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Filtered Search Results
Medchemexpress LLC SR-BI/SCARB1 protein (human, HEK293, C-His tag) | >95.0% | 100 UG
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Recombinant human SR-BI/SCARB1 protein produced in HEK293 mammalian cells and supplied as a lyophilized C-terminal His-tagged protein for biochemical and cell-based studies of HDL-mediated cholesterol transport and lipid/receptor interactions.
- Expressed in HEK293 mammalian cells.
- C-terminal His tag for purification and detection.
- Purity >95% by reducing SDS-PAGE.
- Molecular weight 70-90 kDa (approx.).
- Lyophilized formulation with stabilizers (trehalose or mannitol, and Tween 80).
- Store at -20°C; after reconstitution stable at 4°C for 1 week.
Non-distribution item offered as a customer accommodation; additional freight charges may apply.
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eMolecules 263355-05-1 | 3-Fluoro-2-methylphenyl magnesium bromide, 0.5 M in THF | Synthonix - Stock | MFCD01311483 | 213.332 | C7H6BrFMg | 0.000 | [Br-].Cc1c(F)cccc1[Mg+] | 100ml | 437237240
3-Fluoro-2-methylphenyl magnesium bromide, 0.5 M in THF | Synthonix - Stock | 263355-05-1 | MFCD01311483 | 213.332 | C7H6BrFMg | 0.000 | [Br-].Cc1c(F)cccc1[Mg+] | 100ml | 437237240
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Medchemexpress LLC PNU112455A hydrochloride | 21886-12-4 | 99.6% | 301.75 | 1 ML
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PNU112455A hydrochloride is an ATP-competitive inhibitor of CDK2 and CDK5. It binds to the ATP site of CDK2 and CDK5 with Km values of 3.6 μM and 3.2 μM, respectively. This product is intended for research use only and is not sold to patients.
- ATP-competitive CDK2 and CDK5 inhibitor.
- Binds to the ATP site of CDK2 and CDK5.
- Km for CDK2: 3.6 μM.
- Km for CDK5: 3.2 μM.
- Purity: 99.56%.
- Appearance: Solid, Light yellow to yellow.
- Shipping: Room temperature in continental US.
- Storage: 4°C, sealed storage, away from moisture. In solvent: -80°C for 6 months; -20°C for 1 month.
Non-distribution item offered as a customer accommodation; additional freight charges may apply.
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eMolecules 118486-95-6 | 5-Methyl-2-(tributylstannyl)furan | Synthonix - Stock | MFCD01319081 | 371.152 | C17H32OSn | 97.000 | CCCC[Sn](CCCC)(CCCC)c1ccc(C)o1 | 5g | 525920518
5-Methyl-2-(tributylstannyl)furan | Synthonix - Stock | 118486-95-6 | MFCD01319081 | 371.152 | C17H32OSn | 97.000 | CCCC[Sn](CCCC)(CCCC)c1ccc(C)o1 | 5g | 525920518
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eMolecules 18925-10-5 | Allylzinc bromide, 0.50 M in THF | Synthonix186.360 | C3H5BrZn | 0.000 | [Br-].[Zn+]CC=C | 100ml | 627353790
Allylzinc bromide, 0.50 M in THF | Synthonix | 18925-10-5186.360 | C3H5BrZn | 0.000 | [Br-].[Zn+]CC=C | 100ml | 627353790
Non-distribution item offered as a customer accommodation; additional freight charges may apply.
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eMolecules 737797-40-9 | 5-Acetoxypentylzinc bromide, 0.50 M in THF | Synthonix274.460 | C7H13BrO2Zn | 0.000 | [Br-].CC(=O)OCCCCC[Zn+] | 50ml | 532652598
5-Acetoxypentylzinc bromide, 0.50 M in THF | Synthonix | 737797-40-9274.460 | C7H13BrO2Zn | 0.000 | [Br-].CC(=O)OCCCCC[Zn+] | 50ml | 532652598
Non-distribution item offered as a customer accommodation; additional freight charges may apply.
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Medchemexpress LLC Givinostat hydrochloride | 199657-29-9 | MFCD28502062 | 98.1% | 457.95 | 100 MG
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Givinostat hydrochloride is a Histone Deacetylase (HDAC) inhibitor that can penetrate the blood-brain barrier (BBB). It is known to inhibit HDAC1 and HDAC3, and has shown efficacy in suppressing inflammatory responses and inhibiting cell proliferation in various studies.
- Inhibits HDAC1 (IC50: 198 nM) and HDAC3 (IC50: 157 nM)
- Penetrates the blood-brain barrier (BBB)
- Suppresses LPS-induced IL-1β production
- Decreases IL-6 secretion in PBMCs
- Inhibits JS-1 cell proliferation
Non-distribution item offered as a customer accommodation; additional freight charges may apply.
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Medchemexpress LLC BI-9627 (hydrochloride) | 1422252-46-7 | 98.01% | 392.80 | 100 MG
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Small and/or specialty supplier based on Federal laws and SBA requirements.
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BI-9627 hydrochloride is a potent sodium-hydrogen exchanger isoform 1 (NHE1) inhibitor with IC50 values of 6 nM in intracellular pH recovery (pHi) and 31 nM in human platelet swelling assays. It exhibits over 30-fold selectivity against NHE2 and shows no measurable inhibitory activity against the NHE3 isoform. This compound demonstrates low DDI potential, excellent pharmacokinetics in rat and dog, and remarkably potent activity in the isolated heart model of ischemia-reperfusion injury.
- Decreases autophagy in HTR-8/SVneo cells
- Significantly reduces the pHi of human sperm
- Partially reverses the effect of DMA
- Prolongs Ca2+ recovery time in KO hiPSC-CMs
- For research use only
Non-distribution item offered as a customer accommodation; additional freight charges may apply.
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eMolecules 1013082-37-5 | Tributyl(3,5-dimethylphenyl)stannane | Synthonix - Stock395.218 | C20H36Sn | 0.000 | CCCC[Sn](CCCC)(CCCC)c1cc(C)cc(C)c1 | 1g | 505099297
Tributyl(3,5-dimethylphenyl)stannane | Synthonix - Stock | 1013082-37-5395.218 | C20H36Sn | 0.000 | CCCC[Sn](CCCC)(CCCC)c1cc(C)cc(C)c1 | 1g | 505099297
Non-distribution item offered as a customer accommodation; additional freight charges may apply.
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eMolecules 1135389-59-1 | (1,3-Dioxolan-2-ylmethyl)zinc bromide, 0.50 M in THF | Synthonix | MFCD07698709 | 232.380 | C4H7BrO2Zn | 0.000 | [Br-].[Zn+]CC1OCCO1 | 25ml | 627353592
(1,3-Dioxolan-2-ylmethyl)zinc bromide, 0.50 M in THF | Synthonix | 1135389-59-1 | MFCD07698709 | 232.380 | C4H7BrO2Zn | 0.000 | [Br-].[Zn+]CC1OCCO1 | 25ml | 627353592
Non-distribution item offered as a customer accommodation; additional freight charges may apply.
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eMolecules 1272412-64-2 | 4-(Tributylstannyl)quinoline | Synthonix - Stock | MFCD18325178 | 418.212 | C21H33NSn | 90.000 | CCCC[Sn](CCCC)(CCCC)c1ccnc2ccccc12 | 5g | 525924408
4-(Tributylstannyl)quinoline | Synthonix - Stock | 1272412-64-2 | MFCD18325178 | 418.212 | C21H33NSn | 90.000 | CCCC[Sn](CCCC)(CCCC)c1ccnc2ccccc12 | 5g | 525924408
Non-distribution item offered as a customer accommodation; additional freight charges may apply.
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Medchemexpress LLC Gabapentin hydrochloride | 60142-95-2 | 98.0% | C9H18ClNO2 | 100 MG
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Small and/or specialty supplier based on Federal laws and SBA requirements.
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Gabapentin hydrochloride is a potent, orally active P/Q type Ca2+ channel blocker. It inhibits neuronal Ca2+ influx and reduces neurotransmitter release. This GABA analog can be used to relieve neuropathic pain.
- Potent, orally active P/Q type Ca2+ channel blocker
- Inhibits neuronal Ca2+ influx
- Reduces neurotransmitter release
- GABA analog for neuropathic pain relief
- Inhibits K+-induced Ca2+ increase in synaptosomes
- Decreases K+-evoked release of aspartate and glutamate
- Reduces K+-evoked noradrenaline release
- Improves cognitive performance in animal models
- Provides analgesic effects in animal models
Non-distribution item offered as a customer accommodation; additional freight charges may apply.
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eMolecules 517920-79-5 | 2,4-Difluorophenylzinc bromide, 0.50 M in THF | Synthonix | MFCD02260152 | 258.370 | C6H3BrF2Zn | 0.000 | [Br-].Fc1ccc([Zn+])c(F)c1 | 50ml | 532652750
2,4-Difluorophenylzinc bromide, 0.50 M in THF | Synthonix | 517920-79-5 | MFCD02260152 | 258.370 | C6H3BrF2Zn | 0.000 | [Br-].Fc1ccc([Zn+])c(F)c1 | 50ml | 532652750
Non-distribution item offered as a customer accommodation; additional freight charges may apply.
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eMolecules 27490-32-0 | Tributyl(methoxymethyl)stannane | Synthonix - Stock | MFCD28505600 | 335.119 | C14H32OSn | 95.000 | CCCC[Sn](CCCC)(CCCC)COC | 500mg | 505099293
Tributyl(methoxymethyl)stannane | Synthonix - Stock | 27490-32-0 | MFCD28505600 | 335.119 | C14H32OSn | 95.000 | CCCC[Sn](CCCC)(CCCC)COC | 500mg | 505099293
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AdipoGen Boc-Cys-OH2
Chemical. CAS 10389-65-8. Formula C16H28N2O8S2. MW 440.53. Synthetic. Amino acid protected by tert-butoxycarbonyl Boc group. Used as a reactant in peptide synthesis. Used to obtain asymmetric cystine peptides by enzymatic catalysis with immobilized papain. Used as educt for obtaining S-isoacyl dipeptide building blocks.
Non-distribution item offered as a customer accommodation; additional freight charges may apply.
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