Alfa Chemistry. - Products
Alfa Chemistry is an ISO 9001:2015 Certified Supplier of various building blocks, reagents, catalysts, nanomaterials, reference materials, and research chemicals. In-stock products can be shipped quickly.
| Product | Description | |
|---|---|---|
| Fmoc-N-Me-Ile-OH | Building block for introduction of N-α-methyl-isoleucine amino-acid residues by Fmoc SPPS. Uses: Peptide synthesis. Group: Amino acids. Alternative Names: Fmoc-N-Me-Ile-OH, N-α-Fmoc-N-α-methyl-L-isoleucine. CAS No. 138775-22-1. Mole weight: 367.44. Catalog: ACM138775221. |  |
| Fmoc-N-Me-Leu-OH | Building block for introduction of N-α-methyl-leucine amino-acid residues by Fmoc SPPS. Uses: Peptide synthesis. Group: Amino acids. Alternative Names: Fmoc-N-Me-Leu-OH, N-α-Fmoc-N-α-methyl-L-leucine. CAS No. 103478-62-2. Molecular formula: C22H25NO4. Mole weight: 367.44. Catalog: ACM103478622. | |
| Fmoc-N-Me-Met-OH | Building block for introduction of N-α-methyl-methionine amino-acid residues by Fmoc SPPS. Uses: Peptide synthesis. Group: Amino acids. Alternative Names: Fmoc-N-Me-Met-OH, N-α-Fmoc-N-α-methyl-L-methionine. CAS No. 84000-12-4. Mole weight: 385.48. Catalog: ACM84000124. | |
| Fmoc-N-Me-Phe-OH | Building block for introduction of N-α-methyl-phenylalanine amino-acid residues by Fmoc SPPS. Uses: Peptide synthesis. Group: Amino acids. Alternative Names: Fmoc-N-Me-Phe-OH, N-α-Fmoc-N-α-methyl-L-phenylalanine. CAS No. 77128-73-5. Molecular formula: C25H23NO4. Mole weight: 401.45. Catalog: ACM77128735. | |
| Fmoc-N-Me-Val-OH | Building block for introduction of N-α-methyl-valine amino-acid residues by Fmoc SPPS. Uses: Peptide synthesis. Group: Amino acids. Alternative Names: Fmoc-N-Me-Val-OH, N-α-Fmoc-N-α-methyl-L-valine. CAS No. 84000-11-3. Mole weight: 353.41. Catalog: ACM84000113. | |
| Fmoc-Nva-OH | Standard building block for introduction of norvaline amino-acid residues by Fmoc SPPS. Uses: Peptide synthesis. Group: Amino acids. Alternative Names: Fmoc-Nva-OH, N-α-Fmoc-L-norvaline. CAS No. 135112-28-6. Mole weight: 339.39. Catalog: ACM135112286. | |
| Fmoc-Orn(Boc)-OH | Standard building block for introduction of ornithine amino-acid residues by Fmoc SPPS. Uses: Peptide synthesis. Group: Amino acids. Alternative Names: Fmoc-Orn(Boc)-OH, N-α-Fmoc-N-δ-t.-Boc-L-ornithine. CAS No. 109425-55-0. Mole weight: 454.52. Catalog: ACM109425550. | |
| Fmoc-Orn(Mtt)-OH | The side-chain Mtt group can be selectively removed with 1% TFA in DCM or DCM/HFIP/TFE/TES (6.5:2:1:0.5) , making this an excellent derivative for the synthesis by Fmoc SPPS. of branched peptides, peptides modified at the ornithine side-chain , for the construction of templates and multifunctionalized resins for combinatorial synthesis. Uses: Peptide synthesis. Group: Amino acids. Alternative Names: Fmoc-Orn(Mtt)-OH, N-α-Fmoc-N-δ-4-methyltrityl-L-ornithine, Fmoc-(Nd-4-methyltrityl)-L-ornithine. CAS No. 343770-23-0. Molecular formula: C40H38N2O4. Mole weight: 610.74. Catalog: ACM343770230. | |
| Fmoc-PABA-OH | Standard building block for introduction of p-aminobenzoic acid residues by Fmoc SPPS. Uses: Peptide synthesis. Group: Amino acids. Alternative Names: Fmoc-PABA-OH, N-α-Fmoc-p-aminobenzoic acid,Fmoc-4-Abz-OH. CAS No. 185116-43-2. Mole weight: 359.37. Catalog: ACM185116432. | |
| Fmoc-Phe(4-Cl)-OH | Standard building block for introduction of 4-chlorophenylalanine residues by Fmoc SPPS. Uses: Peptide synthesis. Group: Amino acids. Alternative Names: Fmoc-Phe(4-Cl)-OH, N-α-Fmoc-4-chloro-L-phenylalanine. CAS No. 175453-08-4. Mole weight: 421.87. Catalog: ACM175453084. | |
| Fmoc-Phe(4-NO?)-OH | Cleavage and Deprotection Protocols for Fmoc SPPS. Uses: Peptide synthesis. Group: Amino acids. Alternative Names: Fmoc-Phe(4-NO2)-OH, N-α-Fmoc-4-nitro-L-phenylalanine. CAS No. 95753-55-2. Mole weight: 432.43. Catalog: ACM95753552. | |
| Fmoc-Phe-OH | High purity Fmoc-protected amino acid for research and process production of peptides, with very low levels of dipeptide, free-amino acids and acetic acid impurities. Standard building block for introduction of phenylalanine amino-acid residues by Fmoc SPPS. Uses: Peptide synthesis. Group: Amino acids. Alternative Names: Fmoc-Phe-OH, N-α-Fmoc-L-phenylalanine. CAS No. 35661-40-6. Molecular formula: C24H21NO4. Mole weight: 387.43. Catalog: ACM35661406. | |
| Fmoc-Phg-OH | Standard building block for introduction of phenylglcine residues by Fmoc SPPS. Uses: Peptide synthesis. Group: Amino acids. Alternative Names: Fmoc-Phg-OH, N-α-Fmoc-L-phenylglycine. CAS No. 102410-65-1. Mole weight: 373.4. Catalog: ACM102410651. | |
| Fmoc-Pro-OH | High purity Fmoc-protected amino acid for research and process production of peptides, with very low levels of dipeptide, free-amino acids and acetic acid impurities. Standard building block for introduction of proline amino-acid residues by Fmoc SPPS. Uses: Peptide synthesis. Group: Amino acids. Alternative Names: Fmoc-Pro-OH, N-α-Fmoc-L-proline. CAS No. 71989-31-6. Molecular formula: C20H19NO4. Mole weight: 337.37. Catalog: ACM71989316. | |
| Fmoc-propargyl-Gly-OH | Building block for the introduction by Fmoc SPPS. of an amino acid bearing an alkyne side chain. Such derivatives are useful tools for the synthesis of cyclic peptides by an alkyne-alkyne Glaser coupling, involving Cu(OAc)2/pyridine and heating to 60 °Cusing microwaves. Uses: Peptide synthesis. Group: Amino acids. Alternative Names: (S)-2-(Fmoc-amino)-4-pentynoic acid, Fmoc-L-2-propargylglycine. CAS No. 198561-07-8. Molecular formula: C20H17NO4. Mole weight: 335.35. Canonical SMILES: OC(=O)[C@H](CC#C)NC(=O)OCC1c2ccccc2-c3ccccc13. Catalog: ACM198561078. | |
| Fmoc-Rink Amide AM Resin [183599-10-2] | Fmoc-Rink Amide AM resin is an acid labile amide forming resin ;100-200 mesh size. 1% DVB. ;Substitution: 0.3 to 0.8 mmol/g ;Loading and Cleavage Procedures. Group: Peptide synthesis resins. CAS No. 183599-10-2. Catalog: ACM183599102-1. | |
| Fmoc-Rink Amide MBHA Resin [431041-83-7] | 100-200 mesh size. 1% DVB. ;Substitution: 0.3 to 0.8 mmol/g ;Loading and Cleavage Procedures ; Group: Peptide synthesis resins. CAS No. 431041-83-7. Catalog: ACM431041837-1. | |
| Fmoc-(S)-2-(4-pentenyl)Ala-OH | Building block for introduction of α-n-pentenyl-alanine peptides by Fmoc SPPS. Uses: Fmoc-(s)-2-(4-pentenyl)ala-oh is a fmoc-protected amino acid that can be used to create peptide libraries. Group: Amino acids. Alternative Names: (S)-N-Fmoc-α-4-n-pentenylalanine, Fmoc-(S)-2-(4-pentenyl)alanine, Fmoc-(S)-2-amino-2-methyl-hept-6-enoic acid. CAS No. 288617-73-2. Molecular formula: C23H25NO4. Mole weight: 379.45. Catalog: ACM288617732. | |
| Fmoc-Sar-OH | Standard building block for introduction of sarcosine amino-acid residues by Fmoc SPPS. Uses: Peptide synthesis. Group: Amino acids. Alternative Names: Fmoc-Sar-OH, N-α-Fmoc-sarcosine, Fmoc-N-Me-Gly-OH, Fmoc-Nalpha-methylglycine. CAS No. 77128-70-2. Molecular formula: C18H17NO4. Mole weight: 311.33. Catalog: ACM77128702. | |
| Fmoc-Sec(pMeOBzl)-OH | Building block for the introduction of selenocysteine during Fmoc SPPS. Selenocysteine derivatives can undergo enantiomerization during coupling and can form dehydroalanine and β-piperidinylalanine containing side products during subsequent chain elongation. Therefore, activation methods, such as HBTU or PyBOP which involve the addition of a tertiary, base should be avoided for addition of the Sec and all subsequent residues. Cleavage and side-chain deprotection of Sec-containing peptides can be effected using tFA-m-cresol-thioanisole-EDT-water (80:5:5:5:5) or TFA-water-DCM-TIS (89:5:51) at 4 °C. As the Se-pMeOBzl bond is stable to TFA, these methods result in the formation of the corresponding Sev(pMeOBzl) peptide. Peptides containing two Sec(pMeOBzl) residues can be oxidized directly to the corresponding selenocystinyl peptides by treatment with 5-10% DMSO in TFA. Uses: Peptide synthesis. Group: Amino acids. Alternative Names: Fmoc-Sec(pMeOBzl)-OH, Fmoc-Sec(Mob)-OH, Fmoc-S-4-methoxybenzyl selenocysteine. CAS No. 150308-80-8. Molecular formula: C26H25NO5Se. Mole weight: 510.44. Catalog: ACM150308808. | |
| Fmoc-Ser(Ac3AcNH-α-Gal)-OH | The O-glycosidic linkage and the O-acetyl protection in this building block is stable to both piperidine and TFA , making it completely compatible with standard protocols in Fmoc solid phase peptide synthesis. Removal of the acetyl protecting groups is best carried out by treatment of the peptidyl resin with methanolic ammonia prior to cleavage. Uses: Peptide synthesis. Group: Amino acids. Alternative Names: Fmoc-Ser(Ac3AcNH-α-Gal)-OH, N-α-Fmoc-O-(2-acetamido-2-deoxy-3,4,6-tri-O-acetyl-α-D-galactopyranosyl)-L-serine. CAS No. 120173-57-1. Mole weight: 656.63. Catalog: ACM120173571-1. | |
| Fmoc-Ser(Ac3AcNH-ß-Glc)-OH | The O-glycosidic linkage and the O-acetyl protection in this building block are stable to both piperidine and TFA, making it completely compatible with standard protocols in Fmoc solid phase peptide synthesis. Removal of the acetyl-protecting groups is best carried out by treatment of the peptidyl resin with methanolic ammonia prior to cleavage. Uses: Peptide synthesis. Group: Amino acids. Alternative Names: Fmoc-Ser(Ac3AcNH-ß-Glc)-OH, N-α-Fmoc-O-(2-Acetamido-2-deoxy-tri-O-acetyl-β-D-glucopyranosyl)-L-serine. CAS No. 160067-63-0. Molecular formula: C32H36N2O13. Mole weight: 656.63. Catalog: ACM160067630. | |
| Fmoc-ser-otbu | Heterocyclic Organic Compound. Alternative Names: Fmoc-Ser-OtBu, 110797-35-8, Nalpha-[(9H-Fluoren-9-ylmethoxy)carbonyl]-L-serine tert-Butyl Ester, SureCN2367138, CTK8A9229, ANW-16197, ZINC02386078, AKOS015838093, Nalpha-Fmoc-L-serine tert-Butyl Ester, KB-52154, AM20120698, F0516, I14-61024, L-Serine, N-[(9H-fluoren-9-ylmethoxy)carbonyl]-, 1,1-dimethylethyl ester. CAS No. 110797-35-8. Molecular formula: C22H25NO5. Mole weight: 383.44. Purity: >98.0%(LC)(N). IUPACName: tert-butyl (2S)-2-(9H-fluoren-9-ylmethoxycarbonylamino)-3-hydroxypropanoate. Canonical SMILES: CC (C) (C)OC (=O)C (CO)NC (=O)OCC1C2=CC=CC=C2C3=CC=CC=C13. Density: 1.217g/cm³. Catalog: ACM110797358. | |
| Fmoc-ser(tbu)-bt | Heterocyclic Organic Compound. Alternative Names: 1126433-40-6, Fmoc-Ser(tBu)-Bt, ZINC32602733, AKOS015950366, RP08112, FT-0685790, 9H-fluoren-9-ylmethyl N-[(2S)-1-(1,2,3-benzotriazol-1-yl)-3-(tert-butoxy)-1-oxopropan-2-yl]carbamate. CAS No. 1126433-40-6. Molecular formula: C28H28N4O4. Mole weight: 484.56. Purity: 0.96. IUPACName: 9H-fluoren-9-ylmethyl N-[(2S)-1-(benzotriazol-1-yl)-3-[(2-methylpropan-2-yl)oxy]-1-oxopropan-2-yl]carbamate. Canonical SMILES: CC (C) (C)OCC (C (=O)N1C2=CC=CC=C2N=N1)NC (=O)OCC3C4=CC=CC=C4C5=CC=CC=C35. Catalog: ACM1126433406. | |
| Fmoc-ser(trt)-oh | Heterocyclic Organic Compound. CAS No. 111051-56-4. Purity: 0.96. Catalog: ACM111051564. | |
| FMOC-ß-ALA-OH | Standard building block for introduction of β-alanine amino-acid residues by Fmoc SPPS. Uses: Peptide synthesis. Group: Amino acids. Alternative Names: FMOC-ß-ALA-OH, N-β-Fmoc-β-alanine. CAS No. 35737-10-1. Molecular formula: C18H17NO4. Mole weight: 311.33. Catalog: ACM35737101. | |
| Fmoc-Thi-OH | Standard building block for introduction of thienylalanine by Fmoc SPPS. Useful replacement for Phe. Uses: Peptide synthesis. Group: Amino acids. Alternative Names: Fmoc-Thi-OH, N-α-Fmoc-β-thienyl-L-alanine. CAS No. 130309-35-2. Mole weight: 393.46. Catalog: ACM130309352. | |
| Fmoc-thioproline | A building block for the introduction of thiaproline (Thz) during Fmoc SPPS. Thz has been employed as a masked cysteine residue to prevent self-ligation during native chemical ligation reactions (NCL) of peptide thioesters bearing an N-terminal Cys residue. Once ligation is complete, the N-terminal Cys residue of the resultant peptide is unmasked by ring-opening the Thz residue by treatment with methoxyamine, thereby enabling its subsequent ligation to another peptide thioester fragment. Uses: Peptide synthesis. Group: Amino acids. Alternative Names: Fmoc-thioproline, Fmoc-thiaproline,Fmoc-thiazolidine-4-carboxylic acid. CAS No. 133054-21-4. Mole weight: 333.43. Catalog: ACM133054214. | |
| Fmoc-Thr[GalNAc(Ac)3-α-D]-OH | The O-glycosidic linkage and the O-acetyl protection in this building block is stable to both piperidine and TFA , making it completely compatible with standard protocols in Fmoc solid phase peptide synthesis. Removal of the acetyl protecting groups is best carried out by treatment of the peptidyl resin with methanolic ammonia prior to cleavage. Uses: Peptide synthesis. Group: Amino acids. Alternative Names: Fmoc-O-β-(2-acetamido-2-deoxy-3,4,6-tri-O-acetyl-α-D-galactopyranosyl)-L-threonine. CAS No. 116783-35-8. Mole weight: 670.66. Canonical SMILES: CC (N[C@@H]1[C@@H] (OC (C)=O)[C@@H] (OC (C)=O)[C@@H] (COC (C)=O)O[C@@H]1O[C@H] (C)[C@H] (NC (OCC2C3=C (C4=C2C=CC=C4)C=CC=C3)=O)C (O)=O)=O. Catalog: ACM116783358-1. | |
| Fmoc-Thr(ß-D-GlcNAc(Ac)3)-OH | Fmoc-Thr(GlcNAc)3(Ac) is a complex molecule that belongs to the family of Fmoc-protected amino acids. It is typically used in the synthesis of peptides and serves as an important building block. The molecule has a beta configuration of GlcNAc(Ac)3, which refers to three N-acetylated glucosamine residues, and an acetyl group attached to the beta carboxyl group of the threonine residue. Since their introduction in the 1980s, Fmoc-protected amino acids have become important in the field of peptide synthesis, and Fmoc-Thr(GlcNAc)3(Ac) is no exception. Uses: Fmoc-thr(glcnac)3(ac) has several applications in scientific experiments. it is a useful building block in the synthesis of peptide therapeutics. it can also be used in the synthesis of glycopeptides, which are peptides with one or more sugar units attached. Group: Amino acids. Alternative Names: Fmoc-Thr(GlcNAc)3(Ac). CAS No. 160168-40-1. Molecular formula: C33H38N2O13. Mole weight: 670.7. Purity: Peak Area by HPLC ≥95%. IUPACName: (2S,3R)-3-[(2R,3R,4R,5S,6R)-3-acetamido-4,5-diacetyloxy-6-(acetyloxymethyl)oxan-2-yl]oxy-2-(9H-fluoren-9-ylmethoxycarbonylamino)butanoic acid. Canonical SMILES: CC (C (C (=O)O)NC (=O)OCC1C2=CC=CC=C2C3=CC=CC=C13)OC4C (C (C (C (O4)COC (=O)C)OC (=O)C)OC (=O)C)NC (=O)C. Density: 1.38±0.1g g/mL at 20 °C(lit.). Catalog: ACM160168401. | |
| Fmoc-thr(tbu)-bt | Heterocyclic Organic Compound. Alternative Names: 1126433-39-3, Fmoc-Thr(tBu)-Bt, ZINC32602754, AKOS015950343, RP08114, FT-0685702, 9H-fluoren-9-ylmethyl N-[(2S,3R)-1-(1,2,3-benzotriazol-1-yl)-3-(tert-butoxy)-1-oxobutan-2-yl]carbamate. CAS No. 1126433-39-3. Molecular formula: C29H30N4O4. Mole weight: 498.59. Purity: 0.96. IUPACName: 9H-fluoren-9-ylmethyl N-[(2S,3R)-1-(benzotriazol-1-yl)-3-[(2-methylpropan-2-yl)oxy]-1-oxobutan-2-yl]carbamate. Canonical SMILES: CC (C (C (=O)N1C2=CC=CC=C2N=N1)NC (=O)OCC3C4=CC=CC=C4C5=CC=CC=C35)OC (C) (C)C. Catalog: ACM1126433393. | |
| Fmoc-Thr(Trt)-OH | The side-chain Trt group can be selectively removed with 1% TFA in DCM containing 5% TIS, enabling the side-chain hydroxyl group to be selectively modified whilst the derivative is attached to the solid support. This is an excellent derivative for synthesizing phosphothreonine-containing peptides and peptides modified at the threonine side-chain. The use of trityl-protected amino acids resulted in purer products than when standard t-Bu-protected amino acids were utilized. Uses: Fmoc solid-phase peptide synthesis. Group: Amino acids. Alternative Names: Fmoc-Thr(Trt)-OH, N-α-Fmoc-O-trityl-L-threonine. CAS No. 133180-01-5. Molecular formula: C38H33NO5. Mole weight: 583.7. Catalog: ACM133180015. | |
| Fmoc-Tic-OH | Standard building block for introduction of Tic amino-acid residues by Fmoc SPPS. Uses: Peptide synthesis. Group: Amino acids. Alternative Names: Fmoc-Tic-OH, N-1-Fmoc-L-1,2,3,4,-tetrahydro-isoquinoline-3-carboxylic acid. CAS No. 136030-33-6. Mole weight: 399.44. Catalog: ACM136030336. | |
| Fmoc-Trp(Boc)-Ser(psiMe,Mepro)-OH | This pseudoproline dipeptide is undoubtedly the most effective and simplest to use tool for overcoming aggregation and enhancing peptide quality in Fmoc SPPS for peptide containing the Trp-Ser dipeptide motif. It consists of a dipeptide in which the serine residue has been reversibly protected as a structure-breaking proline-like TFA-labile oxazolidine. The reason the pseudoproline residue is introduced as a dipeptide is because it avoids the need to acylate the hindered oxazolidine nitrogen. This has the added advantage of extending the peptide chain by two residues in one step. The serine residue is regenerated during the normal TFA-mediated cleavage reaction. Uses: Peptide synthesis. Group: Amino acids. Alternative Names: Fmoc-Trp(Boc)-Ser(psiMe,Mepro)-OH. CAS No. 908601-15-0. Mole weight: 653.72. Catalog: ACM908601150. | |
| Fmoc-Trp(Boc)-Thr(psiMe,Mepro)-OH | This pseudoproline dipeptide is undoubtedly the most effective and simplest to use tool for overcoming aggregation and enhancing peptide quality in Fmoc SPPS for peptide containing the Trp-Thr dipeptide motif. It consists of a dipeptide in which the threonine residue has been reversibly protected as a structure-breaking proline-like TFA-labile oxazolidine. The reason the pseudoproline residue is introduced as a dipeptide is because it avoids the need to acylate the hindered oxazolidine nitrogen. This has the added advantage of extending the peptide chain by two residues in one step. The threonine residue is regenerated during the normal TFA-mediated cleavage reaction. Uses: Peptide synthesis. Group: Amino acids. Alternative Names: Fmoc-Trp(Boc)-Thr(psiMe,Mepro)-OH. CAS No. 936707-21-0. Mole weight: 667.75. Catalog: ACM936707210. | |
| Fmoc-Trp-OH | Building block for introduction of typtophan by Fmoc SPPS. Superceded by Fmoc-Trp(Boc)-OH. Uses: Peptide synthesis. Group: Amino acids. Alternative Names: Fmoc-Trp-OH, N-α-Fmoc-L-tryptophan. CAS No. 35737-15-6. Mole weight: 426.46. Catalog: ACM35737156. | |
| Fmoc-Tyr(Me)-OH | Standard building block for introduction of O-methyl-tyrosine amino-acid residues by Fmoc SPPS. Uses: Peptide synthesis. Group: Amino acids. Alternative Names: Fmoc-Tyr(Me)-OH, N-α-Fmoc-O-methyl-L-tyrosine. CAS No. 77128-72-4. Molecular formula: C25H23NO5. Mole weight: 417.45. Catalog: ACM77128724. | |
| Fmoc-Tyr-OH | A useful derivative for the synthesis of phosphotyrosine peptides by the global Fmoc SPPS phosphorylation methodology. Uses: Peptide synthesis. Group: Amino acids. Alternative Names: Fmoc-Tyr-OH, N-α-Fmoc-L-tyrosine. CAS No. 92954-90-0. Molecular formula: C24H21NO5. Mole weight: 403.43. Catalog: ACM92954900. | |
| Fmoc-Tyr(SO3nP)-OH | A novel derivative for the synthesis of sulfotyrosine-containing peptides by Fmoc SPPS. The sulfate neopentyl group is stable to TFA, and thus protects the sulfotyrosine residue from degradation during the cleavage reaction, but is easily cleaved post-cleavage by treatment of the peptide with aqueous ammonium acetate. Uses: Peptide synthesis. Group: Amino acids. Alternative Names: Fmoc-Tyr(SO3nP)-OH, N-Fmoc-O-(2,2 dimethylpropylsulfo)-L-tyrosine. CAS No. 878408-63-0. Molecular formula: C29H31NO8S. Mole weight: 553.62. IUPACName: (2S)-3-[4- (2, 2-dimethylpropoxysulfonyloxy)phenyl]-2- (9H-fluoren-9-ylmethoxycarbonylamino)propanoic acid. Canonical SMILES: CC (C) (C)COS (=O) (=O)OC1=CC=C (C=C1)CC (C (=O)O)NC (=O)OCC2C3=CC=CC=C3C4=CC=CC=C24. Catalog: ACM878408630. | |
| Fmoc-tyr(tbu)-bt | Heterocyclic Organic Compound. Alternative Names: 1126433-42-8, Fmoc-Tyr(tBu)-Bt, AKOS015950379, RP08123, FT-0685792, 9H-fluoren-9-ylmethyl N-[(2S)-1-(1,2,3-benzotriazol-1-yl)-3-[4-(tert-butoxy)phenyl]-1-oxopropan-2-yl]carbamate. CAS No. 1126433-42-8. Molecular formula: C34H32N4O4. Mole weight: 472.57. Purity: 0.96. IUPACName: 9H-fluoren-9-ylmethyl N-[(2S)-1-(benzotriazol-1-yl)-3-[4-[(2-methylpropan-2-yl)oxy]phenyl]-1-oxopropan-2-yl]carbamate. Canonical SMILES: CC (C) (C)OC1=CC=C (C=C1)CC (C (=O)N2C3=CC=CC=C3N=N2)NC (=O)OCC4C5=CC=CC=C5C6=CC=CC=C46. Catalog: ACM1126433428. | |
| Fmoc-Tyr(tBu)-OH | High purity Fmoc-protected amino acid for research and process production of peptides, with very low levels of dipeptide, free-amino acids and acetic acid impurities. Standard building block for introduction of tyrosine amino-acid residues by Fmoc SPPS. Uses: Fmoc-tyr(tbu)-oh novabiochem®. cas 71989-38-3, molar mass 459.55 g/mol. Group: Amino acids. Alternative Names: Fmoc-Tyr(tBu)-OH, N-α-Fmoc-O-t.-butyl-L-tyrosine. CAS No. 71989-38-3. Molecular formula: C28H29NO5. Mole weight: 459.53. Purity: Peak Area by HPLC ≥95%. Catalog: ACM71989383. | |
| Fmoc-Tyr(tBu)-Ser(psiMe,Mepro)-OH | This pseudoproline dipeptide is undoubtedly the most effective and simplest to use tool for overcoming aggregation and enhancing peptide quality in Fmoc SPPS for peptide containing the Tyr-Ser dipeptide motif. It consists of a dipeptide in which the serine residue has been reversibly protected as a structure-breaking proline-like TFA-labile oxazolidine. The reason the pseudoproline residue is introduced as a dipeptide is because it avoids the need to acylate the hindered oxazolidine nitrogen. This has the added advantage of extending the peptide chain by two residues in one step. The serine residue is regenerated during the normal TFA-mediated cleavage reaction. Uses: Peptide synthesis. Group: Amino acids. Alternative Names: Fmoc-Tyr(tBu)-Ser(psiMe,Mepro)-OH. CAS No. 878797-09-2. Mole weight: 586.67. Catalog: ACM878797092. | |
| Fmoc-val-bt | Heterocyclic Organic Compound. Alternative Names: 1126433-37-1, Fmoc-Val-Bt, ZINC32602753, AKOS015950320, RP08103, FT-0685699, 9H-fluoren-9-ylmethyl N-[(2S)-1-(1,2,3-benzotriazol-1-yl)-3-methyl-1-oxobutan-2-yl]carbamate. CAS No. 1126433-37-1. Molecular formula: C26H24N4O3. Mole weight: 440.51. Purity: 0.96. IUPACName: 9H-fluoren-9-ylmethyl N-[(2S)-1-(benzotriazol-1-yl)-3-methyl-1-oxobutan-2-yl]carbamate. Canonical SMILES: CC (C)C (C (=O)N1C2=CC=CC=C2N=N1)NC (=O)OCC3C4=CC=CC=C4C5=CC=CC=C35. Catalog: ACM1126433371. | |
| Fmoc-Val-OH | High purity Fmoc-protected amino acid for research and process production of peptides, with very low levels of dipeptide, free-amino acids and acetic acid impurities. Standard building block for introduction of valine amino-acid residues by Fmoc SPPS. Uses: Peptide synthesis. Group: Amino acids. Alternative Names: Fmoc-Val-OH, N-α-Fmoc-L-valine. CAS No. 68858-20-8. Molecular formula: C20H21NO4. Mole weight: 339.39. Catalog: ACM68858208. | |
| Folic Acid | A vitamin needed to synthesize DNA, conduct DNA repair and methylate DNA, it also acts as a cofactor in biological reactions involving folate. Group: Promotional products. Alternative Names: Folic acid. CAS No. 59-30-3. Molecular formula: C19H19N7O6. Mole weight: 441.4. Appearance: Solid. Purity: 95+%. IUPACName: (2S) -2- [ [4- [ (2-Amino-4-oxo-3H-Pteridin-6-yl) methylamino] benzoyl] amino] pentanedioic acid. Canonical SMILES: C1=CC (=CC=C1C (=O)NC (CCC (=O)O)C (=O)O)NCC2=CN=C3C (=N2)C (=O)NC (=N3)N. Density: 1.4704 g/cm³. Catalog: ACM59303-3. | |
| Follicle Booster | Biomimetic signal peptide (acetyl tetrapeptide-3) combined with a red clover extract rich in Biochanin A. Uses: Hair tonics, hair serums, eye lash serums, anti-hair loss formulas, scalp treatments. Group: Hair actives. CAS No. 107-88-0 / 7732-18-5 / 9004-54-0 / 827306-88-7 / 85085-25-2. Appearance: Colorless transparent liquid. Catalog: CI-HC-0209. | |
| Fomivirsen | Fomivirsen (ISIS-2922 free base) is an antisense 21 mer phosphorothioate oligonucleotide. Fomivirsen is an antiviral agent that is used CMV research, incluiding in AIDs. Fomivirsen binds to and degrades the mRNAs encoding CMV immediate-early 2 protein, thus inhibiting virus proliferation. Group: Inhibitors. Alternative Names: Isis 2922. CAS No. 144245-52-3. Molecular formula: C204H263N63O114P20S20. Mole weight: 6682.4. Purity: 0.96. IUPACName: Fomivirsen. Catalog: ACM144245523. | |
| Forchlorfenuron | Forchlorfenuron is a plant growth regulator. It has been approved for use on kiwi fruit and grapes in the USA, and it has been associated with exploding watermelons in China. Group: Heterocyclic organic compound. Alternative Names: KT-30;N-(2-chloropyridin-4-yl)-N-phenylurea;1-(2-chloropyridin-4-yl)-3-phenylurea;N-(2-Chloro-4-pyridyl)-N-phenylurea;fulmet. CAS No. 68157-60-8. Molecular formula: C12H10ClN3O. Mole weight: 247.68. Appearance: White to off white crystals. Density: 1.415 g/cm³. Catalog: ACM68157608. | |
| Forchlorfenuron-d5 | Forchlorfenuron-d5 is the deuterium labeled Forchlorfenuron. Forchlorfenuron is plant growth regulator and cytokinin; can be used to increase fruit size of fruits, such as kiwi fruit and grapes. Group: Isotope-labeled environmental contaminants. CAS No. 1398065-87-6. Molecular formula: C12H5D5ClN3O. Mole weight: 252.71. Canonical SMILES: [2H]C1=C ([2H])C ([2H])=C ([2H])C ([2H])=C1NC (NC2=CC=NC (Cl)=C2)=O. Catalog: ACM1398065876. | |
| Formaldehyde, DAIH derivative | Heterocyclic Organic Compound. Alternative Names: Formaldehyde, DAIH derivative, 2-Diphenylacetyl-3-(methylene-hydrazono)indan-1-one, 2-Diphenylacetyl-indan-1,3-dione-1-methylidenehydrazone, 1119449-21-6. CAS No. 1119449-21-6. Molecular formula: C24H18N2O2. Mole weight: 366.41. Purity: 0.96. IUPACName: (3Z)-2- (2, 2-diphenylacetyl)-3- (methylidenehydrazinylidene)inden-1-one. Canonical SMILES: C=NN=C1C (C (=O)C2=CC=CC=C21)C (=O)C (C3=CC=CC=C3)C4=CC=CC=C4. Catalog: ACM1119449216. | |
| Formamidine Hydrobromide (99.99%, trace metals basis) | Organohalide based perovskites have emerged as an important class of material for solar cell applications. Our perovskites precursors with extremely low water contents are useful for synthesizing mixed cation or anion perovskites needed for the optimization of the band gap, carrier diffusion length and power conversion efficiency of perovskites based solar cells. Group: Bromide salts. Alternative Names: FABr (99.99%, trace metals basis) Formamidinium Bromide (99.99%, trace metals basis). CAS No. 146958-06-7. Molecular formula: CH4N2 HBr. Mole weight: 124.97. Appearance: White to Almost white powder to crystal. Purity: ≥99%,anhydrous. Catalog: ACM146958067-2. | |
| Formamidinium Lead Iodide | Formamidinium Lead Iodide (FAPbI3) is a novel perovskite solar cell material that exhibits excellent thermal stability and superior photovoltaic performance. Group: Iodide salts. Alternative Names: FA lead iodide, FAI PbI2, alpha-phase FAPbI3, Black formamidinium lead iodide, Formamidinium triiodoplumbate, Lead(II) Iodide/Formamidine Hydroiodide (1:1) Complex, PbI2/FAI (1:1) Complex, Plumbate(1-), triiodo-, hydrogen, compd. with methanimidamide (1:1:1), CH(NH2)2PbI3, α-[HC(NH2)2]PbI3, CH4N2.H.PbI3. CAS No. 1451592-07-6. Molecular formula: CH5IN2-PbI2. Mole weight: 632.98. Appearance: Black crystals or powder. Purity: 2N99%FormamidiniumLeadIodide|3N99. 9%FormamidiniumLeadIodide|4N99. 99%FormamidiniumLeadIodide|5N99. 999%FormamidiniumLeadIodide. Catalog: ACM1451592076-1. | |
| For-met-leu-pna | Heterocyclic Organic Compound. Alternative Names: FOR-MET-LEU-PNA. CAS No. 111150-07-3. Molecular formula: C18H26N4O5S. Mole weight: 410.49. Catalog: ACM111150073. | |
| Formic acid, octylester | Heterocyclic Organic Compound. Alternative Names: Octyl formate, n-Octyl formate, Octyl methanoate, n-Octyl methanoate, 1-Octyl formate, Octyl alcohol, formate, FORMIC ACID, OCTYL ESTER, FEMA No. 2809, W280909_ALDRICH, Octyl alcohol, formate (6CI), EINECS 203-959-5, NSC 404473, BRN 1755259, NSC404473, LS-3009, 4-02-00-00031 (Beilstein Handbook Reference), 112-32-3. CAS No. 112-32-3. Molecular formula: C9H18 O2. Mole weight: 158.27. Purity: PURIFIED. IUPACName: octyl formate. Canonical SMILES: CCCCCCCCOC=O. Density: 0.875g/cm³. ECNumber: 203-959-5. Catalog: ACM112323. | |
| Formononetin-8-C-Beta-D-Apiofuranosyl-(1->6)-O-Beta-D-Glucopyranoside | Flavonoids. CAS No. 1147858-78-3. Molecular formula: C27H30O13. Mole weight: 562.5. Appearance: Powder. Purity: 0.98. Catalog: ACM1147858783. | |
| FORODESINE | Forodesine (BCX-1777) is a highly potent and orally active purine nucleoside phosphorylase (PNP) inhibitor with IC50 values ranging from 0.48 to 1.57 nM for human, mouse, rat, monkey and dog PNP. Forodesine is a potent human lymphocyte proliferation inhibitor. Forodesine could induce apoptosis in leukemic cells by increasing the dGTP levels. Group: Inhibitors. CAS No. 209799-67-7. Molecular formula: C11H14N4O4. Mole weight: 266.26. Appearance: White to Yellow Solid. Purity: 0.95. Canonical SMILES: O=C1C (NC=C2[C@@H]3N[C@H] (CO)[C@@H] (O)[C@H]3O)=C2NC=N1. Catalog: ACM209799677. | |
| Fosalvudine tidoxil | Fosalvudine tidoxil is an orally active nucleoside reverse transcriptase inhibitor (NRTI). Fosalvudine tidoxil is a prodrug derived from Alovudine (HY-B1516). Fosalvudine tidoxil is less toxic than Alovudine and can be used for the research of HIV-1 infection. Group: Inhibitors. Alternative Names: FOSALVUDINE TIDOXIL. CAS No. 763903-67-9. Molecular formula: C35H64FN2O8PS. Mole weight: 722.935. Canonical SMILES: O=P (OC[C@H]1O[C@@H] (N (C (N2)=O)C=C (C)C2=O)C[C@@H]1F) (OCC (OCCCCCCCCCC)CSCCCCCCCCCCCC)O. Catalog: ACM763903679. | |
| Fosamprenavir-d4 | Fosamprenavir-d4 is deuterium labeled Fosamprenavir. Group: Isotope-labeled synthetic intermediates. Alternative Names: Amprenavir phosphate-d4; GW 433908-d4. CAS No. 1133702-41-6. Molecular formula: C25H32D4N3O9PS. Mole weight: 589.63. Canonical SMILES: O=C (O[C@H]1CCOC1)N[C@@H] (CC2=CC=CC=C2)[C@H] (OP (O) (O)=O)CN (CC (C)C)S (=O) (C3=C ([2H])C ([2H])=C (C ([2H])=C3[2H])N)=O. Catalog: ACM1133702416. | |
| Fosinopril | Fosinopril (SQ28555 free acid) is the ester proagent of angiotensin-converting enzyme (ACE) inhibitor with an IC50 value of 0.18 μM. Fosinopril demonstrates a non-competitive inhibition effect on ACE activity with an Ki value of 1.675 μM. Group: Inhibitors. Alternative Names: Fosinopril. CAS No. 98048-97-6. Molecular formula: C30H46NO7P. Mole weight: 563.66. Appearance: Crystalline solid. Canonical SMILES: O=C (O)[C@H]1N (C (C[P@@] (CCCCC2=CC=CC=C2) (O[C@H] (OC (CC)=O)C (C)C)=O)=O)C[C@H] (C3CCCCC3)C1. Density: 1.173 g/cm³. Catalog: ACM98048976. | |
| Fosinoprilat acyl-β-D-glucuronide | Heterocyclic Organic Compound. Alternative Names: trans-4-Cyclohexyl-1-[[hydroxy(4-phenylbutyl)phosphinyl]acetyl]-L-proline β-D-Glucopyranuronosyl Ester. CAS No. 113411-09-9. Molecular formula: C29H42NO11P. Mole weight: 611.62. Appearance: N/A. Purity: 0.96. IUPACName: (2S, 3S, 4S, 5R, 6S) -6-[ (2S, 4S) -4-cyclohexyl-1-[2-[hydroxy (4-phenylbutyl) phosphoryl]acetyl]pyrrolidine-2-carbonyl]oxy-3, 4, 5-trihydroxyoxane-2-carboxylic acid. Canonical SMILES: C1CCC (CC1)C2CC (N (C2)C (=O)CP (=O) (CCCCC3=CC=CC=C3)O)C (=O)OC4C (C (C (C (O4)C (=O)O)O)O)O. Catalog: ACM113411099. | |
| Foy 251 | FOY 251, an anti-proteolytic active metabolite Camostate (HY-13512), acts as a proteinase inhibitor. FOY 251 inhibits SARS-CoV-2 infection in cells assay. Group: Inhibitors. Alternative Names: 4-[[4-[ (Aminoiminomethyl) amino]benzoyl]oxy]-benzeneacetic Acid Monomethanesulfonat;FOY 251;4-(4-guanidinobenzoyloxy)phenylacetic acid; 4-[[4-[ (Aminoiminomethyl) amino]benzoyl]oxy]-benzeneacetic Acid Monomethanesulfonate. CAS No. 71079-09-9. Molecular formula: C17H19N3O7S. Mole weight: 409.413660 [g/mol]. Appearance: White Solid. Purity: 0.96. IUPACName: 2-[4-[4- (diaminomethylideneamino) benzoyl]oxyphenyl]acetic acid; methanesulfonic acid. Canonical SMILES: O=C (O)CC1=CC=C (OC (C2=CC=C (NC (N)=N)C=C2)=O)C=C1. CS (=O) (O)=O. Density: 1.36g/cm³. Catalog: ACM71079099. | |
| FR-179642 | FR-179642 is a cyclic peptide and an important intermediate in producing micafungin. Group: Others. Alternative Names: FR-133303; FR 133303; FR133303; FR-179642; FR 179642; FR179642; Micafungin FR-179642 impurity; Pneumocandin M1. CAS No. 168110-44-9. Molecular formula: C35H52N8O20S. Mole weight: 936.9. Appearance: Solid powder. Purity: >98%. IUPACName: 5-((1S, 2S)-2-((2R, 6S, 9S, 11R, 12R, 14aS, 15S, 16S, 20S, 23S, 25aS)-9-amino-20-((R)-3-amino-1-hydroxy-3-oxopropyl)-2, 11, 12, 15-tetrahydroxy-6-((R)-1-hydroxyethyl)-16-methyl-5, 8, 14, 19, 22, 25-hexaoxotetracosahydro-1H-dipyrrolo[2, 1-c:2', 1'-l][1, 4, 7, 10, 13, 16]hexaazacyclohenicosin-23-yl)-1, 2-dihydroxyethyl)-2-hydroxyphenyl hydrogen sulfate. Canonical SMILES: C[C@@H] (O)[C@@H]1NC (=O)[C@@H] (N)C[C@@H] (O)[C@@H] (O)NC (=O)[C@@H]2[C@@H] (O)[C@@H] (C)CN2C (=O)[C@@H] (NC (=O)[C@@H] (NC (=O)[C@@H]3C[C@@H] (O)CN3C1=O)[C@H] (O)[C@@H] (O)c4ccc (O)c (OS (=O) (=O)O)c4)[C@H] (O)CC (=O)N. Catalog: ACM168110449. | |
| FR 901464 | FR901464 is a potent spliceosome inhibitor and a potential agent for colorectal cancer in combination therapy. Group: Inhibitors. Alternative Names: FR 901464; FR-901464; FR901464; WB 2663B. CAS No. 146478-72-0. Molecular formula: C27H41NO8. Mole weight: 507.62. Appearance: Solid powder. Purity: >98%. IUPACName: (2S,E)-5-(((2R,5S,6S)-6-((2E,4E)-5-((4R,5R,7S)-4,7-dihydroxy-7-methyl-1,6-dioxaspiro[2.5]octan-5-yl)-3-methylpenta-2,4-dien-1-yl)-2,5-dimethyltetrahydro-2H-pyran-3-yl)amino)-5-oxopent-3-en-2-yl acetate. Canonical SMILES: C[C@H]1CC ([C@H] (O[C@H]1C/C=C (\C)/C=C/[C@@H]2[C@H] (C3 (C[C@@] (O2) (C)O)CO3)O)C)NC (=O)/C=C/[C@H] (C)OC (=O)C. Catalog: ACM146478720. | |
| Freon | Heterocyclic Organic Compound. CAS No. 11126-05-9. Catalog: ACM11126059. | |
| Fucoxanthin | Fucoxanthin is a naturally occurring compound found in brown seaweed, such as wakame, hijiki, and brown algae. It is a type of carotenoid and is known for its antioxidant properties. Fucoxanthin has been shown to have potential anti-inflammatory, anti-tumor, and anti-obesity effects. Uses: 1. fucoxanthin is a brown seaweed pigment that is used as a dietary supplement to promote weight loss. 2. it has anti-inflammatory properties and may help reduce the risk of chronic diseases such as cancer and heart disease. 3. fucoxanthin may also have potential as a natural food preservative due to its antioxidant properties. 4. studies have shown that fucoxanthin may improve insulin sensitivity and help regulate blood sugar levels. 5. it has been found to have antibacterial and antiviral properties and may be useful in the development of new treatments for infections. Group: Heterocyclic organic compound. Alternative Names: (3S,3'S,5R,5'R,6S,6'R)-6',7'-Didehydro-5,6-epoxy-4',5',6,7-tetrahydro-3,3',5'-trihydroxy-,-caroten-8(5H)-one. CAS No. 3351-86-8. Molecular formula: C42H58O6. Mole weight: 658.9. Appearance: Powder. Purity: 95%+. IUPACName: [(1S,3R)-3-hydroxy-4-[(3E,5E,7E,9E,11E,13E,15E)-18-[(1R,3S,6S)-3-hydroxy-1,5,5-trimethyl-7-oxabicyclo[4.1.0]heptan-6-yl]-3,7,12,16-tetramethyl-17-oxooctadeca-1,3,5,7,9,11,13,15-octaenylidene]-3,5,5-trimethylcyclohexyl] acetate. Canonical SMILES: CC (=CC=CC=C (C)C=CC=C (C)C (=O)CC12C (CC (CC1 (O2)C)O | |
| Full Area Coverage PdS2 Layers on Sapphire | Alfa Chemisry used chemical vapor deposition to grow full-area PdS2 layers on c-cut sapphire substrates. The sample size is 1 cm and the entire sample surface contains PdS2 sheets. Uses: Optoelectronic devices, microelectronic devices, biological sensing, chemical sensing and other fields. Group: 2d thin films. CAS No. 12137-75-6. Appearance: transparent. Purity: 99.9995% purity. Catalog: ACM12137756. | |
| Fullerene | Fullerene is a 3-dimensional, spherical molecule consisting of 60 carbon atoms. It is unique in that it is able to engage in strong antioxidant activities (quenching free radicals) without being inactivated in the process like other antioxidants such as vitamin C. Dynamic viscosity =10,000 mPas. Uses: Anti-aging and anti-wrinkle creams, anti-blemished skin treatments, skin-whitening treatments, face masks, sun care & after sun products. Group: Skin actives. CAS No. 99685-96-8 / 9067-32-7 / 107-88-0 / 7732-18-5. Appearance: Brown, viscous liquid, odorless. Catalog: CI-SC-1039. | |
| Fullerene C78 | Fullerene C78 is a molecule made up of 78 carbon atoms arranged in a series of interlocking hexagons and pentagons, forming a structure that looks similar to a rugby ball. C70 is actually a 37-sided polygon consisting of 12 pentagons and 25 hexagons. Group: Renewable & alternative energy. Alternative Names: FULLERENE C78;FULLERENECARBON 78, 95.0%;Fullerene-C78,min.95%;Fullerene - C78, min. 95%. CAS No. 136316-32-0. Molecular formula: C78. Mole weight: 936.83. Appearance: Solid. Purity: 2N99% Fullerene C78|3N99.9% Fullerene C78|4N99.99% Fullerene C78|5N99.999% Fullerene C78. IUPACName: tetracontacyclo[25.6.5.516, 28.44, 32.35, 11.321, 34.28, 10.212, 15.222, 35.229, 31.113, 20.124, 38.02, 6.014, 19.017, 25.018, 23.030, 37.033, 36.547, 54.446, 53.448, 58.126, 51.150, 52.03, 45.07, 42.09, 61.039, 40.041, 43.044, 63.049, 76.055, 78.056, 62.057, 68.059, 64.060, 67.065, 69.066, 71.070, 73.072, 75.074, 77]octaheptaconta-1, 3(45), 4(48), 5(61), 6, 8, 10, 12, 14, 16, 18, 20, 22, 24(39), 25, 27(38), 28, 30, 32, 34(42), 35(40), 36, 41(43), 44(63), 46, 49(76), 50(77), 51, 53, 55(78), 56(62), 57, 59, 64, 66, 68, 70(73), 71, 74-nonatriacontaene. Canonical SMILES: C12=C3C4=C5C6=C7C8=C9C% 10=C% 11C% 12=C% 13C% 14=C% 15C% 16=C% 12C% 12=C% 17C% 18=C% 16C% 16=C% 19C% 20=C (C1=C5C (=C% 18% 20) C% 17=C6C8=C% 11% 12) C1=C5C% 19=C6C8=C% 11C5=C5C (=C21) C1=C3C2=C3C% 12=C1C1=C5C% 11=C5C% 11=C8C (=C% 14C8=C% 11C% 11=C% 14C (=C% 12C1=C% 115) C1=C3C (= | |
| Fullerene Powder | Fullerene Powder is available in several forms including sublimed, mixed, mixed refined, hydroxylated and mixed hydrogenated. Fullerenes are also known by the names Buckminsterfullerene and Fullerite. Fullerene Powder is generally immediately available in most volumes. Group: Nanoparticles & nanopowders. Alternative Names: Buckyballs; Buckminsterfullerene; (C60-Ih)[5, 6]Fullerene; [60]fullerene; C6-; Fullerenepowder; Footballene. CAS No. 115383-22-7. Molecular formula: C70. Mole weight: 840.749. Appearance: Black powder. Purity: 99% | 99.9% | 99.99% | 99.999%. IUPACName: (C\{70}-D \{5h(6)}) fullerene. Canonical SMILES: C12=C3C4=C5C6=C7C8=C9C% 10=C% 11C% 12=C% 13C% 10=C% 10C8=C5C1=C% 10C1=C% 13C5=C8C1=C2C1=C3C2=C3C% 10=C% 13C% 14=C3C1=C8C1=C3C5=C% 12C5=C8C% 11=C% 11C9=C7C7=C9C6=C4C2=C2C% 10=C4C (=C29) C2=C6C (=C8C8=C9C6=C4C% 13=C9C (=C% 141) C3=C85) C% 11=C27. Density: 3.51g/cm³. Catalog: ACM115383227. | |
| Fumagillin | Fumagillin(NSC9168) is an antimicrobial compound first isolated in 1949 from the fungus Aspergillus fumigatu. Fumagillin can inhibits HIV-1 infection through the inhibition of HIV-1 viral protein R (Vpr) activity. Group: Inhibitors. Alternative Names: NSC9168; NSC 9168; NSC-9168; Fumidil B; Fumagillin, trade name: Fumagilina; Fugillin; Fumidil. CAS No. 23110-15-8. Molecular formula: C26H34O7. Mole weight: 458.55 g/mol. Appearance: Solid powder. Purity: ≥98%. IUPACName: (2E,4E,6E,8E)-10-(((3R,4S,5S,6R)-5-methoxy-4-((2R)-2-methyl-3-(3-methylbut-2-en-1-yl)oxiran-2-yl)-1-oxaspiro[2.5]octan-6-yl)oxy)-10-oxodeca-2,4,6,8-tetraenoic acid. Canonical SMILES: O=C (O)/C=C/C=C/C=C/C=C/C (O[C@H] (CC1)[C@@H] (OC)[C@H] ([C@@]2 (C)OC2C/C=C (C)\C)[C@]31CO3)=O. Catalog: ACM23110158. | |
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