Benzamides
N-Methylhippuric acid, 99%, Thermo Scientific™
CAS: 2568-34-5 Molecular Formula: C10H11NO3 Molecular Weight (g/mol): 193.20 MDL Number: MFCD00144940 InChI Key: PKCSYDDSNIJRIX-UHFFFAOYSA-N Synonym: benzoylsarcosine,n-methylhippuric acid,n-benzoyl-n-methylglycine,n-benzoylsarcosine,glycine, n-benzoyl-n-methyl,2-n-methylbenzamido acetic acid,sarcosine, n-benzoyl,2-benzoyl methyl amino acetic acid,chembl66391,2-n-methyl-1-phenylformamido acetic acid PubChem CID: 75728 IUPAC Name: 2-[benzoyl(methyl)amino]acetic acid SMILES: CN(CC(O)=O)C(=O)C1=CC=CC=C1
N-Benzylbenzamide, 99%
CAS: 1485-70-7 Molecular Formula: C14H13NO Molecular Weight (g/mol): 211.26 MDL Number: MFCD00003070 InChI Key: LKQUCICFTHBFAL-UHFFFAOYSA-N Synonym: benzamide, n-phenylmethyl,n-benzyl-benzamide,phenyl-n-benzylcarboxamide,benzoylbenzylamine,n∼1∼-benzylbenzamide,benzamide, n-benzyl,n-phenylmethyl benzamide,acmc-1bx9y,n-benzylbenzamide,lkqucicfthbfal-uhfffaoysa PubChem CID: 73878 IUPAC Name: N-benzylbenzamide SMILES: O=C(NCC1=CC=CC=C1)C1=CC=CC=C1
Anthranilamide, 99+%
CAS: 88-68-6 Molecular Formula: C7H8N2O Molecular Weight (g/mol): 136.15 MDL Number: MFCD00007981 InChI Key: PXBFMLJZNCDSMP-UHFFFAOYSA-N Synonym: anthranilamide,benzamide, 2-amino,o-aminobenzamide,2-carbamoylaniline,aminobenzamide,anthranilimidic acid,benzamide, o-amino,anthranilic acid amide,anthranilamide van,o-aminobenzamide van PubChem CID: 6942 IUPAC Name: 2-aminobenzamide SMILES: C1=CC=C(C(=C1)C(=O)N)N
Sigma Aldrich Fine Chemicals Biosciences Sodium hippurate hydrate >=99% | 532-94-5 | MFCD00149113 | 100G
Sodium hippurate hydrate >=99% | Purity: >=99% | 532-94-5 | MFCD00149113 | 100G
Sigma Aldrich Fine Chemicals Biosciences Sodium hippurate hydrate >=99% | 532-94-5 | MFCD00149113 | 1KG
Sodium hippurate hydrate >=99% | Purity: >=99% | 532-94-5 | MFCD00149113 | 1KG
Sigma Aldrich Fine Chemicals Biosciences Sodium hippurate hydrate >=99% | 532-94-5 | MFCD00149113 | 25G
Sodium hippurate hydrate >=99% | Purity: >=99% | 532-94-5 | MFCD00149113 | 25G
Sigma Aldrich Benzamide
MilliporeSigma Sigma Organics products encompass a wide range of quality reagents, solvents, catalysts, and building blocks for organic synthesis. From benchtop discovery to process development and scale-up, Sigma Organics solutions are built to meet the needs of synthetic chemists.
TARGETMOL CHEMICALS INC CERALASERTIB 10MG
Also available in 1 mg 5 mg 50 mg and bulk. Please contact Fisher for quotes. Ceralasertib (AZD6738) is an orally active and selective ATR kinase inhibitor with IC50 of 1 nM. purity: 99%
TARGETMOL CHEMICALS INC CCG-1423 50MG
Also available in 5 mg 10 mg 25 mg 100 mg 200 mg 500 mg 1 mL 10 mM (in DMSO) and bulk. Please contact Fisher for quotes. CCG-1423 a selective RhoA pathway inhibitor suppresses SRF-mediated transcription. purity: 99%
TARGETMOL CHEMICALS INC NECROSTATIN-1 50MG
Also available in 5 mg 10 mg 25 mg 100 mg 200 mg 500 mg 1 mL 10 mM (in DMSO) and bulk. Please contact Fisher for quotes. Necrostatin-1 (Necrostatin 1) is a specific RIP1 inhibitor and inhibits TNF-(alpha)-induced necroptosis (EC50 490 nM in Jurkat cells). purity: 99%
TARGETMOL CHEMICALS INC SOFOSBUVIR 500MG
Also available in 5 mg 10 mg 50 mg 100 mg 1000 mg 1 mL 10 mM (in DMSO) and bulk. Please contact Fisher for quotes. Sofosbuvir (GS 7977) is a uridine monophosphate analog inhibitor of hepatitis C virus (HCV) polymerase NS5B that is used as an antiviral agent in the treatment of chronic hepatitis C. purity: 99%
TARGETMOL CHEMICALS INC HQNO 25MG
Also available in 5 mg 10 mg 50 mg 100 mg 1 mL 10 mM (in DMSO) and bulk. Please contact Fisher for quotes. HQNO is a natural product isolated from P. aeruginosaand is a potent inhibitor of electron transport chain(Kd of 64 nM for complex III). It also is a potent mitochondrial NDH-2 inhibitorin many species. purity: 99%
TARGETMOL CHEMICALS INC DEMETHYLZEYLASTERAL 25MG
Also available in 5 mg 10 mg 50 mg 100 mg 1 mL 10 mM (in DMSO) and bulk. Please contact Fisher for quotes. Demethylzeylasteral (Demethylzeylasteral (T-96)) has strong immunosuppressive activity can be used in the fields of organ transplantation and autoimmune disorders. The risk of elevated serum concentrations of estradiol due to the inhibition of estradiol glucuronidation by Demethylzeylasteral. Demethylzeylasteral increases both activation and inactivation time constants of Ca(2+) currents can inhibit significantly the sperm acrosome reaction initiated by progesterone. purity: 99%
TARGETMOL CHEMICALS INC CORYLIFOL A 10MG
Also available in 1 mg 5 mg 25 mg 50 mg 100 mg 500 mg 1 mL 10 mM (in DMSO) and bulk. Please contact Fisher for quotes. 1. Corylifol A (Corylinin) displays cytotoxic activity against HepG2 and Hep3B hepatocellular carcinoma cell lines with IC50 values of 4.6 and 13.5 ug/ml respectively. 2. Corylifol A and Biochanin A can be the potential uncouplers of neuronal nitric oxide synthase-postsynaptic density protein-95. 3. Corylifol A and bavachin are strong inhibitors of UDP-glucuronosyltransferase 1A1 (UGT1A1) with the inhibition kinetic parameters (Ki) values lower than 1 uM.4. Corylifol A and bakuchiol are naturally occurring potent inhibitors of hCE2 with low Ki values ranging from 0.62uM to 3.89 uM. 5. Corylifol A shows an inhibitory effect on IL-6-induced STAT3 promoter activity in Hep3B cells with IC50 values of 0.81 ± 0.15 uu it also inhibits STAT3 phosphorylation induced by IL-6 in Hep3B cells suggests that corylifol A has antiinflammatory activity. purity: 99%
TARGETMOL CHEMICALS INC TAFAMIDIS 25MG
Also available in 5 mg 10 mg 50 mg 100 mg 1 mL 10 mM (in DMSO) and bulk. Please contact Fisher for quotes. Tafamidis (Fx-1006A) is a kinetic stabilizer of transthyretin (TTR) that prevents amyloidogenesis by wild-type and mutant TTRs. It binds to TTR with negative cooperativity (Kd1 3 nM; Kd2 278 nM) to stabilize the TTR dimer-dimer interface and inhibit tetrameric dissociation. Tafamidis stabilizes wild-type and clinically significant V30M and V122I mutant TTR amyloidogenic homotetramers (EC50s 2.7-3.2 uM) under fibril-promoting denaturing and physiological conditions in vitro. It stabilizes TTR heterotetramers containing wild-type and mutant subunits ex vivo in human plasma derived from patients carrying V30M or V1221 mutations when used at a concentration of 7.2 uM. Formulations containing tafamidis have been used for the treatment of familial amyloid polyneuropathy. purity: 99%