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| Product | Description | |
|---|---|---|
| PSN 375963 hydrochloride | PSN 375963 hydrochloride. Group: Biochemicals. Grades: Purified. CAS No. 388575-52-8. Pack Sizes: 10mg, 50mg. US Biological Life Sciences. |  Worldwide |
| PSNCBAM-1 | PSNCBAM-1 is an allosteric, non-competitive antagonist of CB-1 (IC50= 45 and 209 nM) with hypophagic effects in vivo, potentially an anti-obesity agents. Alternative Names: PSNCBAM 1; PSNCBAM1; N-(4-Chlorophenyl)-N'-(3-(6-(1-pyrrolidinyl)-2-pyridinyl)phenyl)urea. Grades: ≥99% by HPLC. CAS No. 877202-74-9. Molecular formula: C22H21ClN4O. Mole weight: 392.88. |  |
| Psora 4 | Psora 4. Group: Biochemicals. Grades: Purified. CAS No. 724709-68-6. Pack Sizes: 10mg, 50mg. US Biological Life Sciences. | Worldwide |
| Psora-4 | Psora-4 is a potent and selective inhibitor of Kv1.3 (voltage-gated potassium channels) with an EC50 of 3 nM[1]. Psora-4 has immunosuppressive activity and inhibits proliferation of human and rat myelin-specific effector memory T cells in vitro[2]. Uses: Scientific research. Category: Signaling pathways. Alternative Names: 5-(4-Phenylbutoxy)psoralen. CAS No. 724709-68-6. Pack Sizes: 1 mg; 5 mg; 10 mg. Product ID: HY-108583. |  |
| Psoralen | Psoralen is a photoactive probe that has been used to investigate nucleic acid structure and function. It intercalates into DNA and, when activated by ultraviolet radiation, can create covalent interstrand crosslinks, inducing apoptosis. Alternative Names: Ficusin; Furocoumarin. Grades: 97 %. (HPLC). CAS No. 66-97-7. Molecular formula: C11H6O3. Mole weight: 186.16. | |
| Psoralen | Psoralen. Group: Biochemicals. Grades: Highly Purified. CAS No. 66-97-7. Pack Sizes: 10mg, 25mg, 50mg, 100mg. Molecular Formula: C11H6O3. US Biological Life Sciences. | Worldwide |
| Psoralen | Psoralen (Ficusin) is a coumarin isolated from the seeds of Fructus Psoraleae. Psoralen exhibits a wide range of biological properties, including anti-cancer, antioxidant, antidepressant, anticancer, antibacterial, and antiviral, et al[1]. Uses: Scientific research. Category: Signaling pathways. Alternative Names: Ficusin. CAS No. 66-97-7. Pack Sizes: 10 mM * 1 mL in DMSO; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-N0053. | |
| Psoralen Azide | Psoralen Azide is a chemical compound used in biomedical research to study DNA damage and repair pathways. It is commonly used to crosslink DNA and proteins, as well as to label proteins with azide groups for subsequent click chemistry reactions. Alternative Names: 4'-Azidomethyl-4,5',8-trimethylpsoralen; 3-(Azidomethyl)-2,5,9-trimethyl-7H-furo[3,2-g][1]benzopyran-7-one. Grades: ≥97%. CAS No. 1489190-74-0. Molecular formula: C15H13N3O3. Mole weight: 283.28. | |
| Psoralen-C2 CEP | Psoralen-C2 CEP is an innovative biomedical compound, used for studying a myriad of skin afflictions, particularly psoriasand vitiligo. It is derived from psoralen, an organic constituent inherent to select flora. Alternative Names: 2-[4'-(hydroxymethyl)-4,5',8-trimethylpsoralen]-ethyl-1-O-(2-cyanoethyl)-(N,N-diisopropyl)-phosphoramidite; Psoralen C2 Phosphoramidite; Phosphoramidous acid, bis(1-methylethyl)-, 2-cyanoethyl 2-[(2,5,9-trimethyl-7-oxo-7H-furo[3,2-g][1]benzopyran-3-yl)methoxy]ethyl ester; 2-Cyanoethyl (2-((2,5,9-trimethyl-7-oxo-7H-furo[3,2-g]chromen-3-yl)methoxy)ethyl) diisopropylphosphoramidite; Psoralen C-2 CED phosphoramidite. Grades: 95%. CAS No. 126221-83-8. Molecular formula: C26H35N2O6P. Mole weight: 502.55. | |
| Psoralen C6 Phosphoramidite | Psoralen C6 Phosphoramidite is an indispensable compound, finding extensive employment in DNA synthesis and modification. This remarkable product effectively facilitates the incorporation of psoralen derivatives into oligonucleotides, thereby enabling the research of an extensive array of afflictions encompassing cancer and dermatological conditions. Alternative Names: 6-[4'-(Hydroxymethyl)-4,5',8-trimethylpsoralen]-hexyl-1-O-(2-cyanoethyl)-(N,N-diisopropyl)-phosphoramidite; Phosphoramidous acid, N,N-bis(1-methylethyl)-, 2-cyanoethyl 6-[(2,5,9-trimethyl-7-oxo-7H-furo[3,2-g][1]benzopyran-3-yl)methoxy]hexyl ester; Psoralen C-6 CED phosphoramidite; 2-Cyanoethyl 6-[(2,5,9-trimethyl-7-oxo-7H-furo[3,2-g][1]benzopyran-3-yl)methoxy]hexyl N,N-bis(1-methylethyl)phosphoramidite; Phosphoramidous acid, bis(1-methylethyl)-, 2-cyanoethyl 6-[(2,5,9-trimethyl-7-oxo-7H-furo[3,2-g][1]benzopyran-3-yl)methoxy]hexyl ester; Psoralen-C6 CEP. CAS No. 518046-08-7. Molecular formula: C30H43N2O6P. Mole weight: 558.65. | |
| psoralen synthase | This microsomal cytochrome P-450-dependent enzyme is specific for (+)-marmesin, and to a much lesser extent 5-hydroxymarmesin, as substrate. Furanocoumarins protect plants from fungal invasion and herbivore attack. (+)-Columbianetin, the angular furanocoumarin analogue of the linear furanocoumarin (+)-marmesin, is not a substrate for the enzyme but it is a competitive inhibitor. Group: Enzymes. Synonyms: CYP71AJ1. Enzyme Commission Number: EC 1.14.13.102. 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-0701; psoralen synthase; EC 1.14.13.102; CYP71AJ1. Cat No: EXWM-0701. |  |
| Psoralidin | Psoralidin is a dual inhibitor of COX-2 and 5-LOX, regulates ionizing radiation (IR)-induced pulmonary inflammation.Anti-cancer, anti-bacterial, and anti-inflammatory properties[1]. Psoralidin significantly downregulates NOTCH1 signaling. Psoralidin also greatly induces ROS generation[2]. Uses: Scientific research. Category: Signaling pathways. CAS No. 18642-23-4. Pack Sizes: 10 mM * 1 mL in DMSO; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg; 500 mg. Product ID: HY-N0232. | |
| Psoralidin | Psoralidin is a furanocoumarin natural product used in Chinese medicine. Psoralidin, a PTP1B inhibitor, has been shown to have anticancer activity with a variety of mechanisms proposed. Psoralidin induces ROS generation in androgen-independent prostate cancer cells, leading to inhibition of cell proliferation. Psoralidin has been found to downregulate NOTCH1 signaling, causing growth arrest in both breast cancer stem cells and breast cancer cells. Uses: Anticancer and chemopreventive properties. Alternative Names: 3,9-Dihydroxy-2-(3-methyl-2-butenyl)-6H-benzofuro[3,2-c][1]benzopyran-6-one; 3,9-Dihydroxy-2-prenylcoumestan. Grades: >98%. CAS No. 18642-23-4. Molecular formula: C20H16O5. Mole weight: 336.34. | |
| Psoralidin | Psoralidin. Group: Biochemicals. Grades: Plant Grade. CAS No. 18642-23-4. Pack Sizes: 20mg. Molecular Formula: C20H16O5, Molecular Weight: 336.34. US Biological Life Sciences. | Worldwide |
| Psoromic acid | Psoromic acid is a selective inhibitor of Rab geranylgeranyl transferase and P. falciparum fatty acid synthesis (FAS) II enzymes. Alternative Names: 10-formyl-9-hydroxy-3-methoxy-4,7-dimethyl-6-oxobenzo[b][1,4]benzodioxepine-1-carboxylic acid; NSC 92186; Parellic Acid; Psoromsaeure; Sulcatic acid; Sqamaric. Grades: ≥95%. CAS No. 7299-11-8. Molecular formula: C18H14O8. Mole weight: 358.30. | |
| Psoromic acid | Psoromic acid is a potent and selective RabGGTase (Rab geranylgeranyl transferase) inhibitor with an IC50 value of 1.3 μM. Psoromic acid is an antioxidative agent. Psoromic acid exhibits a competitive type of HMGR inhibition and mixed type of ACE (angiotensin converting enzyme) inhibition[1][2]. Uses: Scientific research. Category: Natural products. Alternative Names: Parellic acid. CAS No. 7299-11-8. Pack Sizes: 500 μg. Product ID: HY-130199. | |
| Psp124B I | One unit of the enzyme is the amount required to hydrolyze 1 μg of Lambda DNA (HindIII-digest) in 1 hour at 37°C in a total reaction volume of 50 μl. Applications: After 20-fold overdigestion with enzyme more than 90% of the dna fragments can be ligated and recut. Group: Restriction Enzymes. Purity: 1000U; 5000U. GAGCT↑C C↓TCGAG. Activity: 20000u.a./ml. Appearance: 10 X SE-buffer G. Storage: -20°C. Form: Liquid. Source: Pseudomonas species 124B. Pack: 10 mM Tris-HCl (pH 7.5); 250 mM NaCl; 0,1 mM EDTA; 7 mM 2-mercaptoethanol; 100 μg/ml BSA; 50% glycerol. Cat No: ET-1151RE. | |
| Psp6 I | One unit of the enzyme is the amount required to hydrolyze 1 μg of Lambda DNA (dcm-) in 1 hour at 55°C in a total reaction volume of 50 μl. Applications: After 3-fold overdigestion with enzyme 95% of the dna fragments can be ligated and recut. Group: Restriction Enzymes. Purity: 100U; 500U. ↑CCWGG GGWCC&darr. Activity: 1000-3000u.a./ml. Appearance: 10 X SE-buffer B. Storage: -20°C. Form: Liquid. Source: Pseudomonas species 6. Pack: 10 mM Tris-HCl (pH 7.5); 100 mM KCl; 0.1 mM EDTA; 7 mM 2-mercaptoethanol; 200 μg/ml BSA; and 50% glycerol. Cat No: ET-1152RE. | |
| PspC I | One unit of the enzyme is the amount required to hydrolyze 1 μg of Lambda DNA in 1 hour at 37°C in a total reaction volume of 50 μl. Applications: After 20-fold overdigestion with enzyme more than 90% of the dna fragments can be ligated and recut. ligation is better in presence of 10% peg. Group: Restriction Enzymes. Purity: 2000U; 10000U. CAC↑GTG GTG↓CAC. Activity: 20000u.a./ml. Appearance: 10 X SE-buffer B, BSA. Storage: -20°C. Storage at -70°C is recommended for periods longer than 30 days. Form: Liquid. Source: Pseudomonas species C. Pack: 10 mM Tris-HCl (pH 7.5); 50 mM KCl; 0.1 mM EDTA; 7 mM 2-mercaptoethanol; 200 μg/ml BSA; and 50% glycerol. Cat No: ET-1153RE. | |
| PspE I | One unit of the enzyme is the amount required to hydrolyze 1 μg of Lambda DNA in 1 hour at 37°C in a total reaction volume of 50 μl. Applications: After 10-fold overdigestion with enzyme more than 90% of the dna fragments can be ligated and recut. Group: Restriction Enzymes. Purity: 2000U; 10000U. G↑GTNACC CCANTG↓G. Activity: 10000u.a./ml. Appearance: 10 X SE-buffer B. Storage: -20°C. Form: Liquid. Source: Pseudomonas species E. Pack: 10 mM Tris-HCl (pH 7.5); 50 mM NaCl; 0,1 mM EDTA; 7 mM 2-mercaptoethanol; 200 μg/ml BSA; 50% glycerol. Cat No: ET-1154RE. | |
| PspL I | One unit of the enzyme is the amount required to hydrolyze 1 μg of Lambda DNA (HindIII-digest) in 1 hour at 37°C in a total reaction volume of 50 μl. Applications: After 2-fold overdigestion with enzyme more than 95% of the dna fragments can be ligated and recut. Group: Restriction Enzymes. Purity: 200U; 1000U. C↑GTACG GCATG↓C. Activity: 2000-5000u.a./ml. Appearance: 10 X SE-buffer Y, BSA. Storage: -20°C. Form: Liquid. Source: Pseudomonas species L. Pack: 10 mM Tris-HCl (pH 7.5); 100 mM NaCl; 0.1 mM EDTA; 7 mM 2-mercaptoethanol; 100 μg/ml BSA; 50% glycerol. Cat No: ET-1155RE. | |
| PspN4 I | One unit of the enzyme is the amount required to hydrolyze 1 μg of Lambda DNA in 1 hour at 37°C in a total reaction volume of 50 μl. Applications: After 10-fold overdigestion with enzyme more than 95% of the dna fragments can be ligated and recut. Group: Restriction Enzymes. Purity: 1000U; 5000U. GGN↑NCC CCN↓NGG. Activity: 10000u.a./ml. Appearance: 10 X SE-buffer Y. Storage: -20°C. Form: Liquid. Source: Pseudomonas species N4. Pack: 10 mM Tris-HCl (pH 7.5); 50 mM KCl; 0,1 mM EDTA; 7 mM 2-mercaptoethanol; 200 μg/ml BSA; 50% glycerol. Cat No: ET-1156RE. | |
| PspOM I | One unit of the enzyme is the amount required to hydrolyze 1 μg of Lambda DNA (BamHI-digest) in 1 hour at 37°C in a total reaction volume of 50 μl. Applications: After 10-fold overdigestion with enzyme more than 95% of the dna fragments can be ligated and recut. Group: Restriction Enzymes. Purity: 1500U; 7500U. G↑GGCCC CCCGG↓G. Activity: 10000u.a./ml. Appearance: 10 X SE-buffer Y. Storage: -20°C. Form: Liquid. Source: An E.coli strain that carries the cloned PspOM I gene from Pseudomonas species OM2164. Pack: 20 mM Tris-HCl (pH 7.5); 50 mM NaCl; 0,1 mM EDTA; 1 mM DTT; 200 μg/ml BSA; and 50% glycerol. Cat No: ET-1157RE. | |
| PspPP I | One unit of the enzyme is the amount required to hydrolyze 1 μg of Lambda DNA/HindIII in 1 hour at 37°C in a total reaction volume of 50 μl. Applications: After 5-fold overdigestion with enzyme more than 70% of the dna fragments can be ligated and more than 80% of these can be recut. Group: Restriction Enzymes. Purity: 100U; 500U. RG↑GWCCY YCCWG↓GR. Activity: 2000-5000u.a./ml. Appearance: 10 X SE-buffer Y, BSA. Storage: -20°C. Form: Liquid. Source: Pseudomonas species PP. Pack: 10 mM Tris-HCl (pH 7.5); 200 mM NaCl; 0.1 mM EDTA; 7 mM 2-mercaptoethanol; 200 μg/ml BSA; 50% glycerol. Cat No: ET-1158RE. | |
| PspX I | One unit of the enzyme is the amount required to hydrolyze 1 μg of Lambda DNA (HindIII-digest) in 1 hour at 37°C in a total reaction volume of 50 μl. Applications: After 20-fold overdigestion with enzyme more than 90% of the dna fragments can be ligated and recut. Group: Restriction Enzymes. Purity: 200U; 1000U. VC↑TCGAGB BGAGCT↓CV. Activity: 10000u.a./ml. Appearance: 10 X SE-buffer Y, BSA. Storage: -20°C. Form: Liquid. Source: An E.coli strain that carries the cloned PspX I gene from Pseudomonas species A1-1. Pack: 10 mM Tris-HCl (pH 7.5); 200 mM KCl; 0.1 mM EDTA; 7 mM 2 -mercaptoethanol, 200 μg/ml BSA; 50% glycerol. Cat No: ET-1159RE. | |
| Psr I | One unit of the enzyme is the amount required to hydrolyze 1 μg of T7 DNA in 1 hour at 30°C in a total reaction volume of 50 μl. Applications: After 2-fold overdigestion with enzyme more than 70% of dna fragments can be ligated. of these 80% can be recut. in the presence of 10% peg ligation is better. Group: Restriction Enzymes. Purity: 100U; 500U. ↑(N)7GAACNNNNNNTAC(N)12↑ ↓(N)12CTTGNNNNNNATG(N)7&darr. Activity: 1000-2000u.a./ml. Appearance: 10 X SE-buffer Y, BSA. Storage: -20°C. Form: Liquid. Source: Pseudomonas stutzeri N2. Pack: 10 mM Tris-HCl (pH 7.5); 50 mM KCl; 0,1 mM EDTA; 7 mM 2-mercaptoethanol; 200 μg/ml BSA, 50% glycerol. Cat No: ET-1160RE. | |
| Pss-(1-propylmethacrylate)-heptaisobuty& | Pss-(1-propylmethacrylate)-heptaisobuty&. Alternative Names: PSS-(1-PROPYLMETHACRYLATE)-HEPTAISOBUTY&;3-(3,5,-HEPTAISOBUTYLPENTACYCLO(9.5(3,9);3-(3,5,7,9,11,13,15-heptaisobutylpentacyclo[9.5.13,9.15,15.17,13]octasiloxan-1-yl)propylmethacrylate;pss-(1-propylmethacrylate)-heptaisobutyl substituted;METHACRYLOXYPROPYL. CAS No. 307531-94-8. Molecular formula: C35H74O14Si8. Mole weight: 943.6g/mol. IUPAC Name: 3-[3,5,7,9,11,13,15-heptakis(2-methylpropyl)-2,4,6,8,10,12,14,16,17,18,19,20-dodecaoxa-1,3,5,7,9,11,13,15-octasilapentacyclo[9.5.1.13,9.15,15.17,13]icosan-1-yl]propyl 2-methylprop-2-enoate. SMILES: CC(C)C[Si]12O[Si]3(O[Si]4(O[Si](O1)(O[Si]5(O[Si](O2)(O[Si](O3)(O[Si](O4)(O5)CC(C)C)CC(C)C)CC(C)C)CC(C)C)CC(C)C)CC(C)C)CCCOC(=O)C(=C)C. InChI: InChI=1S/C35H74O14Si8/c1-27(2)20-51-38-50(19-17-18-37-35(36)34(15)16)39-52(21-28(3)4)43-54(41-51,23-30(7)8)47-57(26-33(13)14)48-55(42-51,24-31(9)10)44-53(40-50,22-29(5)6)46-56(45-52,49-57)25-32(11)12/h27-33H,15,17-26H2,1-14,16H3. |  |
| PSS-(1-Propylmethacrylate)-Heptaisobutyl substituted | PSS-(1-Propylmethacrylate)-Heptaisobutyl substituted is a monomer used to produce coatings in the form of films or beads that are resistant to organic solvents and acids. Alternative Names: Methacryloxypropylheptaisobutyl-T8-silsesquioxane; 3-(3,5,7,9,11,13,15-heptaisobutylpentacyclo[9.5.13,9.15,15.17,13]octasiloxan-1-yl)propylmethacrylate. CAS No. 307531-94-8. Molecular formula: C35H74O14Si8. Mole weight: 943.64. | |
| Pss-(2-(3 4-epoxycyclohexyl)ethyl)-hept& | Pss-(2-(3 4-epoxycyclohexyl)ethyl)-hept&. Alternative Names: PSS-(2-(3 4-EPOXYCYCLOHEXYL)ETHYL)-HEPT&;1-(2-(3,4-EPOXYCYCLOHEXYL)ETHYL-3,5,7,9,11 -ISOBUTYLPENTACYCLO-(9.5.)OCTASILOXAN;1-[2-(3,4-epoxycyclohexyl)ethyl]-3,5,7,9,11,13,15-isobutylpentacyclo-[9.5.1.13,9.15,15.17,13]octasiloxane;pss-[2-(3,4-epoxycyclohexyl. CAS No. 445379-56-6. Molecular formula: C36H76O14Si8. Mole weight: 957.67. Purity: 96%. IUPAC Name: AC1MW6NE. | |
| Pss-(2 3-propanediol)propoxy-heptaisobu& | Pss-(2 3-propanediol)propoxy-heptaisobu&. Alternative Names: PSS-(2 3-PROPANEDIOL)PROPOXY-HEPTAISOBU&;1-(2,3-PROPANEDIOL)PROPOXY-3,5,7,9,11,13, 15-ISOBUTYLPENTACYCLO-(9.5.)OCTASILOXA;pss-(2,3-propanediol)propoxy-heptaisobutyl substituted;1,2-Propanediolisobutyl-POSS(R),POSS(R)-1,2-propanediol-isobutylsubstituted,1-. CAS No. 480439-49-4. Molecular formula: C34H76O16Si8. Mole weight: 965.646. Purity: 96%. IUPAC Name: AC1N8M4T. SMILES: CC(C)C[Si]12O[Si]3(O[Si]4(O[Si](O1)(O[Si]5(O[Si](O2)(O[Si](O3)(O[Si](O4)(O5)CC(C)C)CC(C)C)CC(C)C)CC(C)C)CC(C)C)CC(C)C)CCCOCC(CO)O. | |
| Pss-[2-[(Chloromethyl)Phenyl]Ethyl]-Heptaisobutyl Substituted | Pss-[2-[(Chloromethyl)Phenyl]Ethyl]-Heptaisobutyl Substituted. Alternative Names: 1-Chlorobenzylethyl-3,5,7,9,11,13,15-Heptaisobutylpentacyclo[9.5.1.1(3,9).1(5,15).1(7,13)]Ctasiloxane. Molecular formula: C37H73ClO12Si8. Mole weight: 970.11 g/mol. | |
| Pss-(2-(trans-3 4-cyclohexanediol)ethyl& | Pss-(2-(trans-3 4-cyclohexanediol)ethyl&. Alternative Names: PSS-(2-(TRANS-3 4-CYCLOHEXANEDIOL)ETHYL&;1-(2-TRANS-CYCLOHEXANEDIOL)ETHYL-3,5,7,9, 15-ISOBUTYLPENTACYCLO-OCTASILOXANE;1-(2-trans-cyclohexanediol)ethyl-3,5,7,9,11,13,15-isobutylpentacyclo-[9.5.1.13,9.15,15.17,13]octasiloxane;pss-(2-(trans-3,4-cyclohexaned. CAS No. 480439-48-3. Molecular formula: C36H78O15Si8. Mole weight: 975.685. Purity: 96%. IUPAC Name: AC1MUI3F. | |
| Pss-(3-(2-aminoethyl)amino)propyl-hepta& | Pss-(3-(2-aminoethyl)amino)propyl-hepta&. Alternative Names: PSS-(3-(2-AMINOETHYL)AMINO)PROPYL-HEPTA&;1-(3-(2-AMINOETHYL)AMINO)PROPYL-3,5,7,9,11 -ISOBUTYLPENTACYCLO-(9.5.)OCTASILOXAN;1-[3-(2-aminoethyl)amino]propyl-3,5,7,9,11,13,15-isobutylpentacyclo-[9.5.1.1(3,9).1(5,15).1(7,13)]octasiloxane;pss-[3-(2-aminoethyl)a. CAS No. 444315-16-6. Molecular formula: C33H76N2O12Si8. Mole weight: 917.653. Purity: 96%. IUPAC Name: AC1NCUKU. SMILES: CC(C)C[Si]12O[Si]3(O[Si]4(O[Si](O1)(O[Si]5(O[Si](O2)(O[Si](O3)(O[Si](O4)(O5)CC(C)C)CC(C)C)CC(C)C)CC(C)C)CC(C)C)CC(C)C)CCCNCCN. | |
| Pss-(3-glycidyl)propoxy-heptaisobutyl s& | Pss-(3-glycidyl)propoxy-heptaisobutyl s&. Alternative Names: PSS-(3-GLYCIDYL)PROPOXY-HEPTAISOBUTYL S&;1-(3-GLYCIDYL)PROPOXY-3,5,7,9,11,13,15-ISOBUTYLPENTACYCLO-(9.5.)OCTASILOXANE;pss-(3-glycidyl)propoxy-heptaisobutyl substituted;Glycidylisobutyl-POSS(R),POSS(R)-Glycidyl-isobutylsubstituted,1-(3-Glycidyl)propoxy-3,5. CAS No. 444315-17-7. Molecular formula: C34H74O14Si8. Mole weight: 931.6g/mol. IUPAC Name: 1,3,5,7,9,11,13-heptakis(2-methylpropyl)-15-[3-(oxiran-2-ylmethoxy)propyl]-2,4,6,8,10,12,14,16,17,18,19,20-dodecaoxa-1,3,5,7,9,11,13,15-octasilapentacyclo[9.5.1.13,9.15,15.17,13]icosane. SMILES: CC(C)C[Si]12O[Si]3(O[Si]4(O[Si](O1)(O[Si]5(O[Si](O2)(O[Si](O3)(O[Si](O4)(O5)CC(C)C)CC(C)C)CC(C)C)CC(C)C)CC(C)C)CC(C)C)CCCOCC6CO6. InChI: InChI=1S/C34H74O14Si8/c1-27(2)20-50-37-49(17-15-16-35-18-34-19-36-34)38-51(21-28(3)4)42-53(40-50,23-30(7)8)46-56(26-33(13)14)47-54(41-50,24-31(9)10)43-52(39-49,22-29(5)6)45-55(44-51,48-56)25-32(11)12/h27-34H,15-26H2,1-14H3. | |
| PSS-(3-Hydroxypropyl)-heptaisobutyl substituted | PSS-(3-Hydroxypropyl)-heptaisobutyl substituted. Molecular formula: C31H70O13Si8. Mole weight: 875.6g/mol. IUPAC Name: 3-[3,5,7,9,11,13,15-heptakis(2-methylpropyl)-2,4,6,8,10,12,14,16,17,18,19,20-dodecaoxa-1,3,5,7,9,11,13,15-octasilapentacyclo[9.5.1.13,9.15,15.17,13]icosan-1-yl]propan-1-ol. SMILES: CC(C)C[Si]12O[Si]3(O[Si]4(O[Si](O1)(O[Si]5(O[Si](O2)(O[Si](O3)(O[Si](O4)(O5)CC(C)C)CC(C)C)CC(C)C)CC(C)C)CC(C)C)CC(C)C)CCCO. InChI: InChI=1S/C31H70O13Si8/c1-25(2)18-46-33-45(17-15-16-32)34-47(19-26(3)4)38-49(36-46,21-28(7)8)42-52(24-31(13)14)43-50(37-46,22-29(9)10)39-48(35-45,20-27(5)6)41-51(40-47,44-52)23-30(11)12/h25-32H,15-24H2,1-14H3. | |
| Pss-(3-mercapto)propyl-heptaisobutyl su& | Pss-(3-mercapto)propyl-heptaisobutyl su&. Alternative Names: PSS-(3-MERCAPTO)PROPYL-HEPTAISOBUTYL SU&;1-(3-MERCAPTO)PROPYL-3,5,7,9,11,13,15-ISO BUTYLPENTACYCLO-OCTASILOXANE;pss-(3-mercapto)propyl-heptaisobutyl substituted;Mercaptopropylisobutyl-POSS(R),POSS(R)-Mercaptopropyl-isobutylsubstituted,1-(3-Mercapto)propyl. CAS No. 480438-85-5. Molecular formula: C31H70O12SSi8. Mole weight: 891.636. Purity: 96%. IUPAC Name: AC1N7LY5. SMILES: CC(C)C[Si]12O[Si]3(O[Si]4(O[Si](O1)(O[Si]5(O[Si](O2)(O[Si](O3)(O[Si](O4)(O5)CC(C)C)CC(C)C)CC(C)C)CC(C)C)CC(C)C)CC(C)C)CCCS. | |
| Pss-(3-tosyloxypropyl)-heptaisobutyl su& | Pss-(3-tosyloxypropyl)-heptaisobutyl su&. CAS No. 871126-43-1. Molecular formula: C38H76O15SSi8. Mole weight: 1015.72346;g/mol. Purity: 96%. IUPAC Name: PSS-(3-Tosyloxypropyl)-heptaisobutyl substituted. SMILES: CC(C)C[Si]12O[Si]3(O[Si]4(O[Si](O1)(O[Si]5(O[Si](O2)(O[Si](O3)(O[Si](O4)(O5)CC(C)C)CC(C)C)CC(C)C)CC(C)C)CC(C)C)CC(C)C)CCCOS(=O)(=O)C6=CC=CC=C6. | |
| Pss-chloropropyl-heptaisobutyl substitu& | Pss-chloropropyl-heptaisobutyl substitu&. Alternative Names: PSS-CHLOROPROPYL-HEPTAISOBUTYL SUBSTITU&;1-CHLOROPROPYL-3,5,7,9,11,-ISOBUTYLPENTA-CYCLO-(9.5.1.1(3,9).)OCTASILOXANE, 97%;pss-chloropropyl-heptaisobutyl substituted;Chloropropylisobutyl-PSS,PSS-Chloropropyl-isobutylsubstituted,1-Chloropropyl-3,5,7,9,11,13. CAS No. 480438-84-4. Molecular formula: C31H69ClO12Si8. Mole weight: 894.015. Purity: 96%. IUPAC Name: Chloropropylisobutyl-PSS. SMILES: CC(C)C[Si]12O[Si]3(O[Si]4(O[Si](O1)(O[Si]5(O[Si](O2)(O[Si](O3)(O[Si](O4)(O5)CC(C)C)CC(C)C)CC(C)C)CC(C)C)CC(C)C)CC(C)C)CCCCl. | |
| PSS-Cyanopropyldimethylsilyloxy-Heptacyclopentyl substituted | PSS-Cyanopropyldimethylsilyloxy-Heptacyclopentyl substituted. Uses: For analytical and research use. CAS No. 352538-80-8. Mole weight: 1042.80. Catalog: AP352538808. |  |
| Pss-(diphenylvinylsilyloxy)heptaclopent& | Pss-(diphenylvinylsilyloxy)heptaclopent&. Alternative Names: PSS-(DIPHENYLVINYLSILYLOXY)HEPTACLOPENT&;pss-diphenylvinylsilyloxy-heptacyclopentyl substituted;(Diphenylvinylsilyloxy)heptacyclopentylpentacyclooctasiloxane,Diphenylvinylsilyloxy-POSS(R). CAS No. 312693-49-5. Molecular formula: C49H76O13Si9. Mole weight: 1125.9g/mol. IUPAC Name: ethenyl-[(3,5,7,9,11,13,15-heptacyclopentyl-2,4,6,8,10,12,14,16,17,18,19,20-dodecaoxa-1,3,5,7,9,11,13,15-octasilapentacyclo[9.5.1.13,9.15,15.17,13]icosan-1-yl)oxy]-diphenylsilane. SMILES: C=C[Si](C1=CC=CC=C1)(C2=CC=CC=C2)O[Si]34O[Si]5(O[Si]6(O[Si]7(O[Si](O5)(O[Si](O3)(O[Si](O7)(O[Si](O6)(O4)C8CCCC8)C9CCCC9)C1CCCC1)C1CCCC1)C1CCCC1)C1CCCC1)C1CCCC1. InChI: InChI=1S/C49H76O13Si9/c1-2-63(41-23-5-3-6-24-41,42-25-7-4-8-26-42)50-71-60-68(47-35-17-18-36-47)54-65(44-29-11-12-30-44)51-64(43-27-9-10-28-43)52-66(56-68,45-31-13-14-32-45)58-70(62-71,49-39-21-22-40-49)59-67(53-64,46-33-15-16-34-46)57-69(55-65,61-71)48-37-19-20-38-48/h2-8,23-26,43-49H,1,9-22,27-40H2. | |
| PSS-Diphenylvinylsilyloxy-heptacyclopentyl substituted | PSS-Diphenylvinylsilyloxy-heptacyclopentyl substituted. Uses: For analytical and research use. CAS No. 312693-49-5. Mole weight: 1125.89. Catalog: AP312693495. | |
| Pss-dodecaphenyl substituted | Pss-dodecaphenyl substituted. Alternative Names: PSS-DODECAPHENYL SUBSTITUTED;DODECAPHENYL-PSS;Dodecaphenyl-POSS(R). CAS No. 18923-59-6. Molecular formula: C72H60O18Si12. Mole weight: 1550.26. Purity: 96%. IUPAC Name: dodeca(phenylsilasesquioxane). SMILES: C1=CC=C(C=C1)[Si]23O[Si]4(O[Si]5(O[Si](O2)(O[Si]6(O[Si]7(O[Si]8(O[Si](O6)(O[Si](O3)(O[Si](O4)(O[Si](O8)(O[Si](O7)(O5)C9=CC=CC=C9)C1=CC=CC=C1)C1=CC=CC=C1)C1=CC=CC=C1)C1=CC=CC=C1)C1=CC=CC=C1)C1=CC=CC=C1)C1=CC=CC=C1)C1=CC=CC=C1)C1=CC=CC=C1)C1=CC=CC=C1. | |
| PSS-Methacryl substituted. Cage mixture, n=8, 10, 12 | PSS-Methacryl substituted. Cage mixture, n=8, 10, 12. | |
| Pss-octa(2-(4-cyclohexenyl)ethyldimethy& | Pss-octa(2-(4-cyclohexenyl)ethyldimethy&. Alternative Names: PSS-OCTA(2-(4-CYCLOHEXENYL)ETHYLDIMETHY&;Octacyclohexenylethyldimethylsilyloxy-POSS(R),POSS(R)-Octacyclohexenyl)ethyldimethylsilyloxysubstituted. CAS No. 136849-03-1. Molecular formula: C80H152O20Si16. Mole weight: 1883.4g/mol. Purity: 96%. IUPAC Name: 2-cyclohex-3-en-1-ylethyl-[[3,5,7,9,11,13,15-heptakis[[2-cyclohex-3-en-1-ylethyl(dimethyl)silyl]oxy]-2,4,6,8,10,12,14,16,17,18,19,20-dodecaoxa-1,3,5,7,9,11,13,15-octasilapentacyclo[9.5.1.13,9.15,15.17,13]icosan-1-yl]oxy]-dimethylsilane. SMILES: C[Si](C)(CCC1CCC=CC1)O[Si]23O[Si]4(O[Si]5(O[Si](O2)(O[Si]6(O[Si](O3)(O[Si](O4)(O[Si](O5)(O6)O[Si](C)(C)CCC7CCC=CC7)O[Si](C)(C)CCC8CCC=CC8)O[Si](C)(C)CCC9CCC=CC9)O[Si](C)(C)CCC1CCC=CC1)O[Si](C)(C)CCC1CCC=CC1)O[Si](C)(C)CCC1CCC=CC1)O[Si](C)(C)CCC1CCC=CC1. InChI: InChI=1S/C80H152O20Si16/c1-101(2,65-57-73-41-25-17-26-42-73)81-109-89-110(82-102(3,4)66-58-74-43-27-18-28-44-74)92-113(85-105(9,10)69-61-77-49-33-21-34-50-77)94-111(90-109,83-103(5,6)67-59-75-45-29-19-30-46-75)96-115(87-107(13,14)71-63-79-53-37-23-38-54-79)97-112(91-109,84-104(7,8)68-60-76-47-31-20-32-48-76)95-114(93-110,86-106(11,12)70-62-78-51-35-22-36-52-78)99-116(98-113,100-115)88-108(15,16)72-64-80-55-39-24-40-56-80/h17-25,27,29,31,33,35,37,39,73-80H,26,28,30,32,34,36,38,40-72H2,1-16H3. | |
| PSS-Octa[2-(4-cyclohexenyl)ethyldimethylsilyloxy] substituted | PSS-Octa[2-(4-cyclohexenyl)ethyldimethylsilyloxy] substituted. Uses: For analytical and research use. CAS No. 136849-03-1. Mole weight: 1883.42. Catalog: AP136849031. | |
| Pss-octa(2-trichlorosilylethyl)substit& | Pss-octa(2-trichlorosilylethyl)substit&. Alternative Names: PSS-OCTA(2-TRICHLOROSILYLETHYL) SUBSTIT&;1,3,5,7,9,11,13,15-OCTA(2-TRICHLOROSILY&;pss-octa(2-trichlorosilylethyl) substituted;Octa(trichlorosilylethyl)-POSS(R),POSS(R)-Octa(trichlorosilylethyl)substituted,1,3,5,7,9,11,13,15-Octa(2-trichlorosilyl)ethyl)pen. CAS No. 214675-88-4. Molecular formula: C16H32Cl24O12Si16. Mole weight: 1716.66. Purity: 96%. IUPAC Name: PSS-Octa(2-trichlorosilylethyl) substituted. SMILES: C(C[Si](Cl)(Cl)Cl)[Si]12O[Si]3(O[Si]4(O[Si](O1)(O[Si]5(O[Si](O2)(O[Si](O3)(O[Si](O4)(O5)CC[Si](Cl)(Cl)Cl)CC[Si](Cl)(Cl)Cl)CC[Si](Cl)(Cl)Cl)CC[Si](Cl)(Cl)Cl)CC[Si](Cl)(Cl)Cl)CC[Si](Cl)(Cl)Cl)CC[Si](Cl)(Cl)Cl. | |
| Pss-octa((3-hydroxypropyl)dimethylsilox& | Pss-octa((3-hydroxypropyl)dimethylsilox&. Alternative Names: PSS-OCTA((3-HYDROXYPROPYL)DIMETHYLSILOX&;POSS(R)-Octahydroxypropyldimethylsilyl;PSS-Octa[(3-hydroxypropyl)dimethylsiloxy] substituted,POSS-Octahydroxypropyldimethylsilyl. CAS No. 288290-32-4. Molecular formula: C40H104O28Si16. Mole weight: 1482.61. | |
| Pss-octa((3-propylglycidylether)dimethy& | Pss-octa((3-propylglycidylether)dimethy&. Alternative Names: PSS-OCTA((3-PROPYLGLYCIDYLETHER)DIMETHY&;PSS-Octa[(3-glycidyloxypropyl)dimethylsiloxy]substituted. CAS No. 136864-48-7. Molecular formula: C64H136O36Si16. Mole weight: 1931.12. | |
| PSS-Octakis(dimethylsilyloxy) substituted | PSS-Octakis(dimethylsilyloxy) substituted. Uses: For analytical and research use. CAS No. 125756-69-6. Mole weight: 1017.97. Catalog: AP125756696. | |
| PSS-Octaphenyl Substituted | PSS-Octaphenyl Substituted. CAS No. 5256-79-1. Molecular formula: C48H40O12Si8. Mole weight: 1033.51g/mol. IUPAC Name: 1,3,5,7,9,11,13,15-octakis-phenyl-2,4,6,8,10,12,14,16,17,18,19,20-dodecaoxa-1,3,5,7,9,11,13,15-octasilapentacyclo[9.5.1.13,9.15,15.17,13]icosane. SMILES: C1=CC=C(C=C1)[Si]23O[Si]4(O[Si]5(O[Si](O2)(O[Si]6(O[Si](O3)(O[Si](O4)(O[Si](O5)(O6)C7=CC=CC=C7)C8=CC=CC=C8)C9=CC=CC=C9)C1=CC=CC=C1)C1=CC=CC=C1)C1=CC=CC=C1)C1=CC=CC=C1. InChI: InChI=1S/C48H40O12Si8/c1-9-25-41(26-10-1)61-49-62(42-27-11-2-12-28-42)52-65(45-33-17-5-18-34-45)54-63(50-61,43-29-13-3-14-30-43)56-67(47-37-21-7-22-38-47)57-64(51-61,44-31-15-4-16-32-44)55-66(53-62,46-35-19-6-20-36-46)59-68(58-65,60-67)48-39-23-8-24-40-48/h1-40H. | |
| PSS-Octavinyl substituted | PSS-Octavinyl substituted. CAS No. 69655-76-1. Molecular formula: C16H24O12Si8. Mole weight: 633g/mol. IUPAC Name: 1,3,5,7,9,11,13,15-octakis(ethenyl)-2,4,6,8,10,12,14,16,17,18,19,20-dodecaoxa-1,3,5,7,9,11,13,15-octasilapentacyclo[9.5.1.13,9.15,15.17,13]icosane. SMILES: C=C[Si]12O[Si]3(O[Si]4(O[Si](O1)(O[Si]5(O[Si](O2)(O[Si](O3)(O[Si](O4)(O5)C=C)C=C)C=C)C=C)C=C)C=C)C=C. InChI: InChI=1S/C16H24O12Si8/c1-9-29-17-30(10-2)20-33(13-5)22-31(11-3,18-29)24-35(15-7)25-32(12-4,19-29)23-34(14-6,21-30)27-36(16-8,26-33)28-35/h9-16H,1-8H2. | |
| Pss-trivinylsilyloxy-heptacyclopentyl s& | Pss-trivinylsilyloxy-heptacyclopentyl s&. Alternative Names: PSS-TRIVINYLSILYLOXY-HEPTACYCLOPENTYL S&;(TRIVINYLSILYOXY)HEPTACYCLOPENTYLPENTAC&;1-(trivinylsilyloxy)-3,5,7,9,11,13,15-heptacyclopentylpentacyclo[9.5.1.13,9.15,15.17,13]octasiloxane;pss-trivinylsilyloxy-heptacyclopentyl substituted;Trivinylsilyloxy-POSS(. CAS No. 352538-79-5. Molecular formula: C41H72O13Si9. Mole weight: 1025.78. Purity: 96%. IUPAC Name: AC1N9QRU. SMILES: C=C[Si](C=C)(C=C)O[Si]12O[Si]3(O[Si]4(O[Si]5(O[Si](O3)(O[Si](O1)(O[Si](O5)(O[Si](O4)(O2)C6CCCC6)C7CCCC7)C8CCCC8)C9CCCC9)C1CCCC1)C1CCCC1)C1CCCC1. | |
| PSS-Trivinylsilyloxy-Heptacyclopentyl substituted | PSS-Trivinylsilyloxy-Heptacyclopentyl substituted. Uses: For analytical and research use. CAS No. 352538-79-5. Mole weight: 1025.77. Catalog: AP352538795. | |
| Pss-vinyl-heptaisobutyl substituted | Pss-vinyl-heptaisobutyl substituted. Alternative Names: PSS-VINYL-HEPTAISOBUTYL SUBSTITUTED;1-VINYL-3,5,7,9,11,13,-ISOBUTYLPENTACYCL0-(9.5.1.1(3,9).1(5,15).1(7)OCTASILOXANE;1-vinyl-3,5,7,9,11,13,15-isobutylpentacyclo-[9.5.1.13,9.15,15.17,13]octasiloxane;MonovinylIsobutyl-POSS(R),POSS(R)-Monovinyl-isobutylsubst. CAS No. 444315-18-8. Molecular formula: C30H66O12Si8. Mole weight: 843.527. Purity: 96%. SMILES: CC(C)C[Si]12O[Si]3(O[Si]4(O[Si](O1)(O[Si]5(O[Si](O2)(O[Si](O3)(O[Si](O4)(O5)C=C)CC(C)C)CC(C)C)CC(C)C)CC(C)C)CC(C)C)CC(C)C. | |
| Pst I | One unit of the enzyme is the amount required to hydrolyze 1 μg of Lambda DNA in 1 hour at 37°C in a total reaction volume of 50 μl. Applications: After 20-fold overdigestion with enzyme 90% of the dna fragments can be ligated and recut. Group: Restriction Enzymes. Purity: 4000U; 20000U. CTGCA↑G G↓ACGTC. Activity: 20000u.a./ml. Appearance: 10 X SE-buffer O, BSA. Storage: -20°C. Form: Liquid. Source: An E.coli strain that carries the cloned Pst I gene from Providencia stuartii. Pack: 10 mM Tris-HCl (pH 7.5); 200 mM NaCl; 0,1 mM EDTA; 7 mM 2-mercaptoethanol; 200 μg/ml BSA; 50% glycerol. Cat No: ET-1161RE. | |
| PstN I | One unit of the enzyme is the amount required to hydrolyze 1 μg of Lambda DNA in 1 hour at 37°C in a total reaction volume of 50 μl. Applications: After 5-fold overdigestion with enzyme > 95% of lambda dna fragments can be ligated with t4 dna ligase and recut. Group: Restriction Enzymes. Purity: 500 U; 2500U. CAGNNN↑CTG GTC↓NNNGAC. Activity: 5000-10000u.a./ml. Appearance: 10 X SE-buffer Y. Storage: -20°C. Form: Liquid. Source: Pseudomonas stutzeri 217. Pack: 10 mM Tris-HCl (pH 7.5); 100 mM NaCl; 0.1 mM EDTA; 7 mM 2-mercaptoethanol; 200 μg/ml BSA, 50% glycerol. Cat No: ET-1162RE. | |
| p-Styryltrimethoxysilane / (4-Vinylphenyl)trimethoxysilane | p-Styryltrimethoxysilane / (4-Vinylphenyl)trimethoxysilane. CAS No. 18001-13-3. Cenik is your partner of choice for specialised chemicals. We don't just provide products - we supply solutions to your technical and regulatory specifications. |  |
| Psychimicin | Psychimicin is an antibacterial peptide isolated from Oiketicus kirbyi. It has activity against gram-positive bacteria, gram-negative bacteria and fungi. Alternative Names: Ile-Asn-Asn-Trp-Val-Arg-Val-Pro-Pro-Cys-Asp-Gln-Val-Cys-Ser-Arg-Thr-Asn-Pro-Glu-Lys-Asp-Glu-Cys-Cys-Arg-Ala-His-Gly-His-Ala-Phe-His-Ala-Thr-Cys-Ser-Gly-Gly-Met-Gln-Cys-Tyr-Arg-Arg. | |
| Psychosine | Psychosine (Galactosylsphingosine), a substrate of the galactocerebrosidase (GALC) enzyme, is a potential biomarker for Krabbe disease[1]. Psychosine is a highly cytotoxic lipid, capable of inducing cell death in a wide variety of cell types including, most relevantly to globoid cell leukodystrophy (GLD), oligodendrocytes. Psychosine causes cell death at least in part via apoptosis. Psychosine also is an inhibitor of PKC[1]. Uses: Scientific research. Category: Signaling pathways. Alternative Names: Galactosylsphingosine. CAS No. 2238-90-6. Pack Sizes: 1 mg; 5 mg. Product ID: HY-136490. | |
| Psychosine-d5 | Psychosine-d5 is deuterium labeled Psychosine. Psychosine, a substrate of the galactocerebrosidase (GALC) enzyme, is a potential biomarker for Krabbe disease. Psychosine is a highly cytotoxic lipid, capable of inducing cell death in a wide variety of cell. Uses: Scientific research. Category: Signaling pathways. Alternative Names: Galactosylsphingosine-d5. CAS No. 2260670-12-8. Pack Sizes: 100 μg; 500 μg; 1 mg. Product ID: HY-136490S. | |
| psychosine sulfotransferase | This enzyme belongs to the family of transferases, specifically the sulfotransferases, which transfer sulfur-containing groups. Group: Enzymes. Synonyms: PAPS:psychosine sulphotransferase; 3'-phosphoadenosine 5'-phosphosulfate-psychosine sulphotransferase. Enzyme Commission Number: EC 2.8.2.13. CAS No. 37259-76-0. 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-3371; psychosine sulfotransferase; EC 2.8.2.13; 37259-76-0; PAPS:psychosine sulphotransferase; 3'-phosphoadenosine 5'-phosphosulfate-psychosine sulphotransferase. Cat No: EXWM-3371. | |
| Psychotridine | Psychotridine is an alkaloid that has been found in P. forsteriana and has diverse biological activities. It inhibits ADP-, collagen-, or thrombin-induced aggregation of washed isolated human platelets. Alternative Names: Isopsychotridine; 1,1',1'',1''',1''''-Pentamethyl-2,2',2'',2''',2'''',3,3',3'',3''',3'''',8,8',8'',8''',8'''',8a,8a',8a'',8a''',8a''''-icosahydro-1H,1'H,1''H,1'''H,1''''H-3a,7':3a',3a'':7'',3a''':7''',3a''''-quinquepyr rolo[2,3-b]indole; Stereoisomer of 2,2',2'',2''',2'''',3,3',3'',3''',3'''',8,8',8'',8''',8'''',8a,8'a,8' 'a,8'''a,8''''a-eicosahydro-1,1',1'',1''',1''''-pentamethyl-3a(1H),7':3'a,3''a(1'H,1''H):7'',3'''a(1'''H):7''',3''''a(1''''H)-quinquepyrrolo[2,3-b]indole. Grades: >95% by HPLC. CAS No. 52617-25-1. Molecular formula: C55H62N10. Mole weight: 863.15. | |
| Psyle A | Psyle A is an antibacterial peptide isolated from Psychotria leptothyrsa. It has anti-cancer activity and cytotoxicity. Alternative Names: Gly-Ile-Ala-Cys-Gly-Glu-Ser-Cys-Val-Phe-Leu-Gly-Cys-Phe-Ile-Pro-Gly-Cys-Ser-Cys-Lys-Ser-Lys-Val-Cys-Tyr-Phe-Asn. Molecular formula: C128H187N31O35S6. Mole weight: 2912.4. | |
| Psyle C | Psyle C is an antibacterial peptide isolated from Psychotria leptothyrsa. It has anti-cancer activity and cytotoxicity. Alternative Names: Lys-Leu-Cys-Gly-Glu-Thr-Cys-Phe-Lys-Phe-Lys-Cys-Tyr-Thr-Pro-Gly-Cys-Ser-Cys-Ser-Tyr-Pro-Phe-Cys-Lys. | |
| Psyle E | Psyle E is an antibacterial peptide isolated from Psychotria leptothyrsa. It has anti-cancer activity and cytotoxicity. Alternative Names: Gly-Val-Ile-Pro-Cys-Gly-Glu-Ser-Cys-Val-Phe-Ile-Pro-Cys-Ile-Ser-Ser-Val-Leu-Gly-Cys-Ser-Cys-Lys-Asn-Lys-Val-Cys-Tyr-Arg-Asp. | |
| Psyllium Husk 95% | Psyllium Husk 95%. |  CA, FL & NJ |
| Psyllium seed gum | Psyllium seed gum comes from plants of the Plantago genus and is cultivated mainly in the Mediterranean and India. It is a soluble dietary fiber. Its structure is a backbone of D-xylopyranosyl units linked (1-4) and (1-3) with the 4-linked units bearing side chains. The side chains consist of α-L-arabinofuranosyl units linked (1-3) and (1-2) and β-D-xylopyranosyl units linked (1-3) and (1-2) and the α-D-Galap-(1-2)-α-L-Rhap aldobiuronic acid units linked (1-2) to the main chain. Uses: Cathartics. Alternative Names: Psyllium gum; Psyllium; Bistop D 2074; Foodmaid P 100; Fudomeido; Gums, psyllium-seed; Healthy Gum; Inagel A 400; Isabgol; Isapol husk mucilage; Isogel; Ispaghule gum; Isubgol; Metamucil; PG 020; PG 200; Plantaben; Plantaglucide; PO Gum; Psyllium mucilloid; RG 500; Soallium PG 200; VIS TOP D 2074; VIS TOP D 2701. Grades: ≥90%. CAS No. 8063-16-9. | |
| Psyllium Seed Husk Powder | Psyllium Seed Husk Powder. Applications: Psyllium husks are mostly available in health food stores.psyllium may be bought in standard preparations in dry seed or husk form, to be mixed with water as needed.psyllium is also an ingredient in some commercially prepared laxatives.psyllium can also be bought in capsules, tablets, and wafers forms. Group: Others. Purity: 98% Fiber. Appearance: Off-white powder. Psyllium Seed Husk Powder. Cat No: EXTC-167. | |
| p-Synephrine | p-Synephrine is an organic compound, found in multiple biofluids, such as urine and blood. Uses: Scientific research. Category: Signaling pathways. CAS No. 614-35-7. Pack Sizes: 10 mM * 1 mL in DMSO; 50 mg. Product ID: HY-113236. | |
| PT109 | PT109 is an orally active, blood-brain barrier permeable multi-kinase inhibitor. By inhibiting PTBP1, PT109 promotes the switch of pyruvate kinase isoform from PKM2 to PKM1, thereby effectively inhibiting the proliferation and migration of glioblastoma multiforme and inducing its reprogramming into oligodendrocytes. PT109 also targets and regulates key signaling molecules such as JNK, SGK1, GSK3β to exert neuroprotective effects including promoting neurogenesis, inducing synapse formation and alleviating neuroinflammation. In Alzheimer's disease models, PT109 exhibits significant efficacy in improving spatial learning ability, along with excellent in vivo pharmacokinetic properties. PT109 can be used to investigate metabolic reprogramming of glioblastoma multiforme and neuroprotective mechanisms of Alzheimer's disease[1][2]. Uses: Scientific research. Category: Signaling pathways. CAS No. 2059104-90-2. Pack Sizes: 10 mM * 1 mL in DMSO; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-167832. | |
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