A directory of where to buy chemicals in the USA, including: distributors, industrial manufacturers, bulk supplies and wholesalers of raw ingredients & finished goods.
The enzyme catalyses the first step in the aerobic styrene degradation pathway. It forms a two-component system with a reductase (StyB) that utilizes NADH to reduce flavin-adenine dinucleotide, which is then transferred to the oxygenase. Group: Enzymes. Synonyms: StyA; SMO; NSMOA. Enzyme Commission Number: EC 1.14.14.11. 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-0908; styrene monooxygenase; EC 1.14.14.11; StyA; SMO; NSMOA. Cat No: EXWM-0908.
Styrene Oxide
Styrene Oxide. CAS No. 96-09-3. Molecular formula: C8H8O.
Highly specific. Group: Enzymes. Synonyms: SOI. Enzyme Commission Number: EC 5.3.99.7. CAS No. 124541-89-5. 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-5515; styrene-oxide isomerase; EC 5.3.99.7; 124541-89-5; SOI. Cat No: EXWM-5515.
Styrenesulfonic acid, sodium salt
Styrenesulfonic acid, sodium salt. Alternative Names: Sodium p-styrenesulfonate. CAS No. 2695-37-6. Purity: 90% (stabilized with TBC). Product ID: ACM2695376-1. Molecular formula: C8H7NaO3S. Mole weight: 206.2. Alfa Chemistry - ISO 9001:32057 Certified.
Styron g 9001
Styron g 9001. CAS No. 9010-92-8. Molecular formula: C12H14O2. Mole weight: 190.24g/mol. IUPAC Name: 2-methylprop-2-enoic acid;styrene. SMILES: CC(=C)C(=O)O.C=CC1=CC=CC=C1. InChI: InChI=1S/C8H8.C4H6O2/c1-2-8-6-4-3-5-7-8;1-3(2)4(5)6/h2-7H,1H2;1H2,2H3,(H,5,6).
Styryl 9m
Styryl 9m. Alternative Names: STYRYL 6M;STYRYL 9;STYRYL 9M;2-([3-(2-[4-(DIMETHYLAMINO)PHENYL]ETHENYL)-5,5-DIMETHYL-2-CYCLOHEXEN-1-YLIDENE]METHYL)-3-METHYLBENZOTHIAZOLIUM PERCHLORATE;2-[(3-((E)-2-[4-(DIMETHYLAMINO)PHENYL]ETHENYL)-5,5-DIMETHYL-2-CYCLOHEXEN-1-YLIDENE)METHYL]-3-METHYL-1,3. CAS No. 82988-08-7. Molecular formula: C27H31ClN2O4S. Mole weight: 515.06.
Styryl 9M
Styryl 9M is a fluorescent dye. Alternative Names: 2-([3-(2-[4-(Dimethylamino)phenyl]ethenyl)-5,5-dimethyl-2-cyclohexen-1-ylidene]methyl)-3-methylbenzothiazolium perchlorate; 2-[[3-[2-[4-(Dimethylamino)phenyl]ethenyl]-5,5-dimethyl-2-cyclohexen-1-ylidene]methyl]-3-methylbenzothiazolium perchlorate. CAS No. 82988-08-7. Molecular formula: C27H31ClN2O4S. Mole weight: 515.065.
Styryl-D-beta-homoalanine hydrochloride
Styryl-D-beta-homoalanine hydrochloride. Group: Biochemicals. Alternative Names: D-b-HomoAla(styryl)-OH·HCl; (R)-3-Amino-(6-phenyl)-5-hexenoic acid hydrochloride. Grades: Highly Purified. CAS No. 270596-35-5. Pack Sizes: 25mg, 50mg, 100mg, 250mg, 500mg. US Biological Life Sciences.
Worldwide
Styrylethyltrimethoxysilane
Styrylethyltrimethoxysilane. Alternative Names: STYRYLETHYLTRIMETHOXYSILANE; Styrylethyltrimethoxysilane95%; styrylethyltrimethoxysilane 95%. Grades: 95%. CAS No. 134000-44-5. Molecular formula: C13H20O3Si. Mole weight: 252.38.
Styryl Phenol Ethoxylates
Styryl Phenol Ethoxylates. CAS No. 70880-56-7.
SU0268
SU0268 is a potent and specific inhibitor of 8-Oxoguanine DNA glycosylase 1 (OGG1). SU0268 regulates inflammatory responses during Pseudomonas aeruginosa infection[1][2][3]. Uses: Scientific research. Category: Signaling pathways. CAS No. 2210228-45-6. Pack Sizes: 10 mM * 1 mL in DMSO; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-139056.
SU056
SU056 is a YB-1 inhibitor. SU056 induces cell-cycle arrest, apoptosis, and inhibits cell migration in ovarian cancer cells. SU056 interacts with YB-1 and inhibits and its associated downstream proteins and pathways. SU056 can enhance the cytotoxic effects of Paclitaxel (HY-B0015)[1]. Uses: Scientific research. Category: Signaling pathways. CAS No. 2376580-08-2. Pack Sizes: 10 mM * 1 mL in DMSO; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-150231.
SU 10603
SU 10603 is a specific inhibitor of P45017α (P450c17; CYP17A1)[1]. Uses: Scientific research. Category: Signaling pathways. CAS No. 786-97-0. Pack Sizes: 1 mg; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-116643.
SU11274
SU11274 is a selective Met inhibitor with IC50 of 10 nM, but has no effects on PGDFRβ, EGFR or Tie2. Uses: Scientific research. Category: Signaling pathways. Alternative Names: PKI-SU11274. CAS No. 658084-23-2. Pack Sizes: 10 mM * 1 mL in DMSO; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-12014.
SU 11274
SU 11274. Group: Biochemicals. Grades: Purified. CAS No. 658084-23-2. Pack Sizes: 10mg, 50mg. US Biological Life Sciences.
Worldwide
SU11652
SU11652 is a potent receptor tyrosine kinase (RTK) inhibitor. SU11652 also inhibits several members of the split kinase family of RTKs, including VEGFR, FGFR, PDGFR, and Kit. SU11652 can be uesd for spontaneous cancers expressing Kit mutations research[1]. Uses: Scientific research. Category: Signaling pathways. CAS No. 326914-10-7. Pack Sizes: 10 mM * 1 mL in DMSO; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-112452.
SU1261
SU1261 is an IKK inhibitor with Ki values of 10 nM and 680 nM for IKKα and IKKβ, respectively. SU1261 can inhibit non-canonical NF-κB signaling in U2OS osteosarcoma cells[1]. Uses: Scientific research. Category: Signaling pathways. CAS No. 3061890-98-7. Pack Sizes: 5 mg; 10 mg; 25 mg. Product ID: HY-169053.
SU14813
SU14813 is a multi-targeted receptor tyrosine kinases inhibitor with IC50s of 50, 2, 4, 15 nM for VEGFR2, VEGFR1, PDGFRβ and KIT. Uses: Scientific research. Category: Signaling pathways. CAS No. 627908-92-3. Pack Sizes: 10 mM * 1 mL in DMSO; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-10501.
SU1498
SU1498 (AG 1498) is a selective inhibitor of the VEGFR2; inhibits Flk-1 with an IC50 of value of 700 nM[1]. Uses: Scientific research. Category: Signaling pathways. Alternative Names: AG 1498; Tyrphostin SU 1498. CAS No. 168835-82-3. Pack Sizes: 10 mM * 1 mL in DMSO; 1 mg; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-19326.
SU 16f
SU 16f. Group: Biochemicals. Grades: Highly Purified. CAS No. 251356-45-3. Pack Sizes: 10mg. US Biological Life Sciences.
Worldwide
SU212
SU212 is a podophyllotoxin-derived ENO1 inhibitor and AMPK activator. SU212 can selectively induce oxidative phosphorylation, reduce glycolysis activity and glucose uptake in tumor cells, and directly bind to ENO1 without affecting these pathways in normal cells. SU212 induces apoptosis and promotes ENO1 degradation via proteasomal and autophagic pathways without inhibiting the catalytic activity. SU212 leads to mitotic arrest and apoptosis in TNBC (triple-negative breast cancer) cells by activating AMPK, demonstrating potent anti-tumor activity in vitro. SU212 inhibits tumor growth and metastasis in syngeneic, xenograft, and diabetic mouse models, exhibiting an excellent safety profile. SU212 can be used in research on t TNBC, diabetes, and fatty liver disease[1][2]. Uses: Scientific research. Category: Signaling pathways. CAS No. 1262219-89-5. Pack Sizes: 10 mM * 1 mL in DMSO; 5 mg; 10 mg; 25 mg. Product ID: HY-179578.
SU 3327
SU 3327. Group: Biochemicals. Grades: Purified. CAS No. 40045-50-9. Pack Sizes: 10mg, 50mg. US Biological Life Sciences.
Worldwide
SU 3327
SU 3327 is a selective inhibitor of c-Jun N-terminal kinase (JNK) (IC50 = 0.7 μM) with selectivity over p38 MAPK and Akt. SU 3327 inhibits the interaction between JNK and JIP (IC50 = 239 nM). Alternative Names: SU 3327; SU3327; SU-3327; 5-[(5-Nitro-2-thiazolyl)thio]-1,3,4thiadiazol-2-amine. Grades: ≥99% by HPLC. CAS No. 40045-50-9. Molecular formula: C5H3N5O2S3. Mole weight: 261.3.
SU 4312
SU 4312. Group: Biochemicals. Grades: Purified. CAS No. 5812-7-7. Pack Sizes: 10mg. US Biological Life Sciences.
Worldwide
SU 4312
SU 4312 is a potent and selective inhibitor of VEGFR and PDGFR tyrosine kinases (IC50 = 0.8 and 19.4 μM, respectively) wirth selectivity over EGFR and c-Src tyrosine kinases. Alternative Names: SU4312; SU-4312; 3-[[4-(dimethylamino)phenyl]methylene]-1,3-dihydro-2H-indol-2-one; 2H-Indol-2-one, 3-[[4-(dimethylamino)phenyl]methylene]-1,3-dihydro-; 2-Indolinone, 3-[p-(dimethylamino)benzylidene]-; 3-(4-Dimethylaminobenzylidenyl)-2-indolinone; 3-[[4-(Dimethylamino)phenyl]methylidene]-2,3-dihydro-1H-indol-2-one; DMBI; NSC 86429. Grades: ≥95%. CAS No. 5812-7-7. Molecular formula: C17H16N2O. Mole weight: 264.33.
SU 4942
SU 4942 is a modulator of tyrosine kinase signal transduction, targeting VEGF and ECGF. Alternative Names: SU 4942; SU-4942; SU4942. 3-(4-Bromobenzylidene)indoline-2-one. CAS No. 76086-99-2. Molecular formula: C15H10BrNO. Mole weight: 300.155.
SU 5201
SU 5201 is an inhibitor of IL-2 production. Alternative Names: (3Z)-3-[(3,4-Dichlorophenyl)methylidene]-1H-indol-2-one; NSC 247030; NSC-247030; NSC247030; SU 5201; SU5201; SU-5201. CAS No. 114727-43-4. Molecular formula: C15H9Cl2NO. Mole weight: 290.143.
SU 5205
SU5205 is a VEGFR2 inhibitor. Alternative Names: 3-(4-fluorobenzylidene)indolin-2-one; SU 5205; SU-5205; SU5205. CAS No. 3476-86-6. Molecular formula: C15H10FNO. Mole weight: 239.249.
SU 5214
SU 5214 is a modulator of tyrosine kinase signal transduction. Alternative Names: SU 5214; SU5214; SU-5214; (3Z)-3-o-Anisylideneoxindole; 3-(2-Methoxy-benzylidene)-3H-indol-2-ol; (3Z)-3-[(2-methoxyphenyl)methylidene]-1H-indol-2-one. CAS No. 186611-04-1. Molecular formula: C16H13NO2. Mole weight: 251.285.
SU5402
SU5402 is a potent and selective vascular endothelial growth factor receptor (VEGFR) and fibroblast growth factor receptor (FGFR) inhibitor. Alternative Names: SU-5402; SU 5402. Grades: 0.98. CAS No. 215543-92-3. Molecular formula: C17H16N2O3. Mole weight: 296.32054.
SU 5402
A potent and selective inhibitor of fibroblast growth factor receptor (FGFR) (IC50 = 0.03uM for FGFR1) and vascular endothelial growth factor receptors (VEGFR) (IC50 = 0.02uM for VEGFR2). In addition, integrin β4-induced differentiation of neural stem cells was attenuated by SU 5402. Group: Biochemicals. Grades: Highly Purified. CAS No. 215543-92-3. Pack Sizes: 500ug. US Biological Life Sciences.
Worldwide
SU 5402
SU 5402 is a potent multi-targeted receptor tyrosine kinase inhibitor with IC50 of 20 nM, 30 nM, and 510 nM for VEGFR2, FGFR1, and PDGFRβ, respectively. Uses: Scientific research. Category: Signaling pathways. CAS No. 215543-92-3. Pack Sizes: 10 mM * 1 mL in DMSO; 1 mg; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-10407.
SU 5402
SU5402 is a potent multi-targeted receptor tyrosine kinase inhibitor with IC50 of 20 nM, 30 nM, and 510 nM for VEGFR2, FGFR1, and PDGF-Rβ, respectively. Group: Inhibitors. CAS No. 215543-92-3. Pack Sizes: 10mg. Product ID: S7667. Formula: C17H16N2O3. Smiles: CC1=CNC(=C1CCC(=O)O)C=C2C3=CC=CC=C3NC2=O. Storage Conditions: 2 years -80 in solvent.
United States; Europe
SU 5402 2-hydroxyethyl ester
SU 5402 2-hydroxyethyl ester. Group: Biochemicals. Alternative Names: 2-[(1,2-Dihydro-2-oxo-3H-indol-3-ylidene)methyl]-4-methyl-1H-pyrrole-3-propanoic acid 2-hydroxyethyl ester. Grades: Highly Purified. CAS No. 258831-78-6. Pack Sizes: 5mg, 10mg, 25mg, 50mg, 100mg. Molecular Formula: C19H20N2O4. US Biological Life Sciences.
Worldwide
SU5408
A potent, selective and cell-permeable inhibitor of VEGFR2 kinase(IC50= 70 nM) with little or no effect against receptors for platelet-derived growth factor, epidermal growth factor, or insulin-like growth factor (IC50 > 100 μM). Alternative Names: SU-5408; SU 5408; SU5408; ethyl 2,4-dimethyl-5-[(2-oxo-1H-indol-3-ylidene)methyl]-1H-pyrrole-3-carboxylate; VEGFR2 Kinase Inhibitor I; IN1018. CAS No. 15966-93-5. Molecular formula: C18H18N2O3. Mole weight: 310.35.
SU 5614
SU4984 is a FLT3 inhibitor that induces growth arrest, apoptosis, and cell cycle arrest in Ba/F3 and AML cell lines expressing a constitutively activated FLT3. It also exhibits inhibitory effects on C-KIT, VEGFR, and PDGFRβ. Alternative Names: SU5614; SU 5614; SU5614; (3Z)-5-chloro-3-[(3,5-dimethyl-1H-pyrrol-2-yl)methylidene]-1H-indol-2-one. CAS No. 1055412-47-9. Molecular formula: C15H13ClN2O. Mole weight: 272.73.
SU6656
SU6656 is a Src family kinases inhibitor with IC50s of 280, 20, 130, 170 nM for Src, Yes, Lyn, and Fyn, respectively. SU6656 inhibits FAK phosphorylation at Y576/577, Y925, Y861 sites. SU6656 also inhibits p-AKT. Uses: Scientific research. Category: Signaling pathways. CAS No. 330161-87-0. Pack Sizes: 10 mM * 1 mL in DMSO; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-B0789.
SU 6668
SU 6668. Group: Biochemicals. Grades: Purified. CAS No. 252916-29-3. Pack Sizes: 10mg, 50mg. US Biological Life Sciences.
Worldwide
SU9516
SU9516 is a potent CDK2 inhibitor, with an IC50 of 22 nM, and also shows inhibitory effects on CDK1 and CDK4, with IC50s of 40, 200 nM, respectively. Uses: Scientific research. Category: Signaling pathways. CAS No. 377090-84-1. Pack Sizes: 10 mM * 1 mL in DMSO; 1 mg; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-18629.
SU 9516
SU 9516. Group: Biochemicals. Grades: Purified. CAS No. 377090-84-1. Pack Sizes: 10mg, 50mg. US Biological Life Sciences.
Worldwide
SUAM-14746
SUAM-14746 is a prolyl oligopeptidase inhibitor that inhibited breast cancer cell growth in a cytostatic manner without inducing lethality. Alternative Names: 3-({4-[2-(E)-Styrylphenoxy]butanoyl}-L-4-hydroxyprolyl)thiazolidine. CAS No. 126898-09-7. Molecular formula: C26H30N2O4S. Mole weight: 466.59.
Suavioside A
Suavioside A is extracted from the leaves of Rubus suavissimus. It has sweet taste and may be used as a sweetener. Alternative Names: 17-(β-D-Glucopyranosyloxy)kaurane-3β,16α-diol. Grades: 98.0%. CAS No. 133740-37-1. Molecular formula: C26H44O8. Mole weight: 484.63.
Subasumstat
Subasumstat (TAK-981) is a first in class and selective inhibitor of the SUMOylation enzymatic cascade, with potential immune-activating and antineoplastic activities[1][2]. Uses: Scientific research. Category: Signaling pathways. Alternative Names: TAK-981. CAS No. 1858276-04-6. Pack Sizes: 10 mM * 1 mL in DMSO; 1 mg; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg; 200 mg; 500 mg. Product ID: HY-111789.
Subasumstat (TAK-981)
Subasumstat (TAK-981) is a novel, selective inhibitor of the SUMOylation enzymatic cascade with potential immune-activating and antineoplastic activities. Group: Inhibitors. CAS No. 1858276-04-6. Pack Sizes: 5mg. Product ID: S8829. Formula: C25H28ClN5O5S2. Smiles: CC1=C(C=C(S1)C(=O)C2=CN=CN=C2NC3CC(C(C3)O)COS(=O)(=O)N)C4C5=C(CCN4)C=CC(=C5)Cl. Storage Conditions: 3 years -20°C powder.
Subconfluentic acid is a depside metabolite from the lichen Haematomma pachycarpum. Alternative Names: 4-Carboxy-3-methoxy-5-pentylphenyl 2-hydroxy-4-methoxy-6-(2-oxopentyl)benzoate. CAS No. 108548-74-9. Molecular formula: C26H32O8. Mole weight: 472.53.
Subdidymic acid
Subdidymic acid is biosynthesized in the North American lichen Cladonia leporina, a representative of the Cladoniaceae. Alternative Names: 2-Dibenzofurancarboxylic acid, 3-hydroxy-7-methoxy-1,9-dipropyl-; 3-hydroxy-7-methoxy-1,9-dipropyldibenzo[b,d]furan-2-carboxylic acid. CAS No. 86820-01-1. Molecular formula: C20H22O5. Mole weight: 342.39.
Subdivaricatic acid
Subdivaricatic acid is a compound from Ramalina americana. CAS No. 132396-93-1. Molecular formula: C19H20O7. Mole weight: 360.36.
Suberect Spatholobus Stem Extract
Suberect Spatholobus Stem Extract. Applications: Used for women health care products, dietary supplements, for irregular menstruation, dysmenorrhea, amenorrhea. Group: Others. Synonyms: Suberect Spatholobus Stem Extract; Spatholobus suberectusDunn. Purity: 5:1 By TLC. Appearance: Brown red fine powder. Storage: 2 years under well storage situation and stored away from direct sun light. Source: Stem. Species: Spatholobus suberectusDunn. Suberect Spatholobus Stem Extract; Spatholobus suberectusDunn; plant extract. Pack: 20KG-25KG/Drum with double plastic bag of foodstuff inside. Cat No: EXTW-091.
Suberic acid
500g Pack Size. Group: Organics, Research Organics & Inorganics. Formula: C8H14O4. CAS No. 505-48-6. Prepack ID 16326556-500g. Molecular Weight 174.19. See USA prepack pricing.
Suberic acid
100g Pack Size. Group: Organics, Research Organics & Inorganics. Formula: C8H14O4. CAS No. 505-48-6. Prepack ID 16326556-100g. Molecular Weight 174.19. See USA prepack pricing.
Suberic acid
Suberic acid (CAS# 505-48-6) is used in the preparation of reduction-sensitive micelles affecting their cellular uptake. This has potential application in delivery of anticancer drugs. It is also used in the fluorescent detection of amidinium-carboxylate and amidinium formation. Alternative Names: octanedioic acid. CAS No. 505-48-6. Molecular formula: C8H14O4. Mole weight: 174.19.
Suberic Acid
Suberic Acid is used in the preparation of reduction-sensitive micelles affecting their cellular uptake. This has potential application in delivery of anticancer drugs. It is also used in the fluorescent detection of amidinium-carboxylate and amidinium formation. Group: Biochemicals. Alternative Names: Octanedioic Acid; Suberic Acid; 1,6-Dicarboxyhexane; 1,6-Hexanedicarboxylic Acid; 1,8-Octanedioic Acid; Cork Acid; Hexa methyl enedicarboxylic Acid; NSC 25952; NSC 53777. Grades: Highly Purified. CAS No. 505-48-6. Pack Sizes: 10g. US Biological Life Sciences.
Suberic acid monomethyl ester. Group: Biochemicals. Grades: Highly Purified. CAS No. 3946-32-5. Pack Sizes: 2g, 5g, 10g, 25g, 50g. Molecular Formula: C9H16O4. US Biological Life Sciences.
Worldwide
Suberic Acid Monomethyl Ester
Suberic Acid Monomethyl Ester. CAS No: 3946-32-5
Sarchem Laboratories New Jersey NJ
Suberic Dihydrazide
White crystalline, 98%. Synonym: Octanedioic dihydrazide. CAS No. 20247-84-1. Pack Sizes: Typically in stock: 5g, 25g. Mole weight: 202.26. MP/BP: M.P. 186-188. Order No: FR-0278.
Suberoylanilide hydroxamic acid b-D-glucuronide is a highly efficacious inhibitor, aiding in studying cancer, with a distinct focus on histone deacetylases (HDACs). Alternative Names: 1-O-[[1,8-Dioxo-8-(phenylamino)octyl]amino]-b-D-Glucopyranuronic acid. CAS No. 863456-50-2. Molecular formula: C20H28N2O9. Mole weight: 440.44.
A potent, selective, cell permeable histone deacetylase inhibitor (HDAC). Displays anti-angiogenic activity by interfering with VEGF signaling in human umbilical vein endothelial cells (HUVECs). Induces differentiation in uman breast cancer cells. Group: Biochemicals. Alternative Names: SAHA; N-Hydroxy-N-phenyloctanediamide; N-Hydroxy-N-phenyloctanediamide; Zolinza; Suberoylanilide-hydroxamic acid, Vorinostat. Grades: Highly Purified. CAS No. 149647-78-9. Pack Sizes: 100mg. US Biological Life Sciences.