VD/VDR-vd-vdr.com

SU11274 is a highly specific inhibitor of c-Met , with in vitro IC50 for the Met enzyme at 0.012 ¦Ìmol/L. The inhibitor did not affect other tyrosine kinase oncoproteins, including BCR-ABL, TEL-JAK2, TEL-PDGF_R, or TEL-ABL. Inhibition of the Met kinase activity by SU11274 led to time- and dose-dependent reduced cell growth.

June 21, 2017

prudect name : SU11274 is a highly specific inhibitor of c-Met , with in vitro IC50 for the Met enzyme at 0.012 ¦Ìmol/L. The inhibitor did not affect other tyrosine…

📌

0💬 read more

prudect name : SU11272Synonyms: CAS NO: NOMolecular Formula: Molecular Weight: Purity: 98% minSolubility: Storage: −20°C

prudect name : SU11272 Synonyms: CAS NO: NOMolecular Formula: Molecular Weight: Purity: 98% minSolubility: Storage: −20°C web site: www.medchemexpress.com

📌

0💬 read more

Sitafloxacin is a new-generation, broad-spectrum oral fluoroquinolone antibiotic.It is very active against many Gram-positive, Gram-negative and anaerobic clinical isolates, including strains resistant to other fluoroquinolones, was recently approved in Japan for the treatment of respiratory and urinary tract infections. Sitafloxacin is active against methicillin-resistant staphylococci, Streptococcus pneumoniae and other streptococci with reduced susceptibility to levofloxacin and other quinolones and enterococci

prudect name : Sitafloxacin is a new-generation, broad-spectrum oral fluoroquinolone antibiotic.It is very active against many Gram-positive, Gram-negative and anaerobic clinical isolates, including strains resistant to other fluoroquinolones, was recently…

📌

0💬 read more

Skf 38393 Hydrochloride; Skf 38393A; ()-1-Phenyl-2,3,4,5-Tetrahydro-(1H)-3-Benzazepine-7,8-Diol Hydrochloride

prudect name : Skf 38393 Hydrochloride; Skf 38393A; ()-1-Phenyl-2,3,4,5-Tetrahydro-(1H)-3-Benzazepine-7,8-Diol HydrochlorideSKF 38393 hydrochloride Synonyms: CAS NO: 62717-42-4Molecular Formula: C16H18ClNO2Molecular Weight: 291.78Purity: 98% minSolubility: DMSOStorage: -20¡æ web site: www.medchemexpress.com

📌

0💬 read more

(5S)-Methyl 5-C-[4-chloro-3-[(4-ethoxyphenyl)methyl]phenyl]-1-thio-beta-L-xylopyranoside

prudect name : (5S)-Methyl 5-C-[4-chloro-3-[(4-ethoxyphenyl)methyl]phenyl]-1-thio-beta-L-xylopyranosideSotagliflozin;LP 802034; LX 4211 Synonyms: CAS NO: 1018899-04-1Molecular Formula: C21H25ClO5SMolecular Weight: 424.94Purity: 98% minSolubility: In DMSOStorage: -20 oC web site: www.medchemexpress.com

📌

0💬 read more

prudect name : sitafloxacin isomer III(RRS)Synonyms: CAS NO: 127254-10-8Molecular Formula: C19H18CIF2N3O3Molecular Weight: 409.81Purity: ≥97%Solubility: Storage:

prudect name : sitafloxacin isomer III(RRS) Synonyms: CAS NO: 127254-10-8Molecular Formula: C19H18CIF2N3O3Molecular Weight: 409.81Purity: ≥97%Solubility: Storage: −20°C 2 years web site: www.medchemexpress.com

📌

0💬 read more

prudect name : sitafloxacin isomer I(SSR)Synonyms: CAS NO: 127254-11-9Molecular Formula: C19H18CIF2N3O3Molecular Weight: 409.81Purity: ≥97%Solubility: Storage:

prudect name : sitafloxacin isomer I(SSR) Synonyms: CAS NO: 127254-11-9Molecular Formula: C19H18CIF2N3O3Molecular Weight: 409.81Purity: ≥97%Solubility: Storage: −20°C 2 years web site: www.medchemexpress.com

📌

0💬 read more

SP600125 is a broad-spectrum JNK inhibitor for JNK1, JNK2 and JNK3 with IC50 of 40 nM, 40 nM and 90 nM, respectively; 10-fold greater selectivity against MKK4, 25-fold greater selectivity against MKK3, MKK6, PKB, and PKC¦Á, and 100-fold selectivity against ERK2, p38, Chk1, EGFR etc

prudect name : SP600125 is a broad-spectrum JNK inhibitor for JNK1, JNK2 and JNK3 with IC50 of 40 nM, 40 nM and 90 nM, respectively; 10-fold greater selectivity against MKK4,…

📌

0💬 read more

SCR7 is a molecule that inhibits joining of DSBs in cell-free repair system; inhibits NHEJ(nonhomologous end-joining) in a Ligase IV-dependent manner within cells, and activates the intrinsic apoptotic pathway.

prudect name : SCR7 is a molecule that inhibits joining of DSBs in cell-free repair system; inhibits NHEJ(nonhomologous end-joining) in a Ligase IV-dependent manner within cells, and activates the intrinsic…

📌

0💬 read more

SB-743921 is a second generation, highly potent and active KSP inhibitor with Ki of 0.1 nM; no affinity to MKLP1, Kin2, Kif1A, Kif15, KHC, Kif4 and CENP-E.

prudect name : SB-743921 is a second generation, highly potent and active KSP inhibitor with Ki of 0.1 nM; no affinity to MKLP1, Kin2, Kif1A, Kif15, KHC, Kif4 and CENP-E.SB…

📌

0💬 read more