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| Product | Description | |
|---|---|---|
| RETRA | ?98% (HPLC), solid. Group: Fluorescence/luminescence spectroscopy. |  |
| RETRA | RETRA is a mutant p53-dependent activator of p73 that suppresses mutant p53-bearing cancer cells. RETRA increases the expression level of p73, and a release of p73 from the blocking complex with mutant p53, which produces tumor-suppressor effects [1]. Uses: Scientific research. Group: Signaling pathways. CAS No. 1036069-26-7. Pack Sizes: 5 mg; 10 mg. Product ID: HY-108636. |  |
| RETRA hydrochloride | RETRA hydrochloride. Group: Biochemicals. Grades: Purified. CAS No. 1173023-52-3. Pack Sizes: 10mg, 50mg. US Biological Life Sciences. |  Worldwide |
| Retro-2 | ?98% (HPLC). Group: Fluorescence/luminescence spectroscopy. | |
| Retro-2 | A cell-permeable tricyclic imine compound that inhibits the endosome-to-Golgi retrograde transport, but not cellular uptake, of CtxB, StxB without affecting cellular uptake/trafficking of Tf or EGF. Group: Fluorescence/luminescence spectroscopy. | |
| Retro-2 | Retro-2 is a selective inhibitor of retrograde protein trafficking at the endosome-trans-Golgi network interface. Retro-2 is an ebolavirus (EBOV) infection inhibitor with an EC 50 of 12.2 μM in HeLa cells. Retro-2 induces cell autophagy [1] [2] [3]. Uses: Scientific research. Group: Signaling pathways. CAS No. 1201652-50-7. Pack Sizes: 1 mg; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-122571. | |
| Retrochalcone | Retrochalcone. Group: Biochemicals. CAS No. 34221-41-5. Pack Sizes: 5mg. US Biological Life Sciences. | Worldwide |
| Retrocyclin-1 | Retrocyclin-1, a theta-defensin, is a circular octadecapeptide containing an internal trisulfide ladder. In addition to its antimicrobial activity, it has a significant in vitro ability to protect human cells from infection with the T- and M-tropic strains of HIV-1. Retrocyclin is a small molecule HIV-1 entry inhibitor. Synonyms: RC-100; Cyclo(-Gly-Ile-Cys-Arg-Cys-Ile-Cys-Gly-Arg-Gly-Ile-Cys-Arg-Cys-Ile-Cys-Gly-Arg) (Disulfide bridge: Cys3-Cys16, Cys5-Cys14, Cys7-Cys12); cyclo[L-arginyl-L-cysteinyl-L-isoleucyl-L-cysteinyl-glycyl-L-arginyl-glycyl-L-isoleucyl-L-cysteinyl-L-arginyl-L-cysteinyl-L-isoleucyl-L-cysteinyl-glycyl-L-arginyl-glycyl-L-isoleucyl-L-cysteinyl] (2->11),(4->9),(13->18)-tris(disulfide). Grade: ≥95%. CAS No. 724760-19-4. Molecular formula: C74H128N30O18S6. Mole weight: 1918.39. |  |
| Retrocyclin-2 | Retrocyclin-2 is a synthetic antimicrobial peptide. It has activity against viruses. Synonyms: 1-[3-[tetrakis(3-guanidinopropyl)-tetrakis[(1S)-1-methylpropyl]-octadecaoxo-[?]yl]propyl]guanidine. Molecular formula: C78H137N33O18S6. Mole weight: 2017.5. | |
| Retrocyclin-3 | Retrocyclin-3 is a synthetic antimicrobial peptide. It has activity against viruses. Synonyms: 1-[3-[pentakis(3-guanidinopropyl)-tetrakis[(1S)-1-methylpropyl]-octadecaoxo-[?]yl]propyl]guanidine. Molecular formula: C82H146N36O18S6. Mole weight: 2116.7. | |
| retro-Methyl-α-ionol | An intermediate for synthesizing β-Damascenone. Group: Biochemicals. Alternative Names: (6Z). Grades: Highly Purified. CAS No. 945426-65-3. Pack Sizes: 50mg. US Biological Life Sciences. | Worldwide |
| Retronecine | analytical standard. Group: Natural compounds. | |
| Retrorsine | ?90% (HPLC). Group: Fluorescence/luminescence spectroscopy. | |
| retroviral ribonuclease H | Comments: Retroviral reverse transcriptase is a multifunctional enzyme responsible for viral replication. To perform this task the enzyme combines two distinct activities. The polymerase domain (EC 2.7.7.49, RNA-directed DNA polymerase) occupies the N-terminal two-thirds of the reverse transcriptase whereas the ribonuclease H domain comprises the C-terminal remaining one-third. The RNase H domain of Moloney murine leukemia virus and Human immunodeficiency virus display two metal binding sites. Group: Enzymes. Synonyms: RT/RNase H; retroviral reverse transcriptase RNaseH; HIV RNase H. Enzyme Commission Number: EC 3.1.26.13. CAS No. 9050-76-4. 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-3589; retroviral ribonuclease H; EC 3.1.26.13; 9050-76-4; RT/RNase H; retroviral reverse transcriptase RNaseH; HIV RNase H. Cat No: EXWM-3589. |  |
| RET (V804L), active, GST tagged human | recombinant, expressed in baculovirus infected Sf9 cells, ?70% (SDS-PAGE), buffered aqueous glycerol solution. Group: Fluorescence/luminescence spectroscopy. | |
| Reumycin | It is originally isolated from Act. sp. Reumycin is toxic to Airy carcinoma, sarcoma-180, sarcoma-37, lymphosarcoma and other tumor cells. Synonyms: Reumitsin; Rheumygin; 1-demethyltoxoflavin; NSC 99733; 6-Methylpyrimido(5,4-e)-as-triazine-5,7(1H,6H)-dione. CAS No. 5016-18-2. Molecular formula: C6H5N5O2. Mole weight: 179.14. | |
| Reutericyclin | Reutericyclin (Reutericycline), a unique tetramic acid, is an antibiotic produced by some strains of Lactobacillus reuteri. Reutericyclin (Reutericycline) exhibits a broad inhibitory spectrum including Lactobacillus spp. , Bacillus subtilis , B. cereus , Enterococcus faecalis , Staphylococcus aureus , and Listeria innocua [1] [2]. Uses: Scientific research. Group: Natural products. Alternative Names: Reutericycline. CAS No. 303957-69-9. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-103249. | |
| Reuterin | Reuterin is a broad-spectrum antimicrobial agent active against Gram positive and Gram negative bacteria, as well as yeasts, moulds and protozoa. Reuterin is produced by specific strains of Lactobacillus reuteri during anaerobic metabolism of glycerol. Reuterin also demonstrates potent antimicrobial activity against a broad panel of human and poultry meat campylobacter spp. Isolates[1][2]. Uses: Scientific research. Group: Natural products. Alternative Names: 3-Hydroxypropionaldehyde; 3-Hydroxypropanal. CAS No. 2134-29-4. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-N8461. | |
| Revaprazan hydrochloride | Revaprazan hydrochloride. Group: Biochemicals. Alternative Names: 4-(3,4-Dihydro-1-methyl-2(1H)-isoquinolinyl)-N-(4-fluorophenyl)-5,6-dimethyl-2-pyrimidinamine hydrochloride; 5,6-Dimethyl-2-(4-fluorophenylamino)-4-(1-methyl-1,2,3,4-tetrahydroisoquinolin-2-yl)pyrimidine hydrochloride; Revaprazan hydrochloride. Grades: Highly Purified. CAS No. 178307-42-1. Pack Sizes: 1g, 2g, 5g, 10g, 25g. Molecular Formula: C22H24ClFN4. US Biological Life Sciences. | Worldwide |
| Revaprazan hydrochloride | Revaprazan hydrochloride is a novel acid pump antagonist ( APA ). Revaprazan hydrochloride reduces COX-2 expression and has significant anti-inflammatory actions activities in H. pylori infection [1]. Uses: Scientific research. Group: Signaling pathways. CAS No. 178307-42-1. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-N7067. | |
| Revefenacin | Revefenacin (TD-4208; GSK1160724) is a potent mAChR antagonist; has a high affinity on M3 receptor with a K i of 0.18 nM. Uses: Scientific research. Group: Signaling pathways. Alternative Names: TD-4208; GSK1160724. CAS No. 864750-70-9. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-15851. | |
| Revefenacin | Revefenacin is a synthetic anticholinergic agent that is used as a once daily, nebulized inhalant for maintenance treatment of patients with chronic obstructive pulmonary disease. Revefenacin has not been implicated in causing liver enzyme elevations or clinically apparent acute liver injury. Alternative Names: TD-4208. Yupelri. GSK-1160724. CAS No. 864750-70-9. Product ID: API864750709. Molecular formula: C35H43N5O4. Mole weight: 597.7. EINECS: 811-471-4. SMILES: CN(CCN1CCC(CC1)OC(=O)NC2=CC=CC=C2C3=CC=CC=C3)C(=O)C4=CC=C(C=C4)CN5CCC(CC5)C(=O)N. Appearance: Solid Powder. Category: Other APIs. |  |
| REV-ERB? Agonist, GSK4112 | The REV-ERB? Agonist, GSK4112 controls the biological activity of REV-ERB?. This small molecule/inhibitor is primarily used for Biochemicals applications. Group: Fluorescence/luminescence spectroscopy. | |
| REV-ERB Agonist II, SR9009 | A pyrrolidinecarbamate compound that acts as a specific REV-ERB-alpha/beta agonist. Exhibits a direct and reversible binding (Kd = 800nM REV-ERB-alpha) and shows excellent selectivity over a panel of 46 other nuclear receptors. Potently increases REV-ERB-dependent repressor activity (IC50 = 670 and 800nM in Gal4-REV-ERB-alpha and beta transfected HEK 293 cells) and reduces BMAL1 mRNA in HepG2 cells (IC50 = 710nM). Shown to cross the blood-brain barrier and exhibit desirable pharmacokinetic properties. A 7-day administration of SR9009 (100mg/kg, i.p., b.i.d.) causes a significant weight and fat loss in C57BL6 mice with concomitant reduction in plasma glucose and free fatty acid levels, and alters circadian pattern. 217739, CAS # 1379686-30-2, acts as a specific REV-ERB-α/ β agonist that exhibits a direct and reversible binding (Kd = 800nM). Group: Biochemicals. Grades: Highly Purified. CAS No. 1379686-30-2. Pack Sizes: 25mg. Molecular Formula: C??H??ClN?O?S. US Biological Life Sciences. | Worldwide |
| Reveromycin A | solid. Group: Fluorescence/luminescence spectroscopy. | |
| Reveromycin A | The dominant analogue of complex of spiroketals isolated from streptomyces sp. It is an inhibitor of the mitogenic activity of EGF and a G1 phase cell cycle inhibitor. It selectively inhibits isoleucyl-trna synthetase. It has anti-proliferation effect on human cell lines KB and K562, and has potent antifungal activity. Synonyms: (-)-Reveromycin A; [2S-[2α(1E,3E),3β,6α[8S*(2E,4E,6R*,7R*,8E),9R*]]]-butanedioic acid mono[3-butyl-8-(9-carboxy-6-hydroxy-3,7-dimethyl-2,4,8-nonatrienyl)-2-(4-carboxy-3-methyl-1,3-butadienyl)-9-methyl-1,7-dioxaspiro[5.5]undec-3-yl] Ester; Butanedioic Acid Mono[(2S,3R,6S,8R,9S)-3-butyl-8-[(2E,4E,6S,7S,8E)-9-carboxy-6-hydroxy-3,7-dimethyl-2,4,8-nonatrienyl]-2-[(1E,3E)-4-carboxy-3-methyl-1,3-butadienyl]-9-methyl-1,7-dioxaspiro[5.5]undec-3-yl] Ester. Grade: >99% by HPLC. CAS No. 134615-37-5. Molecular formula: C36H52O11. Mole weight: 660.79. | |
| Reveromycin A | Reveromycin A, a benzoquinoid antibiotic isolated from the genus Streptomyces , is a selective inhibitor of protein synthesis in eukaryotic cells. Reveromycin A inhibits bone resorption by inducing apoptosis specifically in osteoclasts. Reveromycin A has antiproliferative activity against tumor cell lines and antifungal activity [1] [2]. Uses: Scientific research. Group: Natural products. CAS No. 134615-37-5. Pack Sizes: 1 mg. Product ID: HY-129337. | |
| Reveromycin A | Reveromycin A. Uses: Designed for use in research and industrial production. Additional or Alternative Names: (2E,6E,8E)-10-[3-butyl-2-[(1E,3E)-4-carboxy-3-methylbuta-1,3-dienyl]-3-(3-carboxypropanoyloxy)-9-methyl-1,7-dioxaspiro[5.5]undecan-8-yl]-5-hydroxy-4,8-dimethyldeca-2,6,8-trienoic acid. Appearance: Lyophilized. CAS No. 134615-37-5. Molecular formula: C36H52O11. Mole weight: 660.8. Purity: 0.99. Canonical SMILES: CCCCC1(CCC2(CCC(C(O2)CC=C(C)C=CC(C(C)C=CC(=O)O)O)C)OC1C=CC(=CC(=O)O)C)OC(=O)CCC(=O)O. Product ID: ACM134615375. Alfa Chemistry ISO 9001:2015 Certified. |  |
| Reveromycin A | Reveromycin A, the dominant analogue of a complex of spiroketals isolated from a Streptomyces sp., is an inhibitor of the mitogenic activity of epidermal growth factor (EGF). It is a G1 phase cell cycle inhibitor, selectively inhibiting isoleucyl-tRNA synthetase. Reveromycin A displays antiproliferative behavior against human cell lines KB and K562 as well as potent antifungal activity. More recently it has been shown to inducing apoptosis in osteoclasts thus inhibiting bone resorption. Group: Biochemicals. Grades: Highly Purified. CAS No. 134615-37-5. Pack Sizes: 250ug. US Biological Life Sciences. | Worldwide |
| Reveromycin B | Reveromycin B is an much less active analogue of reveromycin A formed by rearrangement of the 6to6 spiroketal to a 5to6 spiroketal. Lacking much of the biological activity of reveromycin A, the reveromycin B is a useful negative control in resolving the mode of action of this class. Group: Biochemicals. Grades: Highly Purified. CAS No. 144860-68-4. Pack Sizes: 250ug. US Biological Life Sciences. | Worldwide |
| Reveromycin B | Reveromycin B is a polyketide antibiotic isolated from Streptomyces, which can inhibit mitotic activity. Synonyms: BDBM50217842; ZINC49871994. Grade: >98% by HPLC. CAS No. 144860-68-4. Molecular formula: C36H52O11. Mole weight: 660.79. | |
| Reveromycin C | Reveromycin C is a polyketide isolated from Streptomyces. It is an antibiotic inhibitor with mitotic activity that responds to EGF. Grade: >95% by HPLC. CAS No. 144860-69-5. Molecular formula: C37H54O11. Mole weight: 674.82. | |
| Reveromycin C | Reveromycin C is a minor analogue of the reveromycin complex isolated from a Streptomyces sp. Published information suggests that reveromycin C exhibits comparable potency to reveromycin A, its butyl homologue. In Microbial Screening Technologies in-house screens Reveromycins C and A had similar biological profiles but Reveromycin C was generally more potent. Group: Biochemicals. Grades: Highly Purified. CAS No. 144860-69-5. Pack Sizes: 250ug. US Biological Life Sciences. | Worldwide |
| Reveromycin C | Reveromycin C. Uses: Designed for use in research and industrial production. Additional or Alternative Names: REVEROMYCIN C. Product Category: Heterocyclic Organic Compound. Appearance: White to tan solid. CAS No. 144860-69-5. Molecular formula: C37H54O11. Mole weight: 674.8. Purity: 0.95. Canonical SMILES: CC(C)CCC1(CCC2(CCC(C)C(C/C=C(\\C)/C=C/C(O)C(C)/C=C/C(=O)O)O2)OC1/C=C/C(=C/C( =O)O)/C)OC(=O)CCC(=O)O. Product ID: ACM144860695. Alfa Chemistry ISO 9001:2015 Certified. | |
| Reveromycin D | Reveromycin D is a bacterial metabolite isolated from Streptomyces. It inhibits EGF-induced mitotic activity in Balb/MK cells and has pH-dependent antifungal activity against Candida albicans. Grade: >95% by HPLC. CAS No. 144860-70-8. Molecular formula: C37H54O11. Mole weight: 674.82. | |
| Reveromycin D | Reveromycin D, the isopentyl analogue, is a minor component of the reveromycin complex isolated from a Streptomyces sp. Published information on reveromycin D suggests that it is more active than its straight chain analogue, reveromycin C. Group: Biochemicals. Grades: Highly Purified. CAS No. 144860-70-8. Pack Sizes: 250ug. US Biological Life Sciences. | Worldwide |
| Reversan | Reversan represents a new class of nontoxic MRP1 inhibitor, which may be clinically useful for the treatment of neuroblastoma. Group: Biochemicals. Alternative Names: N-[3-(4-Morpholinyl)propyl]-5,7-diphenylpyrazolo[1,5-a]pyrimidine-3-carboxamide. Grades: Highly Purified. CAS No. 313397-13-6. Pack Sizes: 10mg. US Biological Life Sciences. | Worldwide |
| Reversan | Reversan (CBLC4H10) is a potent and nontoxic multidrug resistance-associated protein 1 (MRP1) and P-glycoprotein (Pgp) inhibitor[1][2]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: CBLC4H10. CAS No. 313397-13-6. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-107643. | |
| Reversan | ?98% (HPLC). Group: Fluorescence/luminescence spectroscopy. | |
| Reverse T3 | Reverse T3 is a thyroid hormone that can be generated by deiodination of the prohormone thyroxine [1]. Reverse T3 inhibits the increase of sodium current generated by other thyroid hormone analogs in neonatal rat myocytes [2]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: 3,5,3-Triiodothyronine. CAS No. 5817-39-0. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg. Product ID: HY-W010696. | |
| Reverse Transcriptase from HIV, Recombinant | Chromatographically purified heterodimer composed of 66kDa and 51kDa subunits. Supplied as a solution in 10mM potassium phosphate, pH 7.4, 1mM DTT and 20% glycerol. Primarily for AIDS research purposes; this enzyme has less fidelity than the AMV enzyme in other applications such as the preparation of cDNA from mRNA for cloning purposes. Applications: Hiv reverse transcriptase is used for research on the aids primer. however it can be substituted for amv reverse transcriptase, which is mainly used to transcribe mrna into double stranded cdna, that can be inserted into prokaryotic vectors. the enzyme can also be used with either single stranded dna or rna templates to mak...or labeling the termini of dna fragments with protruding 5' termini. the enzyme can also be used to sequence dnas by the dideoxy chain termination method of sanger when the klenow fragment of e. coli dna polymerase i, or the t7 dna polymerase yield unsatisfactory results. Group: Enzymes. Synonyms: Reverse transcriptase; RT. Enzyme Commission Number: EC 2.7.7.49. CAS No. 9068-38-6. Purity: Chromatographically purified. RT. Mole weight: 66 kDa and 51 kDa. Activity: > 5,000 units per mg protein. Storage: Store at -20°C. Form: A solution in 10mM potassium phosphate, pH 7.4, 1mM DTT and 20% glycerol. Source: E. coli. Species: HIV. Reverse transcriptase; RT. Cat No: NATE-0987. | |
| Reverse Transcriptase from Moloney Murine Leukemia Virus, Recombinant | This Reverse Transcriptase has exceptionally strong strand displacement activity and enables efficient preparation of cDNA up to 12 kb in length. It is robust, versatile and well-suited for applications requiring full-length cDNA such as preparation of cDNA libraries and other techniques involving first strand cDNA synthesis (RT-PCR, preparation of cDNA probes, real-time quantitative RT-PCR). It can be used for performing a reverse transcription reaction with any RNA template including GC-rich templates and RNAs with high levels of secondary structure. This enzyme is a modified, recombinant MMLV (Moloney Murine Leukemia Virus) reverse transcriptase and is v...ptases tested; 4. highly specific: low rates of non-specific annealing, even on incompletely denatured rna; 5. works on challenging templates: excellent results even with gc-rich templates and templates with high levels of secondary structure 6. highly sensitive: use less of your precious rna samples; 7. demonstrated success with reverse transcription reaction times of 30 min. (60 min. for longer transcripts). Applications: Rt-pcr; first strand cdna synthesis; cdna probe preparation; synthesis of cdna libraries with a high proportion of full-length cdnas. Group: Enzymes. Synonyms: Reverse transcriptase; RT. RT. Storage: Storage at-20°C. Source: E. coli. Spec | |
| Reverse transcriptase-IN-1 | Reverse transcriptase-IN-1 (Compound 12z), a diarylbenzopyrimidine (DABP) analogue, is a potent, orally active HIV-1 nonnucleoside reverse transcriptase inhibitor. Reverse transcriptase-IN-1 has antiviral activity with EC 50 values of 3.4 nM, 4.3 nM and 3.6 nM for HIV-1 III B , E138K and K103N mutants, respectively. Reverse transcriptase-IN-1 also has an IC 50 of 13.7 nM against HIV-1 reverse transcriptase enzyme [1]. Uses: Scientific research. Group: Signaling pathways. CAS No. 2380001-43-2. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-130241. | |
| Reversin 121 | ?97% (HPLC), powder. Group: Fluorescence/luminescence spectroscopy. | |
| Reversin 205 | ?98% (HPLC), film. Group: Fluorescence/luminescence spectroscopy. | |
| Reversine | ?98% (HPLC), solid. Group: Fluorescence/luminescence spectroscopy. | |
| Reversine | Reversine is a novel class of ATP-competitive Aurora kinase inhibitor with IC 50 s of 400, 500 and 400 nM for Aurora A , Aurora B and Aurora C , respectively. Uses: Scientific research. Group: Signaling pathways. CAS No. 656820-32-5. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 50 mg; 100 mg. Product ID: HY-14711. | |
| Reversine (2-(4-Morpholinoanilino)-6-cyclohexylaminopurine) | A cell-permeable, potent, and selective human A3 adenosine receptor antagonist (Ki = 0.66uM) and an aurora kinase inhibitor (IC??'s of 30-550 nM for blast colony formation assay). Induces dedifferentiation in murine C2C12 myoblasts. The cells were also shown to regain multipluripotency following removal of the compound. Group: Biochemicals. Grades: Highly Purified. CAS No. 656820-32-5. Pack Sizes: 1mg, 5mg. US Biological Life Sciences. | Worldwide |
| Revised PVOC Mixture | certified reference material, 2000 ?g/mL each component in methanol. Group: Certified reference materials (crms). | |
| Revumenib | Revumenib (SNDX-5613) is a potent and specific Menin-MLL inhibitor with a binding K i of 0.149 nM and a cell based IC 50 of 10-20 nM. Revumenib can be used for the research of MLL-rearranged (MLL-r) acute leukemias, including acute lymphoblastic leukemia (ALL) and acute myeloid leukemia (AML) [1]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: SNDX-5613. CAS No. 2169919-21-3. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-136175. | |
| Rexamino | Rexamino. Uses: Designed for use in research and industrial production. Additional or Alternative Names: 4,5-Dihydro-4-phenyl-. Product Category: Heterocyclic Organic Compound. CAS No. 52883-35-9. Molecular formula: C9H10N2O. Mole weight: 162.19. Purity: 0.96. IUPACName: 4-phenyl-4,5-dihydro-1,3-oxazol-2-amine. Canonical SMILES: C1C(N=C(O1)N)C2=CC=CC=C2. Density: 1.264g/cm³. Product ID: ACM52883359. Alfa Chemistry ISO 9001:2015 Certified. | |
| Reynoutrin | Reynoutrin is a flavonoid glycoside isolated from the herbs of Saururus chinensis. Uses: Antioxidant. Synonyms: Quercetin 3-beta-D-xylopyranoside. Grade: 95%. CAS No. 549-32-6. Molecular formula: C20H18O11. Mole weight: 434.35. | |
| Rezafungin | Rezafungin. Uses: For analytical and research use. Group: Impurity standards. CAS No. 1396640-59-7. Molecular formula: C63H85N8O17+. Mole weight: 1226.41. Catalog: APB1396640597. | |
| Rezafungin | Rezafungin, a next-generation, broad-spectrum and long-lasting echinocandin, has potent antifungal activity against Candida spp., Aspergillus spp. and Pneumocystis spp. Synonyms: Biafungin; CD101; SP-3025; 2-{[(2R,6S,9S,11R,12S,14aS,15S,16S,20S,23S,25aS)-23-[(1S,2S)-1,2-Dihydroxy-2-(4-hydroxyphenyl)ethyl]-2,11,15-trihydroxy-6,20-bis[(1R)-1-hydroxyethyl]-16-methyl-5,8,14,19,22,25-hexaoxo-9-({[4''-(pentyloxy)-1,1':4',1''-terphenyl-4-yl]carbonyl}amino)tetracosahydro-1H-dipyrrolo[2,1-c:2',1'-l][1,4,7,10,13,16]hexaazacyclohenicosin-12-yl]oxy}-N,N,N-trimethylethanaminium. Grade: ≥95%. CAS No. 1396640-59-7. Molecular formula: C63H85N8O17+. Mole weight: 1226.39. | |
| Rezafungin acetate | Rezafungin acetate (Biafungin acetate) is a next-generation, broad-spectrum, and long-lasting echinocandin. Rezafungin acetate shows potent antifungal activity against Candida spp. , Aspergillus spp. , and Pneumocystis spp. [1] [2]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: Biafungin acetate; CD101 acetate; SP-3025 acetate. CAS No. 1631754-41-0. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-108009A. | |
| Rezafungin Impurity 1 | Rezafungin Impurity 1. Uses: For analytical and research use. Group: Impurity standards. CAS No. 1396639-48-7. Molecular formula: C63H85N8O17+. Mole weight: 1226.41. Catalog: APB1396639487. | |
| Rezafungin Impurity 2 | Rezafungin Impurity 2. Uses: For analytical and research use. Group: Impurity standards. CAS No. 1396640-55-3. Molecular formula: C63H85N8O17+. Mole weight: 1226.41. Catalog: APB1396640553. | |
| Rezafungin Impurity 9 | Rezafungin Impurity 9. Uses: For analytical and research use. Group: Impurity standards. CAS No. 1672717-33-7. Molecular formula: C63H86N9O17+. Mole weight: 1241.43. Catalog: APB1672717337. | |
| Rezatapopt | Rezatapopt (PC14586) is an orally active antineoplastic agent. Rezatapopt binds to a pocket created by the TP53 Y220C mutation. Rezatapopt restores p53 tumor suppressor functions by stabilization of the p53 protein structure. Rezatapopt demonstrates tumor inhibition and regression in mouse models with established human tumor xenografts harboring the TP53 Y220C mutation [1] [2] [3] [4]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: PC14586. CAS No. 2636846-41-6. Pack Sizes: 10 mM * 1 mL; 1 mg; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-156633. | |
| Rezorstobart | Rezorstobart is an anti- KLRB1 human IgG1 κ monoclonal antibody [1]. Recommend Isotype Controls: Human IgG1 kappa, Isotype Control (HY-P99001). Uses: Scientific research. Group: Inhibitory antibodies. CAS No. 2762201-86-3. Pack Sizes: 1 mg; 5 mg; 10 mg. Product ID: HY-P990760. | |
| Rezvilutamide | Rezvilutamide (SHR3680) is an orally active androgen receptor antagonist. Rezvilutamide (SHR3680) is used for the study of prostate cancer [1] [2]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: SHR3680. CAS No. 1572045-62-5. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 50 mg; 100 mg. Product ID: HY-137448. | |
| RF9 | RF9 is a potent and selective Neuropeptide FF receptor antagonist, with K i values of 58 and 75 nM for hNPFF1R and hNPFF2R , respectively [1] [2]. Uses: Scientific research. Group: Signaling pathways. CAS No. 876310-60-0. Pack Sizes: 1 mg; 5 mg. Product ID: HY-107382. | |
| RF 9 | RF 9 is a potent and selective Neuropeptide FF receptor antagonist, with Kis of 58±5 and 75±9 nM for hNPFF1R and hNPFF2R, respectively. It displays selectivity over several related receptors including NPY Y1 GPR10, GPR54, GPR103 and the opioid receptors. Synonyms: 2-Adamantanecarbonyl-Arg-Phe-NH2. Grade: ≥96%. CAS No. 876310-60-0. Molecular formula: C26H38N6O3. Mole weight: 482.62. | |
| RF9 (1-Adamantanecarbonyl-Arg-Phe-NH2) | Selective NPFF receptor antagonist (Ki values are 58 and 75nM at hNPFF1 and hNPFF2 receptors respectively). Displays selectivity over several related receptors including NPY Y1 GPR10, GPR54, GPR103 and the opioid receptors. Blocks NPFF-induced hypothermia and increases in atrial blood pressure and heart rate, and prevents opioid-induced tolerance associated with hyperalgesia in vivo. Group: Biochemicals. Alternative Names: 1-Adamantanecarbonyl-Arg-Phe-NH2. Grades: Highly Purified. CAS No. 876310-60-0. Pack Sizes: 1mg. Molecular Formula: C??H??N?O?, Molecular Weight: 482.62 free base. US Biological Life Sciences. | Worldwide |
| R-Fexofenadine (R-Carboxyterfenadine, R-Terfenadinecarboxyl ate) | A metabolite of of terfenadine, a H1-Histamine receptor antagonist. Group: Biochemicals. Alternative Names: R-Carboxyterfenadine, R-Terfenadinecarboxyl ate. Grades: Highly Purified. Pack Sizes: 10mg. US Biological Life Sciences. | Worldwide |
| r-(-)-Flecainide | r-(-)-Flecainide. Uses: Designed for use in research and industrial production. Additional or Alternative Names: N-[(2R)-2-Piperidinylmethyl]-2,5-bis(2,2,2-trifluoroethoxy)benzamide; (R)-Flecainide; (-)-Flecainide. Product Category: Heterocyclic Organic Compound. CAS No. 99495-90-6. Molecular formula: C17H20F6N2O3. Mole weight: 414.34. Product ID: ACM99495906. Alfa Chemistry ISO 9001:2015 Certified. | |
| R-(-)-Flecainide | R-(-)-Flecainide. Group: Biochemicals. Alternative Names: N-[ (2R) -2-Piperidinylmethyl]-2, 5-bis (2, 2, 2-trifluoroethoxy) benzamide; (R)-Flecainide; (-)-Flecainide. Grades: Highly Purified. CAS No. 99495-90-6. Pack Sizes: 1mg, 2mg, 5mg, 10mg. Molecular Formula: C17H20F6N2O3. US Biological Life Sciences. | Worldwide |
| R-(?)-Fluoxetine hydrochloride | analytical standard. Group: Antidepressants standards. | |
| RFP Expressing Glomerular Microvascular Endothelial Cells, Human (Frozen) | RFP-HGMECs were selected from Zeocin resistant HGMECs after transfection with RFP- expressing Lentiviral particles. Cells are shipped in proliferating culture with >90% confluence (cells are provided at passages 3-5). ENDO-Growth medium containing 5% serum and growth supplement are recommended for cell culture. Cells have an average population doubling level of >16 when cultured. Group: Biologicals. Grades: Cell Culture Grade. Pack Sizes: 1ml. US Biological Life Sciences. | Worldwide |
| RFP Expressing Glomerular Microvascular Endothelial Cells, Human (T-25 flask) | RFP-HGMECs were selected from Zeocin resistant HGMECs after transfection with RFP- expressing Lentiviral particles. Cells are shipped in proliferating culture with >90% confluence (cells are provided at passages 3-5). ENDO-Growth medium containing 5% serum and growth supplement are recommended for cell culture. Cells have an average population doubling level of >16 when cultured. Group: Biologicals. Grades: Cell Culture Grade. Pack Sizes: T-25 flask. US Biological Life Sciences. | Worldwide |
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