JP2000143691A - 還元型コルチゾ―ル接合体 - Google Patents
還元型コルチゾ―ル接合体Info
- Publication number
- JP2000143691A JP2000143691A JP11282460A JP28246099A JP2000143691A JP 2000143691 A JP2000143691 A JP 2000143691A JP 11282460 A JP11282460 A JP 11282460A JP 28246099 A JP28246099 A JP 28246099A JP 2000143691 A JP2000143691 A JP 2000143691A
- Authority
- JP
- Japan
- Prior art keywords
- cortisol
- labeled
- conjugate
- hydrogen
- reduced
- 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.)
- Withdrawn
Links
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- 229960000890 hydrocortisone Drugs 0.000 title claims abstract description 154
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- 238000009903 catalytic hydrogenation reaction Methods 0.000 description 1
- 239000001913 cellulose Substances 0.000 description 1
- 229920002678 cellulose Polymers 0.000 description 1
- 210000001175 cerebrospinal fluid Anatomy 0.000 description 1
- 210000003756 cervix mucus Anatomy 0.000 description 1
- 229910052729 chemical element Inorganic materials 0.000 description 1
- 125000003636 chemical group Chemical group 0.000 description 1
- DHNRXBZYEKSXIM-UHFFFAOYSA-N chloromethylisothiazolinone Chemical compound CN1SC(Cl)=CC1=O DHNRXBZYEKSXIM-UHFFFAOYSA-N 0.000 description 1
- 238000011210 chromatographic step Methods 0.000 description 1
- 229920001436 collagen Polymers 0.000 description 1
- 230000002860 competitive effect Effects 0.000 description 1
- 238000009833 condensation Methods 0.000 description 1
- 230000005494 condensation Effects 0.000 description 1
- 229920001577 copolymer Polymers 0.000 description 1
- 239000003246 corticosteroid Substances 0.000 description 1
- 229960001334 corticosteroids Drugs 0.000 description 1
- OMFXVFTZEKFJBZ-HJTSIMOOSA-N corticosterone Chemical compound O=C1CC[C@]2(C)[C@H]3[C@@H](O)C[C@](C)([C@H](CC4)C(=O)CO)[C@@H]4[C@@H]3CCC2=C1 OMFXVFTZEKFJBZ-HJTSIMOOSA-N 0.000 description 1
- 238000000502 dialysis Methods 0.000 description 1
- 238000010790 dilution Methods 0.000 description 1
- 239000012895 dilution Substances 0.000 description 1
- 201000010099 disease Diseases 0.000 description 1
- BNIILDVGGAEEIG-UHFFFAOYSA-L disodium hydrogen phosphate Chemical compound [Na+].[Na+].OP([O-])([O-])=O BNIILDVGGAEEIG-UHFFFAOYSA-L 0.000 description 1
- 229910000397 disodium phosphate Inorganic materials 0.000 description 1
- 235000019800 disodium phosphate Nutrition 0.000 description 1
- 208000035475 disorder Diseases 0.000 description 1
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- 210000003743 erythrocyte Anatomy 0.000 description 1
- 150000002148 esters Chemical class 0.000 description 1
- RIFGWPKJUGCATF-UHFFFAOYSA-N ethyl chloroformate Chemical compound CCOC(Cl)=O RIFGWPKJUGCATF-UHFFFAOYSA-N 0.000 description 1
- DNJIEGIFACGWOD-UHFFFAOYSA-N ethyl mercaptane Natural products CCS DNJIEGIFACGWOD-UHFFFAOYSA-N 0.000 description 1
- 238000011156 evaluation Methods 0.000 description 1
- GNBHRKFJIUUOQI-UHFFFAOYSA-N fluorescein Chemical compound O1C(=O)C2=CC=CC=C2C21C1=CC=C(O)C=C1OC1=CC(O)=CC=C21 GNBHRKFJIUUOQI-UHFFFAOYSA-N 0.000 description 1
- 238000001506 fluorescence spectroscopy Methods 0.000 description 1
- 239000003193 general anesthetic agent Substances 0.000 description 1
- 239000011521 glass Substances 0.000 description 1
- 229940116332 glucose oxidase Drugs 0.000 description 1
- 235000019420 glucose oxidase Nutrition 0.000 description 1
- 150000004676 glycans Chemical class 0.000 description 1
- 229920000578 graft copolymer Polymers 0.000 description 1
- 125000004404 heteroalkyl group Chemical group 0.000 description 1
- 125000001072 heteroaryl group Chemical group 0.000 description 1
- 229920001519 homopolymer Polymers 0.000 description 1
- 229940088597 hormone Drugs 0.000 description 1
- 239000005556 hormone Substances 0.000 description 1
- 229930195733 hydrocarbon Natural products 0.000 description 1
- 238000005984 hydrogenation reaction Methods 0.000 description 1
- 230000002527 hyperadrenergic effect Effects 0.000 description 1
- 125000002883 imidazolyl group Chemical group 0.000 description 1
- 230000028993 immune response Effects 0.000 description 1
- 210000000987 immune system Anatomy 0.000 description 1
- 230000004054 inflammatory process Effects 0.000 description 1
- 239000003112 inhibitor Substances 0.000 description 1
- 208000014674 injury Diseases 0.000 description 1
- 238000012690 ionic polymerization Methods 0.000 description 1
- 125000000842 isoxazolyl group Chemical group 0.000 description 1
- 238000002372 labelling Methods 0.000 description 1
- 238000011005 laboratory method Methods 0.000 description 1
- 239000004816 latex Substances 0.000 description 1
- 229920000126 latex Polymers 0.000 description 1
- 210000000265 leukocyte Anatomy 0.000 description 1
- 230000037356 lipid metabolism Effects 0.000 description 1
- 239000012280 lithium aluminium hydride Substances 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 150000002739 metals Chemical class 0.000 description 1
- CSJDCSCTVDEHRN-UHFFFAOYSA-N methane;molecular oxygen Chemical group C.O=O CSJDCSCTVDEHRN-UHFFFAOYSA-N 0.000 description 1
- BEGLCMHJXHIJLR-UHFFFAOYSA-N methylisothiazolinone Chemical compound CN1SC=CC1=O BEGLCMHJXHIJLR-UHFFFAOYSA-N 0.000 description 1
- 229960004465 metyrapone Drugs 0.000 description 1
- FJLBFSROUSIWMA-UHFFFAOYSA-N metyrapone Chemical compound C=1C=CN=CC=1C(C)(C)C(=O)C1=CC=CN=C1 FJLBFSROUSIWMA-UHFFFAOYSA-N 0.000 description 1
- 244000005700 microbiome Species 0.000 description 1
- 229910052759 nickel Inorganic materials 0.000 description 1
- 230000036963 noncompetitive effect Effects 0.000 description 1
- 239000012038 nucleophile Substances 0.000 description 1
- 230000000269 nucleophilic effect Effects 0.000 description 1
- UYDLBVPAAFVANX-UHFFFAOYSA-N octylphenoxy polyethoxyethanol Chemical compound CC(C)(C)CC(C)(C)C1=CC=C(OCCOCCOCCOCCO)C=C1 UYDLBVPAAFVANX-UHFFFAOYSA-N 0.000 description 1
- 125000001715 oxadiazolyl group Chemical group 0.000 description 1
- 239000007800 oxidant agent Substances 0.000 description 1
- 125000005429 oxyalkyl group Chemical group 0.000 description 1
- 229910052763 palladium Inorganic materials 0.000 description 1
- 239000008363 phosphate buffer Substances 0.000 description 1
- 229940097886 phosphorus 32 Drugs 0.000 description 1
- 125000004193 piperazinyl group Chemical group 0.000 description 1
- 125000005936 piperidyl group Chemical group 0.000 description 1
- 229910052697 platinum Inorganic materials 0.000 description 1
- 229920000193 polymethacrylate Polymers 0.000 description 1
- 229920001282 polysaccharide Polymers 0.000 description 1
- 239000005017 polysaccharide Substances 0.000 description 1
- 229910052700 potassium Inorganic materials 0.000 description 1
- 239000011591 potassium Substances 0.000 description 1
- 239000003755 preservative agent Substances 0.000 description 1
- 230000002335 preservative effect Effects 0.000 description 1
- 108090000765 processed proteins & peptides Proteins 0.000 description 1
- 102000004196 processed proteins & peptides Human genes 0.000 description 1
- 125000003373 pyrazinyl group Chemical group 0.000 description 1
- JEXVQSWXXUJEMA-UHFFFAOYSA-N pyrazol-3-one Chemical compound O=C1C=CN=N1 JEXVQSWXXUJEMA-UHFFFAOYSA-N 0.000 description 1
- 125000003226 pyrazolyl group Chemical group 0.000 description 1
- 125000005495 pyridazyl group Chemical group 0.000 description 1
- 125000004076 pyridyl group Chemical group 0.000 description 1
- 125000000714 pyrimidinyl group Chemical group 0.000 description 1
- 238000011002 quantification Methods 0.000 description 1
- 125000002294 quinazolinyl group Chemical group N1=C(N=CC2=CC=CC=C12)* 0.000 description 1
- 125000002943 quinolinyl group Chemical group N1=C(C=CC2=CC=CC=C12)* 0.000 description 1
- 230000005855 radiation Effects 0.000 description 1
- 238000010526 radical polymerization reaction Methods 0.000 description 1
- 230000002285 radioactive effect Effects 0.000 description 1
- 238000001055 reflectance spectroscopy Methods 0.000 description 1
- 230000017162 regulation of protein metabolic process Effects 0.000 description 1
- 210000003660 reticulum Anatomy 0.000 description 1
- 230000028327 secretion Effects 0.000 description 1
- 210000000582 semen Anatomy 0.000 description 1
- 150000003384 small molecules Chemical class 0.000 description 1
- 229910000030 sodium bicarbonate Inorganic materials 0.000 description 1
- 235000017557 sodium bicarbonate Nutrition 0.000 description 1
- 229910000029 sodium carbonate Inorganic materials 0.000 description 1
- 239000012475 sodium chloride buffer Substances 0.000 description 1
- 239000002689 soil Substances 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 230000003595 spectral effect Effects 0.000 description 1
- 210000003802 sputum Anatomy 0.000 description 1
- 208000024794 sputum Diseases 0.000 description 1
- 150000003440 styrenes Chemical class 0.000 description 1
- 239000000758 substrate Substances 0.000 description 1
- 238000001356 surgical procedure Methods 0.000 description 1
- 210000004243 sweat Anatomy 0.000 description 1
- 238000003786 synthesis reaction Methods 0.000 description 1
- 229940037128 systemic glucocorticoids Drugs 0.000 description 1
- 210000001138 tear Anatomy 0.000 description 1
- 238000012360 testing method Methods 0.000 description 1
- 239000010409 thin film Substances 0.000 description 1
- 150000007970 thio esters Chemical class 0.000 description 1
- 125000004001 thioalkyl group Chemical group 0.000 description 1
- 150000003573 thiols Chemical class 0.000 description 1
- 230000008733 trauma Effects 0.000 description 1
- 125000001425 triazolyl group Chemical group 0.000 description 1
- 229910052722 tritium Inorganic materials 0.000 description 1
- GPRLSGONYQIRFK-MNYXATJNSA-N triton Chemical compound [3H+] GPRLSGONYQIRFK-MNYXATJNSA-N 0.000 description 1
- DGVVWUTYPXICAM-UHFFFAOYSA-N β‐Mercaptoethanol Chemical compound OCCS DGVVWUTYPXICAM-UHFFFAOYSA-N 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07J—STEROIDS
- C07J5/00—Normal steroids containing carbon, hydrogen, halogen or oxygen, substituted in position 17 beta by a chain of two carbon atoms, e.g. pregnane and substituted in position 21 by only one singly bound oxygen atom, i.e. only one oxygen bound to position 21 by a single bond
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10S—TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10S436/00—Chemistry: analytical and immunological testing
- Y10S436/815—Test for named compound or class of compounds
- Y10S436/817—Steroids or hormones
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Steroid Compounds (AREA)
- Peptides Or Proteins (AREA)
- Preparation Of Compounds By Using Micro-Organisms (AREA)
- Enzymes And Modification Thereof (AREA)
- Measuring Or Testing Involving Enzymes Or Micro-Organisms (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US10283698P | 1998-10-02 | 1998-10-02 | |
| US60/102836 | 1998-10-02 |
Related Child Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2011090267A Division JP2011148821A (ja) | 1998-10-02 | 2011-04-14 | 還元型コルチゾール接合体 |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JP2000143691A true JP2000143691A (ja) | 2000-05-26 |
| JP2000143691A5 JP2000143691A5 (enExample) | 2006-11-24 |
Family
ID=22291927
Family Applications (2)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP11282460A Withdrawn JP2000143691A (ja) | 1998-10-02 | 1999-10-04 | 還元型コルチゾ―ル接合体 |
| JP2011090267A Pending JP2011148821A (ja) | 1998-10-02 | 2011-04-14 | 還元型コルチゾール接合体 |
Family Applications After (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2011090267A Pending JP2011148821A (ja) | 1998-10-02 | 2011-04-14 | 還元型コルチゾール接合体 |
Country Status (8)
| Country | Link |
|---|---|
| US (1) | US6383766B1 (enExample) |
| EP (1) | EP0992512B1 (enExample) |
| JP (2) | JP2000143691A (enExample) |
| AT (1) | ATE312842T1 (enExample) |
| CA (1) | CA2283597C (enExample) |
| DE (1) | DE69928888T2 (enExample) |
| DK (1) | DK0992512T3 (enExample) |
| ES (1) | ES2253866T3 (enExample) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2021162592A (ja) * | 2020-03-30 | 2021-10-11 | ミナリスメディカル株式会社 | 競合法による検体中のステロイドホルモンの測定用キットの安定化方法 |
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|---|---|---|---|---|
| KR100361933B1 (ko) * | 1993-09-08 | 2003-02-14 | 라 졸라 파마슈티칼 컴파니 | 화학적으로정의된비중합성결합가플랫폼분자및그것의콘주게이트 |
| CA2376057A1 (en) * | 1999-06-08 | 2000-12-14 | La Jolla Pharmaceutical Company | Valency platform molecules comprising aminooxy groups |
| NZ511705A (en) * | 2001-05-14 | 2004-03-26 | Horticulture & Food Res Inst | Methods and rapid immunoassay device for detecting progesterone and other steroids |
| JP2004063363A (ja) * | 2002-07-31 | 2004-02-26 | Semiconductor Energy Lab Co Ltd | 電界発光素子用材料、およびそれを用いた電界発光素子 |
| DE102004034008A1 (de) * | 2004-07-14 | 2006-02-09 | Rösner Research GmbH & Co.KG | Verfahren zur Herstellung von Albumin-Corticoid-Konjugaten |
| GB2418665B8 (en) * | 2004-10-04 | 2008-03-25 | Biotrin Intellectual Pty Ltd | Stabilising diluent for a protein-horseradish peroxidase conjugate |
| CN104251903A (zh) * | 2007-11-22 | 2014-12-31 | 特拉斯医药有限公司 | 血液试样的品质评估方法 |
| JP2017150815A (ja) * | 2014-05-29 | 2017-08-31 | 株式会社日立製作所 | 臨床検査キット及び化学物質検出方法 |
| CN119306830B (zh) * | 2023-07-11 | 2025-06-20 | 东莞市朋志生物科技有限公司 | 抗皮质醇抗体、检测皮质醇的试剂和试剂盒 |
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| JPS5634700A (en) * | 1979-08-29 | 1981-04-06 | Teikoku Hormone Mfg Co Ltd | Novel tetrahydrocorticosteroid derivative and antiserum |
| JPS59104388A (ja) * | 1982-11-08 | 1984-06-16 | アボツト・ラボラトリ−ズ | アミノメチルフルオレセイン誘導体 |
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- 1999-09-24 CA CA002283597A patent/CA2283597C/en not_active Expired - Lifetime
- 1999-09-30 US US09/408,931 patent/US6383766B1/en not_active Expired - Lifetime
- 1999-10-01 ES ES99307762T patent/ES2253866T3/es not_active Expired - Lifetime
- 1999-10-01 DK DK99307762T patent/DK0992512T3/da active
- 1999-10-01 AT AT99307762T patent/ATE312842T1/de active IP Right Revival
- 1999-10-01 EP EP99307762A patent/EP0992512B1/en not_active Expired - Lifetime
- 1999-10-01 DE DE69928888T patent/DE69928888T2/de not_active Expired - Lifetime
- 1999-10-04 JP JP11282460A patent/JP2000143691A/ja not_active Withdrawn
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2011
- 2011-04-14 JP JP2011090267A patent/JP2011148821A/ja active Pending
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| EP0003583A1 (en) * | 1978-02-10 | 1979-08-22 | Sin Hang Lee | Compositions for cytochemical investigation, their use and method for the detection of steroid hormone receptors in human tissues |
| JPS5634700A (en) * | 1979-08-29 | 1981-04-06 | Teikoku Hormone Mfg Co Ltd | Novel tetrahydrocorticosteroid derivative and antiserum |
| JPS59104388A (ja) * | 1982-11-08 | 1984-06-16 | アボツト・ラボラトリ−ズ | アミノメチルフルオレセイン誘導体 |
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2021162592A (ja) * | 2020-03-30 | 2021-10-11 | ミナリスメディカル株式会社 | 競合法による検体中のステロイドホルモンの測定用キットの安定化方法 |
| JP7579190B2 (ja) | 2020-03-30 | 2024-11-07 | ミナリスメディカル株式会社 | 競合法による検体中のステロイドホルモンの測定用キットの安定化方法 |
Also Published As
| Publication number | Publication date |
|---|---|
| DE69928888D1 (de) | 2006-01-19 |
| DK0992512T3 (da) | 2008-03-03 |
| HK1027111A1 (en) | 2001-01-05 |
| EP0992512A2 (en) | 2000-04-12 |
| CA2283597C (en) | 2008-02-05 |
| JP2011148821A (ja) | 2011-08-04 |
| CA2283597A1 (en) | 2000-04-02 |
| ES2253866T3 (es) | 2006-06-01 |
| US6383766B1 (en) | 2002-05-07 |
| EP0992512A3 (en) | 2002-04-17 |
| ATE312842T1 (de) | 2005-12-15 |
| DE69928888T2 (de) | 2006-08-24 |
| EP0992512B1 (en) | 2005-12-14 |
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