BOC Sciences provides a wide range of research chemicals and biochemicals including inhibitors, building blocks, GMP Products, impurities and metabolites, APIs for Veterinary, Natural Compounds, ADCs, Stem Cell Molecule and chiral compounds.
| Product | Description | |
|---|---|---|
| BZ-PHE-VAL-ARG-AMC | BZ-PHE-VAL-ARG-AMC is a sensitive fluorogenic substrate for the quantitative determination of thrombin. Alternative Names: N-Benzoyl-Phe-Val-Arg 7-amido-4-methylcoumarin; 4-Methyl-7-(Bz-L-Phe-L-Val-L-Arg-amino)coumarin. CAS No. 88899-22-3. Molecular formula: C37H43N7O6. Mole weight: 681.78. |  |
| Bz-Val-Gly-Arg-AMC | Bz-VGR-AMC acts as a substrate for the tricorn core protease from Thermoplasma acidophilum. Alternative Names: benzoyl-Val-Gly-Arg 4-methyl-7-coumarylamide; benzoyl-Val-Gly-Arg-4-methylcoumaryl-7-amide. CAS No. 87779-49-5. Molecular formula: C30H37N7O6. Mole weight: 591.67. | |
| C14orf49 protein (221-232) | C14orf49 protein (221-232) is a peptide derived from C14orf49 protein. C14orf49 protein is a probable anchoring protein which tethers the nucleus to the cytoskeleton by binding PLEC which can associate with the intermediate filament system. Alternative Names: SYNE3 (221-232). | |
| C14TKL-1 | C14TKL-1 is an endogenous human tachykinin-like peptide and a potent NK1 receptor agonist (EC50 = 1 nM). Alternative Names: H-Arg-His-Arg-Thr-Pro-Met-Phe-Tyr-Gly-Leu-Met-NH2; L-arginyl-L-histidyl-L-arginyl-L-threonyl-L-prolyl-L-methionyl-L-phenylalanyl-L-tyrosyl-glycyl-L-leucyl-L-methioninamide; Chromosome 14 tachykinin-like peptide 1; C14TKL1; C14TKL 1. Grades: ≥95%. CAS No. 1423381-12-7. Molecular formula: C63H98N20O13S2. Mole weight: 1407.71. | |
| C14TKL-1 acetate | C14TKL-1 acetate is an endogenous human tachykinin-like peptide and a potent NK1 receptor agonist (EC50 = 1 nM). Alternative Names: H-Arg-His-Arg-Thr-Pro-Met-Phe-Tyr-Gly-Leu-Met-NH2.CH3CO2H; L-arginyl-L-histidyl-L-arginyl-L-threonyl-L-prolyl-L-methionyl-L-phenylalanyl-L-tyrosyl-glycyl-L-leucyl-L-methioninamide acetate; Chromosome 14 tachykinin-like peptide 1 acetate; C14TKL1 acetate; C14TKL 1 acetate. Grades: ≥95%. Molecular formula: C65H102N20O15S2. Mole weight: 1467.75. | |
| C20-OtBu-Glu-OtBu | C20-OtBu-Glu-OtBu. Alternative Names: (S)-2-(19-tert-Butoxycarbonylnonadecanoylamino)pentanedioic acid 1-tert-butyl ester; (S)-5-(tert-Butoxy)-4-(20-(tert-butoxy)-20-oxoicosanamido)-5-oxopentanoic acid. CAS No. 1119061-70-9. Molecular formula: C33H61NO7. Mole weight: 583.85. | |
| C 21 | C 21 is a selective protein arginine methyltransferase 1 (PRMT1) inhibitor (IC50 = 1.8 μM) with 5-fold selectivity for PRMT1 over PRMT6 and >250-fold selectivity over PRMT3 and CARM1. Alternative Names: C21; C-21; N-Acetyl-L-serylglycyl-N5-(2-chloroethanimidoyl)-L-ornithylglycyl-L-lysylglycylglycyl-L-lysylglycyl-L-leucylglycyl-L-lysylglycylglycyl-L-alanyl-L-lysyl-L-arginyl-L-histidyl-L-arginyl-L-lysyl-L-valine. Grades: >98%. CAS No. 1229236-78-5. Molecular formula: C90H161ClN36O24. Mole weight: 2166.92. | |
| C3a 70-77 | C3A (70-77) is an octapeptide corresponding to the COOH terminal of C3A, shows C3a specificity and 1-2% bioactivity. Alternative Names: Complement 3a (70-77); H-Ala-Ser-His-Leu-Gly-Leu-Ala-Arg-OH; L-alanyl-L-seryl-L-histidyl-L-leucyl-glycyl-L-leucyl-L-alanyl-L-arginine; (2S,5S,8S,14S,17S,20S,23S)-17-((1H-imidazol-4-yl)methyl)-23-amino-2-(3-guanidinopropyl)-20-(hydroxymethyl)-8,14-diisobutyl-5-methyl-4,7,10,13,16,19,22-heptaoxo-3,6,9,12,15,18,21-heptaazatetracosan-1-oic acid; C3a octapeptide. Grades: ≥95%. CAS No. 63555-63-5. Molecular formula: C35H61N13O10. Mole weight: 823.94. | |
| C3a 70-77 2TFA | C3A (70-77) is an octapeptide corresponding to the COOH terminal of C3A, shows C3a specificity and 1-2% bioactivity. Alternative Names: Complement 3a (70-77) 2TFA. Molecular formula: C39H63F6N13O14. Mole weight: 1051.98. | |
| C5a Anaphylatoxin (human) | Complement 5a plays, a central role in host defense, is involved in related functions in sepsis, adult respiratory distress syndrome, rheumatoid arthritis, psoriasis, neurodegeneration and ischemia / reperfusion injury. It has powerful chemoattractant and pro-inflammatory properties. Alternative Names: H-Thr-Leu-Gln-Lys-Lys-Ile-Glu-Glu-Ile-Ala-Ala-Lys-Tyr-Lys-His-Ser-Val-Val-Lys-Lys-Cys-Cys-Tyr-Asp-Gly-Ala-Cys-Val-Asn-Asn-Asp-Glu-Thr-Cys-Glu-Gln-Arg-Ala-Ala-Arg-Ile-Ser-Leu-Gly-Pro-Arg-Cys-Ile-Lys-Ala-Phe-Thr-Glu-Cys-Cys-Val-Val-Ala-Ser-Gln-Leu-Arg-Ala-Asn-Ile-Ser-His-Lys-Asp-Met-Gln-Leu-Gly-Arg-OH (Disulfide bridge: Cys21-Cys47, Cys22-Cys54, Cys34-Cys55). Grades: ≥95%. CAS No. 1816940-05-2. Molecular formula: C350H578N108O107S8. Mole weight: 8267.63. | |
| CA 074 | CA 074 is a potent and selective inhibitor of cathepsin B (Ki = 2-5 nM). It reduces bone metastasis in a 4T1.2 breast cancer model. Uses: Cysteine proteinase inhibitors. Alternative Names: CA-074; CA074; CA 074; N-[[(2S,3S)-3-[(Propylamino)carbonyl]-2-oxiranyl]carbonyl]-L-isoleucyl-L-proline. Grades: ≥98% by HPLC. CAS No. 134448-10-5. Molecular formula: C18H29N3O6. Mole weight: 383.44. | |
| cAC 253 acetate | cAC 253 acetate is an antagonist of amylin, inhibiting 125I adrenomedullin binding with an IC50 value of 25 nM. Grades: >98.0%. Molecular formula: C128H206N42O42S2. Mole weight: 3069.39. | |
| CAD-2 | It is a cell penetrating peptide. Grades: >98%. | |
| Cadherin Peptide, avian Acetate | Cadherins are a class of type-1 transmembrane proteins. Molecular formula: C46H79N17O15. Mole weight: 1110.22. | |
| CADY | CADY is a secondary amphiphilic peptide that has been shown to efficiently deliver short nucleic acids, especially siRNA, but cannot deliver any peptides, even short negatively charged peptides. Alternative Names: Ac-Gly-Leu-Trp-Arg-Ala-Leu-Trp-Arg-Leu-Leu-Arg-Ser-Leu-Trp-Arg-Leu-Leu-Trp-Arg-Ala-cysteamide. Grades: >98%. Molecular formula: C132H205N41O26S. Mole weight: 2814.41. | |
| Caenacin-1 | Caenacin-1 was found in Caenorhabditis elegans. It has antifungal activity. | |
| Caenacin-5 | Caenacin-5 was found in Caenorhabditis elegans. It has antifungal activity. | |
| Caerin 11 | Caerin 11 was found in Litoria peronii. It has antibacterial activity. | |
| Caerin-1.1 | Caerin-1.1 was found in Litoria gilleni. Caerin-1.1 is an antibacterial and antiviral peptide that adopts an alpha helical conformation which can disrupt bacterial membranes. Each caerin displays a different antimicrobial specificity. | |
| Caerin-1.10 | Caerin-1.10 was found in Litoria rothii. Caerin-1.10 is an antibacterial peptide with wide spectrum of activity. | |
| Caerin 1.11 | Caerin 1.11 was produced by Litoria eucnemis. Caerin 1.11 is a cationic amphipathic alpha-helical antimicrobial peptide with weak or no activity against both Gram-positive and Gram-negative bacteria. It is weakly active against E.coli (MIC=25 μM), E.cloacae (MIC=50 μM), K.pneumoniae (MIC=25 μM), and S.haemolyticus (MIC=50 μM). | |
| Caerin 1.12 | Caerin 1.12 is originally isolated from Litoria caerulea. It has antibacterial activity. | |
| Caerin-1.1.2 | Caerin-1.1.2 has antibacterial activity. The source of Caerin-1.1.2 is Litoria caerulea. Grades: >97% by HPLC. Molecular formula: C107H178N30O26. Mole weight: 2300.74. | |
| Caerin 1.13 | Caerin 1.13 is originally isolated from Litoria caerulea. It has antibacterial activity. | |
| Caerin 1.14 | Caerin 1.14 is originally isolated from Litoria caerulea. It has antibacterial activity. | |
| Caerin 1.15 | Caerin 1.15 is originally isolated from Litoria caerulea. It has antibacterial activity. | |
| Caerin-1.17 | Caerin-1.17 was found in Litoria gracilenta. Caerin-1.17 shows significant activity against Gram-positive organisms, but is less effective against Gram-negative organisms. Grades: >95% by HPLC. Molecular formula: C124H206N32O29. Mole weight: 2609.15. | |
| Caerin-1.18 | Caerin-1.18 was found in Litoria gracilenta. It shows significant activity against Gram-positive organisms, but is less effective against Gram-negative organisms. Grades: >96% by HPLC. | |
| Caerin-1.19 | Caerin-1.19 was found in Litoria gracilenta. Caerin-1.19 shows significant activity against Gram-positive organisms, but is less effective against Gram-negative organisms. | |
| Caerin-1.2 | Caerin 1.2 was found in Litoria caerula. Caerin 1.2 is an antibacterial peptide that adopts an alpha helical conformation which can disrupt bacterial membranes. Each caerin displays a different antimicrobial specificity. | |
| Caerin 1.20 | Caerin 1.20 has antibacterial activity. The source of Caerin 1.20 is the skin secretions, hybrid between female Litoria splendida and male Litoria caerulea, Australia. Grades: >98% by HPLC. Molecular formula: C124H201N33O28. Mole weight: 2602.12. | |
| Caerin 1.3 | Caerin 1.3 was found in Litoria caerula. Caerin 1.3 is an antibacterial peptide that adopts an alpha helical conformation which can disrupt bacterial membranes. Each caerin displays a different antimicrobial specificity. | |
| Caerin-1.4 | Caerin-1.4 was found in Litoria gilleni. Caerin-1.4 is an antibacterial and antiviral peptide that adopts an alpha helical conformation which can disrupt bacterial membranes. Each caerin displays a different antimicrobial specificity. | |
| Caerin 1.5 | Caerin 1.5 was found in Litoria caerula. Caerin 1.5 is an antibacterial peptide that adopts an alpha helical conformation which can disrupt bacterial membranes. Each caerin displays a different antimicrobial specificity. | |
| Caerin-1.6 | Caerin 1.6 was found in Litoria chloris. Caerin 1.6 is an antimicrobial peptide that adopts an alpha helical conformation which can disrupt bacterial membranes. | |
| Caerin-1.7 | Caerin 1.7 was found in Litoria chloris. Caerin 1.7 is an antimicrobial peptide that adopts an alpha helical conformation which can disrupt bacterial membranes. | |
| Caerin-1.8 | Caerin 1.8 was found in Litoria chloris. Caerin 1.8 is an antimicrobial peptide that adopts an alpha helical conformation which can disrupt bacterial membranes. | |
| Caerin 1.9 | Caerin 1.9 was found in Litoria chloris. Caerin 1.9 is an antimicrobial peptide that adopts an alpha helical conformation which can disrupt bacterial membranes. Alternative Names: Caerin 1.9; NH2-Gly-Leu-Phe-Gly-Val-Leu-Gly-Ser-Ile-Ala-Lys-His-Val-Leu-Pro-His-Val-Val-Pro-Val-Ile-Ala-Glu-Lys-Leu-NH2. Molecular formula: C124H206N32O28. Mole weight: 2593.2. | |
| Caerin 21 | Caerin 21 was found in Litoria peronii. It has antibacterial activity. | |
| Caerin-2.1 | Caerin 2.1 was found in Litoria splendida. Caerin 2.1 is an antimicrobial peptide that adopts an alpha helical conformation which can disrupt bacterial membranes. Each caerin displays a different antimicrobial specificity. | |
| Caerin-2.2 | Caerin 2.2 was found in Litoria gilleni. Caerin 2.2 is an antimicrobial peptide that adopts an alpha helical conformation which can disrupt bacterial membranes. Each caerin displays a different antimicrobial specificity. | |
| Caerin-2.4 | Caerin 2.4 was found in Litoria caerula. Caerin 2.4 is an antibacterial peptide that adopts an alpha helical conformation which can disrupt bacterial membranes. Each caerin displays a different antimicrobial specificity. | |
| Caerin-2.5 | Caerin 2.5 was found in Litoria gilleni. Caerin 2.5 is an antimicrobial peptide that adopts an alpha helical conformation which can disrupt bacterial membranes. Each caerin displays a different antimicrobial specificity. | |
| Caerin 2.6 | Caerin 2.6 was isolated from Hybrid between female Litoria splendida and male Litoria caerulea. It has antibacterial activity. | |
| Caerin 2.7 | Caerin 2.7 was isolated from Hybrid between female Litoria splendida and male Litoria caerulea. It has antibacterial activity. | |
| Caerin-3.2 | Caerin 3.2 was found in Litoria caerula. Caerin 3.2 is an antibacterial peptide that adopts an alpha helical conformation which can disrupt bacterial membranes. Each caerin displays a different antimicrobial specificity. | |
| Caerin-3.3 | Caerin 3.3 was found in Litoria caerula. Caerin 3.3 is an antibacterial peptide that adopts an alpha helical conformation which can disrupt bacterial membranes. Each caerin displays a different antimicrobial specificity. | |
| Caerin-3.4 | Caerin 3.4 was found in Litoria caerula. Caerin 3.4 is an antibacterial peptide that adopts an alpha helical conformation which can disrupt bacterial membranes. Each caerin displays a different antimicrobial specificity. | |
| Caerin-3.5 | Caerin-3.5 was found in Litoria gracilenta. It shows significant activity against Gram-positive organisms, but is less effective against Gram-negative organisms. | |
| Caerin-4.1 | Caerin 4.1 was found in Litoria caerula. Caerin 4.1 is an antibacterial peptide that adopts an alpha helical conformation which can disrupt bacterial membranes. Each caerin displays a different antimicrobial specificity. Grades: >97% by HPLC. Molecular formula: C104H175N29O31. Mole weight: 2327.67. | |
| Caerin-4.2 | Caerin 4.2 was found in Litoria caerula. Caerin 4.2 is an antibacterial peptide that adopts an alpha helical conformation which can disrupt bacterial membranes. Each caerin displays a different antimicrobial specificity. | |
| Caerin-4.3 | Caerin 4.3 was found in Litoria caerula. Caerin 4.3 is an antibacterial peptide that adopts an alpha helical conformation which can disrupt bacterial membranes. Each caerin displays a different antimicrobial specificity. | |
| Caerulein, desulfated | Caerulein, desulfated is the desulfurated form of Caerulein. Caerulein, a CCK agonist, could be used in paralytic ileus and diagnostic aid in pancreatic malfunction. Alternative Names: 4-Desulfocaerulein; H-Pyr-Gln-Asp-Tyr-Thr-Gly-Trp-Met-Asp-Phe-NH2; L-pyroglutamyl-L-glutaminyl-L-alpha-aspartyl-L-tyrosyl-L-threonyl-glycyl-L-tryptophyl-L-methionyl-L-alpha-aspartyl-L-phenylalaninamide; Pyr-QDYTGWMDF-NH2. Grades: >97% by HPLC. CAS No. 20994-83-6. Molecular formula: C58H73N13O18S. Mole weight: 1272.34. | |
| Caerulein precursor-related fragment Ea | The source of Caerulein precursor-related fragment Ea is Rana esculenta. This peptide has no sequence similarity with antimicrobial peptides isolated from other species of ranid frogs. It potently and selectively inhibits the growth of the Gram-positive bacterium Escherichia coli (minimal inhibitory concentration (MIC<5 microM)). Alternative Names: CPRF-Ea. | |
| Caerulein precursor-related fragment Eb | The source of Caerulein precursor-related fragment Eb is Rana esculenta. This peptide has no sequence similarity with antimicrobial peptides isolated from other species of ranid frogs. It potently and selectively inhibits the growth of the Gram-positive bacterium Escherichia coli (minimal inhibitory concentration (MIC<5 microM)). Alternative Names: CPRF-Eb. | |
| Caerulein precursor-related fragment Ec | The source of Caerulein precursor-related fragment Ec is Rana esculenta. This peptide has no sequence similarity with antimicrobial peptides isolated from other species of ranid frogs. It potently and selectively inhibits the growth of the Gram-positive bacterium Escherichia coli (minimal inhibitory concentration (MIC<5 microM)). Alternative Names: CPRF-Ec. | |
| Caffeic-PH | Caffeic-PH is a derivative of caffeic acid that combines with the dipeptide Pro-His. This compound has been reported to exhibit significant antioxidant properties, including free radical scavenging and lipid peroxidation inhibition activity. It is considered to be a powerful antioxidant in both hydrophilic and lipophilic systems, likely due to the structure of proline that enables histidine to effectively donate electrons. The addition of short peptides like Pro-His to caffeic acid is believed to synergistically enhance its antioxidative activity. This enhanced antioxidant activity contributes to the skin-tightening effect by protecting the skin from oxidative stress, which can lead to skin laxity and wrinkles. Therefore, CA-PH can be used as a potent dermal therapeutic agent and a useful cosmetic ingredient for skin tightening and anti-aging purposes. Alternative Names: Caffeic acid-Pro-His-NH2; CA-proline-histidine amide; CA-Pro-His-NH2; Caffeoyl-prolyl-histidine amide; 1-[3-(3,4-Dihydroxyphenyl)-1-oxo-2-propen-1-yl]-L-prolyl-L-histidinamide; Coumaroyl(3-OH)-Pro-His-NH2; N-(3-Hydroxycoumaroyl)-L-prolyl-L-histidinamide; (S)-N-((S)-1-Amino-3-(1H-imidazol-4-yl)-1-oxopropan-2-yl)-1-(3-(3,4-dihydroxyphenyl)acryloyl)pyrrolidine-2-carboxamide; CA-PH. Grades: ≥95%. CAS No. 1240406-70-5. Molecular formula: C20H23N5O5. Mole weight: 413.43. | |
| Calcineurin Autoinhibitory Peptide | Calcineurin Autoinhibitory Peptide has been found to be a cell-permeable calcineurin inhibitor and could be probably used as an immunosuppressant. Grades: >98%. CAS No. 148067-21-4. Molecular formula: C124H205N39O39S2. Mole weight: 2930.34. | |
| Calcineurin substrate | Calcineurin substrate is a peptide from the regulatory RII subunit of cAMP-dependent protein kinase. Alternative Names: H-Asp-Leu-Asp-Val-Pro-Ile-Pro-Gly-Arg-Phe-Asp-Arg-Arg-Val-Ser-Val-Ala-Ala-Glu-OH; L-alpha-aspartyl-L-leucyl-L-alpha-aspartyl-L-valyl-L-prolyl-L-isoleucyl-L-prolyl-glycyl-L-arginyl-L-phenylalanyl-L-alpha-aspartyl-L-arginyl-L-arginyl-L-valyl-L-seryl-L-valyl-L-alanyl-L-alanyl-L-glutamic acid. Grades: 98%. CAS No. 113873-67-9. Molecular formula: C92H150N28O29. Mole weight: 2112.35. | |
| Calcineurin substrate acetate | Calcineurin substrate acetate is a peptide from the regulatory RII subunit of cAMP-dependent protein kinase. Alternative Names: H-Asp-Leu-Asp-Val-Pro-Ile-Pro-Gly-Arg-Phe-Asp-Arg-Arg-Val-Ser-Val-Ala-Ala-Glu-OH.CH3CO2H; L-α-Aspartyl-L-leucyl-L-α-aspartyl-L-valyl-L-prolyl-L-isoleucyl-L-prolylglycyl-L-arginyl-L-phenylalanyl-L-α-aspartyl-L-arginyl-L-arginyl-L-valyl-L-seryl-L-valyl-L-alanyl-L-alanyl-L-glutamic acid acetate. Grades: ≥95%. Molecular formula: C94H154N28O31. Mole weight: 2172.40. | |
| Calcitermin | Calcitermin is isolated from Homo sapiens. Calcitermin possesses antifungal activity against C.albicans and is also active against E.coli and P.aeruginosa but not L.monocytogenes and S.aureus. | |
| Calcitonin (20-32), salmon | Calcitonin salmon is a synthetic peptide used to treat osteoporosis and other bone conditions. Alternative Names: Gln-Thr-Tyr-Pro-Arg-Thr-Asn-Thr-Gly-Ser-Gly-Thr-Pro-NH2. Molecular formula: C57H91N19O21. Mole weight: 1378.53. | |
| Calcitonin (8-32), salmon | Calcitonin (8-32), salmon is an amylin receptor antagonist with highly selectivity. Alternative Names: H-Val-Leu-Gly-Lys-Leu-Ser-Gln-Glu-Leu-His-Lys-Leu-Gln-Thr-Tyr-Pro-Arg-Thr-Asn-Thr-Gly-Ser-Gly-Thr-Pro-NH2; L-valyl-L-leucyl-glycyl-L-lysyl-L-leucyl-L-seryl-L-glutaminyl-L-alpha-glutamyl-L-leucyl-L-histidyl-L-lysyl-L-leucyl-L-glutaminyl-L-threonyl-L-tyrosyl-L-prolyl-L-arginyl-L-threonyl-L-asparagyl-L-threonyl-glycyl-L-seryl-glycyl-L-threonyl-L-prolinamide; 8-32-Calcitonin (salmon reduced); Calcitonin (salmon reduced), 1-de-L-cysteine-2-de-L-serine-3-de-L-asparagine-4-de-L-leucine-5-de-L-serine-6-de-L-threonine-7-de-L-cysteine-; Salmon calcitonin (8-32). Grades: ≥95%. CAS No. 155069-90-2. Molecular formula: C119H198N36O37. Mole weight: 2725.06. | |
| Calcitonin eel | Calcitonin eel is a peptide hormone produced by the parafollicular C cells of the thyroid or by the ultimobranchial bodies of nonmammalian vertebrates. Alternative Names: Eel calcitonin; Calcitonin (eel); Calcitonin, Eel; Cys-Ser-Asn-Leu-Ser-Thr-Cys-Val-Leu-Gly-Lys-Leu-Ser-Gln-Glu-Leu-His-Lys-Leu-Gln-Thr-Tyr-Pro-Arg-Thr-Asp-Val-Gly-Ala-Gly-Thr-Pro-NH2 [Disulfide bridge: 1-7]; Thyrocalcitonin Eel; L-Cysteinyl-L-seryl-L-asparaginyl-L-leucyl-L-seryl-L-threonyl-L-cysteinyl-L-valyl-L-leucylglycyl-L-lysyl-L-leucyl-L-seryl-L-glutaminyl-L-α-glutamyl-L-leucyl-L-histidyl-L-lysyl-L-leucyl-L-glutaminyl-L-threonyl-L-tyrosyl-L-prolyl-L-arginyl-L-threonyl-L-α-aspartyl-L-valylglycyl-L-alanylglycyl-L-threonyl-L-prolinamide cyclic (1→7)-disulfide; Eel thyrocalcitonin; HC 58; 26-L-Aspartic acid-27-L-valine-29-L-alanine-calcitonin (salmon). Grades: 98%. CAS No. 57014-02-5. Molecular formula: C146H241N43O47S2. Mole weight: 3414.86. | |
| Calcitonin, eel TFA | It is a peptide hormone produced by the parafollicular C cells of the thyroid or by the ultimobranchial bodies of nonmammalian vertebrates. It is used to regulate calcium homeostasis. Alternative Names: Thyrocalcitonin eel (TFA); Cys-Ser-Asn-Leu-Ser-Thr-Cys-Val-Leu-Gly-Lys-Leu-Ser-Gln-Glu-Leu-His-Lys-Leu-Gln-Thr-Tyr-Pro-Arg-Thr-Asp-Val-Gly-Ala-Gly-Thr-Pro-NH2.TFA (Disulfide bridge: Cys1-Cys7); L-cysteinyl-L-seryl-L-asparagyl-L-leucyl-L-seryl-L-threonyl-L-cysteinyl-L-valyl-L-leucyl-glycyl-L-lysyl-L-leucyl-L-seryl-L-glutaminyl-L-alpha-glutamyl-L-leucyl-L-histidyl-L-lysyl-L-leucyl-L-glutaminyl-L-threonyl-L-tyrosyl-L-prolyl-L-arginyl-L-threonyl-L-alpha-aspartyl-L-valyl-glycyl-L-alanyl-glycyl-L-threonyl-L-prolinamide (1->7)-disulfide; Eel Thyrocalcitonin TFA. Grades: >98%. Molecular formula: C146H241N43O47S2.C2HF3O2. Mole weight: 3528.89. | |
| Calcitonin gene-related peptide | Calcitonin gene-related peptide is a member of the calcitonin family of peptides consisting of calcitonin, amylin, adrenomedullin, adrenomedullin 2 (intermedin) and calcitonin - receptor - stimulating peptide. Alternative Names: Calcitonin, pro-; CALCA protein, human; CALC1 protein, human; CGRP1 protein, human. CAS No. 83652-28-2. Molecular formula: C163H266N50O50S2. Mole weight: 3790.28. | |
| Calcitonin gene-related peptide 1 (16-25) | Calcitonin gene-related peptide 1 (16-25) is a peptide derived from Calcitonin gene-related peptide 1. Calcitonin gene-related peptide 1 dilates a variety of vessels including the coronary, cerebral and systemic vasculature. It also elevates platelet cAMP. Alternative Names: Alpha-type CGRP (16-25). | |
| Calcitonin Gene Related Peptide (CGRP) (83-119), rat TFA | α-CGRP (rat) TFA, a member of the calcitonin neuropeptide family, contains 37 amino acids and is an endogenous neuropeptide with vasodilation, cardiovascular, pro-inflammatory and metabolic effects. Alternative Names: Ser-Cys-Asn-Thr-Ala-Thr-Cys-Val-Thr-His-Arg-Leu-Ala-Gly-Leu-Leu-Ser-Arg-Ser-Gly-Gly-Val-Val-Lys-Asp-Asn-Phe-Val-Pro-Thr-Asn-Val-Gly-Ser-Glu-Ala-Phe-NH2.TFA (Disulfide bridge: Cys2-Cys7); CGRP-1 (rat) TFA; L-seryl-L-cysteinyl-L-asparagyl-L-threonyl-L-alanyl-L-threonyl-L-cysteinyl-L-valyl-L-threonyl-L-histidyl-L-arginyl-L-leucyl-L-alanyl-glycyl-L-leucyl-L-leucyl-L-seryl-L-arginyl-L-seryl-glycyl-glycyl-L-valyl-L-valyl-L-lysyl-L-alpha-aspartyl-L-asparagyl-L-phenylalanyl-L-valyl-L-prolyl-L-threonyl-L-asparagyl-L-valyl-glycyl-L-seryl-L-alpha-glutamyl-L-alanyl-L-phenylalaninamide (2->7)-disulfide trifluoroacetic acid; α-CGRP (rat) TFA. Grades: >98%. Molecular formula: C162H262N50O52S2.C2HF3O2. Mole weight: 3920.32. | |
| Calcitonin N-Terminal Flanking Peptide (human) | Calcitonin N-Terminal Flanking Peptide (human) is a synthetic N-procalcitonin (N-PCT) that stimulates the proliferation of normal and tumor human osteoblasts at nanomolar concentrations. Intracerebroventricular administration of N-PCT significantly reduces food intake and body weight gain for at least 48h in conscious, freely moving and unstressed rats fed ad libitum. Alternative Names: N-PCT (human); H-Ala-Pro-Phe-Arg-Ser-Ala-Leu-Glu-Ser-Ser-Pro-Ala-Asp-Pro-Ala-Thr-Leu-Ser-Glu-Asp-Glu-Ala-Arg-Leu-Leu-Leu-Ala-Ala-Leu-Val-Gln-Asp-Tyr-Val-Gln-Met-Lys-Ala-Ser-Glu-Leu-Glu-Gln-Glu-Gln-Glu-Arg-Glu-Gly-Ser-Ser-Leu-Asp-Ser-Pro-Arg-Ser-OH. Grades: 95%. CAS No. 118277-01-3. Molecular formula: C264H426N74O97S. Mole weight: 6220.79. | |
| Calcitonin (rat) | Calcitonin, a peptide hormone involved in calcium and bone metabolism, is effective in treating hypercalcemia caused by bone metastasis, multiple myeloma and osteitis malformation, and is also effective against osteoporosis. Alternative Names: H-Cys-Gly-Asn-Leu-Ser-Thr-Cys-Met-Leu-Gly-Thr-Tyr-Thr-Gln-Asp-Leu-Asn-Lys-Phe-His-Thr-Phe-Pro-Gln-Thr-Ser-Ile-Gly-Val-Gly-Ala-Pro-NH2 (Disulfide bridge: Cys1-Cys7); L-cysteinyl-glycyl-L-asparagyl-L-leucyl-L-seryl-L-threonyl-L-cysteinyl-L-methionyl-L-leucyl-glycyl-L-threonyl-L-tyrosyl-L-threonyl-L-glutaminyl-L-alpha-aspartyl-L-leucyl-L-asparagyl-L-lysyl-L-phenylalanyl-L-histidyl-L-threonyl-L-phenylalanyl-L-prolyl-L-glutaminyl-L-threonyl-L-seryl-L-isoleucyl-glycyl-L-valyl-glycyl-L-alanyl-L-prolinamide (1->7)-disulfide. Grades: ≥95%. CAS No. 11118-25-5. Molecular formula: C148H228N40O46S3. Mole weight: 3399.83. | |
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