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Filtered Search Results
Medchemexpress LLC HY-76299 50mg Medchemexpress, Galanthamine CAS:357-70-0 Purity:>98%
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Medchemexpress, HY-76299 50mg Galanthamine CAS:357-70-0 Galanthamine is a potent acetylcholinesterase (AChE) inhibitor with an IC50 of 500 nM. Purity:>98% Medchemexpress has over 10000 novel life-science reagents, reference compounds, APIs and natural compounds for laboratory and scientific use. Other quantity can also be offered.
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eMolecules 131631-89-5 | Medchem Express | Fuscoside | 5mg | 446264895 | HY-15009 | MFCD00903893 | 449.551 | C26H31N3O4
Pharmablock | 3-bromo-5678-tetrahydroimidazo[12-a]pyridine | 25mg | 788493850 | PBAH082 | 156817-72-0 | MFCD08751337 | 201.067 | C7H9BrN2
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Medchemexpress LLC HY-19544 5mg Medchemexpress, JAK3-IN-1 CAS:1805787-93-2 Purity:>98%
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Medchemexpress, HY-19544 5mg JAK3-IN-1 CAS:1805787-93-2 JAK3-IN-1 is a potent, selective and orally active JAK3 inhibitor with an IC50 of 4.8 nM. JAK3-IN-1 shows over 180-fold more selective for JAK3 than JAK1 (IC50 of 896 nM) and JAK2 (IC50 of 1050 nM). Purity:>98% Medchemexpress has over 10000 novel life-science reagents, reference compounds, APIs and natural compounds for laboratory and scientific use. Other quantity can also be offered.
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eMolecules 1222776-76-2 | Medchem Express | WZ4141 | 1mg | 446257884 | HY-103015 | 279.299 | C16H13N3O2
Medchem Express | Sarpogrelate (hydrochloride) | 10mg | 446258867 | HY-10564 | 135159-51-2 | MFCD00887582 | 465.970 | C24H32ClNO6
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Medchemexpress LLC HY-12026 50mg Medchemexpress, WZ4002 CAS:1213269-23-8 Purity:>98%
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Medchemexpress, HY-12026 50mg WZ4002 CAS:1213269-23-8 WZ4002 is a mutant selective EGFR inhibitor with IC50s of 2, 8, 3 and 2 nM for EGFRL858R, EGFRL858R/T790M, EGFRE746_A750 and EGFRE746_A750/T790M, respectively. Purity:>98% Medchemexpress has over 10000 novel life-science reagents, reference compounds, APIs and natural compounds for laboratory and scientific use. Other quantity can also be offered.
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Apexbio Technology LLC Tamoxifen Citrate 54965-24-1 5g
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Tamoxifen Citrate (CAS 54965-24-1) is a small-molecule antagonist targeting estrogen receptors (ER) It is designed to competitively bind ER thereby modulating estrogen-mediated signal transduction Tamoxifen Citrate exerts its biological activity primarily by inhibiting the transcriptional activity of estrogen-responsive genes leading to reduced synthesis of factors related to cell growth and angiogenesis In in vitro studies Tamoxifen Citrate demonstrates inhibition of cell proliferation with reported IC50 values typically ranging from 3 to 7 M depending on cell line and experimental conditions Based on these pharmacological properties Tamoxifen Citrate holds research potential in studies of estrogen receptor-dependent signaling pathways and anti-tumor strategies particularly in breast cancer models
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Medchemexpress LLC HY-17501A 10mg Medchemexpress, Bambuterol hydrochloride CAS:81732-46-9 Purity:>98%
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Medchemexpress, HY-17501A 10mg Bambuterol hydrochloride CAS:81732-46-9 Bambuterol hydrochloride ((±)-Bambuterol hydrochloride; KWD-2183 hydrochloride) is a long acting beta-adrenoceptor agonist (LABA) used in the treatment of asthma; it also is a prodrug of terbutaline. Purity:>98% Medchemexpress has over 10000 novel life-science reagents, reference compounds, APIs and natural compounds for laboratory and scientific use. Other quantity can also be offered.
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eMolecules 1024448-59-6 | Medchem Express | RN-1747 | 5mg | 552386777 | HY-19976 | MFCD04154169 | 395.86 | C17H18ClN3O4S
Ambeed | (2R3R4R5R6R)-3-Acetamido-6-(acetoxymethyl)tetrahydro-2H-pyran-245-triyl triacetate | 1g | 595927945 | A1246619 | 10385-50-9 | MFCD15144916 | 389.357 | C16H23NO10
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Biotang Inc Rociletinib, Free Base, > 99%, 10MG, AVL-301;CNX-419;CO-1686. M.W. 555.55. C27H28F3N7O3. CAS#1374640-70-6
Rociletinib, Free Base, > 99%, 10MG, AVL-301;CNX-419;CO-1686. M.W. 555.55. C27H28F3N7O3. CAS#1374640-70-6
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Medchemexpress LLC FR194738 FR BS10MM 1ML SOLN
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MedChemExpress | FR194738 free base | 10 mM * 1 mL in DMSO Solution | HY-100303 10 mM * 1 mL in DMSO | Purity: 99.79% | 204067-45-8 | MW: 439.65
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Medchemexpress LLC HY-50709 50mg , A939572 stearoyl-CoA desaturase (SCD) inhibitor;SCD-inhibitor CAS:1032229-33-6 Purity:98%
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Medchemexpress, HY-50709 50mg A939572 stearoyl-CoA desaturase (SCD) inhibitor;SCD-inhibitor CAS:1032229-33-6 Formula:C20H22ClN3O3 IC50: <4 nM (mSCD1), 37 nM (hSCD1) Purity:98% A939572 is a potent, and orally bioavailable SCD1 inhibitor with IC 50 values of <4 nM and 37 nM for mSCD1 and hSCD1 , respectively. Medchemexpress has over 10000 novel life-science reagents, reference compounds, APIs and natural compounds for laboratory and scientific use. Other quantity can also be offered.
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eMolecules 423150-91-8 | Medchem Express | BAY-4931 | 5mg | 788478388 | HY-148352 | MFCD02210727 | 421.84 | C22H16ClN3O4
Ambeed | 5-(Difluoromethyl)-2-fluorobenzonitrile | 100mg | 600846440 | A722620 | 934175-58-3 | MFCD18395398 | 171.122 | C8H4F3N
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Medchemexpress LLC HY-13998 100mg Medchemexpress, ABT-333 Dasabuvir CAS:1132935-63-7 Purity:98%
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Medchemexpress,HY-13998 100mg ABT-333 Dasabuvir CAS:1132935-63-7 Formula:C26H27N3O5S ABT-333 is a nonnucleoside inhibitor of the RNA-dependent RNA polymerase encoded by the HCV NS5B gene, inhibits recombinant NS5B polymerases derived from HCV genotype 1a and 1b clinical isolates, with IC50 between 2.2 and 10.7 nM. Purity:98% Medchemexpress has over 10000 novel life-science reagents, reference compounds, APIs and natural compounds for laboratory and scientific use. Other quantity can also be offered.
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Medchemexpress LLC Tivozanib hydrochloride hydrate | 682745-41-1 | 99.8% | 509.34 | 10 MG
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Tivozanib hydrochloride hydrate is the hydrate hydrochloride form of Tivozanib. It is a selective, orally active inhibitor for vascular endothelial growth factor receptor (VEGFR)-1, 2, and 3, with IC50s of 30, 6.5, and 15 nM, respectively. It exhibits antitumor efficacy.
- Selective, orally active inhibitor for VEGFR-1, 2, and 3.
- Exhibits antitumor efficacy.
- Inhibits the phosphorylation of VEGFR-1, VEGFR-2, and VEGFR-3.
- Inhibits VEGF-induced proliferation and migration of HUVECs.
- Selectively inhibits VEGF-stimulated phosphorylation of MAPKs in endothelial cells.
- Exhibits antitumor efficacy against various cancers in athymic mice models.
- Reversibly suppresses vascular permeability and angiogenesis.
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Sigma Aldrich Fine Chemicals Biosciences Pindolol >=98% (TLC), powder | 13523-86-9 | MFCD00010530 | 250MG
Pindolol >=98% (TLC), powder | Purity: >=98% (TLC) | Mol Wt: 248.32 | 13523-86-9 | MFCD00010530 | 250MG
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