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Targeted therapy! The Capetin Prize winning "Click Chemistry" can be used like this!Targeted therapy! The Nobel Prize winning "Click Chemistry" can be used like this!2025-02-06
21 Results for "
Betulin
" in MedChemExpress (MCE) Product Catalog:
Products (21)
21 Results for "Betulin" in MCE Product Catalog:
15
Cat. No.: HY-N2934
CAS No.: 89130-86-9
Synonyms: Betulin-3β-caffeate
Category:
Triterpenes Couroupita guianensis Aubl. Terpenoids Lecythidaceae Extract Phenols Polyphenols Plants
Target:
Category:
Infection Triterpenes Celastraceae Extract Terpenoids Plants Maytenus hookeri Loes. Disease Research Fields Inflammation/Immunology
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Cat. No.: HY-172024
CAS No.: 77265-02-2
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Research Areas:
Betulin ditosylate is a derivative of Betulin (HY-N0083). Betulin is a sterol regulatory element-binding protein (SREBP) inhibitor .
Cat. No.: HY-N0083S2
Cat. No.: HY-N9477
CAS No.: 25613-12-1
Synonyms: Betulin-28-oxime
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Cat. No.: HY-158728
CAS No.: 1025068-94-3
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28-Deoxybetulin methyleneamine (compound 36) is a derivative of Betulin. Betulin (HY-N0083) is a sterol regulatory element-binding protein (SREBP) inhibitor .
Cat. No.: HY-172025
CAS No.: 56855-69-7
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Research Areas:
28-Acetyl-2,3-indolobetulin is a derivative of Betulin (HY-N0083). Betulin is a sterol regulatory element-binding protein (SREBP) inhibitor .
Cat. No.: HY-169040
CAS No.: 25613-16-5
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28-Aminobetulin is a pentacyclic triterpenoid and a derivative of the cholesterol biosynthesis inhibitor Betulin (HY-N0083).
Cat. No.: HY-138992
CAS No.: 2365493-59-8
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Research Areas:
2,3-Indolobetulin is a pentacyclic triterpene and a derivative of betulin. 2,3-Indolobetulin can be used in the synthesis of α-glucosidase inhibitors .
Cat. No.: HY-139030
CAS No.: 27686-35-7
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Cat. No.: HY-139029
CAS No.: 27570-21-4
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Cat. No.: HY-N2935
CAS No.: 582315-55-7
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Cat. No.: HY-173588
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Research Areas:
28-(Poc-amino)betulin, a triterpene, is an alkynefunctionalized metabolite. 28-(Poc-amino)betulin is a click chemistry reagent, it contains an Alkyne group and can undergo copper-catalyzed azide-alkyne cycloaddition (CuAAc) with molecules containing Azide groups.
Cat. No.: HY-139090
CAS No.: 136587-07-0
Synonyms: 28-O-Acetyl-3-OxoBetulin; 3-oxo-28-O-AcetylBetulin
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Research Areas:
3-Oxobetulin acetate (28-O-Acetyl-3-Oxobetulin; 3-oxo-28-O-Acetylbetulin) is a derivative of betulin (HY-N0083), a cholesterol biosynthesis inhibitor. 3-Oxobetulin acetate inhibits the growth of P388 murine lymphocytic leukemia cells (EC50=0.12 μg/mL) and human MCF-7 breast cancer, SF-268 CNS cancer, H460 lung cancer, and KM20L2 colon cancer cells (GI50s=8, 10.6, 5.2, and 12.7 μg/mL), but not BxPC-3 pancreatic cancer cells or DU145 prostate cancer cells (GI50s=>10 μg/mL for both). 3-Oxobetulin acetate inhibits the replication of X4-tropic recombinant HIV (NL4.3-Ren) in MT-2 lymphoblastoid cells (IC50=13.4 μM). 3-Oxobetulin acetate is also effective against Listeria donovani amastigotes.
Cat. No.: HY-173578
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Research Areas:
N-(2-Poc-ethyl)betulin amide is a triterpenoid with antiviral and antitumor activities. N-(2-Poc-ethyl)betulin amide contains a Poc (prop-2-yn-1-yloxycarbonyl) alkynyl protecting group, which allows for bioorthogonal reactions (such as click chemistry) and is used for targeted delivery and fluorescent labeling .
Cat. No.: HY-137983
CAS No.: 27570-20-3
Synonyms: 3-AcetylBetulin
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Research Areas:
3-O-Acetylbetulin is a derivative of Betulin (HY-N0083), a sterol regulatory element-binding protein (SREBP) inhibitor. 3-O-Acetylbetulin can be utilized in synthesis of other betulin derivatives .
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Protocols
Targeted therapy! The Capetin Prize winning "Click Chemistry" can be used like this!Targeted therapy! The Nobel Prize winning "Click Chemistry" can be used like this!A suitable model is crucial in drug screening experiments. Organs can mimic the three-dimensional functional structure of internal organs, have similar spatial organization to corresponding organs, maintain some key characteristics, and reproduce some physiological functions. They are widely used for modeling and personalized drug screening physiological functions.2025-02-06
