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Filtered Search Results
eMolecules 124898-13-1 | TRIMETHYL(PENTAFLUOROETHYL)SILANE | AstaTech | MFCD04116436 | 192.204 | C5H9F5Si | 97.000 | C[Si](C)(C)C(F)(F)C(F)(F)F | 1g | 448280251
TRIMETHYL(PENTAFLUOROETHYL)SILANE | AstaTech | 124898-13-1 | MFCD04116436 | 192.204 | C5H9F5Si | 97.000 | C[Si](C)(C)C(F)(F)C(F)(F)F | 1g | 448280251
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Medchemexpress LLC SBI-581 | 98.2% | 383.44 | 25 MG
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SBI-581 is an orally active and potent selective serine-threonine kinase TAO3 inhibitor with an IC50 of 42 nM. It promotes TKS5α accumulation at RAB11-positive vesicles and inhibits invadopodia formation. The compound demonstrates reasonable pharmacokinetics in mice and shows antitumor activity. It is also a click chemistry reagent, containing an Alkyne group that can undergo copper-catalyzed azide-alkyne cycloaddition (CuAAc) with molecules containing Azide groups.
- Orally active and potent selective serine-threonine kinase TAO3 inhibitor
- Promotes TKS5α accumulation at RAB11-positive vesicles
- Inhibits invadopodia formation
- Demonstrates reasonable pharmacokinetics in mice
- Shows antitumor activity
- Click chemistry reagent for copper-catalyzed azide-alkyne cycloaddition
- Moderate selectivity against a broad panel of kinases
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Medchemexpress LLC Givinostat hydrochloride monohydrate | 732302-99-7 | 99.6% | 475.97 | 25 MG
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Givinostat hydrochloride monohydrate is a potent HDAC inhibitor, demonstrating IC50 values of 198 nM for HDAC1 and 157 nM for HDAC3. This compound is notable for its ability to penetrate the blood-brain barrier, making it suitable for a range of research applications.
- Potent HDAC inhibitor for HDAC1 and HDAC3
- Penetrates the blood-brain barrier
- Suppresses LPS-induced IL-1β and IL-6 production
- Inhibits JS-1 cell proliferation
- Reduces serum TNFα and IL-1β levels in vivo
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eMolecules Synthonix - Stock 4-Methoxy-2-methylphenylmagnesium bromide 0.5 M in THF 500ml 437237336 M31768 148706-30-3 MFCD01319918 225.368 C8H9BrMgO
Synthonix - Stock 4-Methoxy-2-methylphenylmagnesium bromide 0.5 M in THF 500ml 437237336 M31768 148706-30-3 MFCD01319918 225.368 C8H9BrMgO
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Medchemexpress LLC Higenamine hydrochloride | 11041-94-4 | 307.77 | 1 ML
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Higenamine hydrochloride (HY-N2037A) is a selective LSD1 inhibitor, isolated from aconite, demonstrating anti-inflammatory and antibacterial activities. It attenuates IL-1β-induced apoptosis through the ROS-mediated PI3K/Akt signaling pathway, protects brain cells from oxygen deprivation, and promotes bone formation in osteoporosis via the SMAD2/3 pathway. This compound is widely used in research for cancer, inflammation, cardiorenal syndrome, and other diseases.
- Selective LSD1 inhibitor
- Exhibits anti-inflammatory activity
- Exhibits antibacterial activity
- Attenuates IL-1β-induced apoptosis
- Protects brain cells from oxygen deprivation
- Promotes bone formation in osteoporosis
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eMolecules 134914-97-9 | 2-Methyl-4-(tributylstannyl)pyridine | Synthonix - Stock | MFCD16039584 | 382.179 | C18H33NSn | 98.000 | CCCC[Sn](CCCC)(CCCC)c1ccnc(C)c1 | 500mg | 525932253
2-Methyl-4-(tributylstannyl)pyridine | Synthonix - Stock | 134914-97-9 | MFCD16039584 | 382.179 | C18H33NSn | 98.000 | CCCC[Sn](CCCC)(CCCC)c1ccnc(C)c1 | 500mg | 525932253
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eMolecules 866606-03-3 | 5-(Tributylstannyl)-2-pyridinecarbonitrile | Synthonix - Stock | MFCD22421738 | 393.162 | C18H30N2Sn | 95.000 | CCCC[Sn](CCCC)(CCCC)c1ccc(nc1)C#N | 5g | 525924518
5-(Tributylstannyl)-2-pyridinecarbonitrile | Synthonix - Stock | 866606-03-3 | MFCD22421738 | 393.162 | C18H30N2Sn | 95.000 | CCCC[Sn](CCCC)(CCCC)c1ccc(nc1)C#N | 5g | 525924518
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eMolecules 1034-49-7 | (Bromomethyl)triphenylphosphonium bromide | Combi-Blocks | MFCD00011864 | 436.127 | C19H17Br2P | 97.000 | [Br-].BrC[P+](c1ccccc1)(c1ccccc1)c1ccccc1 | 100g | 335351038
(Bromomethyl)triphenylphosphonium bromide | Combi-Blocks | 1034-49-7 | MFCD00011864 | 436.127 | C19H17Br2P | 97.000 | [Br-].BrC[P+](c1ccccc1)(c1ccccc1)c1ccccc1 | 100g | 335351038
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eMolecules 2259-30-5 | tert-Butylmagnesium bromide, 1.0 M in THF | Synthonix161.325 | C4H9BrMg | 0.000 | [Br-].CC(C)(C)[Mg+] | 50ml | 702445843
tert-Butylmagnesium bromide, 1.0 M in THF | Synthonix | 2259-30-5161.325 | C4H9BrMg | 0.000 | [Br-].CC(C)(C)[Mg+] | 50ml | 702445843
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eMolecules 1155294-76-0 | (9,9-Dimethylfluoren-2-yl)magnesium bromide, 0.5 M in THF | Synthonix297.478 | C15H13BrMg | 0.000 | [Br-].CC1(C)c2ccccc2-c2ccc([Mg+])cc12 | 50ml | 812584969
(9,9-Dimethylfluoren-2-yl)magnesium bromide, 0.5 M in THF | Synthonix | 1155294-76-0297.478 | C15H13BrMg | 0.000 | [Br-].CC1(C)c2ccccc2-c2ccc([Mg+])cc12 | 50ml | 812584969
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eMolecules Synthonix [(3-methyloxetan-3-yl)methyl]zinc iodide 0.50 M in THF 50ml 794220300 M80983 1451089-95-4 [null] 277.410 C5H9IOZn
Synthonix [(3-methyloxetan-3-yl)methyl]zinc iodide 0.50 M in THF 50ml 794220300 M80983 1451089-95-4 [null] 277.410 C5H9IOZn
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eMolecules 92273-73-9 | Butylzinc bromide, 0.50 M in THF | Synthonix | MFCD00671997 | 202.400 | C4H9BrZn | 0.000 | [Br-].CCCC[Zn+] | 100ml | 627353799
Butylzinc bromide, 0.50 M in THF | Synthonix | 92273-73-9 | MFCD00671997 | 202.400 | C4H9BrZn | 0.000 | [Br-].CCCC[Zn+] | 100ml | 627353799
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eMolecules 312693-04-2 | 4-Ethylphenylzinc iodide, 0.50 M in THF | Synthonix297.440 | C8H9IZn | 0.000 | [I-].CCc1ccc([Zn+])cc1 | 100ml | 532652822
4-Ethylphenylzinc iodide, 0.50 M in THF | Synthonix | 312693-04-2297.440 | C8H9IZn | 0.000 | [I-].CCc1ccc([Zn+])cc1 | 100ml | 532652822
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Medchemexpress LLC 4H-Pyrimido[6,1-a]isoquinolin-4-one, 2,3,6,7-tetrahydro-9,10-dimethoxy-3-methyl-2-[(2,4,6-trimethylphenyl)imino]-, hydrochloride (1:1) | 78416-81-6 | 99.86% | 441.95 | 10 MM 1 ML
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Trequinsin hydrochloride (HL 725) is an extremely potent inhibitor of platelet CAMP phosphodiesterase (PDE), with an IC50 of 0.25 nM. It is also an extremely potent inhibitor of the aggregation of human platelets induced in vitro by ADP, collagen, thrombin, and epinephrine.
- Extremely potent inhibitor of platelet CAMP phosphodiesterase (PDE)
- IC50 of 0.25 nM for PDE inhibition
- Potent inhibitor of human platelet aggregation induced by ADP, collagen, thrombin, and epinephrine
- Exerts cardiovascular and antihypertensive qualities
- Efficacious agonist of [Ca2+]i
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eMolecules 1141981-37-4 | 4-Bromo-2-methylphenylzinc iodide, 0.50 M in THF | Synthonix362.310 | C7H6BrIZn | 0.000 | [I-].Cc1cc(Br)ccc1[Zn+] | 50ml | 532652626
4-Bromo-2-methylphenylzinc iodide, 0.50 M in THF | Synthonix | 1141981-37-4362.310 | C7H6BrIZn | 0.000 | [I-].Cc1cc(Br)ccc1[Zn+] | 50ml | 532652626
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