A directory of where to buy chemicals in the USA, including: distributors, industrial manufacturers, bulk supplies and wholesalers of raw ingredients & finished goods.
Search for products or services, then visit the suppliers website for prices or more information.
| Product | Description | |
|---|---|---|
| CTX-712 | CTX-712 is an orally effective CLK 2 inhibitor, with an IC 50 of 1.4 nM, showing anti-tumor activity [1] [2]. Uses: Scientific research. Group: Signaling pathways. CAS No. 2144751-78-8. Pack Sizes: 10 mM * 1 mL; 1 mg; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-144875. |  |
| C-Type Natriuretic Peptide (1-53), human | C-Type Natriuretic Peptide (1-53), human is the 1-53 fragment of C-Type Natriuretic Peptide, which belong to the natriuretic peptide family and is involved in the maintenance of electrolyte-fluid balance and vascular tone. Synonyms: CNP-53 (human); Asp-Leu-Arg-Val-Asp-Thr-Lys-Ser-Arg-Ala-Ala-Trp-Ala-Arg-Leu-Leu-Gln-Glu-His-Pro-Asn-Ala-Arg-Lys-Tyr-Lys-Gly-Ala-Asn-Lys-Lys-Gly-Leu-Ser-Lys-Gly-Cys-Phe-Gly-Leu-Lys-Leu-Asp-Arg-Ile-Gly-Ser-Met-Ser-Gly-Leu-Gly-Cys (Disulfide bond). Grade: ≥95%. CAS No. 141294-77-1. Molecular formula: C251H417N81O71S3. Mole weight: 5801.77. |  |
| C-Type Natriuretic Peptide-22 (human, porcine, rat) trifluoroacetate salt | C-Type natriuretic peptide-22 is an endogenous peptide which has diverse biological activities. CNP-22 acts as a selective agonist of natriuretic peptide receptors (NPRs) 2 and 3 (Kds = 7, 10.8, and >500,000 pM for NPR2, 3, and 1, respectively). The 22 amino acid sequence corresponds to residues 105-126 of its precursors prepro CNP, pro CNP, and CNP-53. Synonyms: CNP-22; glycyl-L-leucyl-L-seryl-L-lysylglycyl-L-cysteinyl-L-phenylalanylglycyl-L-leucyl-L-lysyl-L-leucyl-L-α-aspartyl-L-arginyl-L-isoleucylglycyl-L-seryl-L-methionyl-L-serylglycyl-L-leucylglycyl-L-cysteine cyclic (6→22)-disulfide trifluoroacetate salt. Grade: ≥95%. Molecular formula: C93H157N27O28S3·xCF3COOH. Mole weight: 2197.60. | |
| C-Type Natriuretic Peptide (CNP) (1-22), human | C-Type Natriuretic Peptide (CNP) (1-22), human, a 1-22 fragment of CNP, is a natriuretic peptide receptor B (NPR-B) agonist. C-Type Natriuretic Peptide (CNP) (1-22), human inhibits cAMP synthesis stimulated by the physiological agonists histamine and 5-HT or directly by Forskolin. CNP is a potent, endothelial-derived relaxant and growthinhibitory factor[1][2][3]. Uses: Scientific research. Group: Peptides. CAS No. 127869-51-6. Pack Sizes: 500 ?g; 1 mg; 5 mg; 10 mg. Product ID: HY-P1237. | |
| C-Type Natriuretic Peptide (CNP) (1-22), human | C-type natriuretic peptide is an endogenous peptide found in plasma and cerebrospinal fluid. It is composed of 22 amino acids. C-type natriuretic peptide acts as an agonist of natriuretic peptide receptor NPR2 (NPRB) and exhibits affinity for NPR3 (NPRC). It inhibits L-type calcium currents in myocytes and exhibits antiproliferative effects in cardiac fibroblasts in vitro. Regulates cartilage homeostasis, body fluid volume and exhibits vasodilatory activity in vivo. Synonyms: H-Gly-Leu-Ser-Lys-Gly-Cys(1)-Phe-Gly-Leu-Lys-Leu-Asp-Arg-Ile-Gly-Ser-Met-Ser-Gly-Leu-Gly-Cys(1)-OH; glycyl-L-leucyl-L-seryl-L-lysyl-glycyl-L-cysteinyl-L-phenylalanyl-glycyl-L-leucyl-L-lysyl-L-leucyl-L-alpha-aspartyl-L-arginyl-L-isoleucyl-glycyl-L-seryl-L-methionyl-L-seryl-glycyl-L-leucyl-glycyl-L-cysteine (6->22)-disulfide; Natriuretic peptide, C-type; C-type natriuretic peptide (1-22) (human, rat, swine); Atriopeptin C (pig); C-Type Natriuretic Peptide (32-53) (human, porcine, rat). Grade: ≥95%. CAS No. 127869-51-6. Molecular formula: C93H157N27O28S3. Mole weight: 2197.60. | |
| Cu | Cu. Group: Elements nanoparticles. 99.8% (metal basis). |  |
| Cu | Cu. Group: Nanowires. CAS No. 20427-59-2. Molecular formula: 97.56068 g/mol. 99.5%. | |
| CU-115 | CU-115 is a selective TLR8 inhibitor with IC50 of 1.04 μM. CU-115 was demonstrated that inhibits ssRNA-sensing pathways at low concentrations and does not inhibit other non-endosomal TLR and cytosolic NA-sensing pathways (<5 μ M). Synonyms: N-(4-(3,5-Bis(trifluoromethyl)phenoxy)phenyl)-2-fluoro-6-iodobenzamide. Grade: 98%. CAS No. 2471982-20-2. Molecular formula: C21H11F7INO2. Mole weight: 569.21. | |
| Cu2+-exporting ATPase | A P-type ATPase that undergoes covalent phosphorylation during the transport cycle. The enzyme from the termophilic bacterium Archaeoglobus fulgidus is involved in copper extrusion from the cell. Group: Enzymes. Synonyms: CopB. Enzyme Commission Number: EC 3.6.3.4. 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-4678; Cu2+-exporting ATPase; EC 3.6.3.4; CopB. Cat No: EXWM-4678. |  |
| CU-32 | CU-32 is an inhibitor of cyclic GMP-AMP (cGAMP) synthase (IC50 = 0.45 μM). Synonyms: methyl 4-amino-6-((4-iodophenyl)amino)-1,3,5-triazine-2-carboxylate. Grade: 95%. CAS No. 2400954-16-5. Molecular formula: C11H10IN5O2. Mole weight: 371.13. | |
| CU-32 | CU-32 is a potent cGAS inhibitor with an IC 50 of 0.45 μM. CU-32 decreases IFN-stimulatory DNA-induced production of IFN-β in THP-1 cells [1]. Uses: Scientific research. Group: Signaling pathways. CAS No. 2400954-16-5. Pack Sizes: 1 mg; 5 mg. Product ID: HY-132221. | |
| CU-76 | An inhibitor of cyclic GMP-AMP synthase (IC50 = 0.24 μM). Synonyms: Methyl 4-amino-6-((3,5-difluoro-4-iodophenyl)amino)-1,3,5-triazine-2-carboxylate. Grade: 95%. CAS No. 2400954-58-5. Molecular formula: C11H8F2IN5O2. Mole weight: 407.11. | |
| CuAlMnTi High-Entropy Alloy Ingots | We are engaged in the development, production, and sales of CuAlMnTi High-Entropy Alloy Ingots and provide personalized customization service for high-quality metal powder. CuAlMnTi High-Entropy Alloy is a new alloy with very unique properties. Uses: Used in manufacturing super alloys and electron-beam melting. used in metallurgical, machinery processing, glass, and ceramic industries. used in electronics industry, such as integrated circuits. used in the field of glass coating. Group: High entropy alloys. Pack Sizes: Our CuAlMnTi High-Entropy Alloy Ingot is carefully handled during storage and transportation to preserve the quality of our product in its original condition. 0.99. | |
| CuAlMnTi High-Entropy Alloy Spherical Powder | We are engaged in the development, production and sales of CuAlMnTi high entropy alloy spherical powder, and provide personalized service of high quality metal powder. CuAlMnTi high entropy alloy spherical powder is a new type of alloy with very unique properties. Uses: Cualmnti high-entropy alloy spherical powder is widely used in aerospace parts and auto parts, profile surface spraying, powder metallurgy, nuclear energy and industrial fields. Group: High entropy alloys. | |
| CuAlTiWV High-Entropy Alloy Spherical Powder | CuAlTiWV High-Entropy Alloy Spherical Powder is composed of Cu, Al, Ti, W, V. Alfa Chemistry offers high-quality High-Entropy Alloy with competitive pricing. Uses: Cualtiwv high-entropy alloy spherical powder is widely used in aerospace parts and auto parts, profile surface coating, powder metallurgy, nuclear energy and industrial fields. Group: High entropy alloys. Pack Sizes: Our CuAlTiWV High-Entropy Alloy Spherical Powder is carefully handled during storage and transportation to preserve the quality of our product in its original condition. | |
| CuATSM | CuATSM is a copper complex that scavenges free radicals, inhibits lipid peroxidation and ferroptosis. CuATSM exhibits antioxidant, anti-inflammatory and neuroprotective activities [1] [2]. Uses: Scientific research. Group: Signaling pathways. CAS No. 68341-09-3. Pack Sizes: 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-139827. | |
| CuATSM | CuATSM is a highly potent radical-trapping antioxidant (RTA) and (phosphorus)lipid peroxidation inhibitor, thereby accounting for its ability to inhibit ferroptosis. It is preclinically used as a potential therapy for ALS (amyotrophic lateral sclerosis) and a potential anti-Alzheimer's agent. Synonyms: Cu(II)astm; Copper(II) diacetyl-di(N4-methyl)thiosemicarbazone; [[2,2'-(1,2-Dimethyl-1,2-ethanediylidene)bis[N-methylhydrazinecarbothioamidato]]]copper; [[2,2'-(1,2-Dimethyl-1,2-ethanediylidene)bis[N-methylhydrazinecarbothioamidato]](2-)-N2,N2',S,S']-, (SP-4-2)Copper; [[2,2-Prime-(1,2-Dimethyl-1,2-ethanediylidene)bis[N-methylhydrazinecarbothioamidato]]]copper; (SP-4-2)-[[2,2'-(1,2-dimethyl-1,2-ethanediylidene)bis[N-methylhydrazinecarbothioamidato-κN2,κS]](2-)]-copper; copper-ATSM. Grade: ≥95%. CAS No. 68341-09-3. Molecular formula: C8H14CuN6S2. Mole weight: 321.91. | |
| Cu-ATSM | ?98% (HPLC). Group: Fluorescence/luminescence spectroscopy. |  |
| Cuban Tobacco Fragrance Oil | Cuban Tobacco Fragrance Oil. |  CA, FL & NJ |
| cubebol synthase | Requires Mg2+. The enzyme gives 28% cubebol, 29% (-)-germacrene D, 10% (+)-Δ-cadinene and traces of several other sesquiterpenoids. See also EC 4.2.3.75 (-)-germacrene D synthase and EC 4.2.3.13 (+)-Δ-cadinene synthase. Group: Enzymes. Synonyms: Cop4. Enzyme Commission Number: EC 4.2.3.91. 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-5255; cubebol synthase; EC 4.2.3.91; Cop4. Cat No: EXWM-5255. | |
| Cubeb Pepper Oil | Cubeb essential oilsis a warm, sweet oil with a slight peppery characteristic. Although Cubeb (Piper cubeba) has similarities to Black Pepper (Piper nigrum), Cubeb essential oilsis not as peppery in aroma as Black Pepper Essential Oil. It's a softer, mellower, warming essential oilsthat serves as a middle-base note in fragrancing applications. Cubeb oil is derived from the fruits of the cubebs plants. Cubeb plants are native to Java and Sumatra Islands but are also grown in India, Sri Lanka, and Reunion, too. Uses: Essential Oils, Pharmaceutical. Group: Plant Extracts. INCI Names: Piper Cubeba (Cubeb Pepper) Fruit Oil. Grades: FOOD GRADE. CAS No. 90082-59-0. Pack Sizes: 25 kgs Jerrycan, 200 kg Drums. Product ID: CB-002. Olfactive Profile: Spicy, pepper-like, piperine, mint-like. EC No: 290-148-4. FEMA No: 2339. Origin: Indonesia. |  New Jersey |
| Cubeb Pepper Oil - CO2 | Cubeb essential oilsis a warm, sweet oil with a slight peppery characteristic. Although Cubeb (Piper cubeba) has similarities to Black Pepper (Piper nigrum), Cubeb essential oilsis not as peppery in aroma as Black Pepper Essential Oil. It's a softer, mellower, warming essential oilsthat serves as a middle-base note in fragrancing applications. Cubeb oil is derived from the fruits of the cubebs plants. Cubeb plants are native to Java and Sumatra Islands but are also grown in India, Sri Lanka, and Reunion, too. Uses: Pharmaceutical. Group: Plant Extracts. INCI Names: Piper Cubeba (Cubeb Pepper) Fruit Oil. Grades: FOOD GRADE. CAS No. 90082-59-0 ; 8007-87-2. Pack Sizes: 25 kgs Jerrycan, 200 kg Drums. Product ID: CB-001. Olfactive Profile: Spicy, pepper-like, piperine, mint-like. EC No: 290-148-4. FEMA No: 2339. Origin: Indonesia. | New Jersey |
| Cubenol | Cubenol was used for biological study of antioxidant and antimicrobial activity and comparison of cinnamon leaf and bark essential oils and oleoresins. Cubenol was one of the major components of essential oils isolated from the aerial parts of Artemisia absinthium, Artemisia santonicum and Artemisia spicigera. Group: Biochemicals. Grades: Highly Purified. CAS No. 21284-22-0. Pack Sizes: 10mg, 50mg. Molecular Formula: C15H26O, Molecular Weight: 222.37. US Biological Life Sciences. |  Worldwide |
| Cubic Boron Nitride Nanoparticles | Cubic Boron Nitride Nanoparticles. Group: Nanopowder compounds. CAS No. 7740-42-8. Molecular formula: 24.82 g/mol. Mole weight: BN. 99%. | |
| CU-CPD107 | CU-CPD107 is a a tetrasubstituted imidazole that inhibits R848-induced TLR8 signaling. In the presence of R848, CU-CPD107 acts as a TLR8 signaling inhibitor with IC50 of 13.7 μM. Synonyms: GD0. CAS No. 2573912-32-8. Molecular formula: C16H21IN2O2. Mole weight: 400.26. | |
| CU CPT 22 | CU CPT 22 is a selective TLR1/2 inhibitor (IC50 = 0.58 μM). Synonyms: CU-CPT22; CU-CPT 22; CU-CPT-22; CUCPT22; CUCPT 22; CUCPT-22; 3,4,6-Trihydroxy-2-methoxy-5-oxo-5H-benzocycloheptene-8-carboxylic acid hexyl ester. CAS No. 1416324-85-0. Molecular formula: C19H22O7. Mole weight: 362.37. | |
| CU-CPT22 | ?98% (HPLC). Group: Fluorescence/luminescence spectroscopy. | |
| CU-CPT22 | CU-CPT22 is a potent protein complex of toll-like receptor 1 and 2 (TLR1/2) inhibitor, and competes with the synthetic triacylated lipoprotein (Pam3CSK4) binding to TLR1/2 with a Ki of 0.41 μM. CU-CPT22 blocks Pam3CSK4-induced TLR1/2 activation with an IC50 of 0.58 μM[1]. Uses: Scientific research. Group: Signaling pathways. CAS No. 1416324-85-0. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-108471. | |
| CU CPT 4a | CU CPT 4a is a selective TLR3 inhibitor (IC50 = 3.44 μM in RAW 264.7 cells). Synonyms: CU CPT 4a; CU-CPT-4a; CUCPT4a; N-[(3-Chloro-6-fluorobenzo[b]thien-2-yl)carbonyl]-D-phenylalanine. CAS No. 1279713-77-7. Molecular formula: C18H13ClFNO3S. Mole weight: 377.82. | |
| CU-CPT 4a | CU-CPT 4a (TLR3-IN-1) is a potent, highly selective TLR3 signaling inhibitor. CU-CPT 4a represses the expression of downstream signaling pathways mediated by the TLR3/dsRNA complex, including TNF-α and IL-1β [1]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: TLR3-IN-1. CAS No. 1279713-77-7. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-108473. | |
| CU-CPT-8m | CU-CPT-9m is a TLR8 antagonist with an IC50 of 67 nM. Synonyms: CU-CPT-8m, CU-CPT 8m, CU-CPT8m; 7-(m-tolyl)pyrazolo[1,5-a]pyrimidine-3-carboxamide; 7-(3-methylphenyl) pyrazolo(1,5-a)pyrimidine-3-carboxamide; 7-(3-methylphenyl) pyrazolo[1,5-a]pyrimidine-3-carboxamide; CU-CPT8m. CAS No. 125079-83-6. Molecular formula: C14H12N4O. Mole weight: 252.277. | |
| CU-CPT9a | ?98% (HPLC). Group: Fluorescence/luminescence spectroscopy. | |
| CU-CPT-9a | CU-CPT-9a is a TLR8 antagonist with an IC50 of 0.5 nM. Synonyms: CU-CPT9b; CUCPT9b; CU CPT9b; HY-112667; CS-0059157; HY 112667; CS 0059157; HY112667; CS0059157; 4-(3-methyl-4-oxidanyl-phenyl)quinolin-7-ol; 2-Methyl-4-(7-hydroxyl-4-quinolinyl)-phenol. CAS No. 2162962-69-6. Molecular formula: C16H13NO2. Mole weight: 251.285. | |
| CU-CPT-9b | CU-CPT-9b is a TLR8 inhibitor that inhibits TLR8-mediated proinflammatory signaling in various cell lines and human primary cells. Synonyms: CU-CPT9a; 2-Methyl-4-(7-methoxy-4-quinolinyl)phenol; CU CPT 9a; BCP29122; BCP-29122; CUCPT9a; BCP 29122; 4-(7-methoxy-1H-quinolin-4-ylidene)-2-methylcyclohexa-2,5-dien-1-one; Phenol, 4-(7-methoxy-4-quinolinyl)-2-methyl-; 4-(7-Methoxy-4-quinolinyl)-2-methylphenol. Grade: ≥95%. CAS No. 2165340-32-7. Molecular formula: C17H15NO2. Mole weight: 265.31. | |
| CuCrZr High-Entropy Alloy Ingots | We are engaged in the development, production, and sales of CuCrZr High-Entropy Alloy Ingots and provide personalized customization service for high-quality metal powder. CuCrZr High-Entropy Alloy is a new alloy with very unique properties. Uses: Used in manufacturing super alloys and electron-beam melting. used in metallurgical, machinery processing, glass, and ceramic industries. used in electronics industry, such as integrated circuits. used in the field of glass coating. Group: High entropy alloys. Pack Sizes: Our CuCrZr High-Entropy Alloy Ingot is carefully handled during storage and transportation to preserve the quality of our product in its original condition. 0.99. | |
| CuCrZr High-Entropy Alloy Spherical Powder | We are engaged in the development, production and sales of CuCrZr high entropy alloy spherical powder, and provide personalized service for high quality metal powder. CuCrZr high entropy alloy spherical powder is a new type of alloy with very unique properties. Uses: Cucrzr high-entropy alloy spherical powder is widely used in aerospace parts and auto parts, profile surface spraying, powder metallurgy, nuclear energy and industrial fields. Group: High entropy alloys. | |
| Cucumber Powder | Cucumber powder is made from Cucumis sativus, a widely cultivated plant in the gourd family Cucurbitaceae. Cucumber powder is a great ingredient to help revitalize the skin. Cucumber powder has many benefits for skin, it helps relieve the puffiness of the skin. Cucumber powder also helps remove dead skin cells and tightens skin. Group: Others. Cucumber Powder; Cucumis Sativus Linn. Cat No: EXTC-106. | |
| cucumisin | From the sarcocarp of the musk melon (Cucumis melo). In peptidase family S8 (subtilisin family). Other endopeptidases from plants, which are less well characterized but presumably of serine-type, include euphorbain from Euphorbia cerifera, solanain from horse-nettle Solanum elaeagnifolium, hurain from Hura crepitans and tabernamontanain from Tabernamontana grandiflora. Group: Enzymes. Synonyms: euphorbain; solanain; hurain; tabernamontanain. Enzyme Commission Number: EC 3.4.21.25. CAS No. 82062-89-3. 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-4123; cucumisin; EC 3.4.21.25; 82062-89-3; euphorbain; solanain; hurain; tabernamontanain. Cat No: EXWM-4123. | |
| Cucurbit[5]uril hydrate | Cucurbiturils are macrocyclic molecules made of glycoluril monomers linked by methylene bridges. The oxygen atoms are located along the edges of the band and are tilted inwards, forming a partly enclosed cavity. Cucurbiturils are commonly written as cucurbit[n]uril, where n is the number of glycoluril units. Two common abbreviations are CB[n], or simply CBn. Uses: Host material for supramolecular chemistry. Group: Hydrophilic polymers. Pack Sizes: Packaging 100 mg in glass insert. Mole weight: C30H30N20O10 · xH2O · xKCl · xHCl. O. Cl. [Cl-]. [K+]. O=C1N2CN3C4C5N (CN6C7C8N (CN9C%10C%11N (CN%12C%13C%14N (CN1C%15C2N%16CN4C (=O) N5CN7C (=O) N8CN%10C (=O) N%11CN%13C (=O) N%14CN%15C%16=O) C%12=O) C9=O) C6=O) C3=O. 1S/C30H30N20O10. 2ClH. K. H2O/c51-21-31-1-32-12-14-36 (22 (32)52)4-40-16-18-44 (26 (40)56)8-48-20-19-47 (29 (48)59)7-43-17-15-39 (25 (43)55)3-35 (21)13-11 (31)33-2-34 (12)24 (54)38 (14)6-42 (16)28 (58)46 (18)10-50 (20)30 (60)49 (19)9-45 (17)27 (57)41 (15)5-37 (13)23 (33)53; ; ; ; /h11-20H, 1-10H2; 2*1H; ; 1H2/q; ; ; +1; /p-1/t11-, 12+, 13+, 14-, 15-, 16+, 17+, 18-, 19-, 20+; ; ;. VIWLZIOPOSWHFW-DVJLYPCZSA-M. | |
| Cucurbit[5]uril hydrate | contains acid of crystalization. Group: Hydrophilic polymers. | |
| Cucurbit[6]uril hydrate | Cucurbit[6]uril hydrate. Group: Hydrophilic polymers. CAS No. 80262-44-8. Product ID: 3, 5, 8, 10, 13, 15, 18, 20, 23, 25, 28, 30, 31, 33, 35, 37, 41, 43, 45, 47, 49, 51, 53, 55-tetracosazanonadecacyclo[25.3.3.36, 7.311, 12.316, 17.321, 22.22, 31.226, 33.13, 30.15, 8.110, 13.115, 18.120, 23.125, 28.135, 41.137, 55.143, 45.147, 49.151, 53]hexacontane-34, 36, 38, 39, 40, 42, 44, 46, 48, 50, 52, 54-dodecone. Molecular formula: 996.8g/mol. Mole weight: C36H36N24O12. C1N2C3C4N (C2=O)CN5C6C7N (C5=O)CN8C9C2N (C8=O)CN5C8C%10N (C5=O)CN5C%11C%12N (C5=O)CN5C%13C (N1C5=O)N1CN3C (=O)N4CN6C (=O)N7CN9C (=O)N2CN8C (=O)N%10CN%11C (=O)N%12CN%13C1=O. InChI=1S / C36H36N24O12 / c61-25-37-1-38-14-16-42 (26 (38) 62) 4-46-18-20-50 (30 (46) 66) 8-54-22-24-58 (34 (54) 70) 11-57-23-21-53 (33 (57) 69) 7-49-19-17-45 (29 (49) 65) 3-41 (25) 15-13 (37) 39-2-40 (14) 28 (64) 44 (16) 6-48 (18) 32 (68) 52 (20) 10-56 (22) 36 (72) 60 (24) 12-59 (23) 35 (71) 55 (21) 9-51 (19) 31 (67) 47 (17) 5-43 (15) 27 (39) 63 / h13-24H, 1-12H2. MSBXTPRURXJCPF-UHFFFAOYSA-N. | |
| Cucurbit[6]uril hydrate | contains acid of crystalization. Group: Hydrophilic polymers. | |
| Cucurbit[7]uril | Cucurbit[7]uril is a cyclic organic molecule consisting of seven glycoluril units linked by methylene bridges. It has a rigid barrel-like structure with two identical inlets at both ends to selectively encapsulate guest molecules of appropriate size, shape, and polarity. Cucurbit[7]uril is known for its high binding affinity for a variety of organic and inorganic guests, including drugs, amino acids, peptides, and metal ions. This property makes them promising candidates for various applications in areas such as drug delivery, catalysis, and sensing. Uses: Scientific research. Group: Biochemical assay reagents. Alternative Names: CB7; Carrier CB7. CAS No. 259886-50-5. Pack Sizes: 25 mg; 50 mg. Product ID: HY-104086. | |
| Cucurbit[7]uril hydrate | contains acid of crystalization. Group: Hydrophilic polymers. | |
| Cucurbit[7]uril hydrate | Cucurbiturils are macrocyclic molecules made of glycoluril monomers linked by methylene bridges. The oxygen atoms are located along the edges of the band and are tilted inwards, forming a partly enclosed cavity. Cucurbiturils are commonly written as cucurbit[n]uril, where n is the number of glycoluril units. Two common abbreviations are CB[n], or simply CBn. Uses: Chemists have used cucurbituril for a variety of applications, including drug delivery, asymmetric synthesis, molecular switching, and dye tuning. Group: Hydrophilic polymers. Pack Sizes: Packaging 100 mg in glass insert. Product ID: 3, 5, 8, 10, 13, 15, 18, 20, 23, 25, 28, 30, 33, 35, 36, 38, 40, 42, 46, 48, 50, 52, 54, 56, 58, 60, 62, 64-octacosazadocosacyclo[30.3.3.36, 7.311, 12.316, 17.321, 22.326, 27.22, 36.231, 38.13, 35.15, 8.110, 13.115, 18.120, 23.125, 28.130, 33.140, 46.142, 64.148, 50.152, 54.156, 58.160, 62]heptacontane-39, 41, 43, 44, 45, 47, 49, 51, 53, 55, 57, 59, 61, 63-tetradecone; hydrate. Molecular formula: 1181g/mol. Mole weight: C42H42N28O14 · xH2O · xHCl. O. Cl. O=C1N2CN3C4C5N (CN6C7C8N (CN9C%10C%11N (CN%12C%13C%14N (CN%15C%16C%17N (CN%18C%19C%20N (CN1C%21C2N%22CN4C (=O) N5CN7C (=O) N8CN%10C (=O) N%11CN%13C (=O) N%14CN%16C (=O) N%17CN%19C (=O) N%20CN%21C%22=O) C%18=O) C%15=O) C%12=O) C9=O) C6=O) C3=O. 1S/C42H42N28O14. ClH. H2O/c71-29-43-1-44-16-18-48 (30 (44)72)4-52-20-22-56 (34 (52)76)8-60-24-26-64 (38 (60)80)12-68-28-27-67 (41 (68 | |
| Cucurbit[7]uril hydrate | Cucurbit[7]uril hydrate. Group: Polymers. CAS No. 259886-50-5. Product ID: 3, 5, 8, 10, 13, 15, 18, 20, 23, 25, 28, 30, 33, 35, 36, 38, 40, 42, 46, 48, 50, 52, 54, 56, 58, 60, 62, 64-octacosazadocosacyclo[30.3.3.36, 7.311, 12.316, 17.321, 22.326, 27.22, 36.231, 38.13, 35.15, 8.110, 13.115, 18.120, 23.125, 28.130, 33.140, 46.142, 64.148, 50.152, 54.156, 58.160, 62]heptacontane-39, 41, 43, 44, 45, 47, 49, 51, 53, 55, 57, 59, 61, 63-tetradecone. Molecular formula: 1163g/mol. Mole weight: C42H42N28O14. C1N2C3C4N (C2=O)CN5C6C7N (C5=O)CN8C9C2N (C8=O)CN5C8C%10N (C5=O)CN5C%11C%12N (C5=O)CN5C%13C%14N (C5=O)CN5C%15C (N1C5=O)N1CN3C (=O)N4CN6C (=O)N7CN9C (=O)N2CN8C (=O)N%10CN%11C (=O)N%12CN%13C (=O)N%14CN%15C1=O. InChI=1S / C42H42N28O14 / c71-29-43-1-44-16-18-48 (30 (44) 72) 4-52-20-22-56 (34 (52) 76) 8-60-24-26-64 (38 (60) 80) 12-68-28-27-67 (41 (68) 83) 11-63-25-23-59 (37 (63) 79) 7-55-21-19-51 (33 (55) 75) 3-47 (29) 17-15 (43) 45-2-46 (16) 32 (74) 50 (18) 6-54 (20) 36 (78) 58 (22) 10-62 (24) 40 (82) 66 (26) 14-70 (28) 42 (84) 69 (27) 13-65 (25) 39 (81) 61 (23) 9-57 (21) 35 (77) 53 (19) 5-49 (17) 31 (45) 73 / h15-28H, 1-14H2. ZDOBFUIMGBWEAB-UHFFFAOYSA-N. 99%. | |
| Cucurbit(8)uril | Cucurbit(8)uril. Group: Polymers. Alternative Names: Cucurbit[8]uril; Curcubit[8]uril; Cucurbit[8]uril (CB[8]) hydrate, 99+%; Cucurbit[8]uril hydrate contains acid of crystalization; Cucurbit[8]uril hydrate; 2, 20:3, 19-Dimethano-2, 3, 4a, 5a, 6a, 7a, 8a, 9a, 10a, 11a, 12a, 13a, 14a, 15a, 16a, 17a, 19, 20, 21a, 22a, 23a, 24a, 25a, 26a, 27a, 28a, 29a, 30a, 31a, 32a, 33a, 34a-dotriacontaazabispentaleno[1, 6:5, 6, 7]cycloocta[1, 2, 3:3, 4]pentaleno[1. CAS No. 259886-51-6. Product ID: 3, 5, 8, 10, 13, 15, 18, 20, 23, 25, 28, 30, 33, 35, 38, 40, 41, 43, 45, 47, 51, 53, 55, 57, 59, 61, 63, 65, 67, 69, 71, 73-dotriacontazapentacosacyclo[35. 3. 3. 36, 7. 311, 12. 316, 17. 321, 22. 326, 27. 331, 32. 22, 41. 236, 43. 13, 40. 15, 8. 110, 13. 115, 18. 120, 23. 125, 28. 130, 33. 135, 38. 145, 51. 147, 73. 153, 55. 157, 59. 161, 63. 165, 67. 169, 71]octacontane-44, 46, 48, 49, 50, 52, 54, 56, 58, 60, 62, 64, 66, 68, 70, 72-hexadecone. Molecular formula: 1329.1g/mol. Mole weight: C48H48N32O16. C1N2C3C4N (C2=O)CN5C6C7N (C5=O)CN8C9C2N (C8=O)CN5C8C%10N (C5=O)CN5C%11C%12N (C5=O)CN5C%13C%14N (C5=O)CN5C%15C%16N (C5=O)CN5C%17C (N1C5=O)N1CN3C (=O)N4CN6C (=O)N7CN9C (=O)N2CN8C (=O)N%10CN%11C (=O)N%12CN%13C (=O)N%14CN%15C (=O)N%16CN%17C1=O. InChI=1S / C48H48N32O16 / c81-33-49-1-50-18-20-54 (34 (50) 82) 4-58-22-24-62 (38 (58) 86) 8-66-26-28-70 (42 (66) 90) 12-74-30-32-78 (46 (74) 94) 15-77-31-29-73 (45 (77) 93) 11-69-27-25-65 (41 (69) 89) 7-61-23-2 | |
| Cucurbit[8]uril | Cucurbit[8]uril is a potent, low toxicity and orally active supramolecular inducer of protein heterodimerization. Cucurbit[8]uril induces heterodimerization of methylviologen and naphthalene functionalized proteins. Cucurbit[8]uril can induce energy transfer [1] [2]. Uses: Scientific research. Group: Signaling pathways. CAS No. 259886-51-6. Pack Sizes: 5 mg; 10 mg; 25 mg; 50 mg. Product ID: HY-103689. | |
| Cucurbit[8]uril hydrate | Cucurbiturils are macrocyclic molecules made of glycoluril monomers linked by methylene bridges. The oxygen atoms are located along the edges of the band and are tilted inwards, forming a partly enclosed cavity. Cucurbiturils are commonly written as cucurbit[n]uril, where n is the number of glycoluril units. Two common abbreviations are CB[n], or simply CBn. Uses: Chemists have used cucurbituril for a variety of applications, including drug delivery, asymmetric synthesis, molecular switching, and dye tuning. Group: Hydrophilic polymers. Pack Sizes: Packaging 100 mg in glass insert. Product ID: 3, 5, 8, 10, 13, 15, 18, 20, 23, 25, 28, 30, 33, 35, 38, 40, 41, 43, 45, 47, 51, 53, 55, 57, 59, 61, 63, 65, 67, 69, 71, 73-dotriacontazapentacosacyclo[35. 3. 3. 36, 7. 311, 12. 316, 17. 321, 22. 326, 27. 331, 32. 22, 41. 236, 43. 13, 40. 15, 8. 110, 13. 115, 18. 120, 23. 125, 28. 130, 33. 135, 38. 145, 51. 147, 73. 153, 55. 157, 59. 161, 63. 165, 67. 169, 71]octacontane-44, 46, 48, 49, 50, 52, 54, 56, 58, 60, 62, 64, 66, 68, 70, 72-hexadecone; hydrate. Molecular formula: 1347.1g/mol. Mole weight: C48H48N32O16 · xH2O · xHCl. O. Cl. O=C1N2CN3C4C5N (CN6C7C8N (CN9C%10C%11N (CN%12C%13C%14N (CN%15C%16C%17N (CN%18C%19C%20N (CN%21C%22C%23N (CN1C%24C2N%25CN4C (=O) N5CN7C (=O) N8CN%10C (=O) N%11CN%13C (=O) N%14CN%16C (=O) N%17CN%19C (=O) N%20CN%22C (=O) N%23CN%24C%25=O) C%21=O) C%18=O) C%15=O) C%12=O) C9=O) C6=O) C3=O. 1S/C48H48N32O1 | |
| Cucurbit[8]uril hydrate | contains acid of crystalization. Group: Hydrophilic polymers. | |
| Cucurbitacin A | Cucurbitacin A. Group: Biochemicals. CAS No. 6040-19-3. Pack Sizes: 5mg. US Biological Life Sciences. | Worldwide |
| Cucurbitacin A | Cucurbitacin A is a triterpenoid sterol isolated from rhizomes of Hemsleya amabilis Diels. Synonyms: Cucurbitacin A; 6040-19-3; UNII-83859; MTO77NSC94743; CHEBI:3940. Grade: >98%. CAS No. 6040-19-3. Molecular formula: C32H46O9. Mole weight: 574.711. | |
| Cucurbitacin B | Cucurbitacin B belongs to a class of highly oxidized tetracyclic triterpenoids; could repress cancer cell progression.IC50 value:Target: anticancer natural compoundin vitro: Cucurbitacin-B inhibited growth and modulated expression of cell-cycle regulators in SHSY5Y cells. At the molecular level, we found that Cucurbitacin-B inhibited AKT signaling activation through up-regulation of PTEN. CuB induced apoptosis of A549 cells in a -concentration-dependent manner, as determined by fluorescence microscopy, flow cytometry and transmission electron microscopy. CuB dose-dependently inhibited lung cancer cell proliferation, with cell cycle inhibition and cyclin B1 downregulation. Apoptosis induced by CuB was shown to be associated with cytochrome c release, B-cell lymphoma 2 downregulation and signal transducer and activator of transcription 3 pathway inhibition. CuB inhibited ITGA6 and ITGB4 (integrin α6 and integrin β4), which are overexpressed in breast cancer. Furthermore, CuB also induced the expression of major ITGB1and ITGB3, which are known to cause integrin-mediated cell death. Cuc B treatment caused DNA double-strand breaks (DSBs) without affecting the signal transducer and activator of transcription 3 (STAT3), the potential molecular target for Cuc B. Cuc B triggers ATM-activated Chk1-Cdc25C-Cdk1, which could be reversed by both ATM siRNA and Chk1 siRNA. Cuc B also triggers ATM-activated p53-14-3-3-σ pa |  |
| Cucurbitacin B | Cucurbitacin B. Group: Biochemicals. Alternative Names: Amarin. Grades: Plant Grade. CAS No. 6199-67-3. Pack Sizes: 20mg. Molecular Formula: C32H46O8, Molecular Weight: 558.703. US Biological Life Sciences. | Worldwide |
| Cucurbitacin B | Cucurbitacin B belongs to a class of highly oxidized tetracyclic triterpenoids and is oral active. Cucurbitacin B inhibits tumor cell growth, migration and invasion and cycle arrest, but induces cell apoptosis. Cucurbitacin B has potent anti-inflammatory, antioxidant, antiviral, hypoglycemic, hepatoprotective, neuroprotective activity [1] [2] [3] [4] [5]. Uses: Scientific research. Group: Natural products. CAS No. 6199-67-3. Pack Sizes: 10 mM * 1 mL; 1 mg; 5 mg; 10 mg; 25 mg; 50 mg. Product ID: HY-N0416. | |
| Cucurbitacin B hydrate | ?97% (HPLC). Group: Fluorescence/luminescence spectroscopy. | |
| Cucurbitacin D | Cucurbitacin D. Group: Biochemicals. CAS No. 3877-86-9. Pack Sizes: 5mg. US Biological Life Sciences. | Worldwide |
| Cucurbitacin D | Cucurbitacin D is the active ingredient in Trichosanthes kirilowii and can disrupt the interaction between Hsp90 and two co-chaperones, Cdc37 and p23. Cucurbitacin D is an inflammasome activator. Cucurbitacin D induces cell cycle arrest and cell apoptosis , exhibiting anti-tumor and anti-inflammatory effects [1] [2] [3] [4]. Uses: Scientific research. Group: Natural products. CAS No. 3877-86-9. Pack Sizes: 10 mM * 1 mL; 1 mg; 5 mg; 10 mg. Product ID: HY-N1986. | |
| cucurbitacin Δ23-reductase | Requires Mn2+. Fe2+ or Zn2+ can replace Mn2+ to some extent. Group: Enzymes. Synonyms: NAD(P)H: cucurbitacin B Δ23-oxidoreductase. Enzyme Commission Number: EC 1.3.1.5. CAS No. 37256-38-5. 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-1322; cucurbitacin Δ23-reductase; EC 1.3.1.5; 37256-38-5; NAD(P)H: cucurbitacin B Δ23-oxidoreductase. Cat No: EXWM-1322. | |
| Cucurbitacin E | Cucurbitacin E is a natural compound which from Cucurbitaceae plants. Cucurbitacin E significantly suppresses the activity of the cyclin B1/CDC2 complex. Uses: Designed for use in research and industrial production. Product Category: Inhibitors. Appearance: White powder. CAS No. 18444-66-1. Molecular formula: C32H44O8. Mole weight: 556.67. Purity: 0.98. IUPACName: [(E,6R)-6-[(8S,9R,10R,13R,14S,16R,17R)-2,16-dihydroxy-4,4,9,13,14-pentamethyl-3,11-dioxo-8,10,12,15,16,17-hexahydro-7H-cyclopenta[a]phenanthren-17-yl]-6-hydroxy-2-methyl-5-oxohept-3-en-2-yl] acetate. Canonical SMILES: CC(=O)OC(C)(C)C=CC(=O)C(C)(C1C(CC2(C1(CC(=O)C3(C2CC=C4C3C=C(C(=O)C4(C)C)O)C)C)C)O)O. Product ID: ACM18444661. Alfa Chemistry ISO 9001:2015 Certified. | |
| Cucurbitacin E | Cucurbitacin E. Group: Biochemicals. Alternative Names: Cucurbitacine E; NSC 106399; NSC 521775; α-Elaterin; α-Elaterine; 2,16α,20,25-Tetrahydroxy-9-methyl-19-Nor-9 β,10α-lanosta-1,5,23-triene-3,11,22-trione 25-Acetate. Grades: Highly Purified. CAS No. 18444-66-1. Pack Sizes: 1mg. Molecular Formula: C32H44O8, Molecular Weight: 556.69. US Biological Life Sciences. | Worldwide |
| Cucurbitacin E 2-O-glucoside | Cucurbitacin E 2-O-glucoside. Uses: For analytical and research use. Group: Impurity standards. CAS No. 1398-78-3. Molecular formula: C38H54O13. Mole weight: 718.84. Catalog: APB1398783. | |
| Cucurbitacin I | Cucurbitacin I is a natural selective inhibitor of JAK2/STAT3, with potent anti-cancer activity. Uses: Scientific research. Group: Natural products. Alternative Names: Elatericin B; JSI-124; NSC-521777. CAS No. 2222-7-3. Pack Sizes: 10 mM * 1 mL; 1 mg; 5 mg; 10 mg. Product ID: HY-N1405. | |
| Cucurbitacin I | Cucurbitacin I is a natural selective inhibitor of JAK2/STAT3, with potent anti-cancer activity. Uses: Designed for use in research and industrial production. Additional or Alternative Names: Cucurbitacin I. Product Category: Inhibitors. Appearance: White solid. CAS No. 2222-7-3. Molecular formula: C30H42O7. Mole weight: 514.65. Purity: 0.98. Density: 1.26g/cm³. Product ID: ACM2222073. Alfa Chemistry ISO 9001:2015 Certified. | |
| Cucurbitacin I | Cucurbitacin I. Group: Biochemicals. Grades: Purified. CAS No. 2222-7-3. Pack Sizes: 1mg. US Biological Life Sciences. | Worldwide |
| Cucurbitacin I, Cucumis sativus L. - CAS 2222-07-3 | A cell-permeable and irreversible bitter triterpenoid compound (NCI identifier: NSC 521777) that displays anti-proliferative and antitumor properties both in vitro and in vivo. Group: Fluorescence/luminescence spectroscopy. | |
| Cucurbitacin I hydrate | ?95% (HPLC), solid. Group: Fluorescence/luminescence spectroscopy. | |
| Cucurbitacin Iia | Cucurbitacin IIa is a triterpene isolated from Hemsleya amalils Diels, induces apoptosis of cancer cells, reduces expression of survivin, reduces phospho-Histone H3 and increases cleaved PARP in cancer cells. Uses: Designed for use in research and industrial production. Product Category: Inhibitors. Appearance: White powder. CAS No. 58546-34-2. Molecular formula: C32H50O8. Mole weight: 562.73. Purity: 0.98. IUPACName: [(6R)-6-hydroxy-2-methyl-5-oxo-6-[(2S,3S,8S,9R,10R,13R,14S,16R,17R)-2,3,16-trihydroxy-4,4,9,13,14-pentamethyl-11-oxo-1,2,3,7,8,10,12,15,16,17-decahydrocyclopenta[a]phenanthren-17-yl]heptan-2-yl] acetate. Canonical SMILES: CC(=O)OC(C)(C)CCC(=O)C(C)(C1C(CC2(C1(CC(=O)C3(C2CC=C4C3CC(C(C4(C)C)O)O)C)C)C)O)O. Product ID: ACM58546342. Alfa Chemistry ISO 9001:2015 Certified. Categories: Hemslecin A. | |
| Cucurbitacin IIa | Cucurbitacin IIa is a triterpene isolated from Hemsleya amalils Diels, induces apoptosis of cancer cells, reduces expression of survivin , reduces phospho-Histone H3 and increases cleaved PARP in cancer cells [1]. Uses: Scientific research. Group: Natural products. Alternative Names: Hemslecin A. CAS No. 58546-34-2. Pack Sizes: 1 mg; 5 mg; 10 mg; 20 mg. Product ID: HY-N1988. | |
| Cucurbitacin IIb | Cucurbitacin IIb. Group: Biochemicals. Alternative Names: 23,24-Dihydrocucurbitacin F. Grades: Plant Grade. CAS No. 50298-90-3. Pack Sizes: 10mg. Molecular Formula: C30H48O7, Molecular Weight: 520.698. US Biological Life Sciences. | Worldwide |
Our database is helping our users find suppliers everyday.
