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| Product | Description | |
|---|---|---|
| VEGFR-2-IN-5 hydrochloride | VEGFR-2-IN-5 hydrochloride is a VEGFR2 inhibitor extracted from patent WO2013055780A1, Page 69 [1]. Uses: Scientific research. Group: Signaling pathways. CAS No. 2700435-52-3. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 50 mg; 100 mg. Product ID: HY-18625A. |  |
| VEGFR2/KDR fragment 1 (614-624) |  | |
| VEGFR2 Kinase Inhibitor II | VEGFR2 kinase inhibitor II is a reversible and cell-permeable inhibitor of VEGFR2's kinase activity with IC50 value of 70 nM. It also less potently inhibits the platelet-derived growth factor receptor β (PDGFRβ) with IC50 value of 920 nM, and other related receptor as well as non-receptor tyrosine kinases. Synonyms: (Z)-5-Bromo-3-(4,5,6,7-tetrahydro-1H-indol-2-ylmethylene)-1,3-dihydroindol-2-one. Grades: ≥95%. CAS No. 288144-20-7. Molecular formula: C17H15BrN2O. Mole weight: 343.2. | |
| VEGFR2 Kinase Inhibitor VII, SKLB1002 (VEGFR Tyrosine Kinase Inhibitor XXXV, 6,7-Dimethoxy-4-(5-methyl-1,3,4-thiadiazol-2-ylthio)quinazoline, Vascular Endothelial Growth Factor Receptor 2 Kinase Inhibitor VII) | A cell-permeable quinazoline that acts as a potent, ATP-binding site-targeting, VEGFR2-selective inhibitor (IC50=32nM), while exhibiting much reduced or little activity against 16 other kinases. An effective antiangiogenesis agent (98% inhibition of HUVEC tube formation at 10uM; 80% inhibition of zebrafish embryos intersegmental vessel growth at 2.5uM) that significantly suppresses SW620- and HepG2-derived tumor growth in mice (by 72% and 63%, respectively, in 18 days; 100mg/kg/day; i.p.) in vivo. Group: Biochemicals. Grades: Highly Purified. Pack Sizes: 10mg. US Biological Life Sciences. |  Worldwide |
| VEGFR-IN-1 | VEGFR-IN-1 (compound 3) is a potent angiogenesis inhibitor with IC 50 s of 0.02, 0.18, 0.24 7.3, and 7 μM for KDR , Flt-1 , c-Kit, EGF-R, and c-Src, respectively [1]. Uses: Scientific research. Group: Signaling pathways. CAS No. 269390-69-4. Pack Sizes: 10 mM * 1 mL; 1 mg; 5 mg; 10 mg. Product ID: HY-101219. | |
| VEGFR Tyrosine Kinase Inhibitor II | VEGFR tyrosine kinase inhibitor II is a pyridinyl-anthranilamide compound that potently inhibits the kinase activities of VEGFR2 (KDR), VEGFR1 (FLT1), and c-Kit (IC50 = 20, 180, and 240 nM, respectively). It is potential for cancer treatment for its inhibitory effect of tumor induced angiogenesis. Synonyms: N-(4-Chlorophenyl)-2-[(pyridin-4-ylmethyl)amino]benzamide. Grades: ≥98%. CAS No. 269390-69-4. Molecular formula: C19H16ClN3O. Mole weight: 337.8. | |
| Vegita | Vegita is a metabolite of maneb, a fungicide. Synonyms: Hortocritt; Ethylenethiuramsulfide; Ethylenethiurammonosulfide; ETM(heterocycle); ETEM. Grades: 95%. CAS No. 33813-20-6. Molecular formula: C4H4N2S3. Mole weight: 176.28. | |
| Vejovine (23-82) | Vejovine (23-82) is a new type of antibiotic peptide derived from scorpion venom, which shows significant and effective antibacterial activity against clinical isolates of Gram-negative multi-drug resistant strains of Escherichia coli, Pseudomonas aerμginosa and Acinetobacter baumannii. Synonyms: Gly-Ile-Trp-Ser-Ser-Ile-Lys-Asn-Leu-Ala-Ser-Lys-Ala-Trp-Asn-Ser-Asp-Ile-Gly-Gln-Ser-Leu-Arg-Asn-Lys-Ala-Ala-Gly-Ala-Ile-Asn-Lys-Phe-Val-Ala-Asp-Lys-Ile-Gly-Val-Thr-Pro-Ser-Gln-Ala-Ala-Ser-Met-Thr-Leu-Asp-Glu-Ile-Val-Asp-Ala-Met-Tyr-Tyr-Asp. | |
| VEL-0230 | VEL-0230, also known as NC-2300, is a potent cathespin K inhibitor. VEL-0230 has dual-acting properties that both stimulates bone formation and inhibits loss. VEL-0230 is being studied preclinically for the treatment of diseases involving bone mineral disorders such as bone loss related to multiple myeloma, osteoporosis, bone metastases, and rheumatoid arthritis. Velcura Therapeutics is currently being developed by Velcura Therapeutics. Given VEL- 0230's promotion of bone formation, inhibition of bone loss and reduction of calcium levels, Velcura has chosen Myeloma as its lead indication, as the bone fragility, bone pain, high calcium levels and eventual kidney involvement present serious medical and quality of life issues to affected patients. Synonyms: VEL 0230; VEL0230; NC-2300; NC2300; NC 2300; sodium (2S,3S)-3-(((S)-1-isobutoxy-4-methylpentan-2-yl)carbamoyl)oxirane-2-carboxylate. CAS No. 221144-20-3. Molecular formula: C14H24NNaO5. Mole weight: 309.33. | |
| Velagliflozin | Velagliflozin is an orally available sodium-glucose cotransporter 2 ( SGLT2 ) inhibitor, with anti-diabetic activity. Uses: Scientific research. Group: Signaling pathways. CAS No. 946525-65-1. Pack Sizes: 10 mM * 1 mL; 1 mg; 5 mg. Product ID: HY-109018. | |
| Velagliflozin proline | Velagliflozin proline is an oral sodium-glucose cotransporter 2 ( SGLT2 ) inhibitor with antidiabetic activity. Velagliflozin proline reduces renal glucose reabsorption and stimulates glycosuria, which lowers blood sugar and insulin concentrations [1]. Uses: Scientific research. Group: Signaling pathways. CAS No. 1539295-26-5. Pack Sizes: 10 mM * 1 mL; 1 mg; 5 mg. Product ID: HY-109018A. | |
| Veldoreotide TFA | Veldoreotide (DG3173) TFA a somatostatin analogue, binds to and activate the somatostatin receptors (SSTR) 2, 4, and 5. Veldoreotide TFA inhibits growth hormone (GH) secretion in adenomas compared with Octreotide (HY-P0036). Veldoreotide has the potential to be used as pain modulating agent [1]. Uses: Scientific research. Group: Peptides. Alternative Names: DG3173 TFA; PTR-3173 TFA. CAS No. 2126831-23-8. Pack Sizes: 1 mg; 5 mg; 10 mg. Product ID: HY-P0024A. | |
| Veledimex | Veledimex is used as an immunostimulant drug candidate. Uses: Veledimex is used as an immunostimulant drug candidate. Synonyms: AD-1001; AD1001; AD 1001; INXN-1001;INXN1001; INXN 1001; RG-115932; RG115932; RG 115932; N'-(3,5-dimethylbenzoyl)-N'-[(3R)-2,2-dimethylhexan-3-yl]-2-ethyl-3-methoxybenzohydrazide;(R)-N'-(3,5-dimethylbenzoyl)-N'-(2,2-dimethylhexan-3-yl)-2-ethyl-3-methoxybenzohydrazide. Grades: >98%. CAS No. 1093130-72-3. Molecular formula: C27H38N2O3. Mole weight: 438.61. | |
| Veledimex racemate | Veledimex racemate is the racemate of veledimex. Veledimex is an orally active small molecule diacylhydrazine and controls the expression of the target gene. Synonyms: N'-(3,5-dimethylbenzoyl)-N'-(2,2-dimethylhexan-3-yl)-2-ethyl-3-methoxybenzohydrazide; Veledimex (racemate). CAS No. 755013-59-3. Molecular formula: C27H38N2O3. Mole weight: 438.6. | |
| Veledimex S enantiomer | Veledimex S enantiomer is the S enantiomer of veledimex which is an orally active small molecule diacylhydrazine and controls the expression of the target gene. Synonyms: N'-(3,5-dimethylbenzoyl)-N'-[(3S)-2,2-dimethylhexan-3-yl]-2-ethyl-3-methoxybenzohydrazide; Veledimex (S enantiomer). CAS No. 1093131-03-3. Molecular formula: C27H38N2O3. Mole weight: 438.6. | |
| Veliflapon | Heterocyclic Organic Compound. Alternative Names: (2R)-2-cyclopentyl-2-[4-(quinolin-2-ylmethoxy)phenyl]acetic acid;2-(4-(quinolin-2-yl-methoxy)phenyl)-2-cyclopentylacetic acid;VELIFLAPON. CAS No. 128253-31-6. Molecular formula: C23H23NO3. Mole weight: 361.439. Purity: >98 %. Catalog: ACM128253316. |  |
| Veligrotug | Veligrotug is an IgG1-kappa, anti- IGF1R (insulin-like growth factor 1 receptor, CD221) chimeric monoclonal antibody [1]. Uses: Scientific research. Group: Inhibitory antibodies. CAS No. 2728655-31-8. Pack Sizes: 1 mg; 5 mg; 10 mg. Product ID: HY-P990084. | |
| Veliparib | Veliparib (ABT-888) is a potent inhibitor of PARP1 and PARP2 with Ki of 5.2 nM and 2.9 nM, respectively. In HCT-116 and HT-29 cell lines, the ability of ABT-888 to synergize the effect of the anti-cancer agents, SN38 or oxaliplatin, was determined using the SRB assay. PARP activity was significantly reduced in samples treated with SN38 in combination with ABT-888 (>4 fold at 24 h). Uses: For research used only. Synonyms: (R)-2-(2-methylpyrrolidin-2-yl)-1H-benzo[d]imidazole-4-carboxamide; ABT888; ABT-888; ABT 888; Veliparib. Grades: 0.99. CAS No. 912444-00-9. Molecular formula: C13H16N4O. Mole weight: 244.298. | |
| Veliparib | ABT-888 is a potent, orally bioavailable PARP-1/-2 inhibitor shown to potentiate DNA damaging agents. The ability to potentiate temozolomide (TMZ) and develop a biological marker for PARP inhibition was evaluated in vivo. Group: Biochemicals. Alternative Names: 2-[(2R)-2-Methyl-2-pyrrolidinyl]-1H-benzimidazole-7-carboxamide; A 861695; ABT 888. Grades: Purified. CAS No. 912444-00-9. Pack Sizes: 10mg, 25mg, 50mg. US Biological Life Sciences. | Worldwide |
| Veliparib | Veliparib (ABT-888) is a potent PARP inhibitor, inhibiting PARP1 and PARP2 with K i s of 5.2 and 2.9 nM, respectively [1]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: ABT-888. CAS No. 912444-00-9. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 50 mg; 100 mg; 200 mg. Product ID: HY-10129. | |
| Veliparib dihydrochloride | Veliparib (dihydrochloride) is a potent inhibitor of PARP1 and PARP2 with K i s of 5.2 nM and 2.9 nM in cell-free assays, respectively. Uses: Scientific research. Group: Signaling pathways. Alternative Names: ABT-888 dihydrochloride. CAS No. 912445-05-7. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 50 mg; 100 mg; 200 mg. Product ID: HY-10130. | |
| vellosimine dehydrogenase | Also acts on related alkaloids with an endo-aldehyde group as vellosimine (same stereochemistry at C-16) but only slight activity with exo-aldehydes. Detected in many cell suspension cultures of plants from the family Apocynaceae. Group: Enzymes. Enzyme Commission Number: EC 1.1.1.273. CAS No. 86777-26-6. 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-0180; vellosimine dehydrogenase; EC 1.1.1.273; 86777-26-6. Cat No: EXWM-0180. |  |
| Velnacrine | Heterocyclic Organic Compound. CAS No. 104675-29-8. Molecular formula: C13H14N2O. Mole weight: 214.263 g/mol. Purity: 0.96. IUPACName: 9-amino-1,2,3,4-tetrahydroacridin-1-ol. Canonical SMILES: C1CC(C2=C(C3=CC=CC=C3N=C2C1)N)O. Density: 1.315g/cm³. Catalog: ACM104675298. | |
| Velnacrine-1,2,2-d3 Maleate | 2H Labeled Compounds. Alternative Names: 9-Amino-1,2,3,4-tetrahydro-1-acridinol Maleate;1-Hydroxytacrine Maleate. CAS No. 1219806-48-0. Mole weight: 333.36. Catalog: ACM1219806480. | |
| Velnacrine maleate | Velnacrine maleate (HP 029) is an orally active cholinesterase inhibitor that can be used for the research of Alzheimer's disease [1]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: HP 029; Hydroxytacrine maleate. CAS No. 118909-22-1. Pack Sizes: 25 mg; 50 mg; 100 mg. Product ID: HY-W011246. | |
| Velneperit | Velneperit is a once-daily, oral, centrally acting, small molecule neuropeptide Y (NPY) Y5 receptor antagonist. Uses: An optimized synthetic neuropeptide y (npy) y5 receptor antagonist used in the oral treatment of obesity. Synonyms: S-2367; S 2367; S2367; VelneperitN-[5-(Trifluoromethyl)pyridin-2-yl]-trans-4-(tert-butylsulfonylamino)cyclohexane-1-carboxamide. Grades: ≥98%. CAS No. 342577-38-2. Molecular formula: C17H24F3N3O3S. Mole weight: 407.45. | |
| Velneperit | Velneperit (S-2367) is a novel neuropeptide Y (NPY) Y5 receptor antagonist. Uses: Scientific research. Group: Signaling pathways. Alternative Names: S2367. CAS No. 342577-38-2. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-14423. | |
| Veloutone | Veloutone. CAS No. 65443-14-3. VIGON Item # 502847. Categories: Speciality Ingrdients Suppliers, Fragrances, fruity cyclopentanone, Perfumers. |  America & Internationally |
| Velpatasvir | Velpatasvir (VEL, GS-5816) is a novel pan-genotypic hepatitis C virus (HCV) nonstructural protein 5A (NS5A) inhibitor with activity against genotype 1 (GT1) to GT6 HCV replicons. Velpatasvir is also a SARS-CoV 3CL pro inhibitor with an IC 50 of 2.16 μM [2]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: GS-5816. CAS No. 1377049-84-7. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 50 mg; 100 mg. Product ID: HY-12530. | |
| Velpatasvir | Velpatasvir is a selective Hepatitis C virus NS 5 protein inhibitor originated by Gilead Sciences. It showed pan-genotypic activity and a high barrier to resistance in HCV replicon assays. Uses: Antiviral agents. Synonyms: GS5816; GS-5816; GS 5816; Velpatasvir; methyl ((R)-2-((2S, 4S)-2-(5-(2-((2S, 5S)-1-((methoxycarbonyl)-L-valyl)-5-methylpyrrolidin-2-yl)-1, 11-dihydroisochromeno[4', 3':6, 7]naphtho[1, 2-d]imidazol-9-yl)-1H-imidazol-2-yl)-4-(methoxymethyl)pyrrolidin-1-yl)-2-oxo-1-phenylethyl)carbamate. Grades: >98%. CAS No. 1377049-84-7. Molecular formula: C49H54N8O8. Mole weight: 883.01. | |
| Velpatasvir impurity 1 | Velpatasvir impurity 1. Uses: For analytical and research use. Group: Impurity standards. CAS No. 1378391-45-7. Molecular Formula: C44H53N7O7. Mole Weight: 791.95. Catalog: APB1378391457. |  |
| Velpatasvir impurity 2 | Velpatasvir impurity 2. Uses: For analytical and research use. Group: Impurity standards. CAS No. 1844064-96-5. Molecular Formula: C39H45N7O5. Mole Weight: 691.83. Catalog: APB1844064965. | |
| Veltuzumab | Veltuzumab (IMMU-106) is a humanized anti-CD20 monoclonal antibody. Veltuzumab has low EC 50 value of 0.08-0.09 μg/mL in the Daudi cell line. Veltuzumab can be used for the research of cancer including non-Hodgkin lymphoma (NHL) [1]. Uses: Scientific research. Group: Inhibitory antibodies. Alternative Names: IMMU-106; hA20. CAS No. 728917-18-8. Pack Sizes: 1 mg; 5 mg; 10 mg. Product ID: HY-P99224. | |
| Veltuzumab | Veltuzumab is a humanized anti-CD20 monoclonal antibody. Veltuzumab has been investigated for the treatment of non-Hodgkin's lymphoma. Synonyms: IMMU-106; hA20. CAS No. 728917-18-8. | |
| Velufenacin | Velufenacin is a muscarinic receptor antagonist [1]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: DA-8010. CAS No. 1648737-78-3. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-109196. | |
| Velusetrag | Velusetrag is a selective, 5-HT4receptor agonist. Phase II clinical trials for the treatment of gastroparesis are on-going. Clnical trials for Alzheimer's disease and Constipation were discontinued. Uses: Gastroparesis. Synonyms: UNII-J4VNV64ARB; TD-5108; TD5108; TD 5108; J4VNV64ARB; GTPL8425;N-[(1R,5S)-8-[(2R)-2-hydroxy-3-[methyl(methylsulfonyl)amino]propyl]-8-azabicyclo[3.2.1]octan-3-yl]-2-oxo-1-propan-2-ylquinoline-3-carboxamide. Grades: 98%. CAS No. 866933-46-2. Molecular formula: C25H36N4O5S. Mole weight: 504.65. | |
| Velusetrag | Velusetrag (TD-5108) is an orally active, potent and selective agonist of serotonin 5-HT 4 receptor (5-HT4R) , with a pK i of 7.7. Velusetrag exhibits no affinity (K i >10 μM) for 5-HT 2A and 5-HT 2B receptors. Velusetrag can be used for the research of gastrointestinal diseases and Parkinson's disease [1] [2] [3] [4] [5]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: TD-5108. CAS No. 866933-46-2. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg; 50 mg. Product ID: HY-10457. | |
| Velusetrag hydrochloride | Velusetrag (TD-5108) hydrochloride is an orally active, potent and selective agonist of serotonin 5-HT 4 receptor (5-HT 4 R) , with a pK i of 7.7. Velusetrag hydrochloride exhibits no affinity (K i >10 μM) for 5-HT 2A and 5-HT 2B receptors. Velusetrag hydrochloride can be used for the research of gastrointestinal diseases and Parkinson's disease [1] [2] [3] [4] [5]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: TD-5108 hydrochloride. CAS No. 866933-51-9. Pack Sizes: 5 mg; 10 mg; 25 mg; 50 mg. Product ID: HY-10457A. | |
| Velutin. | Velutin. Group: Biochemicals. Grades: Plant Grade. CAS No. 25739-41-7. Pack Sizes: 20mg. Molecular Formula: C17H14O6, Molecular Weight: 314.29. US Biological Life Sciences. | Worldwide |
| Velvione ® | Velvione ®. CAS No. 37609-25-9. VIGON Item # 501388. Categories: Speciality Ingrdients Suppliers, Fragrances, musk amberol, Perfumers. | America & Internationally |
| Vemircopan | Vemircopan (ALXN2050) is an orally active complement factor D inhibitor. Vemircopan is promising for research of paroxysmal nocturnal hemoglobinuria [1] [2] [3]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: ALXN2050; ACH 0145228; ACH-5228. CAS No. 2086178-00-7. Pack Sizes: 10 mM * 1 mL; 1 mg; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-139588. | |
| Vemurafenib | Vemurafenib / PLX4032 / RG7204 is a novel and potent inhibitor of B-RafV600E with IC50 of 31 nM in cell-free assay. 10-fold selective for B-RafV600E over wild-type B-Raf in enzymatic assays and the cellular. Group: Fluorinated apis. Alternative Names: PLX4032. CAS No. 918504-65-1. Molecular formula: C23H18ClF2N3O3S. Mole weight: 489.92. Appearance: White to off-white solid powder. Purity: >98%. IUPACName: N-[3-[5-(4-chlorophenyl)-1H-pyrrolo[2,3-b]pyridine-3-carbonyl]-2,4-difluorophenyl]propane-1-sulfonamide. Catalog: OFC918504651. | |
| Vemurafenib | Vemurafenib (PLX4032) is a first-in-class, selective, potent inhibitor of B-RAF kinase, with IC 50 s of 31 and 48 nM for RAF V600E and c-RAF-1, respectively [1] [4]. Vemurafenib induces cell autophagy [5]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: PLX4032; RG7204; RO5185426. CAS No. 918504-65-1. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg; 500 mg. Product ID: HY-12057. | |
| Vemurafenib | Vemurafenib is a potent and selective inhibitor of B-RafV600E with IC50 of 13 nM, equally potent to c-Raf-1(Y340D and Y341D mutations), 10-fold selectivity than wild-type B-Raf. Synonyms: PLX4032; PLX 4032; PLX-4032; RG7204 ; RG7204 ; RG 7204 ; RO5185426; RO 5185426 RO5185426 Vemurafenib; Brand name: Zelboraf. Grades: >98%. CAS No. 918504-65-1. Molecular formula: C23H18ClF2N3O3S. Mole weight: 489.92. | |
| Vemurafenib-Analog | BRAF inhibitor is a potent BRAF inhibitor. Synonyms: 2-Propanesulfonamide, N-[2,4-difluoro-3-[[5-(3-pyridinyl)-1H-pyrrolo[2,3-b]pyridin-3-yl]carbonyl]phenyl]-. Grades: >98%. CAS No. 918505-61-0. Molecular formula: C22H18F2N4O3S. Mole weight: 456.47. | |
| Vemurafenib, Free Base (PLX4032) | Vemurafenib selective BRAFV600E kinase inhibitor; an antitumor agent. Vemurafenib functions by inhibiting the proliferation and mitogen-activated protein/extracellular signal-regulated kinase (ERK) kinase and ERK phosphorylation in a panel of tumor cell lines, including melanoma cell lines expressing BRAFV600E or other mutant BRAF proteins altered at codon 600. Group: Biochemicals. Alternative Names: N-[3-[[5-(4-Chlorophenyl)-1H-pyrrolo[2,3-b]pyridin-3-yl]carbonyl]-2,4-difluorophenyl]-1-propanesulfonamide; PLX4032; RG7204; RO51-85426; Zelboraf. Grades: Highly Purified. CAS No. 918504-65-1. Pack Sizes: 25mg, 50mg, 100mg. US Biological Life Sciences. | Worldwide |
| Vemurafenib Impurity 4 | Vemurafenib Impurity 4. Uses: For analytical and research use. Group: Impurity standards. CAS No. 1365986-90-8. Molecular Formula: C23H13D5ClF2N3O3S. Mole Weight: 494.95. Catalog: APB1365986908. | |
| Vemurafenib Impurity 5 | Vemurafenib Impurity 5. Uses: For analytical and research use. Group: Impurity standards. CAS No. 1365986-73-7. Molecular Formula: C23H11D7ClF2N3O3S. Mole Weight: 496.96. Catalog: APB1365986737. | |
| Venadaparib Impurity 1 | Venadaparib Impurity 1. Uses: For analytical and research use. Group: Impurity standards. CAS No. 763111-49-5. Molecular Formula: C21H21FN4O2. Mole Weight: 380.42. Catalog: APB763111495. | |
| Venadaparib Impurity 10 | Venadaparib Impurity 10. Uses: For analytical and research use. Group: Impurity standards. CAS No. 76972-38-8. Molecular Formula: C18H15N3O. Mole Weight: 289.34. Catalog: APB76972388. | |
| Venadaparib Impurity 11 | Venadaparib Impurity 11. Uses: For analytical and research use. Group: Impurity standards. CAS No. 127828-88-0. Molecular Formula: C16H12N2O3. Mole Weight: 280.28. Catalog: APB127828880. | |
| Venadaparib Impurity 12 | Venadaparib Impurity 12. Uses: For analytical and research use. Group: Impurity standards. CAS No. 25947-18-6. Molecular Formula: C10H10N4O2. Mole Weight: 218.22. Catalog: APB25947186. | |
| Venadaparib Impurity 13 | Venadaparib Impurity 13. Uses: For analytical and research use. Group: Impurity standards. CAS No. 618443-91-7. Molecular Formula: C17H16N4O2. Mole Weight: 308.34. Catalog: APB618443917. | |
| Venadaparib Impurity 14 | Venadaparib Impurity 14. Uses: For analytical and research use. Group: Impurity standards. CAS No. 16015-47-7. Molecular Formula: C10H8N2O3. Mole Weight: 204.19. Catalog: APB16015477. | |
| Venadaparib Impurity 15 | Venadaparib Impurity 15. Uses: For analytical and research use. Group: Impurity standards. CAS No. 16015-48-8. Molecular Formula: C11H10N2O3. Mole Weight: 218.21. Catalog: APB16015488. | |
| Venadaparib Impurity 16 | Venadaparib Impurity 16. Uses: For analytical and research use. Group: Impurity standards. CAS No. 28081-52-9. Molecular Formula: C11H10N2O3. Mole Weight: 218.21. Catalog: APB28081529. | |
| Venadaparib Impurity 17 | Venadaparib Impurity 17. Uses: For analytical and research use. Group: Impurity standards. CAS No. 618442-00-5. Molecular Formula: C11H12N4O2. Mole Weight: 232.24. Catalog: APB618442005. | |
| Venadaparib Impurity 18 | Venadaparib Impurity 18. Uses: For analytical and research use. Group: Impurity standards. CAS No. 76972-40-2. Molecular Formula: C17H14N2O3. Mole Weight: 294.31. Catalog: APB76972402. | |
| Venadaparib Impurity 19 | Venadaparib Impurity 19. Uses: For analytical and research use. Group: Impurity standards. CAS No. 32003-14-8. Molecular Formula: C15H12N2O. Mole Weight: 236.27. Catalog: APB32003148. | |
| Venadaparib Impurity 2 | Venadaparib Impurity 2. Uses: For analytical and research use. Group: Impurity standards. CAS No. 76462-38-9. Molecular Formula: C14H9BrN2O. Mole Weight: 301.14. Catalog: APB76462389. | |
| Venadaparib Impurity 20 | Venadaparib Impurity 20. Uses: For analytical and research use. Group: Impurity standards. CAS No. 54145-30-1. Molecular Formula: C10H10N2O. Mole Weight: 174.2. Catalog: APB54145301. | |
| Venadaparib Impurity 21 | Venadaparib Impurity 21. Uses: For analytical and research use. Group: Impurity standards. CAS No. 356790-59-5. Molecular Formula: C13H14N2O3. Mole Weight: 246.27. Catalog: APB356790595. | |
| Venadaparib Impurity 22 | Venadaparib Impurity 22. Uses: For analytical and research use. Group: Impurity standards. CAS No. 68775-82-6. Molecular Formula: C11H10N2O3. Mole Weight: 218.21. Catalog: APB68775826. | |
| Venadaparib Impurity 23 | Venadaparib Impurity 23. Uses: For analytical and research use. Group: Impurity standards. CAS No. 51334-85-1. Molecular Formula: C15H12N2O. Mole Weight: 236.27. Catalog: APB51334851. | |
| Venadaparib Impurity 24 | Venadaparib Impurity 24. Uses: For analytical and research use. Group: Impurity standards. CAS No. 160748-31-2. Molecular Formula: C16H10ClN3O. Mole Weight: 295.73. Catalog: APB160748312. | |
| Venadaparib Impurity 25 | Venadaparib Impurity 25. Uses: For analytical and research use. Group: Impurity standards. CAS No. 16015-59-1. Molecular Formula: C16H13N3O2. Mole Weight: 279.3. Catalog: APB16015591. | |
| Venadaparib Impurity 26 | Venadaparib Impurity 26. Uses: For analytical and research use. Group: Impurity standards. CAS No. 99072-87-4. Molecular Formula: C10H10N4O2. Mole Weight: 218.22. Catalog: APB99072874. | |
| Venadaparib Impurity 27 | Venadaparib Impurity 27. Uses: For analytical and research use. Group: Impurity standards. CAS No. 730951-11-8. Molecular Formula: C11H10N2O4. Mole Weight: 234.21. Catalog: APB730951118. | |
| Venadaparib Impurity 28 | Venadaparib Impurity 28. Uses: For analytical and research use. Group: Impurity standards. CAS No. 28081-54-1. Molecular Formula: C17H14N2O3. Mole Weight: 294.31. Catalog: APB28081541. | |
| Venadaparib Impurity 29 | Venadaparib Impurity 29. Uses: For analytical and research use. Group: Impurity standards. CAS No. 93517-76-1. Molecular Formula: C16H14N2O. Mole Weight: 250.3. Catalog: APB93517761. | |
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