A directory of where to buy chemicals in the USA, including: distributors, industrial manufacturers, bulk supplies and wholesalers of raw ingredients & finished goods.
Thiophene-3-carbonitrile. Group: Biochemicals. Alternative Names: 3-Cyanothiophene. Grades: Highly Purified. CAS No. 1641-09-4. Pack Sizes: 10g, 25g, 50g, 100g. US Biological Life Sciences.
Worldwide
Thiophene-3-carbonitrile ≥97% (GC)
Thiophene-3-carbonitrile ≥97% (GC). Group: Biochemicals. Grades: GC. Pack Sizes: 1g, 5g, 25g, 100g. US Biological Life Sciences.
Worldwide
Thiophene-3-carboxaldehyde
Thiophene-3-carboxaldehyde. Group: Biochemicals. Alternative Names: Thiophene-3-carbaldehydec. Grades: Highly Purified. CAS No. 498-62-4. Pack Sizes: 50g, 100g, 250g, 500g, 1kg. Molecular Formula: C5H4OS. US Biological Life Sciences.
Worldwide
Thiophene-3-carboxylic acid
Thiophene-3-carboxylic acid is a biochemical reagent that can be used as a biological material or organic compound for life science related research. Uses: Scientific research. Group: Biochemical assay reagents. CAS No. 88-13-1. Pack Sizes: 25 g. Product ID: HY-W004615.
Thiophene-3-carboxylic Acid
Thiophene-3-carboxylic Acid. Uses: For analytical and research use. Group: Impurity standards. CAS No. 88-13-1. IUPAC Name: thiophene-3-carboxylic acid. Molecular Formula: C5H4O2S. Mole Weight: 128.15. Catalog: APS88131. SMILES: OC(=O)c1ccsc1. Format: Neat. Shipping: Room Temperature.
Thiophene-3-carboxylic acid 98+% (HPLC)
Thiophene-3-carboxylic acid 98+% (HPLC). Group: Biochemicals. Grades: Reagent Grade. Pack Sizes: 5g, 25g, 100g, 250g. US Biological Life Sciences.
Thiophene appears as a colorless liquid with an unpleasant odor. Insoluble in water and slightly denser than water. Flash point 30°F. Vapors heavier than air. Irritates the skin, eyes, and mucous membranes. Used to make pharmaceuticals and dyes.;Liquid;COLOURLESS LIQUID WITH PUNGENT ODOUR. Group: Electroluminescence materials. CAS No. 110-02-1. Product ID: thiophene. Molecular formula: 84.14g/mol. Mole weight: C4H4S;SCH=CHCH=CH;C4H4S. C1=CSC=C1. InChI=1S/C4H4S/c1-2-4-5-3-1/h1-4H. YTPLMLYBLZKORZ-UHFFFAOYSA-N.
Thiophenium, 1-[4-(1,1-Dimethylethyl)Phenyl]Tetrahydro-, Salt With 4,4,5,5,6,6-Hexafluorodihydro-4H-1,3,2-Dithiazine 1,1,3,3-Tetraoxide
Heterocyclic Organic Compound. CAS No. 1224-63-1. Catalog: ACM1224631.
Thiophosphoryl chloride
100g Pack Size. Group: Building Blocks, Inorganic Chemicals, Salts. Formula: Cl3PS. CAS No. 3982-91-0. Prepack ID 75254135-100g. Molecular Weight 169.4. See USA prepack pricing.
Thiophthalazone. Group: Biochemicals. Grades: Highly Purified. Pack Sizes: 1g. US Biological Life Sciences.
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Thioproperazine
Thioproperazine is a potent neuroleptic with antipsychotic properties, for the treatment of all types of acute and chronic schizophrenia, including those which did not respond to the usual neuroleptics; manic syndromes. Uses: Antipsychotic. Synonyms: Sulfenazin; N,N-dimethyl-10-[3-(4-methylpiperazin-1-yl)propyl]phenothiazine-2-sulfonamide. Grades: ≥98%. CAS No. 316-81-4. Molecular formula: C22H30N4O2S2. Mole weight: 446.63.
Thioproperazine
Thioproperazine (RP 7843) is an orally active antipsychotic agent with calming, antiemetic activity. Thioproperazine is effective in promoting the release of dopamine in rat striatum. Thioproperazine can be used in studies of schizophrenia and bipolar disorder [1]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: RP 7843; SKF 5883; Thioperazine. CAS No. 316-81-4. Pack Sizes: 5 mg; 10 mg. Product ID: HY-A0151.
Thioproperazine difumarate
Heterocyclic Organic Compound. Alternative Names: N,N-Dimethyl-10-[3-(4-methyl-1-piperazinyl)propyl]-. CAS No. 123937-18-8. Molecular formula: C30H38N4O10S2. Mole weight: 678.77. Purity: 0.96. Catalog: ACM123937188.
Thioproperazine difumarate
Thioproperazine difumarate. Group: Biochemicals. Alternative Names: N, N-Dimethyl-10-[3- (4-methylpiperazin-1-yl) propyl]phenothiazine-2-sulfonamide. Grades: Highly Purified. CAS No. 123937-18-8. Pack Sizes: 5mg, 10mg, 25mg, 50mg, 100mg. Molecular Formula: C30H38N4O10S2. US Biological Life Sciences.
Worldwide
thiopurine S-methyltransferase
Also acts, more slowly, on thiopyrimidines and aromatic thiols. Not identical with EC 2.1.1.9 thiol S-methyltransferase. Group: Enzymes. Synonyms: mercaptopurine methyltransferase; thiopurine methyltransferase; 6-thiopurine transmethylase; TPMT. Enzyme Commission Number: EC 2.1.1.67. CAS No. 67339-09-7. 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-1968; thiopurine S-methyltransferase; EC 2.1.1.67; 67339-09-7; mercaptopurine methyltransferase; thiopurine methyltransferase; 6-thiopurine transmethylase; TPMT. Cat No: EXWM-1968.
Thioquinapiperifil
Thioquinapiperifil is a phosphodiesterase-5 (PDE-5) inhibitor used as a dietary supplement. Synonyms: KF-31327; KF 31327; KF31327; 3-ethyl-8-[[2-[4-(hydroxymethyl)piperidin-1-yl]phenyl]methylamino]-1H-imidazo[4,5-g]quinazoline-2-thione. Grades: > 95%. CAS No. 220060-39-9. Molecular formula: C24H28N6OS. Mole weight: 448.589.
A flavoprotein (FAD). Group: Enzymes. Synonyms: NADP-thioredoxin reductase; NADPH-thioredoxin reductase; thioredoxin reductase (NADPH); NADPH2:oxidized thioredoxin oxidoreductase. Enzyme Commission Number: EC 1.8.1.9. CAS No. 9074-14-0. TrxR. 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-1653; thioredoxin-disulfide reductase; EC 1.8.1.9; 9074-14-0; NADP-thioredoxin reductase; NADPH-thioredoxin reductase; thioredoxin reductase (NADPH); NADPH2:oxidized thioredoxin oxidoreductase. Cat No: EXWM-1653.
Thioredoxin reductase
Thioredoxin reductase (TrxR) is a biochemical reagent that can be used as a biological material or organic compound for life science related research. Uses: Scientific research. Group: Signaling pathways. Alternative Names: TrxR. CAS No. 9074-14-0. Pack Sizes: 50 μg. Product ID: HY-P2759.
Thioredoxin Reductase (NADPH) from Yeast, Recombinant
Thioredoxin reductase (TrxR/NTR), an enzyme belonging to the flavoprotein family of pyridine nucleotide-disulfide oxidoreductases. Thioredoxin reductase (TrxR), a component of the thioredoxin system, including thioredoxin (Trx) and NADPH, catalyzes the transfer of electrons from NADPH to Trx, acts as a reductant of disulfide-containing proteins and participates in the defense system against oxidative stresses. Thioredoxin reductase (nadph) yeast recombinant produced in e. coli is a single, nonglycosylated, polypeptide chain having a molecular mass of 36 kda. thioredoxin reductase is purified by proprietary chromatographic techniques. Group: Enzymes. Synonyms: NADP-thioredoxin reductase; NADPH-thioredoxin reductase; thioredoxin reductase (NADPH); NADPH. CAS No. 9074-14-0. Purity: Greater than 98.0% as determined by (a) Analysis by RP-HPLC. (b) Analysis by SDS-PAGE. TrxR. Mole weight: 36 kDa. Activity: 5 IU/mg. Stability: NTR although stable at 4°C for 3 weeks, should be stored desiccated below -18°C. Please prevent freeze thaw cycles. Appearance: Sterile Filtered White lyophilized (freeze-dried) powder. Source: E. coli. Species: Yeast. NADP-thioredoxin reductase; NADPH-thioredoxin reductase; thioredoxin reductase (NADPH); NADPH2:oxidized thioredoxin oxidoreductase; thioredoxin-disulfide reductase; NTR; TrxR. Cat No: NATE-0917.
Thioredoxin reductase peptide acetate
Thioredoxin reductase peptide acetate, derived from residues 53-67 in thioredoxin reductase (TrxR), is widely used in research on thioredoxin reductase. Synonyms: L-Tryptophylglycyl-L-leucylglycylglycyl-L-threonyl-L-cysteinyl-L-valyl-L-asparaginyl-L-valylglycyl-L-cysteinyl-L-isoleucyl-L-prolyl-L-lysine acetate salt; Trp-Gly-Leu-Gly-Gly-Thr-Cys-Val-Asn-Val-Gly-Cys-Ile-Pro-Lys acetate salt. Grades: ≥95%. Molecular formula: C68H110N18O20S2. Mole weight: 1563.84.
Thioridazine
Thioridazine is an inhibitor of CYP1A2 and CYP3A2. It is a piperidine typical antipsychotic drug belonging to the phenothiazine drug group and was previously widely used in the treatment of schizophrenia and psychosis. It was developed by Novartis and has been listed, but it was withdrawn worldwide in 2005 because it caused severe cardiac arrhythmias, however, generic versions are available in the US. Uses: Thioridazine was previously widely used in the treatment of schizophrenia and psychosis. Synonyms: 10-((1-Methyl-2-piperidyl)ethyl)-2-(methylthio)-phenothiazin;10-(2-(1-Methyl-2-piperidyl)ethyl)-2-(methylthio)phenothiazine;10H-Phenothiazine, 10-[2-(1-methyl-2-piperidinyl)ethyl]-2-(methylthio)-; Meleril; Mellaril; Melleril; Sonapax; Aldazine. Grades: 98%. CAS No. 50-52-2. Molecular formula: C21H26N2S2. Mole weight: 370.57.
Thioridazine
Thioridazine, an antagonist of the dopamine receptor D2 family proteins, exhibits potent anti-psychotic and anti-anxiety activities. Thioridazine is also a potent inhibitor of PI3K-Akt-mTOR signaling pathways with anti-angiogenic effect. Thioridazine shows antiproliferative and apoptosis induction effects in various types of cancer cells, with specificity on targeting cancer stem cells (CSCs) [1] [2] [3] [4]. Uses: Scientific research. Group: Signaling pathways. CAS No. 50-52-2. Pack Sizes: 5 mg; 10 mg; 25 mg; 50 mg; 100 mg; 200 mg. Product ID: HY-B0965A.
Thioridazine 2-Sulfone
A major metabolite of Thioridazine (THD 2-SO2).ImThioridazine EP Impurity E. Group: Biochemicals. Alternative Names: 10-[2-(1-Methyl-2-piperidinyl)ethyl]-2-(methylsulfonyl)-10H-phenothiazine; (+/-)-Thioridazine-2-sulfone; Imagotan; Inofal; Psychoson; Sulforidazine; Sulphoridazine; TPN 12; Thioridazine-2-sulfone; Thioridazine EP Impurity E. Grades: Highly Purified. CAS No. 14759-06-9. Pack Sizes: 5mg. Molecular Formula: C??H??N?O?S?, Molecular Weight: 402.57. US Biological Life Sciences.
Worldwide
Thioridazine 2-Sulfone
Thioridazine 2-Sulfone. Uses: For analytical and research use. Group: Impurity standards. CAS No. 14759-06-9. Pack Sizes: 5MG. Molecular Formula: C21H26N2O2S2. Mole Weight: 402.57. Catalog: APS14759069. Format: Neat. Shipping: Room Temperature.
Thioridazine 5-Sulfoxide (Mixture of Diastereomers)
Thioridazine 5-Sulfoxide (Mixture of Diastereomers). Uses: For analytical and research use. Group: Impurity standards. CAS No. 7776-5-8. Pack Sizes: 5MG. IUPAC Name: 10-[2-(1-methylpiperidin-2-yl)ethyl]-2-methylsulfanylphenothiazine 5-oxide. Molecular Formula: C21H26N2OS2. Mole Weight: 386.57. Catalog: APS7776058A. SMILES: CSc1ccc2c (c1)N (CCC3CCCCN3C)c4ccccc4S2=O. Format: Neat. Shipping: Room Temperature.
Thioridazine 5-Sulfoxide (Mixture of Diastereomers)
A major metabolite of Thioridazine (THD-5-SO). Group: Biochemicals. Alternative Names: 10-[2-(1-Methyl-2-piperidinyl)ethyl]-2-(methylthio)-10H-phenothiazine. Grades: Highly Purified. CAS No. 7776-5-8. Pack Sizes: 5mg. US Biological Life Sciences.
Worldwide
Thioridazine-d3 5-Sulfoxide
A labeled metabolite of Thioridazine (THD-5-SO). Group: Biochemicals. Alternative Names: 10-[2-(1-Methyl-2-piperidinyl)ethyl]-2-(methylthio)-10H-phenothiazine. Grades: Highly Purified. CAS No. 1330076-56-6. Pack Sizes: 1mg. US Biological Life Sciences.
Dopamine receptor blocker; parent compound of sulforidazine and mesoridazine. Antipsychotic. Group: Biochemicals. Alternative Names: 10-[2-(1-Methyl-d3-2-piperidinyl)ethyl]-2-(methylthio)-10H-phenothiazine Hydrochloride; 2-Methylmercapto-10-[2-(N-methyl-d3-2-piperidyl)ethyl]pheno-thiazine Hydrochloride. Grades: Highly Purified. CAS No. 1189928-36-6. Pack Sizes: 1mg. US Biological Life Sciences.
Worldwide
Thioridazine hydrochloride
Thioridazine hydrochloride, an orally active antagonist of the dopamine receptor D2 family proteins, exhibits potent anti-psychotic and anti-anxiety activities. Thioridazine hydrochloride is also a potent inhibitor of PI3K-Akt-mTOR signaling pathways with anti-angiogenic effect. Thioridazine hydrochloride shows antiproliferative and apoptosis induction effects in various types of cancer cells, with specificity on targeting cancer stem cells (CSCs) [1] [2] [3] [4]. Uses: Scientific research. Group: Signaling pathways. CAS No. 130-61-0. Pack Sizes: 10 mM * 1 mL; 100 mg; 500 mg. Product ID: HY-B0965.
Thioridazine hydrochloride
Thioridazine hydrochloride, an orally active antagonist of the dopamine receptor D2 family proteins, exhibits potent anti-psychotic and anti-anxiety activities. Thioridazine hydrochloride is also a potent inhibitor of PI3K-Akt-mTOR signaling pathways with anti-angiogenic effect. Thioridazine hydrochloride shows antiproliferative and apoptosis induction effects in various types of cancer cells, with specificity on targeting cancer stem cells (CSCs). Group: Inhibitors. CAS No. 130-61-0. Molecular formula: C21H26N2S2.HCl. Mole weight: 407.03. Purity: >99 %. Catalog: ACM130610.
Thioridazine hydrochloride
Thioridazine hydrochloride is a dopamine receptor antagonist displaying antipsychotic activity. Thioridazine induces apoptosis via targeting the PI 3-K/Akt/mTOR/p70 S6K pathway, and induces G1 cell cycle arrest. Thioridazine exhibits anticancer activity in cervical, endometrial and breast cancer cells. Synonyms: 10-[2-(1-Methyl-2-piperidinyl)ethyl]-2-(methylthio)-10H-phenothiazine hydrochloride; Thioridazine HCl; Sonapax hydrochloride; Thioridazine chloride; Mellaril hydrochloride; 10H-Phenothiazine, 10-[2-(1-methyl-2-piperidinyl)ethyl]-2-(methylthio)-, hydrochloride (1:1); 10H-Phenothiazine, 10-[2-(1-methyl-2-piperidinyl)ethyl]-2-(methylthio)-, monohydrochloride; Phenothiazine, 10-[2-(1-methyl-2-piperidyl)ethyl]-2-(methylthio)-, hydrochloride; Phenothiazine, 10-[2-(1-methyl-2-piperidyl)ethyl]-2-(methylthio)-, monohydrochloride; 10-[2-(1-Methylpiperidin-2-yl)ethyl]-2-(methylsulfanyl)-10H-phenothiazine hydrochloride; 2-Methylmercapto-10-[2-(N-methyl-2-piperidyl)ethyl]phenothiazine hydrochloride; Aldazine; Mallorol; Melleretten; Melleril; Melleril (tablet); Novoridazine; NSC 186060; Orsanil; Ridazin; Stalleril; Thioril; Thiozine. Grades: ≥99% by HPLC. CAS No. 130-61-0. Molecular formula: C21H26N2S2.HCl. Mole weight: 407.04.
Thioridazine Hydrochloride
Thioridazine HCl is a dopamine receptor blocker and antipsychotic. It is the parent compound of sulforidazine and mesoridazine. Group: Biochemicals. Alternative Names: 10-[2-(1-Methyl-2-piperidinyl)ethyl]-2-(methylthio)-10H-phenothiazine Hydrochloride; 2-Methylmercapto-10-[2- (N-methyl-2-piperidyl) ethyl]phenothiazine Hydrochloride; Aldazine; Mellaril; Orsanil; Ridazin; Stalleril. Grades: Highly Purified. CAS No. 130-61-0. Pack Sizes: 2.5g. US Biological Life Sciences.
Worldwide
Thiorphan
Thiorphan is a selective NEP (neprilysin) inhibitor with an IC 50 of 6.9 nM [1]. Uses: Scientific research. Group: Signaling pathways. CAS No. 76721-89-6. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg. Product ID: HY-W013375.
Thiorphan
Thiorphan. Group: Biochemicals. Alternative Names: N-[2-(Mercaptomethyl)-1-oxo-3-phenylpropyl]glycine; 2-Mercapto methyl -3-phenyl propionyl aminoacetic acid; D, L-3-Mercapto-2-benzyl propanoyl glycine. Grades: Highly Purified. CAS No. 76721-89-6. Pack Sizes: 25mg, 50mg, 100mg, 250mg, 500mg. Molecular Formula: C12H15NO3S. US Biological Life Sciences.
Worldwide
Thiorphan
Thiorphan is a potent and specific enkephalinase inhibitor with antinociceptive activity. Uses: Protease inhibitors. Synonyms: N-[2-(Mercaptomethyl)-1-oxo-3-phenylpropyl]glycine; 2-Mercaptomethyl-3-phenylpropionylaminoacetic Acid; D,L-3-Mercapto-2-benzylpropanoylglycine; (+/-)-Thiorphan. Grades: > 95%. CAS No. 76721-89-6. Molecular formula: C12H15NO3S. Mole weight: 253.32.
An Enkephalinase inhibitor. Group: Biochemicals. Alternative Names: 2-Mercaptomethyl-3-phenyl-propionylamino-acetic Acid, D, L-3-Mercapto-2-benzyl propanoyl glycine. Grades: Highly Purified. Pack Sizes: 25mg. US Biological Life Sciences.
Worldwide
Thiorphan-methoxyacetophenone
A metabolite of Thiorphan which can be produced in vivo via the metabolism of the prodrug acetorphan. Grades: > 95%. Molecular formula: C21H23NO5S. Mole weight: 401.49.
Thiorphan Methoxyacetophenone Derivative Dicyclohexylamine Salt
Thiorphan derivative. Group: Biochemicals. Alternative Names: N-[2-[[[2-(3-Methoxyphenyl)-2-oxoethyl]thio]methyl]-1-oxo-3-phenylpropyl]glycine Dicyclohexylamine. Grades: Highly Purified. Pack Sizes: 2.5mg. US Biological Life Sciences.
Thiorphan derivative. Group: Biochemicals. Alternative Names: N-[2-[[[2-(3-Methoxyphenyl)-2-oxoethyl]thio]methyl]-1-oxo-3-phenylpropyl]glycine Dicyclohexylamine Ethyl Ester. Grades: Highly Purified. Pack Sizes: 10mg. US Biological Life Sciences.
Worldwide
Thio salicylic acid
Thio salicylic acid. CAS No: 147-93-3
Sarchem Laboratories New Jersey NJ
Thiosalicylic acid
Thiosalicylic acid is an organosulfur compound containing carboxyl and sulfhydryl functional groups. Its molecular formula is C6H4(SH)(CO2H). it is a yellow solid that is slightly soluble in water, ethanol and diethyl ether, and alkanes, but more soluble in DMSO. Group: Heterocyclic organic compound. Alternative Names: 2-Mercaptobenzoic acid. CAS No. 147-93-3. Molecular formula: C7H6O2S. Mole weight: 154.19. Appearance: Pale yellow powder. Purity: 0.99. IUPACName: 2-sulfanylbenzoic acid. Canonical SMILES: C1=CC=C(C(=C1)C(=O)O)S. Density: 1.49g/ml. ECNumber: 205-704-3. Catalog: ACM147933.
Thiosemicarbazide. Group: Biochemicals. Grades: Highly Purified. CAS No. 79-19-6. Pack Sizes: 25g, 50g, 100g, 250g, 500g. Molecular Formula: CH5N3S. US Biological Life Sciences.
Worldwide
Thiosemicarbazide
Thiosemicarbazide is a vitamin B6 antagonist with anti-acne activity. Thiosemicarbazide is also a well-known source in the synthesis of heterocycles, and its derivatives have potential anticancer activity. Thiosemicarbazide (TSC: HL1) reacts with metal salts, urea (U), to prepare Co(II) and Cu(I) metal complexes. Thiosemicarbazide is also used in the fields of media communications and optical storage, and in the spectrophotometric detection of metals [1] [2] [3] [1] [2] [3]. Uses: Scientific research. Group: Signaling pathways. CAS No. 79-19-6. Pack Sizes: 10 mM * 1 mL; 5 g. Product ID: HY-Y0032.
Thiosemicarbazide
Thiosemicarbazide is well-known source in heterocyclic synthesis. Thiosemicarbazide has also been utilized for spectrophotometric detection of metals, gadget applications with respect to media communications and optical storage. Thiosemicarbazide shows anti-orthopoxvirus activity. Group: Inhibitors. CAS No. 79-19-6. Molecular formula: CH5N3S. Mole weight: 91.13. Appearance: Solid. Purity: MP 180-181deg dec. Canonical SMILES: NNC(N)=S. Catalog: ACM79196.
Thiosemicarbazide hydrochloride
Thiosemicarbazide hydrochloride. Group: Biochemicals. Grades: Highly Purified. CAS No. 4346-94-5. Pack Sizes: 10g, 25g, 50g, 100g, 250g. Molecular Formula: CH5N3SHCl. US Biological Life Sciences.
Worldwide
Thiosildenafil
An analog of Sildenafil; a novel pyrazolopyrimidinethio nes as PDE5 inhibitor. Group: Biochemicals. Alternative Names: 5-[2-Ethoxy-5-[ (4-methyl-1-piperazinyl) sulfonyl]phenyl]-1, 6-dihydro-1-methyl-3-propyl-. Grades: Highly Purified. CAS No. 479073-79-5. Pack Sizes: 10mg. US Biological Life Sciences.
Worldwide
Thiosildenafil
Cas No. 479073-79-5.
Thiosophorose
Thiosophorose, distinguished as a notable compound, holds immense recognition in the realm of biomedicine due to its profound potential as an efficacious antiviral agent. Its application in inhibiting the proliferation and replication of specific viruses, including Influenza A and HIV, has proven remarkably encouraging. Moreover, Thiosophorose exhibits invaluable prospects in the continuum of targeted therapeutic measures against viral infections, thereby presenting novel avenues for treatment in the dynamic domain of the biomedical industry. Synonyms: 2-S-b-D-Glucopyranosyl-2-thiol-D-glucopyranose. CAS No. 92051-25-7. Molecular formula: C12H22O10S. Mole weight: 358.4.
Thiostrepton
Natural antibiotic derived from Streptomyces. Group: Biochemicals. Grades: Highly Purified. CAS No. 1393-48-2. Pack Sizes: 10mg, 100mg, 500mg, 1g, 2.5g. US Biological Life Sciences.
Worldwide
Thiostrepton
Thiostrepton is a thiazole antibiotic which selectively inhibits FOXM1. FOXM1 binds to YAP/TEAD complex. YAP/TEAD/FOXM1 complex binding at regulatory regions of genes governing cell cycle may impact cell proliferation [1]. Uses: Scientific research. Group: Peptides. CAS No. 1393-48-2. Pack Sizes: 50 mg. Product ID: HY-B0990.
Thiostrepton
Thiostrepton, a kind of natural peptide thiazole antibiotic, has been found to be effective in restraining the protein synthesis and could also influence the cell cycle and lead to apoptosis in breast cancer cells. It is also resistant to gram-positive bacteria and mycobacteria. Uses: Thiostrepton is a kind of natural peptide thiazole antibiotic that has been found to be effective in restraining the protein synthesis and could also influence the cell cycle and leat to apoptosis in breast cancer cells. Synonyms: Bryamycin; Thiactin. Grades: 98%. CAS No. 1393-48-2. Molecular formula: C72H85N19O18S5. Mole weight: 1664.9.
Thiostrepton (Bryamycin, Thiactin, Alaninamide, Antibiotic X 146, Antibiotic A 8506, Antibiotic 6761-31)
Thiostrepton is a macrocyclic antibiotic incorporating thiazoles and other atypical amino acids. Patented in 1961, thiostrepton has been used as an antibiotic and acts by binding to ribosomes to prevent the binding of the EF-G elongation factor and GTP to the 50S riobsomal subunit. Thiostrepton is an inducer of tipA, a gene that controls the bacterial transcription regulators, TipAL and TipAS, members of the MerR proteins that are central regulators in multidrug resistance. Closely related to siomycin, a recently discovered inhibitor of oncogenic transcription factor-FoxM1. Group: Biochemicals. Alternative Names: Bryamycin, Thiactin, Alaninamide, Antibiotic X 146, Antibiotic A 8506, Antibiotic 6761-31. Grades: Highly Purified. CAS No. 1393-48-2. Pack Sizes: 5mg. US Biological Life Sciences.
Worldwide
thiosulfate dehydrogenase
This enzyme belongs to the family of oxidoreductases, specifically those acting on a sulfur group of donors with a cytochrome as acceptor. Group: Enzymes. Synonyms: tetrathionate synthase; thiosulfate oxidase; thiosulfate-oxidizing enzyme; thiosulfate-acceptor oxidoreductase. Enzyme Commission Number: EC 1.8.2.2. CAS No. 9076-88-4. 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-1655; thiosulfate dehydrogenase; EC 1.8.2.2; 9076-88-4; tetrathionate synthase; thiosulfate oxidase; thiosulfate-oxidizing enzyme; thiosulfate-acceptor oxidoreductase. Cat No: EXWM-1655.
thiosulfate dehydrogenase (quinone)
The reaction can also proceed with ferricyanide as the electron acceptor, but more slowly. Unlike EC 1.8.2.2, thiosulfate dehydrogenase, this enzyme cannot utilize cytochrome c as an acceptor. Group: Enzymes. Synonyms: thiosulfate:quinone oxidoreductase; thiosulphate:quinone oxidoreductase; thiosulfate oxidoreductase, tetrathionate-forming; TQO. Enzyme Commission Number: EC 1.8.5.2. 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-1677; thiosulfate dehydrogenase (quinone); EC 1.8.5.2; thiosulfate:quinone oxidoreductase; thiosulphate:quinone oxidoreductase; thiosulfate oxidoreductase, tetrathionate-forming; TQO. Cat No: EXWM-1677.
thiosulfate-dithiol sulfurtransferase
The enzyme from Chlorella shows very little activity towards monothiols such as glutathione and cysteine (cf. EC 2.8.1.3 thiosulfate-thiolsulfurtransferase). The enzyme probably transfers the sulfur atom onto one thiol group to form -S-S-, and sulfide is spontaneously expelled from this by reaction with the other thiol group. May be identical with EC 2.8.1.1 thiosulfate sulfurtransferase. Group: Enzymes. Synonyms: thiosulfate reductase; TSR. Enzyme Commission Number: EC 2.8.1.5. CAS No. 9059-49-8. 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-3363; thiosulfate-dithiol sulfurtransferase; EC 2.8.1.5; 9059-49-8; thiosulfate reductase; TSR. Cat No: EXWM-3363.
thiosulfate sulfurtransferase
A few other sulfur compounds can act as donors. Group: Enzymes. Synonyms: thiosulfate cyanide transsulfurase; thiosulfate thiotransferase; rhodanese; rhodanase. Enzyme Commission Number: EC 2.8.1.1. CAS No. 9026-4-4. RHOD. 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-3354; thiosulfate sulfurtransferase; EC 2.8.1.1; 9026-04-4; thiosulfate cyanide transsulfurase; thiosulfate thiotransferase; rhodanese; rhodanase. Cat No: EXWM-3354.
thiosulfate-thiol sulfurtransferase
The primary product is glutathione hydrodisulfide, which reacts with glutathione to give glutathione disulfide and sulfide. L-Cysteine can also act as acceptor. Group: Enzymes. Synonyms: glutathione-dependent thiosulfate reductase; sulfane reductase; sulfane sulfurtransferase. Enzyme Commission Number: EC 2.8.1.3. CAS No. 111070-24-7. 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-3361; thiosulfate-thiol sulfurtransferase; EC 2.8.1.3; 111070-24-7; glutathione-dependent thiosulfate reductase; sulfane reductase; sulfane sulfurtransferase. Cat No: EXWM-3361.