JPS61118395A - 新規なタンニン - Google Patents
新規なタンニンInfo
- Publication number
- JPS61118395A JPS61118395A JP60245750A JP24575085A JPS61118395A JP S61118395 A JPS61118395 A JP S61118395A JP 60245750 A JP60245750 A JP 60245750A JP 24575085 A JP24575085 A JP 24575085A JP S61118395 A JPS61118395 A JP S61118395A
- Authority
- JP
- Japan
- Prior art keywords
- formula
- group
- acetone
- galloyl
- tables
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Granted
Links
- 229920001864 tannin Polymers 0.000 title claims description 6
- 239000001648 tannin Substances 0.000 title claims description 6
- 235000018553 tannin Nutrition 0.000 title claims description 6
- 150000001875 compounds Chemical class 0.000 claims abstract description 8
- 239000008103 glucose Substances 0.000 claims abstract 3
- WQZGKKKJIJFFOK-GASJEMHNSA-N Glucose Natural products OC[C@H]1OC(O)[C@H](O)[C@@H](O)[C@@H]1O WQZGKKKJIJFFOK-GASJEMHNSA-N 0.000 claims abstract 2
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims abstract 2
- 125000001424 substituent group Chemical group 0.000 claims abstract 2
- 239000000126 substance Substances 0.000 claims description 10
- 229910052739 hydrogen Inorganic materials 0.000 claims description 8
- 229920001301 Hexahydroxydiphenic acid Polymers 0.000 claims description 3
- 239000001257 hydrogen Substances 0.000 claims 4
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims 2
- 150000002431 hydrogen Chemical class 0.000 claims 2
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 abstract description 26
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 abstract description 15
- 238000004440 column chromatography Methods 0.000 abstract description 3
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 abstract description 3
- 239000003795 chemical substances by application Substances 0.000 abstract description 2
- 244000037364 Cinnamomum aromaticum Species 0.000 abstract 1
- 235000014489 Cinnamomum aromaticum Nutrition 0.000 abstract 1
- 235000021511 Cinnamomum cassia Nutrition 0.000 abstract 1
- 241001480057 Quercus salicina Species 0.000 abstract 1
- 239000003814 drug Substances 0.000 abstract 1
- 229940079593 drug Drugs 0.000 abstract 1
- 239000000463 material Substances 0.000 abstract 1
- 229940022682 acetone Drugs 0.000 description 8
- 241000196324 Embryophyta Species 0.000 description 7
- CSCPPACGZOOCGX-WFGJKAKNSA-N acetone d6 Chemical compound [2H]C([2H])([2H])C(=O)C([2H])([2H])[2H] CSCPPACGZOOCGX-WFGJKAKNSA-N 0.000 description 7
- 239000000843 powder Substances 0.000 description 7
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 6
- 239000013078 crystal Substances 0.000 description 4
- 102000004190 Enzymes Human genes 0.000 description 3
- 108090000790 Enzymes Proteins 0.000 description 3
- 238000000034 method Methods 0.000 description 3
- 241001167018 Aroa Species 0.000 description 2
- 241001124532 Bubalus depressicornis Species 0.000 description 2
- 241001070941 Castanea Species 0.000 description 2
- 235000014036 Castanea Nutrition 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 230000002401 inhibitory effect Effects 0.000 description 2
- CSCPPACGZOOCGX-MICDWDOJSA-N 1-deuteriopropan-2-one Chemical compound [2H]CC(C)=O CSCPPACGZOOCGX-MICDWDOJSA-N 0.000 description 1
- RZVAJINKPMORJF-UHFFFAOYSA-N Acetaminophen Chemical compound CC(=O)NC1=CC=C(O)C=C1 RZVAJINKPMORJF-UHFFFAOYSA-N 0.000 description 1
- 241000209134 Arundinaria Species 0.000 description 1
- 241000157855 Cinchona Species 0.000 description 1
- 235000021513 Cinchona Nutrition 0.000 description 1
- 241000723347 Cinnamomum Species 0.000 description 1
- 229920002607 Sanguiin H-6 Polymers 0.000 description 1
- 241000218220 Ulmaceae Species 0.000 description 1
- 241001106462 Ulmus Species 0.000 description 1
- 241000190020 Zelkova serrata Species 0.000 description 1
- 239000007864 aqueous solution Substances 0.000 description 1
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 description 1
- 235000017803 cinnamon Nutrition 0.000 description 1
- 230000003111 delayed effect Effects 0.000 description 1
- FFZOOOCGCNFHAQ-GWOIDVGPSA-N dnc013647 Chemical compound OC1=C(O)C(O)=CC(C(=O)O[C@@H]2[C@@H]3OC(=O)C4=CC(O)=C(O)C(O)=C4C4=C(O)C(O)=C(O)C=C4C(=O)O[C@H]3[C@@H]3OC(=O)C4=C(OC=5C(=C(O)C=C(C=5)C(=O)O[C@H]5[C@@H]6OC(=O)C7=CC(O)=C(O)C(O)=C7C7=C(O)C(O)=C(O)C=C7C(=O)O[C@H]6[C@@H]6OC(=O)C7=CC(O)=C(O)C(O)=C7C7=C(O)C(O)=C(O)C=C7C(=O)OC[C@H]6O5)O)C(O)=C(O)C(O)=C4C4=C(O)C(O)=C(O)C=C4C(=O)OC[C@H]3O2)=C1 FFZOOOCGCNFHAQ-GWOIDVGPSA-N 0.000 description 1
- 238000000605 extraction Methods 0.000 description 1
- 238000002955 isolation Methods 0.000 description 1
- FFZOOOCGCNFHAQ-UHFFFAOYSA-N lambertianin A Natural products OC1=C(O)C(O)=CC(C(=O)OC2C3OC(=O)C4=CC(O)=C(O)C(O)=C4C4=C(O)C(O)=C(O)C=C4C(=O)OC3C3OC(=O)C4=C(OC=5C(=C(O)C=C(C=5)C(=O)OC5C6OC(=O)C7=CC(O)=C(O)C(O)=C7C7=C(O)C(O)=C(O)C=C7C(=O)OC6C6OC(=O)C7=CC(O)=C(O)C(O)=C7C7=C(O)C(O)=C(O)C=C7C(=O)OCC6O5)O)C(O)=C(O)C(O)=C4C4=C(O)C(O)=C(O)C=C4C(=O)OCC3O2)=C1 FFZOOOCGCNFHAQ-UHFFFAOYSA-N 0.000 description 1
- 239000010985 leather Substances 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 230000007721 medicinal effect Effects 0.000 description 1
- 125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 description 1
- 230000000144 pharmacologic effect Effects 0.000 description 1
- 238000000746 purification Methods 0.000 description 1
- 239000002994 raw material Substances 0.000 description 1
- SGSLDKSUNBFVSD-UHFFFAOYSA-N sanguiin H-6 Natural products Oc1cc(cc(O)c1O)C(=O)OC2OC3COC(=O)c4cc(O)c(O)c(O)c4c5c(O)c(O)c(O)c(Oc6cc(cc(O)c6O)C(=O)OC7OC8COC(=O)c9cc(O)c(O)c(O)c9c%10c(O)c(O)c(O)cc%10C(=O)OC8C%11OC(=O)c%12cc(c(O)c(O)c%12O)c%13c(O)c(O)c(O)cc%13C(=O)OC7%11)c5C(=O)OC3C%14OC(=O)c%15cc(c(O)c(O)c%15O)c%16c(O)c(O)c(O)cc%16C(=O)OC2%14 SGSLDKSUNBFVSD-UHFFFAOYSA-N 0.000 description 1
- 238000000926 separation method Methods 0.000 description 1
- 238000000638 solvent extraction Methods 0.000 description 1
Landscapes
- Saccharide Compounds (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Medicines Containing Plant Substances (AREA)
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP60245750A JPS61118395A (ja) | 1985-10-31 | 1985-10-31 | 新規なタンニン |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP60245750A JPS61118395A (ja) | 1985-10-31 | 1985-10-31 | 新規なタンニン |
Related Parent Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP57170013A Division JPS5959638A (ja) | 1982-09-28 | 1982-09-28 | 新規なタンニン |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS61118395A true JPS61118395A (ja) | 1986-06-05 |
| JPS6249278B2 JPS6249278B2 (enrdf_load_stackoverflow) | 1987-10-19 |
Family
ID=17138236
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP60245750A Granted JPS61118395A (ja) | 1985-10-31 | 1985-10-31 | 新規なタンニン |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPS61118395A (enrdf_load_stackoverflow) |
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP0727217A3 (en) * | 1995-02-10 | 1997-01-15 | Suntory Ltd | Pharmaceutical and cosmetic compositions containing God-type ellagitannin as an active ingredient |
| EP0727218A3 (en) * | 1995-02-10 | 1997-01-15 | Suntory Ltd | Anti-allergic compositions containing God-type ellagitannin as the active ingredient |
-
1985
- 1985-10-31 JP JP60245750A patent/JPS61118395A/ja active Granted
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP0727217A3 (en) * | 1995-02-10 | 1997-01-15 | Suntory Ltd | Pharmaceutical and cosmetic compositions containing God-type ellagitannin as an active ingredient |
| EP0727218A3 (en) * | 1995-02-10 | 1997-01-15 | Suntory Ltd | Anti-allergic compositions containing God-type ellagitannin as the active ingredient |
Also Published As
| Publication number | Publication date |
|---|---|
| JPS6249278B2 (enrdf_load_stackoverflow) | 1987-10-19 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| Rinehart et al. | Didemnins and tunichlorin: novel natural products from the marine tunicate Trididemnum solidum | |
| DE69630145T2 (de) | Taxal derivate, deren herstellung und diese enthaltende pharmazeutische zusammenstellungen | |
| EP1634877A1 (en) | Mixture and compounds from mycelia of antrodia camphorata and use thereof | |
| EP0306282A2 (en) | Antiviral compositions derived from marine sponge epipolasis reiswigi and their methods of use | |
| EP0397175B1 (de) | Substituierte Pyrrolizinverbindungen und deren Anwendung in der Pharmazie | |
| Horton et al. | Synthesis and reactions of unsaturated sugars: Unsaturated sugars through thionocarbonate intermediates and synthesis of a 5-deoxy-6-thiohexose system | |
| Deng et al. | Monoterpenoid coumarins from the peels of Clausena lansium | |
| Pettit et al. | Antineoplastic agents. Part 409: Isolation and structure of montanastatin from a terrestrial actinomycete | |
| JPH01149764A (ja) | ビス−ｓ−アルキルベンゼン誘導体 | |
| JPS58154571A (ja) | 新規タンニン | |
| JPS6222990B2 (enrdf_load_stackoverflow) | ||
| JPS61118395A (ja) | 新規なタンニン | |
| JPS6248677A (ja) | 新タンニン | |
| US5747527A (en) | Furanoeremophilane and eremophilanolide sesquiterpenes for treatment of diabetes | |
| JPS63198678A (ja) | 新規化合物、その製造方法及びその用途 | |
| DE3317702C2 (enrdf_load_stackoverflow) | ||
| JPS62142193A (ja) | 新規なるタンニン | |
| US6476065B2 (en) | Discalamide compounds and their use as anti-proliferative agents | |
| JPS61112068A (ja) | 新規なタンニン | |
| JPH01500516A (ja) | グアイアズレン誘導体及びその使用方法 | |
| JPS58189176A (ja) | １−スルホ−２−アゼチジノン誘導体およびその製造法 | |
| JPS6353993B2 (enrdf_load_stackoverflow) | ||
| US4647412A (en) | Anti-tumor derivatives of butanediol and process of preparation | |
| I Almansour et al. | Antimycobacterial agents: synthesis and biological evaluation of novel 4-(substituted-phenyl)-6-methyl-2-oxo-N-(pyridin-2-yl)-1, 2, 3, 4-tetrahydropyrimidine-5-carboxamide derivatives by using one-pot multicomponent method | |
| JP3524164B2 (ja) | 抗腫瘍性物質アレナスタチンａおよび該化合物を活性成分として含有する抗腫瘍剤 |