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| Product | Description | |
|---|---|---|
| AFM Probe from SWCNT or MWCNT Tip angle from ± 3° to ± 20 ° available | AFM Probe from SWCNT or MWCNT Tip angle from ± 3° to ± 20 ° available. |  |
| Afoxolaner | Afoxolaner is an orally active isoxazoline insecticide/acaricide against Ixodes scapularis in dogs. Afoxolaner acts on the insect γ-aminobutyric acid receptor (GABA) and glutamate receptors, inhibiting GABA & glutamate-regulated uptake of chloride ions, resulting in excess neuronal stimulation and death of the arthropod[1][2]. Uses: Scientific research. Category: Signaling pathways. CAS No. 1093861-60-9. Pack Sizes: 10 mM * 1 mL in DMSO; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-16974. |  |
| Afoxolaner | Afoxolaner is an insecticide and acaricide used in dogs to treat and prevent flea infestations. Used to treat specifically the Sarcoptes scabiei var. canis species. Group: Biochemicals. Grades: Highly Purified. CAS No. 1093861-60-9. Pack Sizes: 500ug, 2.5mg. Molecular Formula: C26H17ClF9N3O3, Molecular Weight: 625.87. US Biological Life Sciences. |  Worldwide |
| Afoxolaner | Afoxolaner is a potent isoxazoline insecticide and acaricide against Ixodes scapularis in dogs. It is indicated for the treatment and prevention of flea infestations, and the treatment and control of tick infestations in dogs and puppies. It is administered orally in meat-flavoured tablets, and poisons fleas once they start feeding. It is used either alone or as a combination treatment with milbemycin oxime. Alternative Names: 4-[5-[3-Chloro-5-(trifluoromethyl)phenyl]-4,5-dihydro-5-(trifluoromethyl)-3-isoxazolyl]-N-[2-oxo-2-[(2,2,2-trifluoroethyl)amino]ethyl]-1-naphthalenecarboxamide; 4-[5-[3-Chloro-5-(trifluoromethyl)phenyl]-5-(trifluoromethyl)-4H-1,2-oxazol-3-yl]-N-[2-oxo-2-(2,2,2-trifluoroethylamino)ethyl]naphthalene-1-carboxamide. Grades: >98%. CAS No. 1093861-60-9. Molecular formula: C26H17ClF9N3O3. Mole weight: 625.87. |  |
| afoxolaner Impurity 1 | afoxolaner Impurity 1. Uses: For analytical and research use. Molecular formula: C26H19ClF9N3O4. Mole weight: 643.89. Catalog: APB12362. |  |
| afoxolaner Impurity 2 | afoxolaner Impurity 2. Uses: For analytical and research use. Molecular formula: C26H15ClF9N3O2. Mole weight: 607.86. Catalog: APB12363. | |
| afoxolaner Impurity 3 | afoxolaner Impurity 3. Uses: For analytical and research use. Molecular formula: C26H18ClF9N2O4. Mole weight: 628.88. Catalog: APB12364. | |
| afoxolaner Impurity 4 | afoxolaner Impurity 4. Uses: For analytical and research use. Molecular formula: C24H15ClF6N2O4. Mole weight: 544.83. Catalog: APB12365. | |
| afoxolaner Impurity 5 | afoxolaner Impurity 5. Uses: For analytical and research use. CAS No. 1308362-48-2. Molecular formula: C22H12ClF6NO3. Mole weight: 487.78. Catalog: APB1308362482. | |
| Afoxolaner (Standard) | Afoxolaner (Standard) is the analytical standard of Afoxolaner. This product is intended for research and analytical applications. Afoxolaner is an orally active isoxazoline insecticide/acaricide against Ixodes scapularis in dogs. Afoxolaner acts on the insect γ-aminobutyric acid receptor (GABA) and glutamate receptors, inhibiting GABA & glutamate-regulated uptake of chloride ions, resulting in excess neuronal stimulation and death of the arthropod[1][2]. Uses: Scientific research. Category: Signaling pathways. CAS No. 1093861-60-9. Pack Sizes: 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-16974R. | |
| Afragilimycin A | It is produced by the strain of Streptomyces neohygroscopicus sub-sp, afragilimycetius 19255. It has anti-gram-positive bacteria and anti-gram-negative bacteria including anaerobic bacteria activity. Alternative Names: Afrigilimycin A; (2S)-4-[(2E,4E,6R)-6-[(1S,2S,3R,5S,6R)-2,5-dimethylspiro[4,9-dioxabicyclo[3.3.1]non-7-ene-6,2'-oxirane]-3-yl]-4-methylhepta-2,4-dienoyl]-1-[(5S,6S)-5-hydroxy-6-methyloxan-2-yl]-2-[(2S)-1-(methylamino)-1-oxopropan-2-yl]-3-oxo-2H-pyrrol-5-olate. CAS No. 76559-69-8. Molecular formula: C32H43N2O9-. Mole weight: 599.69. | |
| African Mango Seed Extract | African Mango Seed Extract. Applications: Used for health care products, dietary supplements, weight loss, reducing blood lipids. Group: Others. Synonyms: African Mango Seed Extract; 9005-80-5; Irvingia GabonensisSeed. CAS No. 9005-80-5. Purity: 20% Phytoprotein By KJELDAHL, 10:1 By TLC. Appearance: Light yellow fine powder. Storage: 2 years under well storage situation and stored away from direct sun light. Source: Seed. Species: Irvingia GabonensisSeed. African Mango Seed Extract; 9005-80-5; Irvingia GabonensisSeed; plant extract. Pack: 20KG-25KG/Drum with double plastic bag of foodstuff inside. Cat No: EXTW-103. |  |
| African Mango Seed P.E. 10:1 | African Mango Seed P.E. 10:1 (Irvingia Gabonensis). |  CA, FL & NJ |
| Aftin-4 | Aftin-4 is an Amyloid-β42 (Aβ42) inducer. Uses: Scientific research. Category: Signaling pathways. CAS No. 866893-90-5. Pack Sizes: 10 mM * 1 mL in DMSO; 2 mg; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-111267. | |
| Aftin-5 | Aftin-5 is an inducer for Amyloid-β 42 (Aβ42). Aftin-5 upregulates Aβ42 and downregulates Aβ38 levels in a β-secretase- and γ-secretase-dependent manner by altering the ultrastructure of mitochondria. Aftin-5 exhibits slightly cytotoxicity in cell SH-SY5Y, HT22, N2a and N2a-AβPP695, with IC50s of 180, 194, 178 and 150 μM, respectively[1]. Uses: Scientific research. Category: Signaling pathways. CAS No. 1461717-05-4. Pack Sizes: 10 mM * 1 mL in DMSO; 1 mg; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-136674. | |
| Afuresertib | Afuresertib (GSK2110183) is an orally bioavailable, selective, ATP-competitive and potent pan-Akt kinase inhibitor with Kis of 0.08/2/2.6 nM for Akt1/Akt2/Akt3, respectively[1][2]. Uses: Scientific research. Category: Signaling pathways. Alternative Names: GSK2110183; LAE002. CAS No. 1047644-62-1. Pack Sizes: 10 mM * 1 mL in DMSO; 1 mg; 5 mg; 10 mg; 50 mg; 100 mg. Product ID: HY-15727. | |
| Afuresertib | Afuresertib, also known as GSK2110183, is an orally bioavailable inhibitor of the serine / threonine protein kinase Akt (protein kinase B) with potential antineoplastic activity. Akt inhibitor GSK2110183 binds to and inhibits the activity of Akt, which may result in inhibition of the PI3K/Akt signaling pathway and tumor cell proliferation and the induction of tumor cell apoptosis. Activation of the PI3K/Akt signaling pathway is frequently associated with tumorigenesis and dysregulated PI3K/Akt signaling may contribute to tumor resistance to a variety of antineoplastic agents. Alternative Names: GSK-2110183; GSK 2110183; GSK2110183; GSK-2110183B; GSK 2110183B; GSK2110183B. Grades: 98%. CAS No. 1047644-62-1. Molecular formula: C18H17Cl2FN4OS. Mole weight: 427.32. | |
| Afuzosin EP Impurity A | Afuzosin EP Impurity A. Uses: For analytical and research use. Alternative Names: N-[3-[(4-amino-6,7-dimethoxyquinazolin-2-yl)methylamino]propyl]furan-2-carboxamide. Molecular formula: C19H23N5O4. Mole weight: 385.42. Catalog: APB03232. | |
| Afuzosin EP Impurity D | Afuzosin EP Impurity D. Uses: For analytical and research use. Alternative Names: N2-(3-aminopropyl)-6,7-dimethoxy-N2-methylquinazolin-2,4-diamine. Molecular formula: C14H21N5O2. Mole weight: 291.35. Catalog: APB03229. | |
| Afuzosin EP Impurity E | Afuzosin EP Impurity E. Uses: For analytical and research use. Alternative Names: N-[3-[(4-amino-6,7-dimethoxyquinazolin-2-yl)methylamino]propyl]formamide. Molecular formula: C15H21N5O3. Mole weight: 319.36. Catalog: APB03228. | |
| Afuzosin EP Impurity F | Afuzosin EP Impurity F. Uses: For analytical and research use. Alternative Names: 6,7-dimethoxy-N2,N2-dimethylquinazoline-2,4-diamine. Molecular formula: C12H16N4O2. Mole weight: 248.28. Catalog: APB03227. | |
| Afuzosin EP Impurity G | Afuzosin EP Impurity G. Uses: For analytical and research use. Alternative Names: N2-[3-[(4-amino-6,7-dimethoxyquinazolin-2-yl)amino]propyl]-6,7-dimethoxy-N2-methylquinazoline-2,4-diamine. Molecular formula: C24H30N8O4. Mole weight: 494.55. Catalog: APB03226. | |
| Afuzosin hydrochloride | Afuzosin hydrochloride. Uses: For analytical and research use. Alternative Names: (2RS)-N-[3-[(4-Amino-6,7-dimethoxyquinazolin-2-yl)methylamino]propyl]oxolan-2-carboxamide hydrochloride. Molecular formula: C19H27N5O4. Mole weight: 389.45. Catalog: APB03234. | |
| Afzelechin | Afzelechin is isolated from the herbs of Celastrus orbiculatus. Uses: Anti-inflammatory activity. Alternative Names: (2R)-2α-(4-Hydroxyphenyl)chroman-3β,5,7-triol; [2R,3S,(+)]-3,4-Dihydro-2-(4-hydroxyphenyl)-2H-1-benzopyran-3,5,7-triol. Grades: 98%. CAS No. 2545-00-8. Molecular formula: C15H14O5. Mole weight: 274.3. | |
| Afzelechin 3-O-xyloside | Afzelechin 3-O-xyloside is purified from the barks of Cassipourea gerrardii. Alternative Names: (2S,3R,4S,5R)-2-[[(2R,3S)-5,7-dihydroxy-2-(4-hydroxyphenyl)-3,4-dihydro-2H-chromen-3-yl]oxy]oxane-3,4,5-triol. Grades: 98.0%. CAS No. 512781-45-2. Molecular formula: C20H22O9. Mole weight: 406.38. | |
| Afzelechin-(4α?8)-epiafzelechin | Afzelechin-(4α→8)-epiafzelechin is a natural compound isolated from the herbs of Cassia javanica. Alternative Names: (2R,3R)-2-(4-hydroxyphenyl)-8-[(2R,3S,4S)-3,5,7-trihydroxy-2-(4-hydroxyphenyl)-3,4-dihydro-2H-chromen-4-yl]-3,4-dihydro-2H-chromene-3,5,7-triol. Grades: 97.5%. CAS No. 1383627-30-2. Molecular formula: C30H26O10. Mole weight: 546.52. | |
| Afzelin | Afzelin. Group: Biochemicals. CAS No. 482-39-3. Pack Sizes: 5mg. US Biological Life Sciences. | Worldwide |
| Afzelin | Afzelin (Kaempferol-3-O-rhamnoside)It is a flavonol glycoside that has anti-inflammatory, anti-oxidative stress response, anti-apoptotic, and anti-cardiac cytotoxic effects. AfzelinIt can reduce mitochondrial damage, enhance mitochondrial biosynthesis, and reduce mitochondria-related proteins. Parkinand PTENinduced putative kinase 1 (putative kinase 1)s level. AfzelinCan be improved D-galactosamine(GalN)/LPSSurvival rate of mice treated with doxorubicin prophylaxis (HY-15142A)Induced cardiotoxicity and scopolamine (HY-N0296)-induced neurological injury. AfzelinAlso inhibits asthma and allergies caused by ovalbumin[1][2][3][4]. Uses: Scientific research. Category: Signaling pathways. Alternative Names: Kaempferol-3-O-rhamnoside. CAS No. 482-39-3. Pack Sizes: 10 mM * 1 mL in DMSO; 1 mg; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-N1441. | |
| Ag | Ag. Purity: 99.9%. | |
| AG-012986 | AG-012986 is a pan-CDK inhibitor with Ki values of 44 nM (CDK1), 9.2 nM (CDK4), 94 nM (CDK2), and IC50 values of 22 nM (CDK5), 4 nM (CDK9). AG-012986 causes apoptosis of T-cells by targeting upstream kinases in the p38 Mitogen-activated protein kinase (MAPK) pathway and impairing cellular survival. AG-012986 induces cell cycle arrest, retinoblastoma protein hypophosphorylation, and reduces Ki-67 expression. AG-012986 exerts antiproliferative activity in tumor cells, demonstrates antitumor efficacy in human xenograft models, and causes retinal and peripheral neurotoxicity, plus immune cell toxicity. AG-012986 can be used for the research of colon carcinoma, non-small cell lung carcinoma, lung carcinoma, breast carcinoma, ovarian tumor, pancreatic carcinoma, osteosarcoma, lymphoma, leukemia, retinotoxicity[1][2][3][4]. Uses: Scientific research. Category: Signaling pathways. CAS No. 486414-35-1. Pack Sizes: 10 mM * 1 mL in DMSO; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-119715. | |
| AG-024322 | AG-024322 is a potent ATP-competitive pan-CDK inhibitor against cell cycle kinases CDK1, CDK2, and CDK4 with Ki values in the 1-3 nM range[1]. AG-024322 displays broad-spectrum anti-tumor activity and clear target modulation in vivo. AG-024322 induces cell apoptosis[3]. Uses: Scientific research. Category: Signaling pathways. CAS No. 837364-57-5. Pack Sizes: 10 mM * 1 mL in DMSO; 1 mg; 5 mg; 10 mg; 25 mg; 50 mg. Product ID: HY-15491. | |
| AG 045572 | AG 045572. Group: Biochemicals. Grades: Purified. CAS No. 263847-55-8. Pack Sizes: 1mg, 10mg. US Biological Life Sciences. | Worldwide |
| AG1024 | AG1024 (Tyrphostin AG 1024) is a reversible, competitive and selective IGF-1R inhibitor with an IC50 of 7 μM. AG1024 inhibits phosphorylation of IR (IC50=57 μM). AG1024 induces apoptosis and has anti-cancer activity[1][2]. Uses: Scientific research. Category: Signaling pathways. Alternative Names: Tyrphostin AG 1024. CAS No. 65678-07-1. Pack Sizes: 10 mM * 1 mL in DMSO; 5 mg; 10 mg; 50 mg; 100 mg. Product ID: HY-10253. | |
| AG-120 (Ivosidenib) | Ivosidenib (AG-120) is an orally available inhibitor of isocitrate dehydrogenase type 1 (IDH1), with potential antineoplastic activity. Group: Inhibitors. CAS No. 1448347-49-6. Pack Sizes: 5mg. Product ID: S8206. Formula: C28H22ClF3N6O3. Smiles: C1CC(=O)N(C1C(=O)N(C2=CC(=CN=C2)F)C(C3=CC=CC=C3Cl)C(=O)NC4CC(C4)(F)F)C5=NC=CC(=C5)C#N. Storage Conditions: 2 years -80 in solvent. |  United States; Europe |
| AG 126 | Tyrphostins are protein tyrosine kinase inhibitors developed to inhibit cell growth through blocking the activity of certain GFRK (growth factor receptor kinases). AG 126 selectively inhibits the phosphorylation of ERK1 and ERK2 at 25-50 μM. It also inhibits the production of TNF-α (tumor necrosis factor-α), attenuating signaling through NF-κB, the induced expression of COX-2 and iNOS, and the inflammatory response in animal models. AG 126 is a poor inhibitor of epidermal GFRK with IC50 of 450 μM and platelet-derived GFRK with IC50 > 100 μM. AG 126 may represent a new approach for the therapy of inflammation. Uses: Anti- inflammation. Alternative Names: AG126; AG-126; Tyrphostin AG 126; UNII-7YA4AMD1JC; Tyrphostin A 10; alpha-Cyano-(3-hydroxy-4-nitro)cinnamonitrile. Grades: 95%. CAS No. 118409-62-4. Molecular formula: C10H5N3O3. Mole weight: 215.16. | |
| AG-13958 | AG-13958 (AG-013958), a potent VEGFR tyrosine kinase inhibitor, is used for treatment of choroidal neovascularization associated with age-related macular degeneration (AMD)[1]. Uses: Scientific research. Category: Signaling pathways. Alternative Names: AG-013958. CAS No. 319460-94-1. Pack Sizes: 1 mg; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-15492. | |
| AG 1406 | AG 1406 is an inhibitor of tyrosine phosphorylation. Alternative Names: 2-[[4-hydroxy-3,5-di(propan-2-yl)phenyl]methylidene]propanedinitrile; Propanedinitrile, [[4-hydroxy-3,5-bis(1-methylethyl)phenyl]methylene]-; CTK2G2659; AG1406; CTK2G 2659; AG 1406; CTK2G-2659; AG-1406. CAS No. 71308-34-4. Molecular formula: C16H18N2O. Mole weight: 254.333. | |
| AG14361 | AG14361 is a potent PARP-1 inhibitor, with a Ki of < 5 nM, and in permeabilized SW620 and intact SW620 cells, the IC50s are 29 nM and 14 nM, respectively. Uses: Scientific research. Category: Signaling pathways. CAS No. 328543-09-5. Pack Sizes: 10 mM * 1 mL in DMSO; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-12032. | |
| AG-1478 | AG-1478 (Tyrphostin AG-1478) is a selective EGFR tyrosine kinase inhibitor with IC50 of 3 nM. AG-1478 has antiviral effects against HCV and encephalomyocarditis virus (EMCV). Uses: Scientific research. Category: Signaling pathways. Alternative Names: Tyrphostin AG-1478; NSC 693255. CAS No. 153436-53-4. Pack Sizes: 10 mM * 1 mL in DMSO; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-13524. | |
| AG-1478 | AG-1478 is a selective EGFR inhibitor with IC50 of 3 nM in cell-free assays, almost no activity on HER2-Neu, PDGFR, Trk, Bcr-Abl and InsR. AG-1478 (Tyrphostin AG-1478) inhibits encephalomyocarditis virus (EMCV) and hepatitis c virus (HCV) by targeting phosphatidylinositol 4-kinase IIIα (PI4KA). Group: Inhibitors. Alternative Names: Tyrphostin AG-1478, NSC 693255. CAS No. 153436-53-4,175178-82-2. Pack Sizes: 5mg. Product ID: S2728. Formula: C16H14ClN3O2. Smiles: COC1=C(C=C2C(=C1)C(=NC=N2)NC3=CC(=CC=C3)Cl)OC. Storage Conditions: 2 years -80 in solvent. | United States; Europe |
| AG-1557 | AG-1557 is an inhibitor of epidermal growth factor receptor (EGFR) tyrosine kinase. Alternative Names: AG-1557; AG 1557; AG1557; N-(3-Iodophenyl)-6,7-dimethoxyquinazolin-4-amine. CAS No. 189290-58-2. Molecular formula: C16H14IN3O2. Mole weight: 407.211. | |
| AG 18 | AG 18. Group: Biochemicals. Grades: Purified. CAS No. 118409-57-7. Pack Sizes: 10mg, 50mg. US Biological Life Sciences. | Worldwide |
| AG 1-X2 ion exchange resin 200-400 acetate | AG 1-X2 ion exchange resin 200-400 acetate. Group: Biochemicals. Grades: Reagent Grade. Pack Sizes: 1g, 5g, 25g. US Biological Life Sciences. | Worldwide |
| AG-270 | AG-270 is an allosteric, noncompetitive, first-in-class, reversible and orally active MAT2A inhibitor, with an IC50 of 14 nM[1]. Uses: Scientific research. Category: Signaling pathways. CAS No. 2201056-66-6. Pack Sizes: 5 mg; 10 mg; 25 mg; 50 mg; 100 mg; 500 mg; 1 g. Product ID: HY-138630. | |
| AG490 | AG490 (Tyrphostin AG490) is a tyrosine kinase inhibitor that inhibits EGFR, Stat-3 and JAK2/3. Uses: Scientific research. Category: Signaling pathways. Alternative Names: Tyrphostin AG490; Tyrphostin B42. CAS No. 133550-30-8. Pack Sizes: 10 mM * 1 mL in DMSO; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg; 200 mg. Product ID: HY-12000. | |
| AG 490 | AG 490. Group: Biochemicals. Grades: Purified. CAS No. 133550-30-8. Pack Sizes: 10mg, 50mg. US Biological Life Sciences. | Worldwide |
| AG-490 | AG-490. Group: Biochemicals. Alternative Names: 2-Cyano-3-(3,4-dihydroxyphenyl)-N-(phenylmethyl)-2-propenamide; Tyrphostin B 42. Grades: Highly Purified. CAS No. 134036-52-5. Pack Sizes: 10mg, 25mg, 50mg, 100mg, 250mg. Molecular Formula: C17H14N2O3. US Biological Life Sciences. | Worldwide |
| AG-490 | Tyrphostin AG490 is a JAK-2 specific inhibitor, which inhibits phosphorylation of EGFR and signal transducer and activator of transcription 3 [STAT-3], and subsequently reduce invasion and adhesion potential of malignant cells. Uses: Antineoplastic agents. Alternative Names: Tyrphostin AG 490; AG-490; AG490. Grades: 0.98. CAS No. 133550-30-8. Molecular formula: C17H14N2O3. Mole weight: 294.31. | |
| AG 494 | AG 494. Group: Biochemicals. Grades: Purified. CAS No. 133550-35-3. Pack Sizes: 10mg, 50mg. US Biological Life Sciences. | Worldwide |
| AG 538 | AG 538. Alternative Names: Tyrphostin; AG538; AG538; AG-538; NSC676485. Grades: ≥95%. CAS No. 133550-18-2. Molecular formula: C16H1NO5. Mole weight: 297.3. | |
| AG 555 | AG 555. Group: Biochemicals. Grades: Purified. CAS No. 133550-34-2. Pack Sizes: 10mg, 50mg. US Biological Life Sciences. | Worldwide |
| AG 556 | AG 556. Group: Biochemicals. Grades: Purified. CAS No. 133550-41-1. Pack Sizes: 10mg, 50mg. US Biological Life Sciences. | Worldwide |
| AG-636 | AG-636 is a potent, reversible, selective and orally active dihydroorotate dehydrogenase (DHODH) inhibitor with an IC50 of 17 nM. AG-636 has strong anticancer effects[1]. Uses: Scientific research. Category: Signaling pathways. CAS No. 1623416-31-8. Pack Sizes: 10 mM * 1 mL in DMSO; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-137463. | |
| AG-7404 | AG-7404 is an orally active, irreversible inhibitor of the picornavirus 3C protease. AG-7404 blocks the processing of viral polyproteins, thereby inhibiting viral replication. AG-7404 has synergistic antiviral activity with capsid inhibitors such as V-073 (HY-104074) or BTA798 (HY-106254) and is effective against V-073-resistant variants. AG-7404 is used in the study of enterovirus infections such as poliovirus[1][2][3]. Uses: Scientific research. Category: Signaling pathways. CAS No. 343565-99-1. Pack Sizes: 1 mg; 5 mg. Product ID: HY-19476. | |
| AG 825 | AG 825. Group: Biochemicals. Grades: Purified. CAS No. 149092-50-2. Pack Sizes: 10mg, 50mg. US Biological Life Sciences. | Worldwide |
| AG 879 | AG 879. Group: Biochemicals. Grades: Purified. CAS No. 148741-30-4. Pack Sizes: 10mg. US Biological Life Sciences. | Worldwide |
| AG-879 | AG-879, a tyrphostin compound, is a dual EGFR/HER2 inhibitor that was administered together with androgen withdrawal therapy. It inhibits nerve growth factor (NGF)-dependent TrkA tyrosine phosphorylation in PC-12 cells (IC50 = ~40 μM), HER2-ErbB2 kinase in several breast and ovarian cancer cell lines (IC50 = ~0.5 μM), and the VEGF receptor FLK1 (IC50 = ~1 μM). Alternative Names: α-Cyano-(3,5-di-t-butyl-4-hydroxy)thiocinnamide. CAS No. 148741-30-4. Molecular formula: C18H24N2OS. Mole weight: 316.5. | |
| AG 99 | AG 99. Group: Biochemicals. Grades: Purified. CAS No. 122520-85-8. Pack Sizes: 10mg, 50mg. US Biological Life Sciences. | Worldwide |
| AGA-(C8R) HNG17, Humanin derivative | AGA-(C8R) HNG17, Humanin derivative, a powerful humanin (HN) derivative, completely inhibits neuronal cell death through Alzheimer's disease-associated insults. Alternative Names: Pro-Ala-Gly-Ala-Ser-Arg-Leu-Leu-Leu-Leu-Thr-Gly-Glu-Ile-Asp-Leu-Pro. Grades: ≥95%. CAS No. 875910-01-3. Molecular formula: C78H134N20O24. Mole weight: 1736.02. | |
| Ag Ag2Se Core-Shell Nanoparticles | Ag Ag2Se Core-Shell Nanoparticles. CAS No. 1302-09-6. Mole weight: 294.6964 g/mol. Purity: 99.9%. | |
| a-Galactosyl-C16-ceramide (GalCer) | Galactosylceramides play an important roles in promoting th. Group: Biochemicals. Alternative Names: GalCer. Grades: Highly Purified. Pack Sizes: 1mg. US Biological Life Sciences. | Worldwide |
| a-Galactosyl-C18-ceramide | Galactosylceramides play an important roles in promoting th. Group: Biochemicals. Grades: Highly Purified. Pack Sizes: 1mg. US Biological Life Sciences. | Worldwide |
| a-Galactosyl-erythro-sphingosine | Galactosylceramides play an important roles in promoting th. Group: Biochemicals. Grades: Highly Purified. Pack Sizes: 1mg. US Biological Life Sciences. | Worldwide |
| Agar | Agar. Synonyms: MACCONKEY AGAR;MACCONKEY AGAR CS;MAC CONKEY AGAR NO 1;MACCONKEY AGAR NO 1, VEGITONE;MACCONKEY BROMOCRESOL PURPLE BROTH;MACCONKEY BROTH PURPLE;MAC CONKEY MUG AGAR. CAS No. 9002-18-0. Product ID: PE-0149. Molecular formula: C14H24O9. Category: Binder Excipients. Product Keywords: Pharmaceutical Excipients; Solid Dosage Form; Binder Excipients; Agar; PE-0149; C14H24O9; 9002-18-0; 9002-18-0. Purity: 0.99. Color: Brownish yellow. EC Number: 232-658-1. Solubility: H2O: 1.5% with heat. Quality Level: 200. Storage: room temp. Application: Substitute for gelatin, isinglass, etc. in making emulsions including photographic, gels in cosmetics, and as thickening agent in foods especially. Melting Point: 85-95 °C. Product Description: Agar chemically consists of two fractions: agarose, a neutral polymer of high gel strength and agaropectin, a non-gelling fraction with sulfated β-1,3-glycosidically linked D-galactose units. |  |
| Agar | Agar. Synonyms: MACCONKEY AGAR;MACCONKEY AGAR CS;MAC CONKEY AGAR NO 1;MACCONKEY AGAR NO 1, VEGITONE;MACCONKEY BROMOCRESOL PURPLE BROTH;MACCONKEY BROTH PURPLE;MAC CONKEY MUG AGAR. CAS No. 9002-18-0. Product ID: PE-0168. Molecular formula: C14H24O9. Category: Filler. Product Keywords: Pharmaceutical Excipients; Solid Dosage Form; Capsule Excipients; Filler; Agar; PE-0168; C14H24O9; 9002-18-0; 9002-18-0. Purity: 0.99. Color: Brownish yellow. EC Number: 232-658-1. Solubility: H2O: 1.5% with heat. Quality Level: 200. Storage: room temp. Application: Substitute for gelatin, isinglass, etc. in making emulsions including photographic, gels in cosmetics, and as thickening agent in foods especially. Melting Point: 85-95 °C. Product Description: Agar chemically consists of two fractions: agarose, a neutral polymer of high gel strength and agaropectin, a non-gelling fraction with sulfated β-1,3-glycosidically linked D-galactose units. | |
| Agar | Agar. Alternative Names: Bengalgelatin. CAS No. 9002-18-0. Product ID: ACM9002180. Molecular formula: C14H24O9. Mole weight: 336.33. IUPAC Name: (2R,3S,4S,5R)-2-(hydroxymethyl)-6-[[(4R,5S)-4-hydroxy-3-methyl-2,6-dioxabicyclo[3.2.1]octan-8-yl]oxy]-4-methoxyoxane-3,5-diol. Canonical SMILES: CC1[C@H]([C@H]2C(C(O1)CO2)OC3[C@@H]([C@H]([C@H]([C@H](O3)CO)O)OC)O)O. Alfa Chemistry - ISO 9001:32057 Certified. |  |
| Agar | Agar is used as an emulsifier, stabilizer, suspending agent, sustained-release agent, tablet binder, thickener and viscosity-increasing agent. Alternative Names: Agar-agar; Agar-agar flake; Agar-agar gum; Bengal gelatin; Bengal gum; Bengal isinglass; Ceylon isinglass; Chinese isinglass; E406; Gelose; Japan agar; Japan isinglass; layor carang; Gelose; Azazoon; Agargel; Agaron gel; Bacto-agar; Bengal isinglass; Ceylon isinglass; Chinese isinglass; Kantenmatsu; Karikorikan; Phytagar; Sabouraud dextrose agar. CAS No. 9002-18-0. Molecular formula: (C12H18O9)n. | |
| Agar | Agar. Synonyms: MACCONKEY AGAR; MACCONKEY AGAR CS; MAC CONKEY AGAR NO 1; MACCONKEY AGAR NO 1, VEGITONE; MACCONKEY BROMOCRESOL PURPLE BROTH; MACCONKEY BROTH PURPLE; MAC CONKEY MUG AGAR. CAS No. 9002-18-0. Product ID: PE-0021. Molecular formula: C14H24O9. Category: Carrier Excipients; Emulsifier Excipients. Product Keywords: Pharmaceutical Excipients; Excipients for Liquid Dosage Form; Semi-Excipients for Solid Dosage Form; Suppository Bases; Micro-drug Delivery Systems; Emulsifier Excipients; Agar; PE-0021; C14H24O9; 9002-18-0; 9002-18-0. Purity: 0.99. Color: Brownish yellow. EC Number: 232-658-1. Solubility: H2O: 1.5% with heat. Quality Level: 200. Storage: room temp. Applications: Substitute for gelatin, isinglass, etc. in making emulsions including photographic, gels in cosmetics, and as thickening agent in foods especially. Melting Point: 85-95 °C. Product Description: Agar chemically consists of two fractions: agarose, a neutral polymer of high gel strength and agaropectin, a non-gelling fraction with sulfated β-1, 3-glycosidically linked D-galactose units. | |
| Agar | Agar. Synonyms: MACCONKEY AGAR;MACCONKEY AGAR CS;MAC CONKEY AGAR NO 1;MACCONKEY AGAR NO 1, VEGITONE;MACCONKEY BROMOCRESOL PURPLE BROTH;MACCONKEY BROTH PURPLE;MAC CONKEY MUG AGAR. CAS No. 9002-18-0. Product ID: PE-0118. Molecular formula: C14H24O9. Category: Lyophilization Reagents. Product Keywords: Pharmaceutical Excipients; Injections & Sterile Formulation; Lyophilization Reagents; Agar; PE-0118; C14H24O9; 9002-18-0; 9002-18-0. Purity: 0.99. Color: Brownish yellow. EC Number: 232-658-1. Solubility: H2O: 1.5% with heat. Quality Level: 200. Storage: room temp. Application: Substitute for gelatin, isinglass, etc. in making emulsions including photographic, gels in cosmetics, and as thickening agent in foods especially. Melting Point: 85-95 °C. Product Description: Agar chemically consists of two fractions: agarose, a neutral polymer of high gel strength and agaropectin, a non-gelling fraction with sulfated β-1,3-glycosidically linked D-galactose units. | |
| Agar | Agar. Synonyms: MACCONKEY AGAR;MACCONKEY AGAR CS;MAC CONKEY AGAR NO 1;MACCONKEY AGAR NO 1, VEGITONE;MACCONKEY BROMOCRESOL PURPLE BROTH;MACCONKEY BROTH PURPLE;MAC CONKEY MUG AGAR. CAS No. 9002-18-0. Pack Sizes: 100, 500 g in poly bottle. Product ID: CDC10-0221. Molecular formula: C14H24O9. Category: Fragrance Agents. Product Keywords: Cosmetic Ingredients; Fragrance Agents; Agar; CDC10-0221; 9002-18-0; C14H24O9; MACCONKEY AGAR; MACCONKEY AGAR CS; MAC CONKEY AGAR NO 1; MACCONKEY AGAR NO 1, VEGITONE; MACCONKEY BROMOCRESOL PURPLE BROTH; MACCONKEY BROTH PURPLE; MAC CONKEY MUG AGAR; 232-658-1; MFCD00081288; 9002-18-0. Purity: 0.99. Color: Brownish yellow. EC Number: 232-658-1. Solubility: H2O: 1.5% with heat. Quality Level: 200. Storage: room temp. Application: Substitute for gelatin, isinglass, etc. in making emulsions including photographic, gels in cosmetics, and as thickening agent in foods especially. Melting Point: 85-95 °C. Product Description: Agar chemically consists of two fractions: agarose, a neutral polymer of high gel strength and agaropectin, a non-gelling fraction with sulfated β-1,3-glycosidically linked D-galactose units. | |
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