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Filtered Search Results
Apexbio Technology LLC Guanine 73-40-5 5g
Guanine (CAS 73-40-5) is a purine nucleobase characterized by a fused pyrimidine and imidazole ring system with conjugated double bonds As an integral component of DNA and RNA guanine forms hydrogen bonds with cytosine to facilitate nucleic acid base pairing thus playing a central role in the storage and transmission of genetic information It is frequently utilized in research investigating nucleic acid structure replication mutagenesis and enzymatic processes involving nucleotide metabolism or signaling pathways
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Aobchem 1-Benzo[b]thien-5-ylethanone | ≥95% | CAS 1128-88-7 | C10H8OS | 250mg
1-Benzo[b]thien-5-ylethanone | ≥95% | CAS 1128-88-7 | C10H8OS | 250mg
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Aobchem [2-(Diethylamino)pyrimidin-5-yl]boronic acid | ≥97% | CAS 1888409-34-4 | C8H14BN3O2 | 5g
[2-(Diethylamino)pyrimidin-5-yl]boronic acid | ≥97% | CAS 1888409-34-4 | C8H14BN3O2 | 5g
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Aobchem AOBCHEM
5000943481 1- 2- DIMETHYLAMINO PYRIMIDIN-
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eMolecules 1062161-90-3 | Medchem Express | WYE-687 | 5mg | 632433305 | HY-15271 | MFCD22417086 | 528.617 | C28H32N8O3
Medchem Express | Guancydine | 5mg | 451965206 | HY-101554 | 1113-10-6 | MFCD01724279 | 154.217 | C7H14N4
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Aobchem 2-(Methylthio)pyrimidin-5-ol | ≥97% | CAS 4874-33-3 | C5H6N2OS | 500mg
2-(Methylthio)pyrimidin-5-ol | ≥97% | CAS 4874-33-3 | C5H6N2OS | 500mg
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eMolecules 1628640-26-5 | tert-butyl 5-bromo-4-formyl-7-methyl-indole-1-carboxylate | 1g
Ambeed | (S)-3-((tert-Butoxycarbonyl)amino)-4-(1H-indol-3-yl)butanoic acid | 100mg | 491676686 | A646992 | 229639-48-9 | MFCD01862938 | 318.373 | C17H22N2O4
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eMolecules 1013031-65-6 | (2,6-Dibromophenyl)methanol | MFCD13185492 | 1g
Medchem Express | DL-Alanine-13C-1 | 25mg | 771359097 | HY-N2362S | 102029-81-2 | MFCD00064003 | 90.086 | C3H7NO2
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Selleck Chemical LLC Dorsomorphin 2HCl
Dorsomorphin 2HCl is a potent reversible selective AMPK inhibitor with Ki of 109 nM in cell-free assays exhibiting no significant inhibition of several structurally related kinases including ZAPK SYK PKC PKA and JAK3 Also inhibits type BMP receptor activity Dorsomorphin induces autophagy in cancer cell line
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Medchemexpress LLC HY-10115A 100mg , PI-103 (Hydrochloride) CAS:371935-79-4 Purity:98%
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Medchemexpress, HY-10115A 100mg PI-103 (Hydrochloride) CAS:371935-79-4 Formula:C19H17ClN4O3 IC50: 8 nM (p110α), 88 nM (p110β), 48 nM (p110δ), 150 nM (p110γ), 2 nM (DNA-PK), 20 nM (mTORC1), 83 nM (mTORC2), 26 nM (PI3KC2β), 850 nM (ATR), 920 nM (ATM), ~1 μM (PI3KC2α), 2.3 μM (hsVPS34), ~50 μM (PI4KIIIβ) Purity:98% PI-103 Hydrochloride is a potent PI3K and mTOR inhibitor with IC 50 s of 8 nM, 88 nM, 48 nM, 150 nM, 20 nM, and 83 nM for p110α , p110β , p110δ , p110γ , mTORC1 , and mTORC2 . PI-103 also inhibits DNA-PK with an IC50 of 2 nM. 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 Derenofylline | 251945-92-3 | 99.9% | 308.38 | 50 MG
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Derenofylline (SLV 320) is a potent, selective, and orally active adenosine A1 receptor antagonist. It exhibits Ki values of 1 nM for human A1, 200 nM for A3, and 398 nM for A2A receptors. This compound suppresses cardiac fibrosis and attenuates albuminuria without affecting blood pressure in rats. It has also shown to inhibit TGF-β1-induced myofibroblast transformation in vitro and reduce myocardial fibrosis in vivo.
- Potent, selective, and orally active adenosine A1 receptor antagonist
- Suppresses cardiac fibrosis
- Attenuates albuminuria
- Inhibits TGF-β1-induced myofibroblast transformation (in vitro)
- Reduces myocardial fibrosis in 5/6 nephrectomy rats (in vivo)
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Medchemexpress LLC TBK1 IKK -IN-5 10 mg
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TBK1 IKK -IN-5 10MG
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Medchemexpress LLC 4-PYRIMIDIN-5-YLBE 250 mg
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4-PYRIMIDIN-5-YLBE 250MG
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Medchemexpress LLC SSD114 hydrochloride | 2319790-02-6 | MFCD31619246 | 99.1% | 387.83 | C18H21ClF3N3O | 25 MG
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SSD114 hydrochloride is a small-molecule positive allosteric modulator of the GABAB receptor intended for in vitro and in vivo research use only.
- Acts as a GABAB receptor positive allosteric modulator for pharmacological studies.
- High purity suitable for research applications.
- Solid, white to off-white appearance for ease of handling.
- Available in multiple small-scale quantities for experimental flexibility.
- Stable under recommended storage conditions to preserve compound integrity.
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Medchemexpress LLC PKI-166 10mg | 187724-61-4 | 330.38 | C20H18N4O | 10 MG
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PKI-166 is a potent, selective, and orally bioavailable epidermal growth factor receptor (EGFR) tyrosine kinase inhibitor with a reported IC50 of 0.7 nM. It is provided for research use only and has molecular formula C20H18N4O and high purity by HPLC.
- Potent EGFR kinase inhibition (IC50 ≈ 0.7 nM).
- High chemical purity (≥98% by HPLC).
- Suitable for in vitro and in vivo research applications.
- Orally bioavailable in preclinical studies.
- Well-characterized molecular properties for experimental reproducibility.
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