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 | |
|---|---|---|
| Cbz-Ser(tBu)-Ser(tBu)-OH | Cbz-Ser(tBu)-Ser(tBu)-OH is a protected dipeptide used in peptide synthesis. The Cbz (Carbobenzyloxy) group serves as a protective group for the N-terminus of the first serine residue, preventing unwanted reactions during the synthesis process. Each Ser (Serine) residue is protected at its hydroxyl side chain by a tBu (tert-butyl) group, ensuring that these reactive groups remain unaltered until selective deprotection is required. The -OH at the C-terminus indicates a free carboxyl group, allowing for further coupling reactions in the peptide chain. This compound is used to incorporate serine residues into peptides, with specific protections to facilitate precise and controlled synthesis. Synonyms: N-(N-((Benzyloxy)carbonyl)-O-(tert-butyl)-L-seryl)-O-(tert-butyl)-L-serine; N-Benzoxycarbonyl-O-tert-butyl-L-seryl-O-tert-butyl-L-serine; SS; Cbz-Ser(OtBu)-Ser(OtBu)-OH; Z-Ser(tBu)-Ser(tBu)-OH. Grade: ≥95%. CAS No. 119439-59-7. Molecular formula: C22H34N2O7. Mole weight: 438.51. |  |
| Cbz-Thr(OtBu)-Phe-Thr(OtBu)-OMe | Cbz-Thr(OtBu)-Phe-Thr(OtBu)-OMe is a protected tripeptide used in peptide synthesis. The Cbz (Carbobenzyloxy) group protects the N-terminus of the threonine (Thr) residue, preventing it from participating in unwanted reactions. The hydroxyl groups on both threonine residues are protected by OtBu (tert-butyl) groups, ensuring these functional groups remain unreactive until selective deprotection is required. Phe (Phenylalanine), positioned in the middle, adds aromatic and hydrophobic properties to the peptide. The OMe (methyl ester) at the C-terminus indicates that the carboxyl group of the final threonine is esterified, which can facilitate further reactions or modifications. This compound is used to incorporate threonine and phenylalanine into peptides, with controlled reactivity through selective protection, enabling precise and efficient peptide synthesis. Synonyms: TFT; Cbz-Thr(tBu)-Phe-Thr(tBu)-OMe; Z-Thr(OtBu)-Phe-Thr(OtBu)-OMe; Methyl N-N-((benzyloxy)carbonyl)-O-(tert-butyl)-L-threonyl-L-phenylalanyl-O-(tert-butyl)-L-threoninate. Grade: ≥95%. Molecular formula: C34H49N3O8. Mole weight: 627.78. | |
| Cbz-Thr-Phe-Thr(tBu)-OMe | Cbz-Thr-Phe-Thr(tBu)-OMe is a protected tripeptide used in peptide synthesis. The Cbz (Carbobenzyloxy) group protects the N-terminus of the first threonine (Thr) residue, preventing it from participating in unwanted reactions during the synthesis process. The side chain of the second threonine residue is protected by a tBu (tert-butyl) group, shielding the hydroxyl group from reactivity until selective deprotection is needed. Phe (Phenylalanine), the middle amino acid, contributes aromatic and hydrophobic properties to the peptide sequence. The OMe (methyl ester) at the C-terminus indicates that the carboxyl group of the second threonine is esterified, which is useful for controlling the reactivity and allowing further modifications or elongation of the peptide chain. This compound is employed to introduce threonine and phenylalanine into peptides, with specific protections to ensure selective and controlled synthesis. Synonyms: TFT; Methyl N-((benzyloxy)carbonyl)-L-threonyl-L-phenylalanyl-O-(tert-butyl)-L-threoninate; Z-Thr-Phe-Thr(tBu)-OMe. Grade: ≥95%. Molecular formula: C30H41N3O8. Mole weight: 571.67. | |
| Cbz-Thr(tBu)-Phe-OH | Cbz-Thr(tBu)-Phe-OH is a protected dipeptide used in peptide synthesis. The Cbz (Carbobenzyloxy) group protects the N-terminus of the threonine residue, preventing reactions at this site during synthesis. The Thr (Threonine) residue is further protected at its hydroxyl side chain by a tBu (tert-butyl) group, ensuring the hydroxyl group remains unreactive until deprotection is desired. Phe (Phenylalanine) is the second amino acid, contributing aromatic character to the peptide. The -OH at the C-terminus signifies a free carboxyl group, which can participate in peptide bond formation. This compound is used to introduce threonine and phenylalanine into peptides with specific protective measures for controlled and selective synthesis. Synonyms: N-((Benzyloxy)carbonyl)-O-(tert-butyl)-L-threonyl-L-phenylalanine; Z-Thr(tBu)-Phe-OH; N-Benzoxycarbonyl-O3-tert-butyl-L-threonyl-L-phenylalanine; TF; L-Phenylalanine, N-[O-(1,1-dimethylethyl)-N-[(phenylmethoxy)carbonyl]-L-threonyl]-. Grade: ≥95%. CAS No. 47732-07-0. Molecular formula: C25H32N2O6. Mole weight: 456.54. | |
| Cbz-Thr(tBu)-Phe-Thr(tBu)-OH | Cbz-Thr(tBu)-Phe-Thr(tBu)-OH is a protected tripeptide used in peptide synthesis. The Cbz (Carbobenzyloxy) group protects the N-terminus of the threonine (Thr) residue, preventing it from reacting during synthesis. Both threonine residues have their side chain hydroxyl groups protected by tBu (tert-butyl) groups, which shield these groups from unwanted reactions until deprotection is desired. Phe (Phenylalanine), the central amino acid in the sequence, adds aromatic and hydrophobic properties to the peptide. The -OH at the C-terminus indicates a free carboxyl group, allowing for further peptide coupling. This compound is used to incorporate threonine and phenylalanine into peptides while maintaining control over the functional groups' reactivity through selective protection. Synonyms: TFT; N-N-((Benzyloxy)carbonyl)-O-(tert-butyl)-L-threonyl-L-phenylalanyl-O-(tert-butyl)-L-threonine; Z-Thr(tBu)-Phe-Thr(tBu)-OH; Cbz-Thr(OtBu)-Phe-Thr(OtBu)-OH. Grade: ≥95%. Molecular formula: C33H47N3O8. Mole weight: 613.75. | |
| Cbz-Tyr(OtBu)-Ser(OtBu)-OMe | Cbz-Tyr(OtBu)-Ser(OtBu)-OMe is a protected dipeptide used in peptide synthesis. The Cbz (Carbobenzyloxy) group protects the N-terminus of the tyrosine (Tyr) residue, preventing it from reacting during synthesis. The hydroxyl group of tyrosine is protected by an OtBu (tert-butyl) group, ensuring it remains unreactive until deprotection is necessary. The Ser (Serine) residue is similarly protected at its hydroxyl group by an OtBu group. The OMe (methyl ester) at the C-terminus indicates that the carboxyl group of the serine is esterified, facilitating further peptide coupling or modification. This compound is used to introduce tyrosine and serine into peptides while controlling the reactivity of their functional groups. Synonyms: Z-Tyr(OtBu)-Ser(OtBu)-OMe; Methyl N-((S)-2-(((benzyloxy)carbonyl)amino)-3-(4-(tert-butoxy)phenyl)propanoyl)-O-(tert-butyl)-L-serinate; YS. Grade: ≥95%. Molecular formula: C29H40N2O7. Mole weight: 528.65. | |
| C(Cbz)-acetic acid | C(Cbz)-acetic acid. Synonyms: 2-Oxo-4-[(benzyloxycarbonyl)amino]pyrimidine-1(2H)-acetic acid. CAS No. 144564-95-4. Molecular formula: C14H13N3O5. Mole weight: 303.27. | |
| Cc-CATH2 | Cc-CATH2 is isolated from Coturnix coturnix. Cc-CATH2 showed considerable reduction of cytotoxic activity compared to other avian cathelicidins, with average IC(50) values of 20.18μm. | |
| Cc-CATH3 | Cc-CATH3 is isolated from Coturnix coturnix. Cc-CATH3 is an avian antimicrobial peptide (AMP) with 29 amino acids in length containing a broad-spectrum antibacterial activity. Cc-CATH3 showed considerable reduction of cytotoxic activity compared to other avian cathelicidins, with average IC(50) values of 17.16 μm. | |
| CcD1 | CcD1 is isolated from Capsicum chinense. It has antifungal activity. | |
| Cc-GRP | Cc-GRP is a peptide with a molecular weight of 7kDa and it was observed to display homology to GRPs. Cc-GRP has antifungal activity. | |
| CCHa2 | CCHa2. Synonyms: H-Gly-Cys-Gln-Ala-Tyr-Gly-His-Val-Cys-Tyr-Gly-Gly-His-NH2. Molecular formula: C57H79N19O16S2. Mole weight: 1350.48. | |
| CCK-4 Acetate | Tetragastrin is a tetrapeptide. Synonyms: CCK-4; CCK4; CCK 4; Gastrin Tetrapeptide; Cholecystokinin Octapeptide (5-8); Cholecystokinin Tetrapeptide; Gastrin (14-17) (human). CAS No. 35144-91-3. Molecular formula: C29H36N6O6S. Mole weight: 596.70. | |
| CCL27 | CCL27 is a chemotactic factor that attracts skin-associated memory T-lymphocytes. It may play a role in mediating homing of lymphocytes to cutaneous sites. Synonyms: C-C Motif Chemokine Ligand 27. | |
| Cc-LTP1 | Cc-LTP1 is produced by Coffea canephora. It has active antifungal activity against Candida albicans. | |
| CCMV Gag-(7-25) | It is a cell penetrating peptide. Synonyms: H-Lys-Leu-Thr-Arg-Ala-Gln-Arg-Arg-Ala-Ala-Ala-Arg-Lys-Asn-Lys-Arg-Asn-Thr-Arg-OH; L-lysyl-L-leucyl-L-threonyl-L-arginyl-L-alanyl-L-glutaminyl-L-arginyl-L-arginyl-L-alanyl-L-alanyl-L-alanyl-L-arginyl-L-lysyl-L-asparagyl-L-lysyl-L-arginyl-L-asparagyl-L-threonyl-L-arginine. Grade: ≥95%. Molecular formula: C93H175N43O25. Mole weight: 2295.70. | |
| C-Cys-Mel | C-Cys-Mel. Synonyms: Gly-Ile-Gly-Ala-Val-Leu-Lys-Val-Leu-Thr-Thr-Gly-Leu-Pro-Ala-Leu-Ile-Ser-Trp-Ile-Lys-Arg-Lys-Arg-Gln-Gln-Cys. | |
| CD20 (188-196) | CD20 (188-196) is a truncated fragment of a membrane phosphoprotein, CD20, which is expressed on the surface of B cells. CD20 receptor is an important target for immunotherapy against B cell lymphoma. Synonyms: B-lymphocyte antigen CD20 (188-196). Grade: >95%. Molecular formula: C46H77N9O12. Mole weight: 948.16. | |
| CD59 glycoprotein precursor (106-114) | CD59 glycoprotein precursor (106-114) is a peptide derived from CD59 glycoprotein precursor which is a potent inhibitor of the complement membrane attack complex (MAC) action. CD59 glycoprotein is involved in signal transduction for T-cell activation complexed to a protein tyrosine kinase. Synonyms: HRF-20 (106-114); Membrane attack complex inhibition factor (106-114). | |
| Cdc25A (80-93) (human) | Cdc25A abundance fluctuates periodically during the cell division cycle and is mainly regulated by the ubiquitin-proteasome system, through the action of two ubiquitin ligase complexes, which later promote complex/cyclosome and Skp1/Cul1/F-box proteins. Due to the presence of the destruction motif (KEN-box) in Cdc25A, ubiquitination and degradation occur at the mitotic outlet and G1, while phosphorylation events modulate the stability of Cdc25A protein in the S phase, both in undisturbed cells and in cells exposed to DNA damage agents or DNA replication inhibitors. Synonyms: H-Thr-Asp-Ser-Gly-Phe-Cys-Leu-Asp-Ser-Pro-Gly-Pro-Leu-Asp-OH. Grade: ≥95%. CAS No. 851538-67-5. Molecular formula: C60H90N14O24S. Mole weight: 1423.52. | |
| CDK2 acetate | CDK2 acetate, a member of the eukaryotic S/T protein kinase family, catalyzes the phosphoryl transfer of ATP γ-phosphate to serine or threonine hydroxyl (denoted as S0/T0) in a protein substrate. Synonyms: H-His-His-Ala-Ser-Pro-Arg-Lys-OH.CH3CO2H; L-histidyl-L-histidyl-L-alanyl-L-seryl-L-prolyl-L-arginyl-L-lysine acetic acid. Grade: ≥95%. Molecular formula: C37H61N15O11. Mole weight: 891.99. | |
| CDK4-R24C (23-32) | CDK4-R24C (23-32) is a peptide derived from CDK4-R24C. The common mutation in CDK4 (CDK4R24C) in melanoma inhibits the interaction with p16INK4A and thus leads to constitutive activation. | |
| CEC1_DROVI Cecropin-1 precursor | CEC1_DROVI Cecropin-1 precursor has antibacterial activity. The source of CEC1_DROVI Cecropin-1 precursor is Drosophila virilis. Grade: >95% by HPLC. Molecular formula: C182H311N61O51. Mole weight: 4169.78. | |
| CEC3_DROVI Cecropin-3 precursor | CEC3_DROVI Cecropin-3 precursor was found in Drosophila virilis. Cecropins have lytic and antibacterial activity against several Gram-positive and Gram-negative bacteria. | |
| CEC4_BOMMO Cecropin | CEC4_BOMMO Cecropin has antibacterial activity. CEC4_BOMMO Cecropin was found in Bombyx mori. Grade: >97% by HPLC. Molecular formula: C172H291N51O43. Mole weight: 3761.46. | |
| CECA1_DROSI Cecropin-A1 precursor | CECA1_DROSI Cecropin-A1 precursor was found in Drosophila simulans. Cecropins have lytic and antibacterial activity against several Gram-positive and Gram-negative bacteria. | |
| CECC_DROTK Cecropin-C precursor | CECC_DROTK Cecropin-C precursor was found in Drosophila takahashii. Cecropins have lytic and antibacterial activity against several Gram-positive and Gram-negative bacteria. | |
| CECD_BOMMO Cecropin-D precursor | CECD_BOMMO Cecropin-D precursor was found in Bombyx mori. Cecropins have lytic and antibacterial activity against several Gram-positive and Gram-negative bacteria. | |
| CECE_BOMMO Antibacterial peptide enbocin precursor | CECE_BOMMO Antibacterial peptide enbocin precursor was found in Bombyx mori. It has antibacterial activity against Gram-positive and Gram-negative bacteria. | |
| Cecropin | Cecropin was found in Oiketicus kirbyi. Cecropins have lytic and antibacterial activity against several Gram-positive and Gram-negative bacteria. | |
| Cecropin-1 | Cecropin-1 was found in Ceratitis capitata. Cecropins have lytic and antibacterial activity against several Gram-positive and Gram-negative bacteria. | |
| Cecropin-2 | Cecropin-2 was found in Ceratitis capitata. Cecropins have lytic and antibacterial activity against several Gram-positive and Gram-negative bacteria. | |
| Cecropin A | Cecropin A is an antibacterial peptide that exists in a variety of organisms including mammals. It has a broad-spectrum antiparasitic and antibacterial activity. Synonyms: Lys-Trp-Lys-Leu-Phe-Lys-Lys-Ile-Glu-Lys-Val-Gly-Gln-Asn-Ile-Arg-Asp-Gly-Ile-Ile-Lys-Ala-Gly-Pro-Ala-Val-Ala-Val-Val-Gly-Gln-Ala-Thr-Gln-Ile-Ala-Lys-NH2; Cecropin A, porcine; P9A Protein; L-lysyl-L-tryptophyl-L-lysyl-L-leucyl-L-phenylalanyl-L-lysyl-L-lysyl-L-isoleucyl-L-alpha-glutamyl-L-lysyl-L-valyl-glycyl-L-glutaminyl-L-asparagyl-L-isoleucyl-L-arginyl-L-alpha-aspartyl-glycyl-L-isoleucyl-L-isoleucyl-L-lysyl-L-alanyl-glycyl-L-prolyl-L-alanyl-L-valyl-L-alanyl-L-valyl-L-valyl-glycyl-L-glutaminyl-L-alanyl-L-threonyl-L-glutaminyl-L-isoleucyl-L-alanyl-L-lysinamide. Grade: ≥95% by HPLC. CAS No. 80451-04-3. Molecular formula: C184H313N53O46. Mole weight: 4003.78. | |
| Cecropin-A | Cecropin-A was found in Culex pipiens pipiens. Cecropins have lytic and antibacterial activity against several Gram-positive and Gram-negative bacteria. | |
| Cecropin A1 | Cecropin A1 was found in Bombyx mori. It has antibacterial activity. | |
| Cecropin-A1 | Cecropin-A1 was found in Drosophila mauritiana. Cecropins have lytic and antibacterial activity against several Gram-positive and Gram-negative bacteria. | |
| Cecropin A (1-7)-Melittin A (2-9) amide | Cecropin A (1-7)-Melittin A (2-9) amide, a synthetic hybrid peptide consisting of parts of the naturally occurring antibiotic peptides cecropin A and melittin, exhibits better antimicrobial activity than the native molecules, but lacks the hemolytic properties of melittin. Its antimicrobial activity is not limited to aerobic microorganisms, but also includes several gram-negative and gram-positive anaerobic microorganisms. With its identified broad-spectrum antibiotic activity, it may represent an effective alternative to ciprofloxacin in the treatment of anthrax infections. Synonyms: CAMEL0; H-Lys-Trp-Lys-Leu-Phe-Lys-Lys-Ile-Gly-Ala-Val-Leu-Lys-Val-Leu-NH2; L-lysyl-L-tryptophyl-L-lysyl-L-leucyl-L-phenylalanyl-L-lysyl-L-lysyl-L-isoleucyl-glycyl-L-alanyl-L-valyl-L-leucyl-L-lysyl-L-valyl-L-leucinamide. Grade: ≥95%. CAS No. 157606-25-2. Molecular formula: C89H152N22O15. Mole weight: 1770.33. | |
| Cecropin-A2 | Cecropin-A2 was found in Aedes albopictus. Cecropins have lytic and antibacterial activity against several Gram-positive and Gram-negative bacteria. Synonyms: H-Gly-Gly-Leu-Lys-Lys-Phe-Gly-Lys-Lys-Leu-Glu-Gly-Val-Gly-Lys-Arg-Val-Phe-Lys-Ala-Ser-Glu-Lys-Ala-Leu-Pro-Val-Ala-Val-Gly-Ile-Lys-Ala-Leu-Gly-Lys-OH. Grade: >97% by HPLC. Molecular formula: C172H298N48O42. Mole weight: 3710.49. | |
| Cecropin-A precursor | Cecropin-A precursor was found in Anopheles gambiae. It has antibacterial activity against several Gram-positive and Gram-negative bacteria. It also has antifungal activity against A.fumigatus, B.cinerea, F.culmorum, F.oxysporum, N.crassa, C.albicans, C.neoformans and S.cerevisiae. | |
| Cecropin-B | Cecropin-B was found in Heliothis virescens. Cecropins have lytic and antibacterial activity against several Gram-positive and Gram-negative bacteria. It also has activity against fungi. | |
| Cecropin B1 | Cecropin B1 was found in Bombyx mori. It has antibacterial activity. | |
| Cecropin-B1 | Cecropin-B1 was found in Culex pipiens pipiens. Cecropins have lytic and antibacterial activity against several Gram-positive and Gram-negative bacteria. | |
| Cecropin-B2 | Cecropin-B2 was found in Culex pipiens pipiens. Cecropins have lytic and antibacterial activity against several Gram-positive and Gram-negative bacteria. | |
| Cecropin B (free acid) | Cecropin B (free acid). Synonyms: Cecropin B, free acid; H-Lys-Trp-Lys-Val-Phe-Lys-Lys-Ile-Glu-Lys-Met-Gly-Arg-Asn-Ile-Arg-Asn-Gly-Ile-Val-Lys-Ala-Gly-Pro-Ala-Ile-Ala-Val-Leu-Gly-Glu-Ala-Lys-Ala-Leu-OH. Grade: ≥95%. CAS No. 203265-23-0. Molecular formula: C176H301N51O42S. Mole weight: 3835.71. | |
| Cecropin B TFA salt | Cecropin B is an antibacterial peptide originally isolated from insects. It has broad-spectrum antiparasitic and antibacterial activities and is also effective against fungi. Synonyms: P9B Protein. Grade: ≥97% by HPLC. Molecular formula: C176H302N52O41S (free base). Mole weight: 3835 (free base). | |
| Cecropin-C | Cecropin-C was found in Heliothis virescens. Cecropins have lytic and antibacterial activity against several Gram-positive and Gram-negative bacteria. It also has activity against fungi. | |
| Cecropin-C type 1 | Cecropin-C type 1 was found in Aedes albopictus. Cecropins have lytic and antibacterial activity against several Gram-positive and Gram-negative bacteria. Synonyms: CECC1. | |
| Cecropin-D | Cecropin-D was found in Hyalophora cecropia. Cecropins have lytic and antibacterial activity against several Gram-positive and Gram-negative bacteria. CAS No. 83652-32-8. | |
| Cecropin-D-like peptide | Cecropin-D-like peptide is an antibacterial peptide isolated from Galleria mellonella. It has activity against gram-positive bacteria and fungi. Synonyms: Glu-Asn-Phe-Phe-Lys-Glu-Ile-Glu-Arg-Ala-Gly-Gln-Arg-Ile-Arg-Asp-Ala-Ile-Ile-Ser-Ala-Ala-Pro-Ala-Val-Glu-Thr-Leu-Ala-Gln-Ala-Gln-Lys-Ile-Ile-Lys-Gly-Gly-Asp. Grade: 96.7%. Molecular formula: C187H309N55O58. Mole weight: 4255.84. | |
| Cecropin P1 | It is the first cecropin family to be isolated from a mammal rather than an insect. It has antiviral and broad-spectrum antibacterial activities. It also has antifungal activity, and has cytotoxic effect on cancer cell lines. Synonyms: H-Ser-Trp-Leu-Ser-Lys-Thr-Ala-Lys-Lys-Leu-Glu-Asn-Ser-Ala-Lys-Lys-Arg-Ile-Ser-Glu-Gly-Ile-Ala-Ile-Ala-Ile-Gln-Gly-Gly-Pro-Arg-OH; Cecropin P1-LI; Cecropin P1 Porcine. Grade: ≥95%. CAS No. 125667-96-1. Molecular formula: C147H253N45O43. Mole weight: 3338.86. | |
| Cecropin-P2 | Cecropin-P2 is from Ascaris suum (Pig roundworm) (Ascaris lumbricoides). It has antibacterial activity against several Gram-positive and Gram-negative bacteria. Cecropin-P2 is weakly active against yeasts. Synonyms: CecP2. | |
| Cecropin-P3 | Cecropin-P3 is from Ascaris suum (Pig roundworm) (Ascaris lumbricoides). It has antibacterial activity against several Gram-positive and Gram-negative bacteria. Cecropin-P3 is weakly active against yeasts. Synonyms: CecP3. | |
| Cecropin-P4 | Cecropin-P4 is from Ascaris suum (Pig roundworm) (Ascaris lumbricoides). Recombinant CecP4 showed antimicrobial activity against both Pseudomona and E. coli, suggesting the broad spectrum of its antimicrobial activity. Synonyms: CecP4. | |
| CEF10 Epstein-Barr Virus LMP2 (426-434) | CEF10 Epstein-Barr Virus LMP2 (426-434) is a peptide that corresponds to aa 426-434 of the LMP2 protein from the Epstein-Barr Virus. Synonyms: H-Cys-Leu-Gly-Gly-Leu-Leu-Thr-Met-Val-OH; LMP2A (426-434); L-cysteinyl-L-leucyl-glycyl-glycyl-L-leucyl-L-leucyl-L-threonyl-L-methionyl-L-valine. CAS No. 152274-91-4. Molecular formula: C39H71N9O11S2. Mole weight: 906.16. | |
| CEF11 Epstein-Barr Virus BMLF1 (280-288) | CEF11 Epstein-Barr Virus BMLF1 (280-288) is a peptide that corresponds to aa 280-288 of the BMLF1 protein from the Epstein-Barr Virus. Synonyms: Gly-Leu-Cys-Thr-Leu-Val-Ala-Met-Leu; H-Gly-Leu-Cys-Thr-Leu-Val-Ala-Met-Leu-OH. CAS No. 183719-29-1. Molecular formula: C40H73N9O11S2. Mole weight: 920.19. | |
| CEF14, EBV Rta Protein 28-37 | It is the HLA A24 restriction epitope of Epstein-Barr virus Rta protein (28-37). Synonyms: Asp-Tyr-Cys-Asn-Val-Leu-Asn-Lys-Glu-Phe; (3S,6S,9R,12S,15S,18S,21S,24S,27S)-3-Amino-24-(4-aminobutyl)-27-[{[(1S)-1-carboxy-2-phenylethyl]imino}(hydroxy)methyl]-4,7,10,13,16,19,22,25-octahydroxy-6-(4-hydroxybenzyl)-12,21-bis(2-hydroxy-2-iminoethyl)-18-isobutyl-15-isopropyl-9-(sulfanylmethyl)-5,8,11,14,17,20,23,26-octaazatriaconta-4,7,10,13,16,19,22,25-octaene-1,30-dioic acid. Grade: ≥95%. CAS No. 216862-58-7. Molecular formula: C55H81N13O18S. Mole weight: 1244.37. | |
| CEF19, Epstein-Barr Virus latent NA-3A 458-466 | It is a single peptide epitope representing the 458-466 residues of Epstein-Barr virus type 1 nuclear antigen 3A protein (B95.8 strain) that significantly affects cytotoxic T lymphocyte (CTL) recognition. Synonyms: L-tyrosyl-L-prolyl-L-leucyl-L-histidyl-L-alpha-glutamyl-L-glutaminyl-L-histidyl-glycyl-L-methionine; Tyr-Pro-Leu-His-Glu-Gln-His-Gly-Met; N-{(5S,8S,11S,14S,17S)-11-(2-Carboxyethyl)-1,4,7,10,13,16,19-heptahydroxy-8-(3-hydroxy-3-iminopropyl)-5,14-bis(1H-imidazol-5-ylmethyl)-17-isobutyl-19-[(2S)-1-(L-tyrosyl)-2-pyrrolidinyl]-3,6,9,12,15,18-hexaazanonadeca-3,6,9,12,15,18-hexaen-1-ylidene}-L-methionine. Grade: ≥95%. CAS No. 157876-41-0. Molecular formula: C49H70N14O14S. Mole weight: 1111.23. | |
| CEF20 acetate | CEF20 acetate, a CEF control peptide pool, is the HLA-A*0201-restricted epitope from cytomegalovirus pp65 (495-503). Synonyms: H-Asn-Leu-Val-Pro-Met-Val-Ala-Thr-Val-OH.CH3CO2H; L-asparagyl-L-leucyl-L-valyl-L-prolyl-L-methionyl-L-valyl-L-alanyl-L-threonyl-L-valine acetic acid. Grade: ≥95%. Molecular formula: C44H78N10O14S. Mole weight: 1003.22. | |
| CEF25 Influenza Virus NP (44-52) | CEF25 Influenza Virus NP (44-52) is a peptide that corresponds to aa 44-52 of Influenza A virus nucleoprotein. NP is a critical component of the viral ribonucleoproteins (vRNP) complex, and the recognized functions of NP include, but are not limited to, organization of RNA packing, nuclear trafficking, and vRNA transcription and replication. Synonyms: H-Cys-Thr-Glu-Leu-Lys-Leu-Ser-Asp-Tyr-OH; L-cysteinyl-L-threonyl-L-alpha-glutamyl-L-leucyl-L-lysyl-L-leucyl-L-seryl-L-alpha-aspartyl-L-tyrosine. CAS No. 152647-27-3. Molecular formula: C46H74N10O17S. Mole weight: 1071.20. | |
| CEF26 Influenza Virus NP (265-274) | CEF26 Influenza Virus NP (265-274) is a peptide that corresponds to aa 265-274 of Influenza A virus nucleoprotein. NP is a critical component of the viral ribonucleoproteins (vRNP) complex, and the recognized functions of NP include, but are not limited to, organization of RNA packing, nuclear trafficking, and vRNA transcription and replication. Synonyms: H-Ile-Leu-Arg-Gly-Ser-Val-Ala-His-Lys-OH; Ile-Leu-Arg-Gly-Ser-Val-Ala-His-Lys. Molecular formula: C43H77N15O11. Mole weight: 980.23. | |
| CEF27, Epstein-Barr Virus BRLF-1 lytic 148-156 | It is the 148-156 amino acid fragment of the BRLF1 protein. BRLF1 is a transcriptional activator that directly binds to GC-rich motif in the promoter of EBV lytic gene. Synonyms: L-Lysine, L-arginyl-L-valyl-L-arginyl-L-alanyl-L-tyrosyl-L-threonyl-L-tyrosyl-L-seryl-; Arg-Val-Arg-Ala-Tyr-Thr-Tyr-Ser-Lys. Grade: ≥95%. CAS No. 254110-79-7. Molecular formula: C51H82N16O14. Mole weight: 1143.32. | |
| CEF27, Epstein-Barr Virus BRLF-1 lytic 148-156 acetate | CEF27, Epstein-Barr Virus BRLF-1 lytic 148-156 acetate is the 148-156 amino acid fragment of the BRLF1 protein. BRLF1 is a transcriptional activator that directly binds to the GC-rich motif in the promoter of EBV lytic gene. Synonyms: L-Arginyl-L-valyl-L-arginyl-L-alanyl-L-tyrosyl-L-threonyl-L-tyrosyl-L-seryl-L-lysine acetate salt; H-Arg-Val-Arg-Ala-Tyr-Thr-Tyr-Ser-Lys-OH.CH3CO2H; L-arginyl-L-valyl-L-arginyl-L-alanyl-L-tyrosyl-L-threonyl-L-tyrosyl-L-seryl-L-lysine acetic acid. Grade: ≥95%. Molecular formula: C53H86N16O16. Mole weight: 1203.35. | |
| CEF2 Influenza Virus PA (46-54) | CEF2 Influenza Virus PA (46-54) is a peptide corresponds to aa 46-54 of the influenza A virus RNA polymerase PA subunit. The PA subunit of the influenza virus polymerase complex is a phosphoprotein that induces proteolytic degradation of coexpressed proteins. Synonyms: H-Phe-Met-Tyr-Ser-Asp-Phe-His-Phe-Ile-OH; Phe-Met-Tyr-Ser-Asp-Phe-His-Phe-Ile. Molecular formula: C60H75N11O14S. Mole weight: 1206.37. | |
| CEF30 Epstein-Barr Virus BRLF1 (134-142) | CEF30 Epstein-Barr Virus BRLF1 (134-142) is a peptide that corresponds to aa 134-142 of the BRLF1 protein from the Epstein-Barr Virus. Synonyms: H-Ala-Thr-Ile-Gly-Thr-Ala-Met-Tyr-Lys-OH; Ala-Thr-Ile-Gly-Thr-Ala-Met-Tyr-Lys. Molecular formula: C42H70N10O13S. Mole weight: 955.2. | |
| CEF3 acetate | CEF3 acetate corresponds to aa 13-21 of the influenza A virus M1 protein, and was first described in the yeast Saccharomyces cerevisiae and has subsequently been identified in a wide range of fungal species including Candida albicans and Schizosaccharomyces pombe. The matrix (M1) protein of influenza A virus is a multifunctional protein that plays essential structural and functional roles in the virus life cycle. Synonyms: H-Ser-Ile-Ile-Pro-Ser-Gly-Pro-Leu-Lys-OH.CH3CO2H; L-seryl-L-isoleucyl-L-isoleucyl-L-prolyl-L-seryl-glycyl-L-prolyl-L-leucyl-L-lysine acetic acid. Grade: ≥95%. Molecular formula: C44H78N10O14. Mole weight: 971.16. | |
| CEF8, Influenza Virus NP 383-391 | CEF8, Influenza Virus NP (383-391) is the 383-391 amino acid fragment of influenza A virus nuclear protein. It is the most important HLA-B*2705 restriction epitope, and is associated with immune escape mediated by cytotoxic T lymphocytes. Synonyms: L-seryl-L-arginyl-L-tyrosyl-L-tryptophyl-L-alanyl-L-isoleucyl-L-arginyl-L-threonyl-L-arginine; Ser-Arg-Tyr-Trp-Ala-Ile-Arg-Thr-Arg. Grade: ≥95%. CAS No. 142479-13-8. Molecular formula: C54H85N19O13. Mole weight: 1208.3699999999999. | |
| cell division cycle 45-like (556-564) | cell division cycle 45-like (556-564). | |
| Cell division cycle protein 27 homolog (760-771) | A peptide fragment of Cell division cycle protein 27 homolog. Cell division cycle protein 27 homolog is a component of the anaphase promoting complex/cyclosome (APC/C), a cell cycle-regulated E3 ubiquitin ligase that controls progression through mitosis and the G1 phase of the cell cycle. Synonyms: Anaphase-promoting complex subunit 3 (760-771); CDC27 homolog (760-771). | |
| Cell Penetrating ARF Peptide (26-44) | It is a cell penetrating peptide corresponding to amino acids 26 to 44 of the ARF tumor suppressor protein fused to nine D-Arginine (D-Arg) residues. Synonyms: H-D-Arg-D-Arg-D-Arg-D-Arg-D-Arg-D-Arg-D-Arg-D-Arg-D-Arg-Lys-Phe-Val-Arg-Ser-Arg-Arg-Pro-Arg-Thr-Ala-Ser-Cys-Ala-Leu-Ala-Phe-Val-Asn-OH; D-arginyl-D-arginyl-D-arginyl-D-arginyl-D-arginyl-D-arginyl-D-arginyl-D-arginyl-D-arginyl-L-lysyl-L-phenylalanyl-L-valyl-L-arginyl-L-seryl-L-arginyl-L-arginyl-L-prolyl-L-arginyl-L-threonyl-L-alanyl-L-seryl-L-cysteinyl-L-alanyl-L-leucyl-L-alanyl-L-phenylalanyl-L-valyl-L-asparagine. Grade: ≥95%. Molecular formula: C149H267N69O33S. Mole weight: 3585.29. | |
| Cellular tumor antigen p53 (153-165) | Cellular tumor antigen p53 (153-165) is amino acids 153 to 165 fragment of Cellular tumor antigen p53. Cellular tumor antigen p53 is any isoform of a protein encoded by TP53 gene. TP53 gene is the most frequently mutated gene in human cancer indicating that the TP53 gene plays a crucial role in preventing cancer formation. Synonyms: Tumor suppressor p53 (153-165); Phosphoprotein p53 (153-165); Antigen NY-CO-13 (153-165); p53 (153-165). | |
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