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| Product | Description | |
|---|---|---|
| CTP synthase (glutamine hydrolysing) | The enzyme contains three functionally distinct sites: an allosteric GTP-binding site, a glutaminase site where glutamine hydrolysis occurs (cf. EC 3.5.1.2, glutaminase), and the active site where CTP synthesis takes place. The reaction proceeds via phosphorylation of UTP by ATP to give an activated intermediate 4-phosphoryl UTP and ADP. Ammonia then reacts with this intermediate generating CTP and a phosphate. The enzyme can also use ammonia from the surrounding solution. Group: Enzymes. Synonyms: UTP-ammonia ligase; cytidine triphosphate synthetase; uridine triphosphate aminase; cytidine 5'-triphosphate synthetase; CTPS (gene name); pyrG (gene name); CTP synthase; UTP:ammonia ligase (ADP-forming). Enzyme Commission Number: EC 6.3.4.2. CAS No. 9023-56-7. 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-5789; CTP synthase (glutamine hydrolysing); EC 6.3.4.2; 9023-56-7; UTP-ammonia ligase; cytidine triphosphate synthetase; uridine triphosphate aminase; cytidine 5'-triphosphate synthetase; CTPS (gene name); pyrG (gene name); CTP synthase; UTP:ammonia ligase (ADP-forming). Cat No: EXWM-5789. |  |
| CTS-1027 | CTS-1027 inhibits individual members of the MMP family that are believed to be important in inflammation and tissue damage. CTS-1027 was specifically designed, however, not to inhibit MMP 1, as inhibition of MMP 1 was believed to be associated with musculoskeletal side effects. Synonyms: RS 130830; Ro 1130830; CTS1027; CTS 1027; RS130830; Ro1130830; RS-130830; Ro-1130830. Grades: >98%. CAS No. 193022-04-7. Molecular formula: C19H20ClNO6S. Mole weight: 425.88. |  |
| CTS-21166 | CTS-21166, the selective BACE1 inhibitor whose structure is not revealed, reduce brain Aβ levels by over 35% and plaque load by 40%. Phase 1 IC50=1.2-3.6 nM (cell line details NA) APP transgenic mice, 4mg/kg i.p. injection for 6 weeks, >35% ↓ brain Aβ, 40% ↓ plaque load. Human patients, 7.5.225 mg i.v. injection dose-dependant ↓ plasma Aβ, 80% ↓ at 225 mg. Synonyms: ATG-Z1; CTS-21166; ZPQ-21166; ATG Z1; CTS 21166; ZPQ 21166; ATGZ1; CTS21166; ZPQ21166. Molecular formula: none. | |
| CT Series Talc | CT Industrial Talcs can be used in a wide range of industrial and specialty applications. CT Industrial Talcs are produced from an extensive depositof high quality platy talc ore. CT series talcs are a cost effective formulating tool for moderate brightness applications. Pack Sizes Available: 50 lbs bags, 2,000 lbs pallets. |  AG&P Mineral Purveyors |
| CTTHWGFTLC, CYCLIC acetate | CTTHWGFTLC, CYCLIC acetate is a cyclic peptide inhibitor for matrix metalloproteinases (MMP-2) and MMP-9. Synonyms: L-Cysteine, L-cysteinyl-L-threonyl-L-threonyl-L-histidyl-L-tryptophylglycyl-L-phenylalanyl-L-threonyl-L-leucyl-, cyclic (1?10)-disulfide acetate; CTT 1 acetate; H-Cys-Thr-Thr-His-Trp-Gly-Phe-Thr-Leu-Cys-OH.CH3CO2H (Disulfide Bridge: Cys1-Cys10); L-cysteinyl-L-threonyl-L-threonyl-L-histidyl-L-tryptophyl-glycyl-L-phenylalanyl-L-threonyl-L-leucyl-L-cysteine (1->10)-disulfide acetic acid acetate. Grades: ≥95%. Molecular formula: C54H75N13O16S2. Mole weight: 1226.39. | |
| CTX-0294885 | CTX-0294885 is a novel broad-spectrum kinase inhibitor. CTx-0294885 exhibits inhibitory activity against a broad range of kinases in vitro. Use of a quantitative proteomics approach confirmed the selectivity of CTx-0294885-bound beads for kinase enrichment. Large-scale CTx-0294885-based affinity purification followed by LC-MS/MS led to the identification of 235 protein kinases from MDA-MB-231 cells, including all members of the AKT family that had not been previously detected by other broad-spectrum kinase inhibitors. CTx-0294885 represents a powerful new reagent for analysis of kinome signaling networks that may facilitate development of targeted therapeutic strategies. Synonyms: CTX-0294885; CTX 0294885; CTX0294885; CTx 0294885. Grades: 98%. CAS No. 1439934-41-4. Molecular formula: C22H24ClN7O. Mole weight: 437.93. | |
| CTX-0294885 hydrochloride | CTX-0294885 hydrochloride is the hydrochloride salt of CTX-0294885 which displays high affinity toward an extensive range of kinases. The evaluation of the binding profile of CTx-0294885 in MDA-MB-231 cells by quantitative MS demonstrated its selective properties as a kinase enrichment reagent. Synonyms: 2-[[5-chloro-2-(4-piperazin-1-ylanilino)pyrimidin-4-yl]amino]-N-methylbenzamide;hydrochloride; CTX-0294885 hydrochloride; CTX 0294885 hydrochloride; CTX0294885 hydrochloride. Molecular formula: C22H25Cl2N7O. Mole weight: 474.39. | |
| CTX1 | CTX1 is a p53 activator that overcomes HdmX-mediated p53 repression. CTX1 exhibits potent anti-cancer activity in a mouse acute myeloid leukemia (AML) model system [1]. Uses: Scientific research. Group: Signaling pathways. CAS No. 501935-96-2. Pack Sizes: 10 mM * 1 mL; 1 mg; 5 mg. Product ID: HY-U00442. |  |
| CTX-471 | CTX-471 is a fully human monoclonal antibody of CD137. CTX-471 has bind affinity for recombinant human, cynomolgus macaque CD137 and mouse CD137 with K d values of 50 nM, 61 nM and 748 nM, respectively. CTX-471 can be used for the research of immunomodulation and cancer [1]. Uses: Scientific research. Group: Inhibitory antibodies. CAS No. 2377152-49-1. Pack Sizes: 1 mg; 5 mg; 10 mg. Product ID: HY-P99178. | |
| 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). Grades: ≥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. Grades: ≥95%. Molecular formula: C93H157N27O28S3·xCF3COOH. Mole weight: 2197.60. | |
| C-Type natriureticpeptide-22 (swine) (9CI) | Heterocyclic Organic Compound. CAS No. 127869-51-6. Molecular formula: C93H157 N27 O28 S3. Mole weight: 2197.6. Catalog: ACM127869516. |  |
| 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). Grades: ≥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%. | |
| 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 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. | |
| 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. | |
| Cuban Tobacco Fragrance Oil | Cuban Tobacco Fragrance Oil. |  CA, FL & NJ |
| Cubebin | Phenylpropanoids. CAS No. 1242843-00-0. Molecular formula: C20H20O6. Mole weight: 356.4. Appearance: White powder. Purity: 0.98. IUPACName: (3R,4R)-3,4-bis(1,3-benzodioxol-5-ylmethyl)oxolan-2-ol. Canonical SMILES: C1C (C (C (O1)O)CC2=CC3=C (C=C2)OCO3)CC4=CC5=C (C=C4)OCO5. Catalog: ACM1242843000. | |
| 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 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 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-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. Grades: ≥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 Essence Water | Natural water infused with cucumber oils/extracts (Cucumis Sativus). Has similar scents and functional properties as hydrosols. Uses: Serums, creams & lotions, toners, skin cleansers, sun- and after-sun care, sunscreens. Group: Skin actives. CAS No. 7732-18-5 / 89998-01-6 / 532-32-1 / 590-00-1 / 77-92-9. Appearance: Clear to slightly pale yellow in color, medium intensity characteristic scent. Catalog: CI-SC-0971. | |
| Cucumber Fruit Extract | Natural Cucumber fruit extract. Contains 20% extract dissolved in water and glycerin. Uses: Creams & lotions, skin cleansers, hair care products, after-sun products, hair moisturizing sprits, hair conditioners and body lotions. Group: Skin actives. CAS No. 56-81-5 / 7732-18-5 / 89998-01-6 / 122-99-6. Appearance: Colorless to light yellow liquid, slight cucumber odor. Catalog: CI-SC-0690. | |
| Cucumber Fruit Extract, USDA Certified Organic | Organic extract from cucumber fruits. Contains 20% extract dissolved in glycerin. Cucumber has a high content in minerals, potassium and sulfur and is being used in skin care to soften and hydrate the skin, especially suitable for after-sun products but also cleansing products to soften the skin. Uses: Creams & lotions, skin cleansers, hair care products, after-sun products, hair moisturizing sprits, hair conditioners and body lotions. Group: Skin actives. CAS No. 56-81-5/89998-01-6. Appearance: Colorless, odorless, viscous liquid. Catalog: CI-SC-0708. | |
| 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. | |
| Cucumis Sativus Extract | Conditioning agent in personal care products. Group: Natural surfactants. Alternative Names: Cucumis Sativus (Cucumber) Extract. CAS No. 89998-01-6. Catalog: ACM89998016. | |
| 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[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[7]uril | Cucurbit[7]uril is a cyclic organic molecule that consists of seven glycoluril units connected by methylene bridges. Cucurbit[7]uril is a pharmaceutical excipient, which can be used in the fields of drug delivery, catalysis, and sensing. Synonyms: 2, 18:3, 17-Dimethano-2, 3, 4a, 5a, 6a, 7a, 8a, 9a, 10a, 11a, 12a, 13a, 14a, 15a, 17, 18, 19a, 20a, 21a, 22a, 23a, 24a, 25a, 26a, 27a, 28a, 29a, 30a-octacosaazabispentaleno[1''''', 6''''':5'''', 6'''', 7'''']cycloocta[1'''', 2'''', 3'''':3''', 4''']pentaleno[1''', 6''':5'', 6'', 7'']cycloocta[1'', 2'', 3'':3', 4']pentaleno[1', 6':5, 6, 7]cycloocta[1, 2, 3-cd:1', 2', 3'-gh]pentalene-1, 4, 6, 8, 10, 12, 14, 16, 19, 21, 23, 25, 27, 29-tetradecone, tetradecahydro-, stereoisomer; stereoisomer of Tetradecahydro-2, 18:3, 17-dimethano-2, 3, 4a, 5a, 6a, 7a, 8a, 9a, 10a, 11a, 12a, 13a, 14a, 15a, 17, 18, 19a, 20a, 21a, 22a, 23a, 24a, 25a, 26a, 27a, 28a, 29a, 30a-octacosaazabispentaleno[1''''', 6''''':5'''', 6'''', 7'''']cycloocta[1'''', 2'''', 3'''':3''', 4''']pentaleno[1''', 6''':5'', 6'', 7'']cycloocta[1'', 2'', 3'':3', 4']pentaleno[1', 6':5, 6, 7]cycloocta[1, 2, 3-cd:1', 2', 3'-gh]pentalene-1, 4, 6, 8, 10, 12, 14, 16, 19, 21, 23, 25, 27, 29-tetradecone; Carrier CB 7; CB 7; CB-7; CB7. Grades: 95%. CAS No. 259886-50-5. Molecular formula: C42H42N28O14. Mole weight: 1162.96. | |
| 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 | 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 remarkably versatile host molecule utilized in a diverse range of drug delivery and catalysis applications. Its unique ability to selectively bind various drug and biomolecule targets with high avidity illustrates its significant potential as a candidate for targeted drug delivery. Furthermore, the catalytic efficacy and promising sensor properties of Cucurbit[8]uril make it a valuable asset in the field of chemical synthesis and detection of diverse analytes. Synonyms: CB[8]; Cucurubituril(8). Grades: 95%. CAS No. 259886-51-6. Molecular formula: C48H48N32O16. Mole weight: 1329.10. | |
| 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 | |
| Cucurbitacin | Cucurbitacin. Uses: For analytical and research use. Group: Impurity standards. CAS No. 2222-7-3. Molecular Formula: C30H42O7. Mole Weight: 514.66. Catalog: APB2222073. |  |
| 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. Grades: >98%. CAS No. 6040-19-3. Molecular formula: C32H46O9. Mole weight: 574.711. | |
| Cucurbitacin A 2-O-Β-D-Glucopyranoside | Terpenoids. CAS No. 1135141-76-2. Molecular formula: C38H56O14. Mole weight: 736.8. Appearance: Oil. Purity: 0.98. Catalog: ACM1135141762. | |
| 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 | 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; 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 C | Cucurbitacin C is a cucurbitacin. Grades: > 95%. CAS No. 5988-76-1. Molecular formula: C32H48O8. Mole weight: 560.72. | |
| 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 D | Source from rhizomes of Hemsleya amabilis Diels. It might be a new therapeutic option for the treatment of endometrial and ovarian cancers, also may be a potential therapeutic agent for β-hemoglobinopathies, including sickle cell anemia and β-thalassemia. And it induces apoptosis through caspase-3 and phosphorylation of JNK in hepatocellular carcinoma cells. Uses: Antitumor, resistance to chemical carcinogens, protect liver. Synonyms: 17-[(3E)-1,5-Dihydroxy-1,5-dimethyl-2-oxohex-3-en-1-yl]-2,16-dihydroxy-4,4,9,14-tetramethylestr-5-ene-3,11-dione. Grades: >98%. CAS No. 3877-86-9. Molecular formula: C30H44O7. Mole weight: 516.67. | |
| Cucurbitacin D | Cucurbitacin D. Group: Biochemicals. CAS No. 3877-86-9. Pack Sizes: 5mg. US Biological Life Sciences. | Worldwide |
| Cucurbitacin D | Cucurbitacin D. Uses: For analytical and research use. Group: Impurity standards. CAS No. 3877-86-9. Molecular Formula: C30H44O7. Mole Weight: 516.68. Catalog: APB3877869. | |
| 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. 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 | Cucurbitacin E is a natural compound which from Cucurbitaceae plants. Cucurbitacin E significantly suppresses the activity of the cyclin B1/CDC2 complex. Group: Inhibitors. CAS No. 18444-66-1. Molecular formula: C32H44O8. Mole weight: 556.67. Appearance: White powder. 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. Catalog: ACM18444661. | |
| 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. Group: Biochemicals. Grades: Purified. CAS No. 2222-7-3. Pack Sizes: 1mg. US Biological Life Sciences. | Worldwide |
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