Chakravarti RN, Chakravarti D (March 1951). "Andrographolide, the active constituent of Andrographis paniculata Nees; a preliminary communication". The Indian Medical Gazette. 86 (3): 96–7. PMC5191793. PMID 14860885.
abcamBiochemicals Andrographolide-ab120636
Wang J, Tan XF, Nguyen VS, Yang P, Zhou J, Gao M, และคณะ (March 2014). "A quantitative chemical proteomics approach to profile the specific cellular targets of andrographolide, a promising anticancer agent that suppresses tumor metastasis". Molecular & Cellular Proteomics. 13 (3): 876–86. doi:10.1074/mcp.M113.029793. PMC3945915. PMID 24445406.
Tan WS, Liao W, Zhou S, Wong WS (September 2017). "Is there a future for andrographolide to be an anti-inflammatory drug? Deciphering its major mechanisms of action". Biochemical Pharmacology. 139: 71–81. doi:10.1016/j.bcp.2017.03.024. PMID 28377280. S2CID 26727535.
Garg A, Agrawal L, Misra RC, Sharma S, Ghosh S (September 2015). "Andrographis paniculata transcriptome provides molecular insights into tissue-specific accumulation of medicinal diterpenes". BMC Genomics. 16 (1): 659. doi:10.1186/s12864-015-1864-y. PMC4557604. PMID 26328761.
Sharma SN, Jha Z, Sinha RK, Geda AK (February 2015). "Jasmonate-induced biosynthesis of andrographolide in Andrographis paniculata". Physiologia Plantarum. 153 (2): 221–9. doi:10.1111/ppl.12252. PMID 25104168.
↑ Srivastava N, Akhila A (August 2010). "Biosynthesis of andrographolide in Andrographis paniculata". Phytochemistry. 71 (11–12): 1298–304. doi:10.1016/j.phytochem.2010.05.022. PMID 20557910.
สิงหาคม 05, 2021
แอนโดรกราโฟไลด, งกฤษ, andrographolide, เป, นสารประกอบแลบเดน, กล, มไดเทอร, นอยด, แยกได, จากลำต, นและใบของฟ, าทะลายโจร, andrographis, paniculata, เป, นสารท, รสขมมากandrographolideช, อตาม, iupac, decahydro, hydroxy, hydroxymethyl, dimethyl, methylene, napthalenyl. aexnodrkraofild xngkvs Andrographolide epnsarprakxbaelbedn klumidethxrphinxyd thiaeykidcaklatnaelaibkhxngfathalayocr Andrographis paniculata 1 aexnodrkraofildepnsarthimirskhmmakaexnodrkraofildAndrographolidechuxtam IUPAC 3 2 Decahydro 6 hydroxy 5 hydroxymethyl 5 8a dimethyl 2 methylene 1 napthalenyl ethylidene dihydro 4 hydroxy 2 3H furanoneelkhthaebiynelkhthaebiyn CAS 5508 58 7 CAS PubChem 5318517ChEBI 65408SMILES O C3OCC O C3 CCC1 C C CCC2C C CO C O CCC12CInChI 1 C20H30O5 c1 12 4 7 16 19 2 9 8 17 23 20 16 3 11 21 14 12 6 5 13 15 22 10 25 18 13 24 h5 14 17 21 23H 1 4 6 11H2 2 3H3ChemSpider ID 16735664khunsmbtisutromelkul C20H30O5mwlomelkul 350 45 g mol 1lksnathangkayphaph aephnhruxprisumrxmbik cakexthanxlhruxemthanxlkhwamhnaaenn 1 2317 k sm 3cudhlxmehlw 230 231 C 503 504 K 446 448 Fkhwamsamarthlalayid in na lalayidnxysarprakxbxunthiekiywkhxngknaelbednthiekiywkhxng 14 dixxksiaexnodrkraofildsarprakxbthiekiywkhxng siehyiynphing 喜炎平 hakmiidrabuepnxun khxmulkhangtnnikhuxkhxmulsar n phawamatrthanthi 25 C 100 kPasthaniyxy ekhmimikarsuksaaexnodrkraofildthungphlkrathbtxkarsngsyyankhxngesll karprbrabbphumikhumkn aelaorkhhlxdeluxdsmxng 2 karsuksaaesdngihehnwaaexnodrkraofild xaccbkbsepktrmkhxngoprtinepahmayrwmthng NF kB aelaaexktinodykarddaeplngomelkul hlngkarthxdrhs 3 4 chiwsngekhraah aekikh chiwsngekhraahkhxngaexnodrkraofild aexnodrkraofild epnsarphunthaninklumidethxrphinaelkhotn sungepnsarchiwsngekhraahkhxngfathalayocr idrbkarxthibayinchwngkhristthswrrs 2010 5 6 aexnodrkraofild epnixosphrinxydthiepnphlitphnthcakthrrmchati odysartngtnkhxngkarsngekhraahixosphrinxydkhux ixosephnethniliphorfxseft IPP aelaidemthilxlliliphorfxseft DMAPP samarthsngekhraahidphanthangwithikrdemwaolnik MVA hruxwithidixxksisilluols DXP 7 cakkartidchlakixosothp C13 khxngsartngtnsahrbthngwithi MVA aela DXP phbwasartngtnkhxngaexnodrkraofild swnihythuksngekhraahphanthang DXP 7 misartngtnkhxngaexnodrkraofild ephiyngelknxythisngekhraahphanwithi MVA karsngekhraahthangchiwphaphkhxngaexnodrkraofild erimtndwykarephim IPP ipyng DMAPP sungsrangecxraniliphor fxseft caknnephimomelkulkhxng IPP xiktwhnungsungihphlepnfarensiliphorfxseft FPP omelkul IPP sudthaycathukephimekhaipin FPP ephuxsrangaeknhlkkhxngidethxrphinihsmburn phnthakhuthimitnkaenidcak DMAPP cathukxxksiidsepnxiphxkisdkxnthicamikarpidwngaehwnsungprakxbepnwnghkehliymsxngwng chudkhxngkarekidxxksiedchnkxtwepnsaraelkhotnhaehliymnxkehnuxcakkarephimklumaexlkxhxl imepnthithrabladbkhxngkarddaeplnghlngkarsngekhraahehlanithnghmd 7 duephim aekikhsiehyiynphingxangxing aekikh Chakravarti RN Chakravarti D March 1951 Andrographolide the active constituent of Andrographis paniculata Nees a preliminary communication The Indian Medical Gazette 86 3 96 7 PMC 5191793 PMID 14860885 abcamBiochemicals Andrographolide ab120636 Wang J Tan XF Nguyen VS Yang P Zhou J Gao M aelakhna March 2014 A quantitative chemical proteomics approach to profile the specific cellular targets of andrographolide a promising anticancer agent that suppresses tumor metastasis Molecular amp Cellular Proteomics 13 3 876 86 doi 10 1074 mcp M113 029793 PMC 3945915 PMID 24445406 Tan WS Liao W Zhou S Wong WS September 2017 Is there a future for andrographolide to be an anti inflammatory drug Deciphering its major mechanisms of action Biochemical Pharmacology 139 71 81 doi 10 1016 j bcp 2017 03 024 PMID 28377280 S2CID 26727535 Garg A Agrawal L Misra RC Sharma S Ghosh S September 2015 Andrographis paniculata transcriptome provides molecular insights into tissue specific accumulation of medicinal diterpenes BMC Genomics 16 1 659 doi 10 1186 s12864 015 1864 y PMC 4557604 PMID 26328761 Sharma SN Jha Z Sinha RK Geda AK February 2015 Jasmonate induced biosynthesis of andrographolide in Andrographis paniculata Physiologia Plantarum 153 2 221 9 doi 10 1111 ppl 12252 PMID 25104168 7 0 7 1 7 2 Srivastava N Akhila A August 2010 Biosynthesis of andrographolide in Andrographis paniculata Phytochemistry 71 11 12 1298 304 doi 10 1016 j phytochem 2010 05 022 PMID 20557910 ekhathungcak https th wikipedia org w index php title aexnodrkraofild amp oldid 9371376, wikipedia, วิกิ หนังสือ, หนังสือ, ห้องสมุด,