JPS61224984A - ビフィドバクテリウム属細菌の増殖剤 - Google Patents
ビフィドバクテリウム属細菌の増殖剤Info
- Publication number
- JPS61224984A JPS61224984A JP60067242A JP6724285A JPS61224984A JP S61224984 A JPS61224984 A JP S61224984A JP 60067242 A JP60067242 A JP 60067242A JP 6724285 A JP6724285 A JP 6724285A JP S61224984 A JPS61224984 A JP S61224984A
- Authority
- JP
- Japan
- Prior art keywords
- genus bifidobacterium
- bacterium belonging
- multiplying agent
- bacterium
- bifidobacterium
- 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
- 241000186000 Bifidobacterium Species 0.000 title claims abstract description 16
- 241000894006 Bacteria Species 0.000 title abstract description 12
- 239000003795 chemical substances by application Substances 0.000 abstract description 8
- 150000001875 compounds Chemical class 0.000 abstract description 5
- 229920001817 Agar Polymers 0.000 abstract description 2
- 239000008272 agar Substances 0.000 abstract description 2
- ZVNUABIDENQZES-UHFFFAOYSA-N 1-(3-phenylpropanoyl)piperidin-2-one Chemical compound C1CCCC(=O)N1C(=O)CCC1=CC=CC=C1 ZVNUABIDENQZES-UHFFFAOYSA-N 0.000 abstract 1
- NGNBDVOYPDDBFK-UHFFFAOYSA-N 2-[2,4-di(pentan-2-yl)phenoxy]acetyl chloride Chemical compound CCCC(C)C1=CC=C(OCC(Cl)=O)C(C(C)CCC)=C1 NGNBDVOYPDDBFK-UHFFFAOYSA-N 0.000 description 9
- 238000006243 chemical reaction Methods 0.000 description 8
- 150000003951 lactams Chemical class 0.000 description 6
- FYSNRJHAOHDILO-UHFFFAOYSA-N thionyl chloride Chemical compound ClS(Cl)=O FYSNRJHAOHDILO-UHFFFAOYSA-N 0.000 description 6
- 238000000034 method Methods 0.000 description 4
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 3
- ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 3
- 239000002253 acid Substances 0.000 description 3
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 2
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 2
- JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical compound C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 description 2
- 150000008065 acid anhydrides Chemical class 0.000 description 2
- 239000003814 drug Substances 0.000 description 2
- 229940079593 drug Drugs 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 210000003608 fece Anatomy 0.000 description 2
- 235000013305 food Nutrition 0.000 description 2
- 210000000936 intestine Anatomy 0.000 description 2
- VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 2
- CTSLXHKWHWQRSH-UHFFFAOYSA-N oxalyl chloride Chemical compound ClC(=O)C(Cl)=O CTSLXHKWHWQRSH-UHFFFAOYSA-N 0.000 description 2
- XUWHAWMETYGRKB-UHFFFAOYSA-N piperidin-2-one Chemical compound O=C1CCCCN1 XUWHAWMETYGRKB-UHFFFAOYSA-N 0.000 description 2
- 239000000843 powder Substances 0.000 description 2
- 230000002062 proliferating effect Effects 0.000 description 2
- 230000001902 propagating effect Effects 0.000 description 2
- 239000011541 reaction mixture Substances 0.000 description 2
- WBYWAXJHAXSJNI-VOTSOKGWSA-M .beta-Phenylacrylic acid Natural products [O-]C(=O)\C=C\C1=CC=CC=C1 WBYWAXJHAXSJNI-VOTSOKGWSA-M 0.000 description 1
- OKDGRDCXVWSXDC-UHFFFAOYSA-N 2-chloropyridine Chemical class ClC1=CC=CC=N1 OKDGRDCXVWSXDC-UHFFFAOYSA-N 0.000 description 1
- WLJVXDMOQOGPHL-PPJXEINESA-N 2-phenylacetic acid Chemical compound O[14C](=O)CC1=CC=CC=C1 WLJVXDMOQOGPHL-PPJXEINESA-N 0.000 description 1
- XMIIGOLPHOKFCH-UHFFFAOYSA-N 3-phenylpropionic acid Chemical compound OC(=O)CCC1=CC=CC=C1 XMIIGOLPHOKFCH-UHFFFAOYSA-N 0.000 description 1
- WBYWAXJHAXSJNI-SREVYHEPSA-N Cinnamic acid Chemical compound OC(=O)\C=C/C1=CC=CC=C1 WBYWAXJHAXSJNI-SREVYHEPSA-N 0.000 description 1
- 206010012735 Diarrhoea Diseases 0.000 description 1
- 208000004232 Enteritis Diseases 0.000 description 1
- RFSUNEUAIZKAJO-ARQDHWQXSA-N Fructose Chemical class OC[C@H]1O[C@](O)(CO)[C@@H](O)[C@@H]1O RFSUNEUAIZKAJO-ARQDHWQXSA-N 0.000 description 1
- 206010021143 Hypoxia Diseases 0.000 description 1
- BPQQTUXANYXVAA-UHFFFAOYSA-N Orthosilicate Chemical compound [O-][Si]([O-])([O-])[O-] BPQQTUXANYXVAA-UHFFFAOYSA-N 0.000 description 1
- OAICVXFJPJFONN-UHFFFAOYSA-N Phosphorus Chemical compound [P] OAICVXFJPJFONN-UHFFFAOYSA-N 0.000 description 1
- PMZURENOXWZQFD-UHFFFAOYSA-L Sodium Sulfate Chemical compound [Na+].[Na+].[O-]S([O-])(=O)=O PMZURENOXWZQFD-UHFFFAOYSA-L 0.000 description 1
- 125000002777 acetyl group Chemical group [H]C([H])([H])C(*)=O 0.000 description 1
- 230000032683 aging Effects 0.000 description 1
- 229910052783 alkali metal Inorganic materials 0.000 description 1
- -1 alkali metal salt Chemical class 0.000 description 1
- 150000001412 amines Chemical class 0.000 description 1
- 230000001093 anti-cancer Effects 0.000 description 1
- 210000000481 breast Anatomy 0.000 description 1
- 229930016911 cinnamic acid Natural products 0.000 description 1
- 235000013985 cinnamic acid Nutrition 0.000 description 1
- 230000007423 decrease Effects 0.000 description 1
- 230000018044 dehydration Effects 0.000 description 1
- 238000006297 dehydration reaction Methods 0.000 description 1
- 238000000855 fermentation Methods 0.000 description 1
- 230000004151 fermentation Effects 0.000 description 1
- 230000007954 hypoxia Effects 0.000 description 1
- JCQLYHFGKNRPGE-FCVZTGTOSA-N lactulose Chemical compound OC[C@H]1O[C@](O)(CO)[C@@H](O)[C@@H]1O[C@H]1[C@H](O)[C@@H](O)[C@@H](O)[C@@H](CO)O1 JCQLYHFGKNRPGE-FCVZTGTOSA-N 0.000 description 1
- 229960000511 lactulose Drugs 0.000 description 1
- PFCRQPBOOFTZGQ-UHFFFAOYSA-N lactulose keto form Natural products OCC(=O)C(O)C(C(O)CO)OC1OC(CO)C(O)C(O)C1O PFCRQPBOOFTZGQ-UHFFFAOYSA-N 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- WBYWAXJHAXSJNI-UHFFFAOYSA-N methyl p-hydroxycinnamate Natural products OC(=O)C=CC1=CC=CC=C1 WBYWAXJHAXSJNI-UHFFFAOYSA-N 0.000 description 1
- 239000012046 mixed solvent Substances 0.000 description 1
- 239000003960 organic solvent Substances 0.000 description 1
- 239000011574 phosphorus Substances 0.000 description 1
- 229910052698 phosphorus Inorganic materials 0.000 description 1
- UHZYTMXLRWXGPK-UHFFFAOYSA-N phosphorus pentachloride Chemical compound ClP(Cl)(Cl)(Cl)Cl UHZYTMXLRWXGPK-UHFFFAOYSA-N 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 description 1
- HNJBEVLQSNELDL-UHFFFAOYSA-N pyrrolidin-2-one Chemical compound O=C1CCCN1 HNJBEVLQSNELDL-UHFFFAOYSA-N 0.000 description 1
- 102200033386 rs886039568 Human genes 0.000 description 1
- 230000001568 sexual effect Effects 0.000 description 1
- 229910052938 sodium sulfate Inorganic materials 0.000 description 1
- 235000011152 sodium sulphate Nutrition 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 238000010189 synthetic method Methods 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
Landscapes
- Micro-Organisms Or Cultivation Processes Thereof (AREA)
- Medicines Containing Material From Animals Or Micro-Organisms (AREA)
- Dairy Products (AREA)
- Confectionery (AREA)
- Coloring Foods And Improving Nutritive Qualities (AREA)
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP60067242A JPS61224984A (ja) | 1985-03-30 | 1985-03-30 | ビフィドバクテリウム属細菌の増殖剤 |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP60067242A JPS61224984A (ja) | 1985-03-30 | 1985-03-30 | ビフィドバクテリウム属細菌の増殖剤 |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS61224984A true JPS61224984A (ja) | 1986-10-06 |
| JPH0468910B2 JPH0468910B2 (enExample) | 1992-11-04 |
Family
ID=13339251
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP60067242A Granted JPS61224984A (ja) | 1985-03-30 | 1985-03-30 | ビフィドバクテリウム属細菌の増殖剤 |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPS61224984A (enExample) |
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP0943609A1 (en) * | 1998-03-18 | 1999-09-22 | Toa Pharmaceutical Co., Ltd. | Azetidine derivative, bifidobacterium division-promoting composition containing the same, and a process for production thereof |
| JPWO2020175690A1 (enExample) * | 2019-02-28 | 2020-09-03 |
-
1985
- 1985-03-30 JP JP60067242A patent/JPS61224984A/ja active Granted
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP0943609A1 (en) * | 1998-03-18 | 1999-09-22 | Toa Pharmaceutical Co., Ltd. | Azetidine derivative, bifidobacterium division-promoting composition containing the same, and a process for production thereof |
| JPWO2020175690A1 (enExample) * | 2019-02-28 | 2020-09-03 |
Also Published As
| Publication number | Publication date |
|---|---|
| JPH0468910B2 (enExample) | 1992-11-04 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| Hollifield Jr et al. | Ferric enterobactin transport system in Escherichia coli K-12. Extraction, assay, and specificity of the outer membrane receptor | |
| Yamamoto et al. | Isolation and structure elucidation of acinetobactin., a novel siderophore from Acinetobacter baumannii | |
| Fujioka et al. | Anti-AIDS agents, 11. Betulinic acid and platanic acid as anti-HIV principles from Syzigium claviflorum, and the anti-HIV activity of structurally related triterpenoids | |
| Rotstein et al. | Succinic acid, a metabolic by-product of Bacteroides species, inhibits polymorphonuclear leukocyte function | |
| Kolenbrander et al. | Inhibition of coaggregation between Fusobacterium nucleatum and Porphyromonas (Bacteroides) gingivalis by lactose and related sugars | |
| Loesche et al. | The predominant cultivable flora of tooth surface plaque removed from institutionalized subjects | |
| Nagabhushan et al. | Mutagenicity of chili extract and capsaicin in short‐term tests | |
| Kass | The antibacterial activity of 3-decynoyl-N-acetylcysteamine: Inhibition in vivo of β-hydroxydecanoyl thioester dehydrase | |
| Braun et al. | The biosynthesis of dihydrosphingosine in cell-free preparations of Hansenula ciferri. | |
| EP0357673A1 (en) | ANTIBIOTIC REUTERIN. | |
| ES8406477A1 (es) | Procedimiento para la preparacion de b-carbolinas | |
| US5352586A (en) | Method of determining the presence of an antibiotic produced by Lactobacillus reuteri | |
| Anding et al. | Nonspecific biosynthesis of hopane triterpenes in a cell-free system from Acetobacter rancens | |
| JPS61224984A (ja) | ビフィドバクテリウム属細菌の増殖剤 | |
| WO1993002185A1 (en) | Acat inhibitor | |
| Knight et al. | The specificity of aneurin and nicotinamide in the growth of Staph. aureus | |
| GB1528763A (en) | Carbocyclic-fused pyridine derivatives | |
| LAUER et al. | Antibiotics from basidiomycetes XXXVIII. 2-Methoxy-5-methyl-1, 4-benzoquinone, a thromboxane A 2 receptor antagonist from Lentinus adhaerens | |
| Noble et al. | Incorporation of propionic acid into a branched-chain fatty acid of the preen gland of the goose | |
| McCormick et al. | On the nature of the reversible isomerizations occurring in the tetracycline family | |
| Field et al. | Effects of fatty acids on growth of Bordetella pertussis in defined medium | |
| JPH0898677A (ja) | ビフィズス菌増殖促進組成物 | |
| US5929109A (en) | Enhancing and stabilizing agent of the activity of Bifidus factor | |
| Cook et al. | Antibiotics produced by fungi, and a new phenomenon in optical resolution | |
| GB1565083A (en) | Pseudomonic acid amides |