- Search results for (base)
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1688 products were found matching "(base)"!
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Item number: TGM-T16103-100mg
Description: ML-9 (free base) suppresses MLCK, PKA, and PKC activity (Ki: 4, 32, and 54 µM, respectively). ML-9 (free base) is a selective and effective inhibitor of Akt kinase, inhibits myosin light-chain kinase (MLCK), and stromal interaction molecule 1 (STIM1) activity. ML-9 (free base) causes autophagy by...
CAS | 110448-31-2 |
MW: | 324.83 D |
From 1,520.00€
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Item number: TGM-T28905-100mg
Description: T-611, a cytomegalovirus replication inhibitor, is used potentially for the treatment of cytomegalovirus infections. Target: Others. Smiles: N(=O)(=O)C=1C(=NC(=NC1C)N2[C@@H](C)COCC2)N3C=CN=C3. References: Sullivan C, Liu Y, Shen J, Curtis A, Newman C, Hock JM, Li X. Novel interactions between FOXM1 and...
Keywords: | T-0902611, T-2611, T0902611, T-902611, T2611, T-611 |
CAS | 350595-60-7 |
MW: | 304.3 D |
From 1,520.00€
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Item number: TGM-T26359-50mg
Description: AA 497, a beta-2 agonist, causes relaxation and suppresses Ca spike frequency. Target: Others. Smiles: C(O)C1=C2C([C@H](O)[C@@H](NC(C)C)CC2)=CC=C1O. References: Kimura I, Katoh H, Kimura M. Difference between adrenergic beta 1- and beta 2-blocking effects on isoproterenol-induced Ca spike suppression in...
Keywords: | AA 497, AA-497, AA497 |
CAS | 59605-49-1 |
MW: | 251.32 D |
From 2,272.00€
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Item number: TGM-T36977-5mg
Description: AS-99 is a first-in-class, potent, and selective ASH1L histone methyltransferase inhibitor (IC50= 0.79 µM, Kd= 0.89 µM) with anti-leukemic activity, blocking cell proliferation, inducing apoptosis and differentiation, downregulating MLL fusion target genes, and reducing the leukemia burden in vivo[1]....
CAS | 2323623-93-2 |
MW: | 593.68 D |
872.00€
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Item number: TGM-T68922-100mg
Description: YM543 free base, a potent and orally active sodium-glucose cotransporter (SGLT) 2 inhibitor, effectively reduces blood glucose levels and is suitable for diabetes research. Target: Others. Smiles: O[C@H]1[C@@H](O[C@H](CO)[C@@H](O)[C@@H]1O)C2=CC(CC3=CC=4C(=C3)C=CC=CC4)=CC=C2O
CAS | 655237-16-4 |
MW: | 396.43 D |
From 1,820.00€
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Item number: TGM-T68934-100mg
Description: VT101 is a TEAD Auto-palmitoylation inhibitor that Selectively Inhibit Proliferation and Tumor Growth of NF2-deficient Mesothelioma. VT101 inhibited the firefly luciferase reporter dose-dependently and had no 204 effect on the Renilla luciferase reporter. Target: Others. Smiles:...
CAS | 65194-64-1 |
MW: | 312.38 D |
From 1,520.00€
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Item number: TGM-T71534L-10mg
Description: CIA-1 (Free base) is a nuclear receptor COUP-TFII inhibitor with IC50 values ranging from 1.2 µM to 7.6 µM in prostate cancer cell lines. CIA-1 (Free base) inhibits tumor growth in a mouse model of prostate cancer xenografts. Target: Gamma-secretase. Smiles:...
Keywords: | CIA-1(Free base) |
CAS | 452087-38-6 |
MW: | 329.42 D |
From 52.00€
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Item number: TGM-T68288-100mg
Description: OB-24 free base is a potent and selective heme oxygenase 1 (HO-1) inhibitor. Target: Others. Smiles: C(C1(CCC2=CC=C(Br)C=C2)OCCO1)N3C=CN=C3
CAS | 940061-39-2 |
MW: | 337.21 D |
From 1,520.00€
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Item number: TGM-T8746L-10mg
Description: I-49 free base (Pyrido[4,3-d]pyrimidin-7(6H)-one, 2-methyl-4-[[(1R)-1-[2-methyl-3-(trifluoromethyl)phenyl]ethyl]amino]-6-(tetrahydro-2H-pyran-4-yl)-) is a novel benzylamino substituted pyridopyrimidinone as SOS1 inhibitor. Target: Raf. Smiles:...
Keywords: | I-49, Pyrido[4,3-d]pyrimidin-7(6H)-one,... |
MW: | 482.92 D |
From 133.00€
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Item number: T8601.1
Tris is one of the most widely used buffers in molecular biology and cell culture due to its low toxicity, stability and buffering capacity. Our USP Grade is very similar in specifications to ultrapure Tris (T8600). Purity: >99.0%, Appearance: White, crystalline powder, Solubility (1M): Colorless, clear,...
CAS | 77-86-1 |
MW: | 121.14 D |
From 63.00€
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Item number: FOR-AIMSB0210
Application: | Escherichia coli medium, auto induction medium (AIM) |
From 18.00€
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Item number: TGM-T11290-100mg
Description: FK-448 Free base is a potent and specific chymotrypsin inhibitor, with an IC50 of 720 nM. Target: Others. Smiles: C(OC1=CC=C(C(=O)N2CCN(C(C)C)CC2)C=C1)(=O)C3C=4C(CCC3)=CC=CC4. References: Fujii S, et al. New synthetic inhibitors of chymotrypsin. J Biochem. 1984 Feb,95(2):319-22.
CAS | 85858-76-0 |
MW: | 406.52 D |
From 1,520.00€
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