GB1226438A - - Google Patents
Info
- Publication number
- GB1226438A GB1226438A GB5742968A GB1226438DA GB1226438A GB 1226438 A GB1226438 A GB 1226438A GB 5742968 A GB5742968 A GB 5742968A GB 1226438D A GB1226438D A GB 1226438DA GB 1226438 A GB1226438 A GB 1226438A
- Authority
- GB
- United Kingdom
- Prior art keywords
- optionally
- carbanilide
- salicylanilide
- prepared
- chlorine
- 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.)
- Expired
Links
- GWEHVDNNLFDJLR-UHFFFAOYSA-N 1,3-diphenylurea Chemical compound C=1C=CC=CC=1NC(=O)NC1=CC=CC=C1 GWEHVDNNLFDJLR-UHFFFAOYSA-N 0.000 abstract 6
- WKEDVNSFRWHDNR-UHFFFAOYSA-N salicylanilide Chemical compound OC1=CC=CC=C1C(=O)NC1=CC=CC=C1 WKEDVNSFRWHDNR-UHFFFAOYSA-N 0.000 abstract 3
- 229950000975 salicylanilide Drugs 0.000 abstract 3
- 229910052801 chlorine Inorganic materials 0.000 abstract 2
- 239000000460 chlorine Substances 0.000 abstract 2
- 125000001309 chloro group Chemical group Cl* 0.000 abstract 2
- 125000005186 naphthyloxy group Chemical group C1(=CC=CC2=CC=CC=C12)O* 0.000 abstract 2
- BFCFYVKQTRLZHA-UHFFFAOYSA-N 1-chloro-2-nitrobenzene Chemical compound [O-][N+](=O)C1=CC=CC=C1Cl BFCFYVKQTRLZHA-UHFFFAOYSA-N 0.000 abstract 1
- KJCVRFUGPWSIIH-UHFFFAOYSA-N 1-naphthol Chemical compound C1=CC=C2C(O)=CC=CC2=C1 KJCVRFUGPWSIIH-UHFFFAOYSA-N 0.000 abstract 1
- XGFJMWKZGVEFBI-UHFFFAOYSA-N 2-naphthalen-1-yloxyaniline Chemical class NC1=CC=CC=C1OC1=CC=CC2=CC=CC=C12 XGFJMWKZGVEFBI-UHFFFAOYSA-N 0.000 abstract 1
- 125000003118 aryl group Chemical group 0.000 abstract 1
- -1 aryl isocyanate Chemical class 0.000 abstract 1
- 229910052799 carbon Inorganic materials 0.000 abstract 1
- 125000004432 carbon atom Chemical group C* 0.000 abstract 1
- 239000003795 chemical substances by application Substances 0.000 abstract 1
- 150000001875 compounds Chemical class 0.000 abstract 1
- USIUVYZYUHIAEV-UHFFFAOYSA-N diphenyl ether Chemical compound C=1C=CC=CC=1OC1=CC=CC=C1 USIUVYZYUHIAEV-UHFFFAOYSA-N 0.000 abstract 1
- 230000002070 germicidal effect Effects 0.000 abstract 1
- 125000005843 halogen group Chemical group 0.000 abstract 1
- 125000004435 hydrogen atom Chemical group [H]* 0.000 abstract 1
- 239000012948 isocyanate Substances 0.000 abstract 1
- 125000005184 naphthylamino group Chemical class C1(=CC=CC2=CC=CC=C12)N* 0.000 abstract 1
- 150000002828 nitro derivatives Chemical class 0.000 abstract 1
- YGSDEFSMJLZEOE-UHFFFAOYSA-N salicylic acid Chemical class OC(=O)C1=CC=CC=C1O YGSDEFSMJLZEOE-UHFFFAOYSA-N 0.000 abstract 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C275/00—Derivatives of urea, i.e. compounds containing any of the groups, the nitrogen atoms not being part of nitro or nitroso groups
- C07C275/28—Derivatives of urea, i.e. compounds containing any of the groups, the nitrogen atoms not being part of nitro or nitroso groups having nitrogen atoms of urea groups bound to carbon atoms of six-membered aromatic rings of a carbon skeleton
- C07C275/32—Derivatives of urea, i.e. compounds containing any of the groups, the nitrogen atoms not being part of nitro or nitroso groups having nitrogen atoms of urea groups bound to carbon atoms of six-membered aromatic rings of a carbon skeleton being further substituted by singly-bound oxygen atoms
- C07C275/34—Derivatives of urea, i.e. compounds containing any of the groups, the nitrogen atoms not being part of nitro or nitroso groups having nitrogen atoms of urea groups bound to carbon atoms of six-membered aromatic rings of a carbon skeleton being further substituted by singly-bound oxygen atoms having nitrogen atoms of urea groups and singly-bound oxygen atoms bound to carbon atoms of the same non-condensed six-membered aromatic ring
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB5742968 | 1968-12-03 |
Publications (1)
Publication Number | Publication Date |
---|---|
GB1226438A true GB1226438A (enrdf_load_stackoverflow) | 1971-03-31 |
Family
ID=10479173
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB5742968A Expired GB1226438A (enrdf_load_stackoverflow) | 1968-12-03 | 1968-12-03 |
Country Status (2)
Country | Link |
---|---|
US (1) | US3706799A (enrdf_load_stackoverflow) |
GB (1) | GB1226438A (enrdf_load_stackoverflow) |
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
FR2411831A1 (fr) * | 1977-12-13 | 1979-07-13 | Sumitomo Chemical Co | Derives de n'-phenyl-n-methyluree, leur preparation et leur utilisation comme agents herbicides et fongicides |
US7547804B2 (en) | 2002-07-15 | 2009-06-16 | Myriad Genetics, Inc. | Compounds, compositions, and methods employing same |
WO2020033019A2 (en) | 2018-04-25 | 2020-02-13 | Charles R. Drew University Of Medicine And Science | Novel mct4 inhibitors and uses thereof |
Families Citing this family (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2006060580A1 (en) * | 2004-11-30 | 2006-06-08 | Myriad Genetics, Inc. | Therapeutic formulations |
CA2592035A1 (en) * | 2004-12-27 | 2006-07-06 | Myriad Genetics, Inc. | Method of treating cancer |
-
1968
- 1968-12-03 GB GB5742968A patent/GB1226438A/en not_active Expired
-
1969
- 1969-12-03 US US881869A patent/US3706799A/en not_active Expired - Lifetime
Cited By (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
FR2411831A1 (fr) * | 1977-12-13 | 1979-07-13 | Sumitomo Chemical Co | Derives de n'-phenyl-n-methyluree, leur preparation et leur utilisation comme agents herbicides et fongicides |
FR2433510A1 (fr) * | 1977-12-13 | 1980-03-14 | Sumitomo Chemical Co | Procede de preparation d'isocyanates de 4-(2-naphtyloxy) phenyle et nouveaux produits ainsi obtenus |
FR2434799A1 (fr) * | 1977-12-13 | 1980-03-28 | Sumitomo Chemical Co | Procede pour preparer des ethers de 2-naphtyle et de 4-aminophenyle, ainsi que des ethers de 2-naphtyle de 4-nitrophenyle et nouveaux produits ainsi obtenus |
US7547804B2 (en) | 2002-07-15 | 2009-06-16 | Myriad Genetics, Inc. | Compounds, compositions, and methods employing same |
WO2020033019A2 (en) | 2018-04-25 | 2020-02-13 | Charles R. Drew University Of Medicine And Science | Novel mct4 inhibitors and uses thereof |
WO2020033019A3 (en) * | 2018-04-25 | 2020-04-02 | Charles R. Drew University Of Medicine And Science | Novel mct4 inhibitors and uses thereof |
US10919878B2 (en) | 2018-04-25 | 2021-02-16 | Charles R. Drew University Of Medicine And Science | MCT4 inhibitors and uses thereof |
Also Published As
Publication number | Publication date |
---|---|
US3706799A (en) | 1972-12-19 |
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Legal Events
Date | Code | Title | Description |
---|---|---|---|
PS | Patent sealed [section 19, patents act 1949] | ||
PCNP | Patent ceased through non-payment of renewal fee |