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Filtered Search Results
![eMolecules 204384-69-0 | (2S)-4-[4-(tert-butoxy)phenyl]-2-({[(9H-fluoren-9-yl)methoxy]carbonyl}amino)butanoic acid | Pharmablock | MFCD01321420 | 473.569 | C29H31NO5 | 97.000 | CC(C)(C)Oc1ccc(CC[C@H](NC(=O)OCC2c3ccccc3-c3ccccc23)C(O)=O)cc1 | 50mg | 855327999](https://assets.fishersci.com/TFS-Assets/CCG/product-images/5000190443.jpg-250.jpg)
eMolecules 204384-69-0 | (2S)-4-[4-(tert-butoxy)phenyl]-2-({[(9H-fluoren-9-yl)methoxy]carbonyl}amino)butanoic acid | Pharmablock | MFCD01321420 | 473.569 | C29H31NO5 | 97.000 | CC(C)(C)Oc1ccc(CC[C@H](NC(=O)OCC2c3ccccc3-c3ccccc23)C(O)=O)cc1 | 50mg | 855327999
(2S)-4-[4-(tert-butoxy)phenyl]-2-({[(9H-fluoren-9-yl)methoxy]carbonyl}amino)butanoic acid | Pharmablock | 204384-69-0 | MFCD01321420 | 473.569 | C29H31NO5 | 97.000 | CC(C)(C)Oc1ccc(CC[C@H](NC(=O)OCC2c3ccccc3-c3ccccc23)C(O)=O)cc1 | 50mg | 855327999
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![eMolecules 2227199-12-2 | tert-butyl cis-N-(4-amino-1-methyl-cyclohexyl)carbamate;hydrochloride | Pharmablock264.790 | C12H25ClN2O2 | 97.000 | Cl.CC(C)(C)OC(=O)N[C@]1(C)CC[C@H](N)CC1 | 500mg | 551225362](https://assets.fishersci.com/TFS-Assets/CCG/product-images/5000473748.jpg-250.jpg)
eMolecules 2227199-12-2 | tert-butyl cis-N-(4-amino-1-methyl-cyclohexyl)carbamate;hydrochloride | Pharmablock264.790 | C12H25ClN2O2 | 97.000 | Cl.CC(C)(C)OC(=O)N[C@]1(C)CC[C@H](N)CC1 | 500mg | 551225362
tert-butyl cis-N-(4-amino-1-methyl-cyclohexyl)carbamate;hydrochloride | Pharmablock | 2227199-12-2264.790 | C12H25ClN2O2 | 97.000 | Cl.CC(C)(C)OC(=O)N[C@]1(C)CC[C@H](N)CC1 | 500mg | 551225362
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Medchemexpress LLC HZX-02-059 | 2240205-30-3 | 99.4% | 487.48 | 25 MG
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HZX-02-059 is a potent methuosis inducer and dual-target PIKfyve/tubulin inhibitor with anticancer activity. It primarily disrupts the balance of endocytosis and exocytosis, leading to the formation of numerous vesicles and inducing cell death. This compound also induces cell vacuolization, promotes apoptosis, downregulates the p53 pathway, inhibits PI3K/AKT phosphorylation, and suppresses c-Myc and NF-κB transcription.
- Potent methuosis inducer
- Dual-target PIKfyve/tubulin inhibitor
- Anticancer activity
- Induces cell vacuolization
- Promotes apoptosis
- Downregulates the p53 pathway
- Inhibits PI3K/AKT phosphorylation
- Inhibits c-Myc and NF-κB transcription
- Broad spectrum of cytotoxicity against various human cancer cell lines
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BIOHIPPO AAV-TH-hM4D(Gi)-mCherry-WPRE-hGH-polyA
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Recombinant adeno associated virus expressing hM4D(Gi) fused to mCherry under the TH promoter with WPRE and hGH polyA elements. The Dre dependent configuration enables expression only after recombination, providing precise chemogenetic control of targeted neurons. Offered under the Biohippo AAVX Series with multiple serotypes available including AAV2/1, AAV2/2, AAV2/5, AAV2/6, AAV2/6m, AAV2/6.2FF, AAV2/7m8, AAV2/8, AAV2/9, AAV2/DJ, AAV2/DJ8, AAV2/Retro, AAV2/PHP.eB, AAV2/PHP.B, AAV2/rh10, AAV2/PHP.S, AAV2/anc80, AAV2/B10, AAV2/olig001, AAV2/BI30, AAV2/BR1, AAV2/MG1.2, AAV1/2, AAV2/MaCPNS1, and AAV2/MaCPNS2. Regular titer is greater than or equal to 2.00E+12 vg per mL, with high titer greater than or equal to 1.00E+13 vg per mL available upon request at no additional cost. Customers may specify preferred serotype and titer when placing orders.
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![eMolecules 64987-85-5 | (2,5-dioxopyrrolidin-1-yl) 4-[(2,5-dioxopyrrol-1-yl)methyl]cyclohexanecarboxylate | Synthonix | MFCD00009634 | 334.328 | C16H18N2O6 | 97.000 | O=C(ON1C(=O)CCC1=O)C1CCC(CN2C(=O)C=CC2=O)CC1 | 5g | 808570424](https://assets.fishersci.com/TFS-Assets/CCG/product-images/5000223899.jpg-250.jpg)
eMolecules 64987-85-5 | (2,5-dioxopyrrolidin-1-yl) 4-[(2,5-dioxopyrrol-1-yl)methyl]cyclohexanecarboxylate | Synthonix | MFCD00009634 | 334.328 | C16H18N2O6 | 97.000 | O=C(ON1C(=O)CCC1=O)C1CCC(CN2C(=O)C=CC2=O)CC1 | 5g | 808570424
(2,5-dioxopyrrolidin-1-yl) 4-[(2,5-dioxopyrrol-1-yl)methyl]cyclohexanecarboxylate | Synthonix | 64987-85-5 | MFCD00009634 | 334.328 | C16H18N2O6 | 97.000 | O=C(ON1C(=O)CCC1=O)C1CCC(CN2C(=O)C=CC2=O)CC1 | 5g | 808570424
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(C)OCCBr | 25g | 487585543](https://assets.fishersci.com/TFS-Assets/CCG/product-images/5000160386.jpg-250.jpg)
eMolecules 86864-60-0 | (2-Bromoethoxy)(tert-butyl)dimethylsilane | Apollo Scientific US - Building Blocks | MFCD00209550 | 239.228 | C8H19BrOSi | 96.000 | CC(C)(C)[Si](C)(C)OCCBr | 25g | 487585543
(2-Bromoethoxy)(tert-butyl)dimethylsilane | Apollo Scientific US - Building Blocks | 86864-60-0 | MFCD00209550 | 239.228 | C8H19BrOSi | 96.000 | CC(C)(C)[Si](C)(C)OCCBr | 25g | 487585543
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Medchemexpress LLC Gamma-Linolenic acid methyl ester | 16326-32-2 | 99.37% | 292.46 | 50 MG
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Gamma-Linolenic acid methyl ester | 16326-32-2 | 99.37% | 292.46 | 50 MG
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![eMolecules 1087798-38-6 | 2-(tert-butoxycarbonylamino)spiro[3.3]heptane-6-carboxylic acid | Pharmablock | MFCD11099888 | 255.314 | C13H21NO4 | 97.000 | CC(C)(C)OC(=O)NC1CC2(C1)CC(C2)C(O)=O | 2.5g | 686931709](https://assets.fishersci.com/TFS-Assets/CCG/product-images/5000490851.jpg-250.jpg)
eMolecules 1087798-38-6 | 2-(tert-butoxycarbonylamino)spiro[3.3]heptane-6-carboxylic acid | Pharmablock | MFCD11099888 | 255.314 | C13H21NO4 | 97.000 | CC(C)(C)OC(=O)NC1CC2(C1)CC(C2)C(O)=O | 2.5g | 686931709
2-(tert-butoxycarbonylamino)spiro[3.3]heptane-6-carboxylic acid | Pharmablock | 1087798-38-6 | MFCD11099888 | 255.314 | C13H21NO4 | 97.000 | CC(C)(C)OC(=O)NC1CC2(C1)CC(C2)C(O)=O | 2.5g | 686931709
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(C)CCOC(=O)ON1C(=O)CCC1=O | 25g | 525085969](https://assets.fishersci.com/TFS-Assets/CCG/product-images/5000470309.jpg-250.jpg)
eMolecules 78269-85-9 | Teoc-OSu | Ambeed | MFCD02683467 | 259.333 | C10H17NO5Si | 97.000 | C[Si](C)(C)CCOC(=O)ON1C(=O)CCC1=O | 25g | 525085969
Teoc-OSu | Ambeed | 78269-85-9 | MFCD02683467 | 259.333 | C10H17NO5Si | 97.000 | C[Si](C)(C)CCOC(=O)ON1C(=O)CCC1=O | 25g | 525085969
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![eMolecules 95408-45-0 | 1,1'-Bis(di-tert-butylphosphino)ferrocene Palladium Dichloride | Accela ChemBio | MFCD08064219 | 651.750 | C26H44Cl2FeP2Pd | 98.000 | [Cl-].[Cl-].[Fe].[Pd++].CC(C)(C)P(c1cccc1)C(C)(C)C.CC(C)(C)P(c1cccc1)C(C)(C)C | 0.1g | 783627424](https://assets.fishersci.com/TFS-Assets/CCG/product-images/5000482280.jpg-250.jpg)
eMolecules 95408-45-0 | 1,1'-Bis(di-tert-butylphosphino)ferrocene Palladium Dichloride | Accela ChemBio | MFCD08064219 | 651.750 | C26H44Cl2FeP2Pd | 98.000 | [Cl-].[Cl-].[Fe].[Pd++].CC(C)(C)P(c1cccc1)C(C)(C)C.CC(C)(C)P(c1cccc1)C(C)(C)C | 0.1g | 783627424
1,1'-Bis(di-tert-butylphosphino)ferrocene Palladium Dichloride | Accela ChemBio | 95408-45-0 | MFCD08064219 | 651.750 | C26H44Cl2FeP2Pd | 98.000 | [Cl-].[Cl-].[Fe].[Pd++].CC(C)(C)P(c1cccc1)C(C)(C)C.CC(C)(C)P(c1cccc1)C(C)(C)C | 0.1g | 783627424
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![eMolecules 95408-45-0 | 1,1'-Bis(di-tert-butylphosphino)ferrocene palladium dichloride | Combi-Blocks | MFCD08064219 | 651.750 | C26H44Cl2FeP2Pd | 97.000 | [Cl-].[Cl-].[Fe].[Pd++].CC(C)(C)P(c1cccc1)C(C)(C)C.CC(C)(C)P(c1cccc1)C(C)(C)C | 1g | 342864249](https://assets.fishersci.com/TFS-Assets/CCG/product-images/default.jpg-250.jpg)
eMolecules 95408-45-0 | 1,1'-Bis(di-tert-butylphosphino)ferrocene palladium dichloride | Combi-Blocks | MFCD08064219 | 651.750 | C26H44Cl2FeP2Pd | 97.000 | [Cl-].[Cl-].[Fe].[Pd++].CC(C)(C)P(c1cccc1)C(C)(C)C.CC(C)(C)P(c1cccc1)C(C)(C)C | 1g | 342864249
1,1'-Bis(di-tert-butylphosphino)ferrocene palladium dichloride | Combi-Blocks | 95408-45-0 | MFCD08064219 | 651.750 | C26H44Cl2FeP2Pd | 97.000 | [Cl-].[Cl-].[Fe].[Pd++].CC(C)(C)P(c1cccc1)C(C)(C)C.CC(C)(C)P(c1cccc1)C(C)(C)C | 1g | 342864249
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Medchemexpress LLC 2-Phenyl-2-(2-pyridyl)acetonitrile | 5005-36-7 | 100.0% | 194.23 | 100 MG
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2-Phenyl-2-(2-pyridyl)acetonitrile is identified as the major metabolite of SC 15396, an antigastrin that inhibits gastric secretion. It is metabolized by the supernatant fraction of rat liver homogenate.
- Major metabolite of SC 15396
- Metabolized by rat liver homogenate supernatant fraction
- Antigastrin
- Inhibits gastric secretion
- Off-white to light brown solid
- High purity
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Medchemexpress LLC α-Methyltyrosine methyl ester hydrochloride | 7361-31-1 | 98.91% | 245.71 | 1 G
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α-Methyltyrosine methyl ester hydrochloride is an orally active, competitive tyrosine hydroxylase inhibitor. It can inhibit the conversion of tyrosine to dopamine and serves as a tool for sympathetic nervous system research. Studies have shown it can induce renal lesions with the formation of calculi in the urinary tract in rats.
- Orally active and competitive tyrosine hydroxylase inhibitor
- Inhibits the conversion of tyrosine to dopamine
- Can be used as a tool for sympathetic nervous system research
- Induces renal lesions with the formation of calculi in the urinary tract in rats
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Medchemexpress LLC 3-Chloro-N-(4-hydroxy-2-oxo-2H-chromen-3-yl)benzamide | 94205-22-8 | C16H10ClNO4 | 100 MG
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Anticancer agent 93 is a 4-Hydroxycoumarin derivative that demonstrates efficacy against lung cancer cells. It inhibits invasion and migration by modulating epithelial-mesenchymal transition (EMT) effectors, making it a potential candidate for cancer research.
- Inhibits A549 cell invasion by approximately 50%
- Significantly inhibits A549 cell migration
- Decreases lung cancer cell motility by downregulating EMT markers
- Reduces expression of N-cadherin and E-cadherin in A549 cells
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Medchemexpress LLC MEDCHEMEXPRESS LLC
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5000723529 7-BROMOHEPTAN-1-AMIN 500MG
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