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Filtered Search Results
Aobchem 5-(4-Fluorophenyl)pyrimidin-2-amine | ≥97% | CAS 31408-40-9 | C10H8FN3 | 250mg
5-(4-Fluorophenyl)pyrimidin-2-amine | ≥97% | CAS 31408-40-9 | C10H8FN3 | 250mg
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Aobchem 5-(4-Bromophenyl)pyrimidin-2-amine | 97% | CAS 31483-56-4 | C10H8BrN3 | 1g
5-(4-Bromophenyl)pyrimidin-2-amine | 97% | CAS 31483-56-4 | C10H8BrN3 | 1g
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eMolecules 1123231-07-1 | (1-(4-(Naphthalen-2-yl)pyrimidin-2-yl)piperidin-4-yl)methanamine | MFCD20527803 | 50mg
Medchem Express | ADRA1D receptor antagonist 1 | 5mg | 778475771 | HY-135270 | 1191908-14-1 | 337.200 | C15H14Cl2N4O
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Medchemexpress LLC Org41841 | 301847-37-0 | 99.8% | 402.53 g/mol | C19H22N4O2S2 | 100 MG
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Org41841 is a small-molecule partial agonist of the luteinizing hormone/choriogonadotropin receptor (LHCGR) and the thyroid-stimulating hormone receptor (TSHR), provided for research use in studies of GPCR signaling and cAMP-mediated receptor responses.
- Partial agonist of LHCGR and TSHR, suitable for receptor pharmacology studies.
- Molecular weight 402.53 g/mol.
- Molecular formula C19H22N4O2S2.
- CAS number 301847-37-0.
- Purity 99.77% with supporting analytical data (COA, LCMS).
- Available in multiple solid sizes and as a DMSO solution format for in vitro use.
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Medchemexpress LLC HY-10683 5mg Medchemexpress, PKI-402 CAS:1173204-81-3 Purity:>98%
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Medchemexpress, HY-10683 5mg PKI-402 CAS:1173204-81-3 PKI-402 is a selective, reversible, ATP-competitive inhibitor of PI3K, including PI3K-α mutants, and mTOR (IC50=2, 3, 7,14 and 16 nM for PI3Kα, mTOR, PI3Kβ, PI3Kδ and PI3Kγ). 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 94222-07-8 | 1-(2-Chloro-4-pyrimidinyl)-4-piperidinol | Synthonix | MFCD09743694 | 213.670 | C9H12ClN3O | 95.000 | OC1CCN(CC1)c1ccnc(Cl)n1 | 500mg | 786490886
1-(2-Chloro-4-pyrimidinyl)-4-piperidinol | Synthonix | 94222-07-8 | MFCD09743694 | 213.670 | C9H12ClN3O | 95.000 | OC1CCN(CC1)c1ccnc(Cl)n1 | 500mg | 786490886
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eMolecules 1684386-71-7 | Medchem Express | VER-246608 | 5mg | 446261363 | HY-12492 | MFCD28411365 | 552.96 | C28H23ClF2N4O4
Ambeed | (R)-N-((S)-(2-(Di(adamantan-1-yl)phosphino)phenyl)(phenyl)methyl)-N2-dimethylpropane-2-sulfinamide | 50mg | 633660985 | A1486500 | 2413724-69-1 | 601.870 | C38H52NOPS
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Medchemexpress LLC HY-114414 5mg Medchemexpress, HDACs/mTOR Inhibitor 1 CAS:2271413-06-8 Purity:>98%
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Medchemexpress, HY-114414 5mg HDACs/mTOR Inhibitor 1 CAS:2271413-06-8 HDACs/mTOR Inhibitor 1 is a dual Histone Deacetylases (HDACs) and mammalian target of Rapamycin (mTOR) target inhibitor for treating hematologic malignancies, with IC 50 s of 0.19 nM, 1.8 nM, 1.2 nM and >500 nM for HDAC1, HDAC6, mTOR and PI3Kα, respectively. HDACs/mTOR Inhibitor 1 stimulates cell cycle arrest in G0/G1 phase and induce tumor cell apoptosis with low toxicity in vivo [1] . 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 1609960-30-6 | Medchem Express | TH287 | 5mg | 446267994 | HY-16965 | MFCD29035111 | 269.13 | C11H10Cl2N4
Medchem Express | E7766 (diammonium salt) | 1mg | 694124877 | HY-111999A | 2242635-03-4 | 780.660 | C24H32F2N12O8P2S2
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Selleck Chemical LLC NIH-12848
NIH-12848 is a specific PI5P4K inhibitor with an IC50 of approximately 1 M but does not inhibit the and PI5P4K isoforms at concentrations up to 100 M
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Medchemexpress LLC HY-101430 5mg Medchemexpress, PGD2-IN-1 CAS:885066-67-1 Purity:>98%
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Medchemexpress, HY-101430 5mg PGD2-IN-1 CAS:885066-67-1 PGD2-IN-1 is an antagonist of DP extracted from patent WO 2006044732 A2, example 15 (d); has an IC 50 of 0.3 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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Apexbio Technology LLC GNF 2 778270-11-4 5mg
GNF 2 (CAS 778270-11-4) is a small-molecule inhibitor targeting Bcr-Abl kinase It is designed to suppress Bcr-Abl-mediated signaling thereby regulating leukemic cell proliferation GNF 2 exerts its biological activity primarily through non-ATP competitive allosteric inhibition at the myristate-binding pocket of Abl In cell-based studies GNF 2 demonstrates inhibitory activity with an IC50 of approximately 138 nM in Ba/F3 p210 cells expressing wild-type Bcr-Abl It also inhibits mutant Bcr-Abl forms (E255V Y253H) and proliferation of K562 and SUP-B15 human leukemia cell lines with IC50 values of 194 273 nM Based on these pharmacological properties GNF 2 holds research potential in chronic myeloid leukemia (CML) pathogenesis and therapeutic response studies involving Bcr-Abl fusion proteins
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Aobchem 4-(5-(Methylthio)pyrimidin-2-yl)thiomorpholine | 95% | CAS 2921694-52-0 | C9H13N3S2 | 1g
4-(5-(Methylthio)pyrimidin-2-yl)thiomorpholine | 95% | CAS 2921694-52-0 | C9H13N3S2 | 1g
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Selleck Chemical LLC WYE-125132 (WYE-132) S2661-5mg
WYE-125132 (WYE-132) is a highly potent ATP-competitive mTOR inhibitor with IC50 of 0 19 nM highly selective for mTOR versus PI3Ks or PI3K-related kinases hSMG1 and ATR
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Aobchem (2-(4-Fluorophenoxy)pyrimidin-5-yl)boronic acid | 97% | C10H8BFN2O3 | 1g
(2-(4-Fluorophenoxy)pyrimidin-5-yl)boronic acid | 97% | C10H8BFN2O3 | 1g
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