# celastrol

> chemical compound

**Wikidata**: [Q5057534](https://www.wikidata.org/wiki/Q5057534)  
**Wikipedia**: [English](https://en.wikipedia.org/wiki/Celastrol)  
**Source**: https://4ort.xyz/entity/celastrol


## References

1. celastrol. ChEBI
2. [CAS Common Chemistry](https://commonchemistry.cas.org/detail?cas_rn=34157-83-0)
3. (9β,13α,14β,20α)-3-Hydroxy-9,13-dimethyl-2-oxo-24,25,26-trinoroleana-1(10),3,5,7-tetraen-29-oic acid. ECHA Substance Infocard database
4. celastrol. PubChem
5. ChEBI release 2020-09-01
6. CELASTROL. ChEMBL
7. IUPHAR/BPS Guide to PHARMACOLOGY
8. CELASTROL. Global Substance Registration System
9. Celastrol. ChemSpider
10. Steroidal alkaloids
11. Taxonomy and chemotaxonomy of some species of celastraceae
12. Antiinflammatory constituents of Celastrus orbiculatus inhibit the NF-kappaB activation and NO production
13. Terpenoids from root bark of Celastrus orbiculatus
14. Celastrol isolated from Tripterygium regelii induces apoptosis through both caspase-dependent and -independent pathways in human breast cancer cells
15. Triterpenoids from Tripterygium wilfordii
16. SARS-CoV 3CLpro inhibitory effects of quinone-methide triterpenes from Tripterygium regelii
17. Novel Quinone Methides from Salacia kraussii with in Vitro Antimalarial Activity
18. Quinone-methide, phenolic and related triterpenoids of plants of Celastraceae: further evidence for the structure ofCelastranhydride
19. Cytotoxic cardenolides and antibacterial terpenoids from Crossopetalum gaumeri
20. Quinone-methide triterpenes and salaspermic acid from Kokoona ochracea
21. Studies on terpenoids and steroids. Part 10. Structures of four new natural phenol is D:A-friedo-24-noroleanane triterpenoids
22. Studies on terpenoids and steroids. Part 3. Structure and synthesis of a new phenolic D:A-friedo-24-noroleanane triterpenoid, zeylasterone, from kokoona zeylanica
23. Structure of new bioactive triterpenes related to 22-β-hydroxy-tingenone
24. New Phenolic and Quinone-methide Triterpenes fromMaytenusSpecies (Celastraceae)
25. Triterpenoid and Phenolic Compounds from Two Chilean Celastraceae
26. Structure and absolute configuration of triterpene dimers from Maytenus scutioides
27. Scutione, a new bioactive norquinonemethide triterpene from Maytenus scutioides (Celastraceae)
28. Crystal structure of orthosphenic acid
29. Sesquiterpenes from Orthosphenia mexicana
30. Antitumor Agents 228. Five New Agarofurans, Reissantins A-E, and Cytotoxic Principles from Reissantia buchananii
31. Antitumor agents. 228. five new agarofurans, Reissantins A-E, and cytotoxic principles from Reissantia buchananii.
32. Biogenetically important quinonemethides and other triterpenoid constituents of Salacia reticulata
33. Antimitotic quinoid triterpenes from Maytenus chuchuhuasca
34. A New Nortriterpene from the Root of Celastrus hypoleucus
35. Antifungal properties of pristimerin and celastrol isolated from Celastrus hypoleucus
36. Antiproliferative terpenoids and alkaloids from the roots of Maytenus vitis-idaea and Maytenus spinosa
37. Friedelanes and triterpenoid quinone methides from Hippocratea excelsa
38. Di- and triterpenoids from Tripterygium hypoglaucum
39. Terpenoids from Tripterigyum hypoglaucum
40. An isoaurone and other constituents from Trichosanthes kirilowii seeds inhibit hypoxia-inducible factor-1 and nuclear factor-kappaB.
41. Terpenoids in transformed root culture of Tripterygium wilfordii
42. D:A-friedo-24-noroleanane triterpenoids from Tripterigium wilfordii
43. A diterpenoid and triterpenes from tissue cultures of Tripterygium wilfordii
44. Terpenoids from Tripterygium wilfordii.
45. Triterpenoid inhibitors of interleukin-1 secretion and tumour-promotion from Tripterygium wilfordii var. regelii
46. Terpenoids from Tripterygium wilfordii
47. Gambogic Acid, a Natural Product Inhibitor of Hsp90
48. Quantitative determination for cytotoxic Friedo-nor-oleanane derivatives from five morphological types of Maytenus ilicifolia (Celastraceae) by reverse-phase high-performance liquid chromatography.
49. Biosynthesis of friedelane and quinonemethide triterpenoids is compartmentalized in Maytenus aquifolium and Salacia campestris
50. Mapping file of InChIStrings, InChIKeys and DTXSIDs for the EPA CompTox Dashboard