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Filtered Search Results
Chemscene CHEMSCENE
5000577787 2-1-TERT-BUTOXYCARBONYL PI 15G
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Chemscene CHEMSCENE
5000577947 3R 4R-1-BENZYLPYRROLIDINE-3 5G
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Chemscene CHEMSCENE
5000578792 R-2-TERT-BUTOXYCARBONYL AM 10G
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Chemscene CHEMSCENE
5000578832 S-BENZYL PYRROLIDINE-2-CA 100G
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Chemscene CHEMSCENE
5000579856 N-TERT-BUTOXYCARBONYL-N-ME 25G
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![eMolecules 170508-14-2 | Methyl 6-((tert-butoxycarbonyl)amino)spiro[3.3]heptane-2-carboxylate | MFCD18425636 | 1g](https://assets.fishersci.com/TFS-Assets/CCG/product-images/502138251.JPG-250.jpg)
eMolecules 170508-14-2 | Methyl 6-((tert-butoxycarbonyl)amino)spiro[3.3]heptane-2-carboxylate | MFCD18425636 | 1g
Pharmablock | 2-(8-chloro-1-naphthyl)-4455-tetramethyl-132-dioxaborolane | 25mg | 783661090 | PBU8171 | 2454397-84-1 | 288.580 | C16H18BClO2
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eMolecules EMOLECULES INC
5000841595 N-1-2R 3R 4R 5R-5-B 25G
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Medchemexpress LLC (Rac)-Juvenile hormone III | 24198-95-6 | MFCD00078044 | 1 MG
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(Rac)-Juvenile hormone III is identified as a cecropia juvenile hormone and a juvenile hormone agonist. It has been observed to induce test insects to retain larval characteristics even after undergoing their final molt into the adult stage. The substance demonstrates juvenile hormone activity in pupae of *Tenebrio molitor* and in last-instar nymphs of *Oncopeltus fasciatus*. Furthermore, it exhibits morphogenetic activity across various insect assays.
- Acts as a cecropia juvenile hormone.
- Functions as a juvenile hormone agonist.
- Induces the retention of larval characteristics in test insects post-molt.
- Exhibits juvenile hormone activity in *Tenebrio molitor* pupae.
- Demonstrates juvenile hormone activity in *Oncopeltus fasciatus* last-instar nymphs.
- Possesses morphogenetic activity in insect assays.
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![Medchemexpress LLC 4-Ethyl-7,8-dihydro-4-hydroxy-1H-pyrano[3,4-f]indolizine-3,6,10_4H_-trione | 102978-40-5 | 100.0% | 263.25 | 25 MG](https://assets.fishersci.com/TFS-Assets/CCG/product-images/5000403452-logo.png-250.jpg){kind=logo}
Medchemexpress LLC 4-Ethyl-7,8-dihydro-4-hydroxy-1H-pyrano[3,4-f]indolizine-3,6,10_4H_-trione | 102978-40-5 | 100.0% | 263.25 | 25 MG
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(rac)-Exatecan Intermediate 1 is an isomer of Exatecan Intermediate 1. Exatecan Intermediate 1 (compound 6) is an intermediate of Exatecan, a camptothecin-based anticancer agent. Exatecan inhibits tumor growth by interfering with the proliferation and division of tumor cells by interacting with DNA. Exatecan is primarily used in research into a variety of cancers including ovarian, lung and breast cancer. For research use only. We do not sell to patients.
- (rac)-Exatecan intermediate 1 is an isomer of exatecan intermediate 1.
- Exatecan intermediate 1 (compound 6) is an intermediate of exatecan, a camptothecin-based anticancer agent.
- Exatecan inhibits tumor growth by interfering with the proliferation and division of tumor cells by interacting with DNA.
- Exatecan is primarily used in research into a variety of cancers including ovarian, lung and breast cancer.
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Medchemexpress LLC (Rac)-Modipafant (UK-74505) | 122956-68-7 | 98.15% | 605.09 | 1 MG
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(Rac)-Modipafant (UK-74505) is an orally active, selective, long-acting irreversible platelet activating factor receptor (PAFR) antagonist. It prevents dengue infection.
- Orally active
- Selective
- Long-acting irreversible platelet activating factor receptor (PAFR) antagonist
- Prevents dengue infection
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Medchemexpress LLC (tert-Butoxycarbonyl)-D-aspartic acid | 62396-48-9 | 99.9% | 233.22 | 25 G
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(tert-Butoxycarbonyl)-D-aspartic acid is an aspartic acid derivative that is used as an ergogenic supplement. It influences anabolic hormone secretion, provides fuel during exercise, enhances mental performance, and helps prevent exercise-induced muscle damage. This compound is recognized as a beneficial ergogenic dietary substance.
- Aspartic acid derivative
- Influences anabolic hormone secretion
- Supports fuel supply during exercise
- Enhances mental performance during stress-related tasks
- Helps prevent exercise-induced muscle damage
- Chemical formula: C9H15NO6
- Appearance: Solid
- Color: White to off-white
- For research use only
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Medchemexpress LLC Rac -Shin2 5Mg | HY-134978-5MG
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Rac -Shin2 5Mg
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Medchemexpress LLC 3'-Azido-3'-deoxyuridine | 70580-88-0 | C9H11N5O5 | 5 MG
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3'-Azido-3'-deoxyuridine is a purine nucleoside analogue with broad antitumor activity, particularly against indolent lymphoid malignancies. Its anticancer mechanisms involve inhibiting DNA synthesis and inducing apoptosis. This product is also a click chemistry reagent, containing an Azide group that can participate in copper-catalyzed azide-alkyne cycloaddition (CuAAc) reactions with alkyne-containing molecules, and strain-promoted alkyne-azide cycloaddition (SPAAC) reactions with DBCO or BCN groups.
- Purine nucleoside analogue
- Exhibits broad antitumor activity
- Inhibits DNA synthesis
- Induces apoptosis
- Click chemistry reagent with Azide group
- Enables copper-catalyzed azide-alkyne cycloaddition (CuAAc) reactions
- Participates in strain-promoted alkyne-azide cycloaddition (SPAAC) reactions
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![Medchemexpress LLC Phenylalanine, N-[(1,1-dimethylethoxy)carbonyl]-N, β,β-trimethyl- | 676487-35-7 | 99.1% | 307.38 | 50 MG](https://assets.fishersci.com/TFS-Assets/CCG/product-images/5000404071-logo.png-250.jpg){kind=logo}
Medchemexpress LLC Phenylalanine, N-[(1,1-dimethylethoxy)carbonyl]-N, β,β-trimethyl- | 676487-35-7 | 99.1% | 307.38 | 50 MG
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(Rac)-Taltobulin intermediate-1 is an intermediate used in the synthesis of Taltobulin. Taltobulin is identified as a common toxin component in Antibody-Drug Conjugate (ADC) preparation and acts as a powerful inhibitor of tubulin. Its mechanism of action involves disrupting tubulin polymerization, leading to mitotic arrest and inducing apoptosis.
- Intermediate in the synthesis of Taltobulin.
- A component of ADC preparation.
- A potent tubulin inhibitor.
- Disrupts tubulin polymerization, induces mitotic arrest, and causes apoptosis.
- Available as solid or in solution.
- White to off-white solid appearance.
- Soluble in DMSO (≥ 100 mg/mL).
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Medchemexpress LLC (Rac)-EBET-1055 | 3031540-65-2 | 97.17% | 923.02 | 5 MG
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(Rac)-EBET-1055 is the racemate of EBET-1055, a bromodomain and extra-terminal (BET) PROTAC degrader.
- Effectively inhibits the growth of pancreatic ductal adenocarcinoma (PDAC).
- Simultaneously modulates cancer-associated fibroblast (CAF) activity, upregulating all reporter gene activities in organoid co-cultures.
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