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| Product | Description | |
|---|---|---|
| pseudotropine acyltransferase | This enzyme exhibits absolute specificity for the exo/3β configuration found in pseudotropine as tropine (tropan-3α-ol;see EC 2.3.1.185, tropine acyltransferase) and nortropine are not substrates. Acts on a wide range of aliphatic acyl-CoA derivatives, including acetyl-CoA, β-methylcrotonyl-CoA andtigloyl-CoA. Group: Enzymes. Synonyms: pseudotropine:acyl-CoA transferase; tigloyl-CoA:pseudotropine acyltransferase; acetyl-CoA:pseudotropine acyltransferase; pseudotropine acetyltransferase; pseudotropine tigloyltransferase; PAT. Enzyme Commission Number: EC 2.3.1.186. CAS No. 138440-78-5, 162535-26-4. 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-2128; pseudotropine acyltransferase; EC 2.3.1.186; 138440-78-5, 162535-26-4; pseudotropine:acyl-CoA transferase; tigloyl-CoA:pseudotropine acyltransferase; acetyl-CoA:pseudotropine acyltransferase; pseudotropine acetyltransferase; pseudotropine tigloyltransferase; PAT. Cat No: EXWM-2128. |  |
| Pseudouridimycin | Pseudouridimycin (PUM) is an antibiotic that selectively inhibits bacterial RNA polymerase (RNAP), with an IC50 of about 0.1 μM and MICs of 4-6 μg/mL. Pseudouridimycin is a C-nucleoside analogue that's effective against both Gram-negative and Gram-positive bacteria. Pseudouridimycin inhibits bacterial growth in vitro and shows activity in a mouse model of purulent streptococcal peritonitis[1][2]. Uses: Scientific research. Category: Signaling pathways. Alternative Names: PUM. CAS No. 1566586-52-4. Pack Sizes: 1 mg. Product ID: HY-125650. |  |
| Pseudouridimycin | Pseudouridimycin is a C-nucleoside analogue that selectively inhibits bacterial RNA polymerase. Pseudouridimycin is an antibiotic found in Streptomyces albus that has activity against Gram-positive and Gram-negative bacteria. Synonyms: PUM; 2,4(1H,3H)-Pyrimidinedione, 5-(5-((N-(aminoiminomethyl)glycyl-N2-hydroxy-L-glutaminyl)amino)-5-deoxy-beta-D-ribofuranosyl)-; (1S)-1,4-Anhydro-5-[(N-carbamimidoylglycyl-N2-hydroxy-L-glutaminyl)amino]-5-deoxy-1-(2,4-dioxo-1,2,3,4-tetrahydro-5-pyrimidinyl)-D-ribitol; D-Ribitol, 5-[[N-(aminoiminomethyl)glycyl-N2-hydroxy-L-glutaminyl]amino]-1,4-anhydro-5-deoxy-1-C-(1,2,3,4-tetrahydro-2,4-dioxo-5-pyrimidinyl)-, (1S)-. Grade: ≥95%. CAS No. 1566586-52-4. Molecular formula: C17H26N8O9. Mole weight: 486.44. |  |
| Pseudouridine | An isomer of the nucleoside uridine found in all species and in many classes of RNA except mRNA. It is formed by enzymes called ? synthases, which post-transcriptionally isomerize specific uridine residues in RNA in a process termed pseudouridylation. Studies suggest that β-Pseudouridine reduces radiation-induced chromosome aberrations in human lymphocytes. Group: Biochemicals. Alternative Names: 5- β-D-Ribofuranosyl-2,4(1H,3H)-Pyrimidinedione; 5-( β-D-Ribofuranosyl)uracil; 5-Ribosyluracil; NSC 162405; Pseudouridine C; β-D-Pseudouridine; Pseudouridine; ?-Uridine. Grades: Highly Purified. CAS No. 1445-07-4. Pack Sizes: 25mg, 50mg, 100mg. Molecular Formula: C9H12N2O6, Molecular Weight: 244.2. US Biological Life Sciences. |  Worldwide |
| Pseudouridine | Pseudouridine is an isomer of uridine and the most abundant modified nucleoside in non-coding RNA. It fine-tunes and stabilizes regional structures in rRNA and tRNA, maintaining their functions in mRNA decoding, ribosome assembly, processing, and translation.Pseudouridine-modified tRNA fragments can inhibit aberrant protein synthesis and hold promise for research on myelodysplastic syndrome (MDS)-related leukemia.[1][2][3][4][5]. Uses: Scientific research. Category: Signaling pathways. CAS No. 1445-07-4. Pack Sizes: 10 mM * 1 mL in DMSO; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-113061. | |
| pseudouridine 5'-phosphatase | Requires Mg2+ for activity. Group: Enzymes. Synonyms: pseudouridine 5'-monophosphatase; 5'-PsiMPase; HDHD1. Enzyme Commission Number: EC 3.1.3.96. 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-3703; pseudouridine 5'-phosphatase; EC 3.1.3.96; pseudouridine 5'-monophosphatase; 5'-PsiMPase; HDHD1. Cat No: EXWM-3703. | |
| Pseudouridine 5'-triphosphate | Pseudouridine 5'-triphosphate. Alternative Names: Pseudouridine 5-Triphosphate, CTK8G2650, 1175-34-4, AG-D-39466. CAS No. 1175-34-4. Purity: 96%. Product ID: ACM1175344. Molecular formula: C9H15N2O15P3. Mole weight: 484.14. IUPAC Name: [[(2R,5S)-5-(2,4-dioxo-1H-pyrimidin-5-yl)-3,4-dihydroxyoxolan-2-yl]methoxy-hydroxyphosphoryl] phosphono hydrogen phosphate. Alfa Chemistry - ISO 9001:32057 Certified. |  |
| Pseudouridine-5'-triphosphate trisodium salt | Pseudouridine-5'-triphosphate trisodium salt, an indispensable compound in the biomedical realm, serves as a synthetically modified nucleoside triphosphate integral to RNA studies. Exhibiting remarkable efficacy in combatting diverse human afflictions - anti-tumor, antiviral, and anticancer among many others - this compound has also been shown to mediate transcriptional regulation in bacterial populations and has been investigated in the context of metabolic syndromes like obesity. Synonyms: Pseudo-UTP sodium salt; Pseudo-UTP trisodium salt; 5-Ribosyl Uracil trisodium salt; sodium ((2R,3S,4R,5S)-5-(2,4-dioxo-1,2,3,4-tetrahydropyrimidin-5-yl)-3,4-dihydroxytetrahydrofuran-2-yl)methyl hydrogen triphosphate; 5'-triphospho-pseudouridine sodium salt; Pseudouridine 5'-triphosphate (trisodium). Grade: ≥97% by AX-HPLC. Molecular formula: C9H12N2Na3O15P3. Mole weight: 550.09. | |
| Pseudouridine-5'-triphosphate Trisodium Salt, 100mM (Liquid) (Pseudo-UTP) | Pseudouridine-5'-triphosphate trisodium salt, 100mM aqueous solution.Uridine analog as ribonucleate nucleotidyltransferase substrate. Group: Biochemicals. Alternative Names: Pseudo-UTP. Grades: Highly Purified. CAS No. 1175-34-4. Pack Sizes: 1mg, 2mg, 5mg, 10mg, 25mg. Molecular Formula: C9H12N2O15P3Na3, Molecular Weight: 550.09. US Biological Life Sciences. | Worldwide |
| pseudouridine kinase | This enzyme belongs to the family of transferases, specifically those transferring phosphorus-containing groups (phosphotransferases) with an alcohol group as acceptor. The systematic name of this enzyme class is ATP:pseudouridine 5'-phosphotransferase. This enzyme is also called pseudouridine kinase (phosphorylating). This enzyme participates in pyrimidine metabolism. Group: Enzymes. Synonyms: pseudouridine kinase (phosphorylating). Enzyme Commission Number: EC 2.7.1.83. CAS No. 62213-40-5. 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-3113; pseudouridine kinase; EC 2.7.1.83; 62213-40-5; pseudouridine kinase (phosphorylating). Cat No: EXWM-3113. | |
| pseudouridylate synthase | The reaction it readily reversible. While the enzymes from Tetrahymena pyriformis and Agrobacterium tumefaciens produce pseudouridine 5'-phosphate the enzyme from Escherichia coli functions as a pseudouridine-5'-phosphate glycosidase in vivo. Group: Enzymes. Synonyms: pseudouridylic acid synthetase; pseudouridine monophosphate synthetase; 5-ribosyluracil 5-phosphate synthetase; pseudouridylate synthetase; upsilonUMP synthetase; uracil hydro-lyase (adding D-ribose 5-phosphate); YeiN; pseudouridine-5'-phosphate glycosidase. Enzyme Commission Number: EC 4.2.1.70. CAS No. 9023-35-2. Storage: Store it at +4 ?C for short term. For long term storage, store it at -20 ?C?-80 ?C. Form: Liquid or lyophilized powder. EXWM-5056; pseudouridylate synthase; EC 4.2.1.70; 9023-35-2; pseudouridylic acid synthetase; pseudouridine monophosphate synthetase; 5-ribosyluracil 5-phosphate synthetase; pseudouridylate synthetase; upsilonUMP synthetase; uracil hydro-lyase (adding D-ribose 5-phosphate); YeiN; pseudouridine-5'-phosphate glycosidase. Cat No: EXWM-5056. | |
| Pseudo Vardenafil | Vardenafil. Group: Biochemicals. Alternative Names: 2-[2-Ethoxy-5- (1-piperidinylsulfonyl) phenyl]-5-methyl-7-propylimidazo[5, 1-f][1, 2, 4]triazin-4 (1H) -one. Grades: Highly Purified. CAS No. 224788-34-5. Pack Sizes: 5mg. US Biological Life Sciences. | Worldwide |
| Pseurotin | Pseurotin A is a secondary metabolite of Aspergillus. It has effective neurogenesis activity in PC12 pheochromocytoma cells, induces multipolar and branched neurites equivalent to β-NGF (an endogenous neurotrophic factor), and also exhibits chitinase inhibition. And it has a synergistic effect with azole antifungal agents. Synonyms: Pseurotin. Grade: >99% by HPLC. CAS No. 58523-30-1. Molecular formula: C22H25NO8. Mole weight: 431.43. | |
| Pseurotin A | Pseurotin A is a fungal metabolite with an unusual hetero-spirocyclic ring system. It has been shown to have potent neuritogenic activity in PC12 phaechromocytoma cells, a useful model for adrenergic neuronal differentiation. Pseurotin A induced multipolar and branching neurites comparable to beta-NGF, an endogenous neurotrophic factor. Pseurotin A is also reported to exhibit chitinase inhibition and displays synergistic activity with azole antifungal agents. Group: Biochemicals. Grades: Highly Purified. CAS No. 58523-30-1. Pack Sizes: 1mg. US Biological Life Sciences. | Worldwide |
| Pseurotin D | Isomeric to pseurotin A. Anticancer and antiparasitic compound. Apomorphine antagonist. Neuroleptic agent. Inhibitor of IgE production. Group: Biochemicals. Grades: Highly Purified. CAS No. 77409-68-8. Pack Sizes: 1mg, 5mg. Molecular Formula: C??H??NO?. US Biological Life Sciences. | Worldwide |
| p-Sexiphenyl | p-Sexiphenyl. Alternative Names: 6P p-6P. CAS No. 4499-83-6. Molecular formula: C36H26. Mole weight: 458.60. Purity: >98.0%(GC). IUPAC Name: 1-phenyl-4-[4-[4-(4-phenylphenyl)phenyl]phenyl]benzene. SMILES: C1=CC=C(C=C1)C2=CC=C(C=C2)C3=CC=C(C=C3)C4=CC=C(C=C4)C5=CC=C(C=C5)C6=CC=CC=C6. InChI: InChI=1S/C36H26/c1-3-7-27(8-4-1)29-11-15-31(16-12-29)33-19-23-35(24-20-33)36-25-21-34(22-26-36)32-17-13-30(14-18-32)28-9-5-2-6-10-28/h1-26H. |  |
| PSI-6206 13C | PSI-6206 13CD3 is the deuterium labeled PSI-6206. PSI-6206 is a potent and selective HCV NS5B polymerase inhibitor. Category: Active pharmaceutical ingredients. CAS No. 1256490-42-2. Product ID: API1256490422. Molecular formula: C10H13FN2O5. Mole weight: 264.23. |  |
| PSI-697 | PSI-697 is an oral P-selectin inhibitor with an IC50 of 125 μM[1]. Uses: Scientific research. Category: Signaling pathways. Alternative Names: P-Selectin Inhibitor. CAS No. 851546-61-7. Pack Sizes: 10 mM * 1 mL in DMSO; 1 mg; 5 mg; 10 mg; 50 mg; 100 mg. Product ID: HY-15526. | |
| PSI-7409 | PSI-7409 is the active 5'-triphosphate metabolite of Sofosbuvir (PSI-7977). Category: Active pharmaceutical ingredients. CAS No. 1015073-42-3. Product ID: API1015073423. Molecular formula: C10H16FN2O14P3. Mole weight: 500.16. | |
| PSI-7409 tetrasodium | PSI-7409 tetrasodium, the active 5'-triphosphate metabolite of sofosbuvir (PSI-7977), exhibits specific inhibitory activity against NS5B polymerases of various genotypes, with IC50s being 1.6 μM for GT 1b_Con1, 2.8 μM for GT 2a_JFH1, 0.7 μM for GT 3a, and 2.6 μM for GT 4a, respectively. Category: Active pharmaceutical ingredients. CAS No. 1621884-22-7. Product ID: API1621884227. Molecular formula: C10H16FN2Na4O14P3. Mole weight: 592.117. | |
| PSI-7409 tetrasodium | PSI-7409 tetrasodium is an active 5'-triphosphate metabolite of sofosbuvir (PSI-7977), inhibiting HCV NS5B polymerases, with IC50s of 1.6, 2.8, 0.7 and 2.6 μM for GT 1b_Con1, GT 2a_JFH1, GT 3a, and GT 4a NS5B polymerases, respectively. Uses: Scientific research. Category: Signaling pathways. CAS No. 1621884-22-7. Pack Sizes: 10 mM * 1 mL in Water; 1 mg; 5 mg; 10 mg; 25 mg. Product ID: HY-15745A. | |
| Psicofuranine | Nucleoside antibiotic. Antitumor compound. Xanthosine monophosphate (XMP) aminase inhibitor. Antimetabolite of the purine biosynthesis. Group: Biochemicals. Alternative Names: 1'-C- (Hydroxymethyl) adenosine; 1'- (Hydroxymethyl) adenosine; 9- β-D-Psicofuranosyl-6-aminopurine; 9- β-D-Psicofuranosyladenine; Angustmycin C; NSC 53104; Psicofuranine; 9- β-D-psicofuranosyl-adenine; 9- β-D-Psicofuranosyl-9H-purin-6-amine. Grades: Highly Purified. CAS No. 1874-54-0. Pack Sizes: 1mg, 5mg. Molecular Formula: C??H??N?O?. US Biological Life Sciences. | Worldwide |
| Psidial A | Psidial A, a natural triterpenoid isolated from the leaves of Psidium guajava L, exhibits the activity to enzyme PTP1B and also reduces tumor growth and stimulates uterus proliferation. Uses: Anti-tumour. Synonyms: (1S,4S,7R,11R,12R)-14,16-dihydroxy-1,5,5-trimethyl-8-methylidene-12-phenyl-19-oxatetracyclo[9.8.0.04,7.013,18]nonadeca-13,15,17-triene-15,17-dicarbaldehyde; 7,9-dihydroxy-2,2,4a- trimethyl-13-methylene-10-phenyl-1,2,2a,3,4,4a,10, 10a,11,12,13,13a-dodecahydrocyclobuta[6,7] cyclonona[b]chromene-6,8-dicarbaldehyde. Grade: >98%. CAS No. 1207181-35-8. Molecular formula: C30H34O5. Mole weight: 474.6. | |
| PSiF-DBT | PSiF-DBT is a conductive polymer that can be used as an active layer with thermal stability and high degree of π-electron delocalization. It has a high mobility of charge carrier around 1×10-3cm2 /(V s) which can be useful in organic electronics. Alternative Names: Poly[2,7-(9,9-dioctyl-dibenzosilole)-alt-4,7-bis(thiophen-2-yl)benzo-2,1,3-thiadiazole], Poly[2,1,3-benzothiadiazole-4,7-diyl-2,5-thiophenediyl(9,9-dioctyl-9H-9-silafluorene-2,7-diyl)-2,5-thiophenediyl]. CAS No. 1004272-92-7. Molecular formula: (C42H46N2S3Si)n. Mole weight: average Mn 10000-80000. | |
| Psi 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 about 50% of the dna fragments can be ligated and of these 95% can be recut. Group: Restriction Enzymes. Purity: 200U; 1000U. TTA↑TAA AAT↓ATT. Activity: 5000u.a./ml. Appearance: 10 X SE-buffer B. Storage: -20°C. Form: Liquid. Source: Pseudomonas species-SE-G49. Pack: 10 mM Tris-HCl (pH 7.5); 200 mM KCl; 0.1 mM EDTA; 7 mM 2-mercaptoethanol; 200 μg/ml BSA; and 50% glycerol. Cat No: ET-1150RE. | |
| PSI Reagent | PSI Reagent. CAS No. 2245335-71-9. Cenik is your partner of choice for specialised chemicals. We don't just provide products - we supply solutions to your technical and regulatory specifications. |  |
| PSMA-11 | PSMA-11 is a small molecule ligand that targets prostate-specific membrane antigen (PSMA) and has the ability to inhibit PSMA activity. PSMA-11 can be used to synthesize 68Ga-PSMA-11, a positron emission tomography (PET) tracer that can be used to image advanced prostate cancer[1][2][3]. Uses: Scientific research. Category: Signaling pathways. Alternative Names: HBED-CC-PSMA. CAS No. 1366302-52-4. Pack Sizes: 10 mM * 1 mL in DMSO; 1 mg; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-125399. | |
| PSMA (27-38) | Prostate-specific membrane antigen (PSMA) is considered an ideal target for antigen-redirected immunotherapy because it is expressed at the surface of prostate cancer cells, present in all tumor stages, and shows an increased expression in androgen-independent and metastatic stages of the disease. Synonyms: Prostate-specific membrane antigen (27-38). | |
| PSMA-ALB-56 | PSMA-ALB-56 is a PSMA-targeting radioligand designed by combining the glutamate-urea PSMA-binding entity and an albumin binder[1]. Uses: Scientific research. Category: Signaling pathways. CAS No. 2306049-48-7. Pack Sizes: 1 mg; 5 mg; 10 mg. Product ID: HY-141536. | |
| PSMA-azide | PSMA-azide is a prostate-specific membrane antigen (PSMA) ligand. PSMA-azide inhibits PSMA-dependent NAAG (N-acetylaspartylglutamic acid) hydrolysis, with an IC50 of 9 nM and a Ki of 1 nM. PSMA-azide contains an Azide group and can undergo copper-catalyzed azide-alkyne cycloaddition reaction (CuAAc) with molecules containing Alkyne groups[1]. Uses: Scientific research. Category: Signaling pathways. CAS No. 2374814-84-1. Pack Sizes: 1 mg; 5 mg. Product ID: HY-160893. | |
| PSMA-BCH | PSMA-BCH (NOTA-PSMA) is a NOTA-conjugated precursor. NOTA is a bifunctional chelate which acts as the framework to construct PET imaging tools[1]. Uses: Scientific research. Category: Signaling pathways. Alternative Names: NOTA-PSMA. CAS No. 1703768-73-3. Pack Sizes: 10 mM * 1 mL in DMSO; 5 mg; 10 mg. Product ID: HY-155483. | |
| PSMA binder-1 | PSMA binder-1 is a ligand for PSMA and can be used to synthesize PSMA targeting molecule, such as Ac-PSMA-trillium[1][2]. Uses: Scientific research. Category: Signaling pathways. CAS No. 2170653-14-0. Pack Sizes: 10 mM * 1 mL in DMSO; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-158123. | |
| PSMA I&S | PSMA I&S is a precursor of the 99mTc-labeled PSMA-targeting ligand[1]. Uses: Scientific research. Category: Signaling pathways. CAS No. 2639475-07-1. Pack Sizes: 1 mg; 5 mg; 10 mg. Product ID: HY-148152. | |
| PSMα2 | PSMα2 is a potent PSM (phenol-soluble modulin) peptide toward mouse neutrophils, led to strong influx of leukocytes[1]. Uses: Scientific research. Category: Peptides. CAS No. 1092844-32-0. Pack Sizes: 5 mg; 10 mg. Product ID: HY-P10629. | |
| PSMα3 | PSMα3 is an inhibitor of NF-κB p65 and p38 MAPK. PSMα3 forms membrane pores and binds to residues of human insulin B chain to inhibit insulin aggregation. PSMα3 forms α-type amyloid-like fibrils to exert cytotoxic effects, and acts as a functional amyloid virulence determinant of Staphylococcus aureus. PSMα3 is applicable to research related to spondyloarthritis, rheumatoid arthritis, insulin-derived amyloidosis, and Staphylococcus aureus infection[1][2][3]. Uses: Scientific research. Category: Signaling pathways. CAS No. 1001405-52-2. Pack Sizes: 5 mg; 10 mg. Product ID: HY-P2358. | |
| PSMA-PEG4 | PSMA-PEG4. Synonyms: (21S,25S)-1-Amino-15,23-dioxo-3,6,9,12-tetraoxa-16,22,24-triazaheptacosane-21,25,27-tricarboxylic acid. CAS No. 2256069-92-6. Molecular formula: C23H42N4O12. Mole weight: 566.60. | |
| PSMA/PSM-P1 (4-12) | This peptide is a tetramer of biotinylated peptide with streptavidin mainly composed of PSMA-derived peptide of LLHETDSAV sequence covering 4-12 and A*0201 molecule. | |
| PSMA-Val-Cit-PAB-MMAE | PSMA-Val-Cit-PAB-MMAE is a small-molecule conjugate targeting PSMA, with Monomethyl auristatin E (MMAE) (HY-15162) as its cytotoxic payload. PSMA-Val-Cit-PAB-MMAE binds to PSMA, thereby being delivered into PSMA-expressing prostate cancer cells. Subsequently, the Val-Cit linker is cleaved under the mediation of cathepsin B, releasing active MMAE. PSMA-Val-Cit-PAB-MMAE inhibits CYP3A4 activity (IC50 = 11.2 μM), induces intracellular ROS production and oxidative stress, disrupts the cytoskeleton through microtubule destabilization, and induces prostate cancer cell death. PSMA-Val-Cit-PAB-MMAE can be used in research related to prostate cancer[1]. Uses: Scientific research. Category: Signaling pathways. CAS No. 2748039-79-2. Pack Sizes: 1 mg; 5 mg; 10 mg. Product ID: HY-141860. | |
| PSM P2 (711-719) | PSM P2 (711-719) is a 9-aa peptide. PSM P2 is a zinc metalloenzyme that resides in membranes. It is mainly expressed in four tissues of the body, including prostate epithelium, the proximal tubules of the kidney, the jejunal brush border of the small intestine and ganglia of the nervous system. Synonyms: Glutamate carboxypeptidase 2 (711-719); N-acetyl-L-aspartyl-L-glutamate peptidase I (711-719); NAAG peptidase (711-719); prostate-specific membrane antigen (PSMA) (711-719). | |
| PSN 375963 | PSN 375963 is a potent GPR119 agonist, with EC50s of 8.4 and 7.9 μM for human and mouse GPR119, respectively. PSN 375963 shows similar potency to the endogenous agonist oleoylethanolamide (OEA)[1][2]. Uses: Scientific research. Category: Signaling pathways. CAS No. 388575-52-8. Pack Sizes: 10 mM * 1 mL in DMSO; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-108258. | |
| PSN 375963 hydrochloride | PSN 375963 hydrochloride. Group: Biochemicals. Grades: Purified. CAS No. 388575-52-8. Pack Sizes: 10mg, 50mg. US Biological Life Sciences. | Worldwide |
| 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 (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 | 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. Synonyms: Ficusin; Furocoumarin. Grade: 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 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. Synonyms: 3,9-Dihydroxy-2-(3-methyl-2-butenyl)-6H-benzofuro[3,2-c][1]benzopyran-6-one; 3,9-Dihydroxy-2-prenylcoumestan. Grade: >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 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. | |
| Psoromic acid | Psoromic acid is a selective inhibitor of Rab geranylgeranyl transferase and P. falciparum fatty acid synthesis (FAS) II enzymes. Synonyms: 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. Grade: ≥95%. CAS No. 7299-11-8. Molecular formula: C18H14O8. Mole weight: 358.30. | |
| 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-(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. | |
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