisin GX; subtilisin E; subtilisin BL; genenase I; esperase; maxatase; alcalase; thermoase PC 10; protease XXVII; thermoase; superase; subtilisin DY; subtilopeptidase; SP 266; savinase 8.0L; savinase 4.0T; kazusase; protease VIII; opticlean; Bacillus subtilis alkaline proteinase; protin A 3L; savinase; savinase 16.0L; savinase 32.0 L EX. |  |
| Subtilisin | Subtilisin (EC 3.4.21.14) is a bacterial serine protease. Subtilisin induces Apoptosis. Subtilisin stimulates the expression of pro-allergic cytokines (IL-1α, IL-33). Subtilisin induces prototypic allergic lung inflammation. Subtilisin exhibits anticancer activity against breast and colon cancer. Subtilisin shows antifouling activity. Subtilisin can be used as a detergent additive[1][2][3][4][5][6]. Uses: Scientific research. Category: Signaling pathways. Alternative Names: EC 3.4.21.14. CAS No. 9014-1-1. Pack Sizes: 50 mg; 100 mg; 200 mg; 500 mg. Product ID: HY-P2729. | |
| Subtilomycin | Subtilomycin is a lantibiotic peptide isolated from Bacillus subtil is MMA7. It has activity against gram-positive bacteria, gram-negative bacteria and fungi. Alternative Names: Thr-Trp-Ala-Thr-Ile-Gly-Lys-Thr-Ile-Val-Gln-Ser-Val-Lys-Lys-Cys-Arg-Thr-Phe-Thr-Cys-Gly-Cys-Ser-Leu-Gly-Ser-Cys-Ser-Asn-Cys-Asn. Mole weight: 3235. | |
| Subtilosin A | Subtilosin A is an antibiotic peptide produced by Bacillus subtilis 168. Alternative Names: SboA protein, Bacillus subtilis; Subtilosin protein, Bacillus amyloliquefaciens; H-Gly-Leu-Gly-Leu-Trp-Gly-Asn-Lys-Gly-Cys-Ala-Thr-Cys-Ser-Ile-Gly-Ala-Ala-Cys-Leu-Val-Asp-Gly-Pro-Ile-Pro-Asp-Gly-Ile-Ala-Gly-Ala-Gly-OH. CAS No. 98914-01-3. Molecular formula: C129H208N36O41S3. Mole weight: 3015.5. | |
| Subtilosin A1 | Subtilosin A1 is an antibacterial peptide isolated from Bacillus subtilis. It has activity against gram-positive bacteria. Alternative Names: Asn-Lys-Gly-Cys-Ala-Thr-Cys-Ser-Thr-Gly-Ala-Ala-Cys-Leu-Val-Asp-Gly-Pro-Ile-Pro-Asp-Phe-Glu-Ile-Ala-Gly-Ala-Thr-Gly-Leu-Phe-Gly-Leu-Trp-Gly. | |
| Suc-AAPF-AMC | Suc-AAPF-AMC is an α-chymotrypsin fluorogenic substrate for the quantitative determination of chymotrypsin activity[1]. Uses: Scientific research. Category: Peptides. Alternative Names: Suc-Ala-Ala-Pro-Phe-AMC. CAS No. 88467-45-2. Pack Sizes: 10 mM * 1 mL in DMSO; 5 mg; 10 mg; 25 mg. Product ID: HY-137811. | |
| Suc-AAPF-pNA | Suc-AAPF-pNA (Suc-Ala-Ala-Pro-Phe-pNA) is a chromogenic p-nitroanilide (pNA) substrate with the Km of 1.7 mM. Cleavage of Suc-AAPF-pNA releases 4-nitroaniline, which is yellow in colour and can be measured spectrophotometrically. Suc-AAPF-pNA can be used for the measurement of free and membrane-bound cathepsin G in human neutrophils[1][2][3]. Uses: Scientific research. Category: Peptides. Alternative Names: Suc-Ala-Ala-Pro-Phe-pNA. CAS No. 70967-97-4. Pack Sizes: 5 mg; 10 mg; 25 mg; 100 mg. Product ID: HY-P2573. | |
| Suc-Ala-Ala-Ala-Ala-Ala-pNA | Suc-Ala-Ala-Ala-Ala-Ala-pNA. Alternative Names: 3-Carboxypropionyl-L-alanyl-L-alanyl-L-alanyl-L-alanyl-L-alanine-p-nitroanilide; N-(3-Carboxy-1-oxopropyl)-L-alanyl-L-alanyl-L-alanyl-L-alanyl-N-(4-nitrophenyl)-L-alaninamide; Suc Ala Ala Ala Ala Ala pNA. Grades: 95%. CAS No. 61043-68-3. Molecular formula: C25H35N7O10. Mole weight: 593.59. | |
| Suc-Ala-Ala-Ala-Ala-Ala-pNA | Suc-Ala-Ala-Ala-Ala-Ala-pNA. Group: Biochemicals. Grades: Reagent Grade. Pack Sizes: 5mg, 25mg, 100mg. US Biological Life Sciences. | Worldwide |
| SUC-ALA-ALA-ALA-AMC | A sensitive fluorogenic substrate for pancreatic elastase. Alternative Names: Suc-Ala-Ala-Ala-7-Amino-4-Methylcoumarin; succinyl-Ala-Ala-Ala-4-methylcoumaryl-7-amide; 4-((S)-1-((S)-1-((S)-1-(4-methyl-2-oxo-2H-chromen-7-ylamino)-1-oxopropan-2-ylamino)-1-oxopropan-2-ylamino)-1-oxopropan-2-ylamino)-4-oxobutanoic acid. CAS No. 73617-90-0. Molecular formula: C23H28N4O8. Mole weight: 488.49. | |
| Suc-Ala-Ala-Ala-pNA | Substrate for Elastase. Alternative Names: Succinyl-L-alanine-L-alanine-L-alanine 4-nitroanilide; Succinyl-Trialanine-4-Nitroanilide; Suc Ala Ala Ala pNA. Grades: ≥ 99% (TLC). CAS No. 52299-14-6. Molecular formula: C19H25N5O8. Mole weight: 451.44. | |
| Suc-Ala-Ala-Ala-pNA | N-Succinyl-Ala-Ala-Ala-p-nitroanilide is a chromogenic substrate for chymotrypsin-like serine protease, pancreatic elastase and serine endopeptidase. Group: Biochemicals. Alternative Names: N-Succinyl-L-alanyl-L-alanyl-L-alanine 4-nitroanilide; N-Succinyl-tri-L-alanine 4-nitroanilide. Grades: Highly Purified. CAS No. 52299-14-6. Pack Sizes: 25mg, 50mg, 100mg. Molecular Formula: C19H25N5O8, Molecular Weight: 451.43. US Biological Life Sciences. | Worldwide |
| Suc-Ala-Ala-Ala-pNA 99+% (TLC) | Suc-Ala-Ala-Ala-pNA 99+% (TLC). Group: Biochemicals. Grades: Reagent Grade. Pack Sizes: 100mg. US Biological Life Sciences. | Worldwide |
| Suc-Ala-Ala-pNA | Suc-Ala-Ala-pNA. Alternative Names: Succinyl-L-alanyl-L-alanine p-nitroanilide; Succinyl-alanyl-alanine-4-nitroanilide. CAS No. 61043-66-1. Molecular formula: C16H20N4O7. Mole weight: 380.36. | |
| Suc-Ala-Ala-Pro-Abu-pNA | Suc-Ala-Ala-Pro-Abu-pNA is a colorimetric substrate for pancreatic elastase. Alternative Names: Elastase Substrate IV, Colorimetric; Suc-AAP-Abu-pNA; N-(3-Carboxypropanoyl)-L-alanyl-L-alanyl-N-{(2S)-1-[(4-nitrophenyl)amino]-1-oxo-2-butanyl}-L-prolinamide. Grades: ≥95%. CAS No. 108392-27-4. Molecular formula: C25H34N6O9. Mole weight: 562.57. | |
| Suc-Ala-Ala-Pro-Ala-pNA | An excellent substrate for porcine pancreatic elastase. Alternative Names: 4-((S)-1-((S)-1-((S)-2-((S)-1-(4-Nitrophenylamino)-1-Oxopropan-2-Ylcarbamoyl)Pyrrolidin-1-Yl)-1-Oxopropan-2-Ylamino)-1-Oxopropan-2-Ylamino)-4-Oxobutanoic Acid; Suc Ala Ala Pro Ala pNA. Grades: 95%. CAS No. 72682-69-0. Molecular formula: C24H32N6O9. Mole weight: 548.55. | |
| Suc-Ala-Ala-Pro-Ala-pNA | Suc-Ala-Ala-Pro-Ala-pNA. Group: Biochemicals. Grades: Reagent Grade. Pack Sizes: 100mg. US Biological Life Sciences. | Worldwide |
| Suc-Ala-Ala-Pro-Arg-pNA | Suc-Ala-Ala-Pro-Arg-pNA. Group: Biochemicals. Grades: Reagent Grade. Pack Sizes: 25mg, 50mg, 100mg. US Biological Life Sciences. | Worldwide |
| Suc-Ala-Ala-Pro-Arg-pNA | Suc-Ala-Ala-Pro-Arg-pNA. Alternative Names: 4-((S)-1-((S)-1-((S)-2-((S)-5-Guanidino-1-(4-Nitrophenylamino)-1-Oxopentan-2-Ylcarbamoyl)Pyrrolidin-1-Yl)-1-Oxopropan-2-Ylamino)-1-Oxopropan-2-Ylamino)-4-Oxobutanoic Acid; Suc Ala Ala Pro Arg pNA. Grades: 95%. CAS No. 131068-47-8. Molecular formula: C27H39N9O9. Mole weight: 633.66. | |
| SUC-ALA-ALA-PRO-GLU-PNA | SUC-ALA-ALA-PRO-GLU-PNA. Alternative Names: Suc-AAPE-pNA; N-(3-Carboxy-1-oxopropyl)-L-alanyl-L-alanyl-L-prolyl-N-(4-nitrophenyl)-L-α-glutamine. Grades: 95%. CAS No. 108929-37-9. Molecular formula: C26H34N6O11. Mole weight: 606.58. | |
| Suc-Ala-Ala-Pro-Lys-pNA | Suc-Ala-Ala-Pro-Lys-pNA. Alternative Names: 4-((S)-1-((S)-1-((S)-2-((S)-6-amino-1-(4-nitrophenylamino)-1-oxohexan-2-ylcarbamoyl)pyrrolidin-1-yl)-1-oxopropan-2-ylamino)-1-oxopropan-2-ylamino)-4-oxobutanoic acid; Suc-AAPK-pNA. Grades: >99%. CAS No. 108929-39-1. Molecular formula: C27H39N7O9. Mole weight: 605.64. | |
| Suc-Ala-Ala-Pro-Met-pNA | Suc-Ala-Ala-Pro-Met-pNA is a sensitive substrate for human pancreatic elastase. Alternative Names: succinyl-Ala-Ala-Pro-Met-p-nitroanilide. CAS No. 72682-73-6. Molecular formula: C26H36N6O9S. Mole weight: 608.66. | |
| Suc-Ala-Ala-Pro-Phe-AMC | Fluorogenic substrate for chymotrypsin. Alternative Names: Suc Ala Ala Pro Phe AMC. Grades: ≥ 99% (HPLC). CAS No. 88467-45-2. Molecular formula: C34H39N5O9. Mole weight: 661.71. | |
| SUC-ALA-ALA-PRO-PHE-PNA | SUC-ALA-ALA-PRO-PHE-PNA. Alternative Names: CATHEPSIN G SUBSTRATE I, COLORIMETRIC; SUCCINYL-L-ALANYL-L-ALANYL-L-PROLYL-L-PHENYLALANINE-4-NITROANILIDE; SUCCINYL-ALA-ALA-PRO-PHE-P-NITROANILIDE; SUC-ALA-ALA-PRO-PHE-PARANITROANILIDE; SUC-ALA-ALA-PRO-PHE-PNA; SUC-AAPF-PNA; N-SUCCINYL-L-ALANYL-L-ALANYL-L-PROL. CAS No. 70967-97-4. Molecular formula: C30H36N6O9. Mole weight: 624.64. | |
| Suc-Ala-Ala-Pro-Phe-SBzl | Carboxypeptidase B is a very sensitive substrate for rat mast cell proteases and chymotrypsin. Alternative Names: Carboxypeptidase B; Protaminase; N-Suc-Ala-Ala-Pro-Phe-SBzl; N-succinyl-Ala-Ala-Pro-Phe-thiobenzyl ester. Grades: 95%. CAS No. 80651-95-2. Molecular formula: C31H38N4O7S. Mole weight: 610.73. | |
| SUC-ALA-ALA-PRO-VAL-AMC | SUC-ALA-ALA-PRO-VAL-AMC is a substrate for human neutrophil elastase. Alternative Names: N-(3-Carboxypropionyl)-L-Ala-L-Ala-L-Pro-L-Val-(4-methyl-2-oxo-2H-1-benzopyran-6-yl)NH2. Grades: 95%. CAS No. 113277-37-5. Molecular formula: C30H39N5O9. Mole weight: 613.66. | |
| Suc-Ala-Glu-Pro-Phe-pNA | Suc-AEPF-pNA can be used as a chromogenic substrate for the peptidylprolyl isomerase Pin1. Alternative Names: Suc-AEPF-pNA. Grades: ≥ 99%. CAS No. 128802-76-6. Molecular formula: C32H38N6O11. Mole weight: 682.69. | |
| Suc-Ala-Glu-Pro-Phe-pNA | Suc-Ala-Glu-Pro-Phe-pNA. Group: Biochemicals. Grades: Reagent Grade. Pack Sizes: 25mg, 50mg, 250mg. US Biological Life Sciences. | Worldwide |
| Suc-Ala-Leu-Pro-Phe-pNA | Suc-Ala-Leu-Pro-Phe-pNA (Suc-ALPF-pNA) is a synthetic polypeptide substrate that targets FK506-binding protein (FKBP). Suc-Ala-Leu-Pro-Phe-pNA can be used to determine peptidyl-prolyl cis-trans isomerase activity via the chymotrypsin-coupled assay. Suc-Ala-Leu-Pro-Phe-pNA serves as a substrate for human FK506-binding protein hFKBP-12 in the chymotrypsin-FKBP coupled PPIase assay. Suc-Ala-Leu-Pro-Phe-pNA is applicable for the detection and research of PPIase activity[1][2]. Uses: Scientific research. Category: Signaling pathways. Alternative Names: Suc-ALPF-pNA. CAS No. 128802-78-8. Pack Sizes: 5 mg; 10 mg. Product ID: HY-P4581. | |
| Suc-Ala-Leu-Pro-Phe-pNA | Suc-Ala-Leu-Pro-Phe-pNA is a substrate for FK-506 binding proteins and cyclophilins, which belong to the group of peptidyl prolyl cis-trans isomerases (PPIases). Alternative Names: Suc-ALPF-PNA; succinyl-Ala-Leu-Pro-Phe-p-nitroanilide; N-succinyl Ala-Leu-Pro-Phe p-nitroanilide; N-Succinyl-L-alanyl-L-Leucyl-L-prolyl-L-phenylalanine 4-nitroanilide. CAS No. 128802-78-8. Molecular formula: C33H42N6O9. Mole weight: 666.72. | |
| Suc-Ala-Phe-Lys-AMC | Suc-Ala-Phe-Lys-AMC is a highly sensitive fluorogenic substrate for plasmin, and is used for determination of gingipain K. Alternative Names: Suc-AFK-AMC; N-(3-Carboxy-1-oxopropyl)-L-alanyl-L-phenylalanyl-N-(4-methyl-2-oxo-2H-1-benzopyran-7-yl)-L-lysinamide; N-Succinyl-Ala-Phe-Lys-MCA; L-Lysinamide, N-(3-carboxy-1-oxopropyl)-L-alanyl-L-phenylalanyl-N-(4-methyl-2-oxo-2H-1-benzopyran-7-yl)-; 4-(((S)-1-(((S)-1-(((S)-6-amino-1-((4-methyl-2-oxo-2H-chromen-7-yl)amino)-1-oxohexan-2-yl)amino)-1-oxo-3-phenylpropan-2-yl)amino)-1-oxopropan-2-yl)amino)-4-oxobutanoic acid. Grades: 95%. CAS No. 73207-91-7. Molecular formula: C32H39N5O8. Mole weight: 621.69. | |
| Suc-Ala-Phe-Pro-Phe-pNA | Suc-Ala-Phe-Pro-Phe-pNA is a substrate for FK-506 binding proteins and cyclophilins, which belong to the group of peptidyl prolyl cis-trans isomerases (PPIases). Alternative Names: Suc-apppa; Succinimidyl-alanyl-phenylalanyl-prolyl-phenylalanine 4-nitroanilide. Grades: >99%. CAS No. 128802-73-3. Molecular formula: C36H40N6O9. Mole weight: 700.75. | |
| Suc-Ala-Pro-Ala-AMC | A sensitive substrate for human neutrophil elastase. Alternative Names: succinyl-Ala-Pro-Ala-MCA; 4-((S)-1-((S)-2-((S)-1-(4-methyl-2-oxo-2H-chromen-7-ylamino)-1-oxopropan-2-ylcarbamoyl)pyrrolidin-1-yl)-1-oxopropan-2-ylamino)-4-oxobutanoic acid. CAS No. 88467-44-1. Molecular formula: C25H30N4O8. Mole weight: 514.53. | |
| Suc-Ala-Pro-Ala-pNA | Suc-Ala-Pro-Ala-pNA is a synthetic peptide substrate that inhibits serine proteases. Suc-Ala-Pro-Ala-pNA has been used in biochemical assays to detect the presence of protease activity. Alternative Names: L-Alaninamide, N-(3-carboxy-1-oxopropyl)-L-alanyl-L-prolyl-N-(4-nitrophenyl)-; Succinyl-Ala-Pro-Ala-p-nitroanilide; Suc-Ala-Pro-Ala-pNA. CAS No. 72682-79-2. Molecular formula: C21H27N5O8. Mole weight: 477.47. | |
| Suc-Ala-Pro-pNA | Suc-Ala-Pro-pNA is a peptide that serves as a substrate to detect the activity and stability of prolyl endopeptidase (PEP)[1]. Uses: Scientific research. Category: Signaling pathways. CAS No. 95632-46-5. Pack Sizes: 5 mg; 10 mg. Product ID: HY-P4490. | |
| Suc-Ala-Pro-pNA | Suc-Ala-Pro-pNA is the chromogenic substrate for prolyl endopeptidase. Alternative Names: Suc-AP-pNA; succinyl-alanyl-proline-p-nitro-anilide; L-Prolinamide, N-(3-carboxy-1-oxopropyl)-L-alanyl-N-(4-nitrophenyl)-; N-(3-Carboxypropanoyl)-L-alanyl-N-(4-nitrophenyl)-L-prolinamide; 4-(((S)-1-((S)-2-((4-nitrophenyl)carbamoyl)pyrrolidin-1-yl)-1-oxopropan-2-yl)amino)-4-oxobutanoic acid. Grades: ≥95%. CAS No. 95632-46-5. Molecular formula: C18H22N4O7. Mole weight: 406.39. | |
| succimimidyl-4-azidobutyrate | Succimimidyl-4-azidobutyrate is a superior biopharmaceutical formulation that can facilitate breakthrough drug development and research efforts. As a chemically mediated linker, it accelerates the synthesis of targeted drugs, ultimately resulting in good precision in drug delivery and modulated drug release. Alternative Names: Azidobutyric acid NHS ester;Azidobutyric Acid NHS Ester; (2,5-dioxopyrrolidin-1-yl) 4-azidobutanoate. Grades: ≥98%. CAS No. 943858-70-6. Molecular formula: C8H10N4O4. Mole weight: 226.19. | |
| Succinaldehydic acid | Succinaldehydic acid is a catabolite of GABA. Uses: Scientific research. Category: Signaling pathways. CAS No. 692-29-5. Pack Sizes: 1 mg; 2.5 mg. Product ID: HY-104071. | |
| SUCCINALDEHYDIC ACID | SUCCINALDEHYDIC ACID. Alternative Names: SUCCINALDEHYDIC ACID; SUCCINIC SEMIALDEHYDE; BETA-FORMYLPROPIONIC ACID; 4-OXO-BUTANOIC ACID; 4-OXOBUTYRIC ACID; 3-formylpropanoicacid; 3-formylpropionicacid; 4-oxo-butanoicaci. CAS No. 692-29-5. Molecular formula: C4H6O3. Mole weight: 102.09. | |
| Succinamic acid | Succinamic acid (CAS# 638-32-4) is a useful research chemical. Alternative Names: 4-amino-4-oxobutanoic acid. CAS No. 638-32-4. Molecular formula: C4H7NO3. Mole weight: 117.10. | |
| Succinamide | Succinamide (CAS# 110-14-5 ) is a useful research chemical. Alternative Names: butanediamide. Grades: 95 %. CAS No. 110-14-5. Molecular formula: C4H8N2O2. Mole weight: 116.12. | |
| succinate-CoA ligase (ADP-forming) | This enzyme belongs to the family of ligases, specifically those forming carbon-sulfur bonds as acid-thiol ligases. This enzyme participates in 4 metabolic pathways: Citric acid cycle, propanoate metabolism, c5-branched dibasic acid metabolism, and reductive carboxylate cycle (CO2 fixation). Group: Enzymes. Synonyms: succinyl-CoA synthetase (ADP-forming); succinic thiokinase; succinate thiokinase; succinyl-CoA synthetase; succinyl coenzyme A synthetase (adenosine diphosphate-forming); succinyl coenzyme A synthetase; A-STK (adenin nucleotide-linked succinate thiokinase); STK; A-SCS. Enzyme Commission Number: EC 6.2.1.5. CAS No. 9080-33-5. A-SCS. 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-5707; succinate-CoA ligase (ADP-forming); EC 6.2.1.5; 9080-33-5; succinyl-CoA synthetase (ADP-forming); succinic thiokinase; succinate thiokinase; succinyl-CoA synthetase; succinyl coenzyme A synthetase (adenosine diphosphate-forming); succinyl coenzyme A synthetase; A-STK (adenin nucleotide-linked succinate thiokinase); STK; A-SCS. Cat No: EXWM-5707. | |
| succinate-CoA ligase (GDP-forming) | Itaconate can act instead of succinate, and ITP instead of GTP. Group: Enzymes. Synonyms: succinyl-CoA synthetase (GDP-forming); succinyl coenzyme A synthetase (guanosine diphosphate-forming); succinate thiokinase; succinic thiokinase; succinyl coenzyme A synthetase; succinate-phosphorylating enzyme; P-enzyme; SCS; G-STK; succinyl coenzyme A synthetase (GDP-forming); succinyl CoA synthetase; succinyl coenzyme A synthetase. Enzyme Commission Number: EC 6.2.1.4. CAS No. 9014-36-2. 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-5698; succinate-CoA ligase (GDP-forming); EC 6.2.1.4; 9014-36-2; succinyl-CoA synthetase (GDP-forming); succinyl coenzyme A synthetase (guanosine diphosphate-forming); succinate thiokinase; succinic thiokinase; succinyl coenzyme A synthetase; succinate-phosphorylating enzyme; P-enzyme; SCS; G-STK; succinyl coenzyme A synthetase (GDP-forming); succinyl CoA synthetase; succinyl coenzyme A synthetase. Cat No: EXWM-5698. | |
| succinate dehydrogenase | A flavoprotein (FAD) complex containing iron-sulfur centres. The enzyme is found in the inner mitochondrial membrane in eukaryotes and the plasma membrane of many aerobic or facultative bacteria and archaea. It catalyses succinate oxidation in the citric acid cycle and transfers the electrons to quinones in the membrane, thus constituting a part of the aerobic respiratory chain (known as complex II). In vivo the enzyme uses the quinone found in the organism - eukaryotic enzymes utilize ubiquinone, bacterial enzymes utilize ubiquinone or menaquinone, and archaebacterial enzymes from the Sulfolobus genus use caldariellaquinone. cf. EC 1.3.5.4, fumarate reductase (quinone). Group: Enzymes. Synonyms: succinate dehydrogenase (quinone); succinate dehydrogenase (ubiquinone); succinic dehydrogenase; complex II (ambiguous); succinate dehydrogenase complex; SDH; succinate:ubiquinone oxidoreductase. Enzyme Commission Number: EC 1.3.5.1. CAS No. 9028-11-9. 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-1385; succinate dehydrogenase; EC 1.3.5.1; 9028-11-9; succinate dehydrogenase (quinone); succinate dehydrogenase (ubiquinone); succinic dehydrogenase; complex II (ambiguous); succinate dehydrogenase complex; SDH; succinate:ubiquinone oxidoreductase. Cat No: EXWM-1385. | |
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