Patent(s) and the Corresponding Patented Drug(s) |
Top |
World Intellectual Property Organization (WIPO) |
Patent ID |
WO2015162615 |
Title |
Quinazoline Scaffold Based Compounds, Pharmaceutical Compositions and Methods of Use Thereof. |
Abstract |
The present invention relates to novel heterocyclic compounds based on a quinazoline scaffold of formula (I), which bind effectively to the mitochondrial translocator protein (TSPO), and counteract cell death processes. These compounds can also stimulate neuronal differentiation. The present invention further relates to pharmaceutical compositions including such compounds, and methods of using these compounds for the prevention and treatment of brain damage resulting from brain injury, especially secondary brain damage due to traumatic brain injury (TBI). The compounds of the invention are also useful in preventing, treating, and curing brain damage due to neurodegenerative diseases, including underlying and associated pathological and mental disorders. The compounds can also be used to prevent and treat brain damage due to infection, toxic challenges, and excessive drug use, e.g., recreational, over the counter, or prescription drugs. These compounds can also prevent heart failure, for example associated with brain injuries and brain diseases. |
Applicant(s) |
Technion Research & Development Foundation Limited |
Representative Drug(s) |
D0S2SS |
Drug Info
|
Ki = 2.5 nM |
Click to Show More |
[1] |
2
|
D0TP7S
|
Drug Info
|
Ki = 2.5 nM
|
[1] |
3
|
D09JTT
|
Drug Info
|
Ki = 60 nM
|
[1] |
4
|
D0K3ZB
|
Drug Info
|
Ki = 60 nM
|
[1] |
5
|
D02UMS
|
Drug Info
|
Ki = 600 nM
|
[1] |
Patent ID |
WO2015040148 |
Title |
Carbazole Compounds for In Vivo Imaging. |
Abstract |
The present invention concerns in vivo imaging and in particular in vivo imaging of translocator protein (TSPO, formerly known as the peripheral benzodiazepine receptor). An indole-based in vivo imaging agent is provided that overcomes problems relating to known TSPO-binding radiotracers. The present invention also provides a precursor compound useful in the synthesis of the in vivo imaging agent of the invention, as well as a method for synthesis of said precursor compound. Other aspects of the invention include a method for the synthesis of the in vivo imaging agent of the invention comprising use of the precursor compound of the invention, a kit for carrying out said method, and a cassette for carrying out an automated version of said method. In addition, the invention provides a radiopharmaceutical composition comprising the in vivo imaging agent of the invention, as well as methods for the use of said in vivo imaging agent. |
Applicant(s) |
Ge Healthcare Limited |
Representative Drug(s) |
D00UDJ |
Drug Info
|
Ki = 3 nM |
Click to Show More |
[2] |
2
|
D01PXI
|
Drug Info
|
Ki = 4 nM
|
[2] |
3
|
D0B3RK
|
Drug Info
|
Ki = 24 nM
|
[2] |
Patent ID |
WO2012041953 |
Title |
In Vivo Imaging Method for Cancer. |
Abstract |
The present invention provides a method useful in the diagnosis and monitoring of cancer wherein there is an abnormal expression of PBR. The method of the invention is particularly useful in evaluating the severity of the cancer, e.g. PBR expression correlates with cell proliferation rates, metastatic potential, tumour aggressiveness, malignancy progression. The method of the invention can therefore be applied in the determination of likely disease progression and in making an associated prognosis. Furthermore, the method of the invention can find use in determining the likely success of certain therapeutic approaches, or in the evaluation of the efficacy of certain proposed new treatments. |
Applicant(s) |
Ge Healthcare Limited |
Representative Drug(s) |
D04SWU |
Drug Info
|
Ki = 0.73 nM |
Click to Show More |
[2] |
2
|
D0L5EG
|
Drug Info
|
Ki = 0.87 nM
|
[2] |
3
|
D02VRI
|
Drug Info
|
Ki = 1.3 nM
|
[2] |
4
|
D0E6TQ
|
Drug Info
|
Ki = 1.5 nM
|
[2] |
5
|
D0RT5D
|
Drug Info
|
Ki = 1.7 nM
|
[2] |
6
|
D0TQ8V
|
Drug Info
|
Ki = 1.9 nM
|
[2] |
7
|
D0K3QX
|
Drug Info
|
Ki = 3.8 nM
|
[2] |
8
|
D0Q5JO
|
Drug Info
|
Ki = 4 nM
|
[2] |
9
|
D0R0OA
|
Drug Info
|
Ki = 5.4 nM
|
[2] |
10
|
D0NF3Y
|
Drug Info
|
Ki = 7.6 nM
|
[2] |
11
|
D0EI2Q
|
Drug Info
|
Ki = 18 nM
|
[2] |
Patent ID |
WO2010106166 |
Title |
Radiolabelled pyridinyl derivatives for in-vivo imaging. |
Abstract |
The present invention provides a novel radiolabeled aryloxyalinine derivative suitable for in vivo imaging. In comparison to known aryloxyalinine derivative in vivo imaging agents, the in vivo imaging agent of the present invention has better properties for in vivo imaging. The in vivo imaging agent of the present invention demonstrates good selective binding to the peripheral benzodiazepine receptor (PBR), in combination with good brain uptake and in vivo kinetics following administration to a subject. |
Applicant(s) |
GE HEALTHCARE LIMITED |
Representative Drug(s) |
D0A5RG |
Drug Info
|
Ki = 0.056 nM |
Click to Show More |
[1] |
2
|
D0TB2L
|
Drug Info
|
Ki = 2.6 nM
|
[1] |
3
|
D06HIJ
|
Drug Info
|
Ki = 3.6 nM
|
[1] |
4
|
D0IY5H
|
Drug Info
|
Ki = 4.2 nM
|
[1] |
Patent ID |
WO2010037851 |
Title |
Indole Derivatives Suitable for Imaging Neuroinflammation. |
Abstract |
The present invention concerns in vivo imaging and in particular in vivo imaging of the peripheral benzodiazepine receptor (PBR). A tetracyclic indole in vivo imaging agent is provided that binds with high affinity to PBR, has good uptake into the brain following administration, and which preferentially binds to tissues expressing higher levels of PBR. The present invention also provides a precursor compound useful in the synthesis of the in vivo imaging agent of the invention, as well as a method for synthesis of said in vivo imaging agent comprising use of said precursor compound, and a kit for carrying out said method. A cassette for the automated synthesis of the in vivo imaging agent is also provided. In addition, the invention provides a radiopharmaceutical composition comprising the in vivo imaging agent of the invention, as well as methods for the use of said in vivo imaging agent. |
Applicant(s) |
Ge Healthcare Limited |
Representative Drug(s) |
D0U0IH |
Drug Info
|
Ki = 0.68 nM |
[2] |
Patent ID |
WO2010015340 |
Title |
Daa-Pyridine As Peripheral Benzodiazepine Receptor Ligand for Diagnostic Imaging and Pharmaceutical Treatment. |
Abstract |
This invention relates to novel compounds suitable for labelling or already labelled by 18F, methods of preparing such a compound, compositions comprising such compounds, kits comprising such compounds or compositions and uses of such compounds, compositions or kits for therapy and diagnostic imaging by positron emission tomography (PET). |
Applicant(s) |
Bayer Schering Pharma Aktiengesellschaft Lehmann |
Representative Drug(s) |
D0TB2L |
Drug Info
|
Ki = 2.6 nM |
Click to Show More |
[1] |
2
|
D06HIJ
|
Drug Info
|
Ki = 3.6 nM
|
[1] |
3
|
D0IY5H
|
Drug Info
|
Ki = 4.2 nM
|
[1] |
Patent ID |
WO1999056736 |
Title |
Apoptosis-Inducing Compounds. |
Abstract |
The present invention relates to pyrrolobenzoxazepines, pyrrolobenzthiazepines and related compounds having the ability to induce apoptosis, to pharmaceutical compositions comprising these compounds and to their use as anti-tumour agents. |
Applicant(s) |
The Provost, Fellows and Scholars of the College of the Holy and Undivided Trinity of Queen |
Representative Drug(s) |
D0GN5R |
Drug Info
|
IC50 = 0.94 nM; Ki = 0.36 nM |
Click to Show More |
[1] |
2
|
D05GJL
|
Drug Info
|
IC50 = 1.3 nM; Ki = 0.52 nM
|
[1] |
3
|
D0G7HK
|
Drug Info
|
IC50 = 1.3 nM; Ki = 0.51 nM
|
[1] |
4
|
D0GY0E
|
Drug Info
|
IC50 = 2.3 nM; Ki = 0.91 nM
|
[1] |
5
|
D08XOA
|
Drug Info
|
IC50 = 3.8 nM; Ki = 1.5 nM
|
[1] |
6
|
D0O8DG
|
Drug Info
|
IC50 = 4 nM; Ki = 1.8 nM
|
[1] |
7
|
D03ENW
|
Drug Info
|
IC50 = 5.1 nM; Ki = 2 nM
|
[1] |
Patent ID |
WO1999006353 |
Title |
Aryloxyaniline Derivatives. |
Abstract |
Aryloxyaniline derivatives represented by the general formula (I), wherein Ar1 and Ar2represent each a substituted or unsubstituted phenyl, pyridyl, or naphthyl group; R1 represents a hydrogen atom, an alkyl group or the like; X1 represents a hydrogen atom, an alkyl group or the like; and Y1 represents a branched or unbranched 1-6 C alkylene group or a single bond, or pharmaceutically acceptable salts thereof. The derivatives can provide medicines having high affinity for MDR exhibiting therapeutic and prophylactic effects on anxiety and associated diseases, depression, and the like. |
Applicant(s) |
Taisho Pharmaceutical Co., Ltd |
Representative Drug(s) |
D04JEH |
Drug Info
|
IC50 = 0.28 nM |
Click to Show More |
[1] |
2
|
D0FR9I
|
Drug Info
|
IC50 = 0.92 nM; Ki = 2.8 nM
|
[1] |
Patent ID |
WO1993011771 |
Title |
Use of Peripheral-Type Benzodiazepine Sites for Treatment of Cns Trauma or Disease. |
Abstract |
It is a purpose of this invention to provide a means of treating various central nervous system (CNS) injuries to prevent or minimize damage to the CNS. A novel use has been found for some previously known compounds which are inhibitory agonists of the peripheral-type BZ receptors. It is another purpose of this invention to provide a means of speeding the recovery of tissue damaged through injury to the CNS. The above described inhibitory agonists of the peripheral-type BZ receptors are useful for this purpose, and provide an easily administrable medication. Additionally, a means is provided for screening for new compounds which will act as inhibitory agonists of the peripheral-type BZ receptors and therefore which can be used for treating CNS injuries and for speeding the recovery of tissue damaged through such injuries. |
Applicant(s) |
Cocensys, Inc |
Representative Drug(s) |
D0FF5C |
Drug Info
|
IC50 = 0.11 nM |
Click to Show More |
[1] |
2
|
D0PE1K
|
Drug Info
|
IC50 = 0.2 nM
|
[1] |
3
|
D06WUT
|
Drug Info
|
IC50 = 4.6 nM
|
[1] |
4
|
D0OB0Q
|
Drug Info
|
IC50 = 9.8 nM
|
[1] |
5
|
D01KPW
|
Drug Info
|
Ki = 28 nM
|
[1] |
6
|
D07KTM
|
Drug Info
|
IC50 = 1500 nM
|
[1] |
7
|
D0AW8P
|
Drug Info
|
IC50 = 10000 nM
|
[1] |
8
|
D0N9DS
|
Drug Info
|
N.A.
|
[1] |
9
|
D0R2XX
|
Drug Info
|
N.A.
|
[1] |
Patent ID |
WO2014138791 |
Title |
Transgenic Non-Human organisms with Non-Functional Tspo Genes. |
Abstract |
The present invention relates to transgenic animal models. Specifically, the present invention relates to transgenic animal models for applications associated with TSPO-related normal physiology, diseases and disorders. The present invention features a transgenic nonhuman animal comprising cells with at least one copy of a non-functional, endogenous TSPO gene. Also disclosed are compounds for investigating or modulating TSPO-related functions. |
Applicant(s) |
Australian Nuclear Science and Technology Organization the University of Sydney |
Representative Drug(s) |
D0HS8T |
Drug Info
|
Ki = 16 nM |
Click to Show More |
[1] |
2
|
D01WQX
|
Drug Info
|
N.A.
|
[1] |
Patent ID |
WO2015113991 |
Title |
Treatment of Degenerations and Light-Induced Damage To The Retina. |
Abstract |
The present invention relates to a compound of the following formula (I): or a pharmaceutically acceptable salt thereof, to be used in the prevention or treatment of light-induced damage and/or a degeneration of the retina in a patient. |
Applicant(s) |
Biocodex |
Representative Drug(s) |
D08ZHA |
Drug Info
|
N.A. |
Click to Show More |
[2] |
2
|
D0JN7L
|
Drug Info
|
N.A.
|
[2] |
Patent ID |
WO2005080334 |
Title |
Novel Heterocyclic Compound. |
Abstract |
Disclosed is a drug having a high affinity for benzodiazepine &ohgr;3 receptors which contains, for example, a compound represented by the formula (1) below as an active constituent and has curative and preventive effects on anxiety and depression. (1) [In the formula, R1 and R2 independently represent a hydrogen atom, an optionally substituted alkyl group, an optionally substituted aryl group or the like; R3 and R4 independently represent a hydrogen atom, an optionally substituted alkyl group or the like; R5, R6, R7 and R8 independently represent a hydrogen atom, an optionally substituted alkyl group, an optionally substituted aryl group or the like; and X represents an oxygen atom, a sulfur atom, NR10 or the like (wherein R10 represents a hydrogen atom, an optionally substituted alkyl group or the like).]. |
Representative Drug(s) |
D08DPU |
Drug Info
|
N.A. |
Click to Show More |
[1] |
2
|
D0AC4P
|
Drug Info
|
N.A.
|
[1] |
Patent ID |
WO2015190568 |
Title |
Medicine for Preventing and/or Treating Stress-Induced Diseases. |
Abstract |
The present invention relates to a medicine for preventing and/or treating stress-induced diseases, said medicine being characterized in that (1S)-2-acetyl-1-(4-chloro-2-methoxyphenyl)-5-fluoro-1,2,3,9-tetrahydrospiro[gama-carboline-4,1'-cyclopropane] is administered at such a specific dose that a brain TSPO occupancy required for the development of the pharmacological activity of the medicine can be obtained. |
Applicant(s) |
Ono Pharmaceutical Co., Ltd |
Representative Drug(s) |
D09GSO |
Drug Info
|
Ki = 0.08 nM |
[2] |
Patent ID |
WO2015037774 |
Title |
[18F]Fluoromethyl Group-Introduced Radiotracer for Positron Emission Tomography for Targeting Brain Neuroinflammation, Synthesis Thereof, and Method for Evaluating Biological Results Using Same. |
Abstract |
The present invention relates to an [18F]fluoromethyl group-introduced radiotracer for positron emission tomography for targeting brain neuroinflammation, a synthesis thereof, and a method for evaluat. |
Applicant(s) |
Bio Imaging Korea Co., Ltd |
Representative Drug(s) |
D0E2XN |
Drug Info
|
Ki = 8.3 nM |
[1] |
Patent ID |
WO2014164678 |
Title |
Translocator Protein Imaging Agents; Methods of Manufacture, and Methods of Use Thereof. |
Abstract |
Radiolabeled 4-phenylquinazoline-2-carboxamides useful as imaging agents for positron emission tomography of translocator protein (TSPO) are described. Methods of detecting TSPO and neuroinflammation using the compounds are described. Also disclosed are radiolabeling methods for selected compounds. |
Applicant(s) |
The United States of America, As Presented By the Secretary, Department of Health and Human Services |
Patent ID |
WO2013076646 |
Title |
A New Diaza-Benzofluoranthene Derivative As Drug. |
Abstract |
The present invention relates to a new 16-tetrazolyl-eburnamenine of formula (I) or pharmaceutically acceptable salt thereof and/or hydrates and/or solvates thereof. The invention also relates to the pharmaceutical compositions containing the compound of formula (I) or hydrates or solvates thereof as active ingredient. The invention also relates to the synthesis of compounds of formula (I), and the chemical and pharmaceutical manufacture of medicaments containing these compounds, as well as the methods of treatment of mammals - including human - with these compounds. There is still further provided methods for the treatment of neurological, neurodegenerative and psychiatric diseases or conditions as well as comprising the step of administering to human, in need of such treatment and/or prophylaxis a pharmaceutical composition comprising a therapeutically effective amount of compound of formula (I) or pharmaceutically acceptable salts thereof alone or together with at least one and a pharmaceutically acceptable carrier and/or diluent. |
Applicant(s) |
Richter Gedeon Nyrt |
Representative Drug(s) |
D0AP1F |
Drug Info
|
N.A. |
[2] |
Patent ID |
WO2015040151 |
Title |
S-Enantiomer of Tetracyclic Indole Derivative As Pbr Ligands. |
Abstract |
The present invention concerns in vivo imaging and in particular in vivo imaging of translocator protein (TSPO, formerly known as the peripheral benzodiazepine receptor). An indole-based in vivo imaging agent is provided that overcomes problems relating to known TSPO-binding radiotracers. The present invention also provides a precursor compound useful in the synthesis of the in vivo imaging agent of the invent ion, as well as a method for synthesis of said precursor compound. Other aspects of the invention include a method for the synthesis of the in vivo imaging agent of the invention comprising use of the precursor compound of the invention, a kit for carrying out said method, and a cassette for carrying out an automated version of said method. In addition, the invention provides a radiopharmaceutical composition comprising the in vivo imaging agent of the invention, as well as methods for the use of said in vivo imaging agent. |
Applicant(s) |
Ge Healthcare Limited |
Patent ID |
WO2015040087 |
Title |
Macrophage Imaging. |
Abstract |
The present invention concerns in vivo imaging and in particular in vivo imaging of activated macrophages. An indole-based in vivo imaging agent labelled with 18F is provided that binds with high affinity to translocator protein (TSPO). Other aspects of the invention include a method of diagnosis and a method of therapy monitoring which comprise the imaging method. In addition, the invention provides the use of the TSPO imaging agent in the methods of the invention. |
Applicant(s) |
Ge Healthcare Limited |
Patent ID |
WO2007103162 |
Title |
Structure Based Drug Design of Steroidogenesis Inhibitors. |
Abstract |
Steroidogenesis begins with the transfer of free cholesterol from intracellular stores into mitochondria. The peripheral-type benzodiazepine receptor (PBR) and steroidogenic acute regulatory protein (StAR) function in this process, functioning together to shuttle cholesterol from outside the mitochondria to the inner mitochondrial membrane. The present invention provides methods of using structure-based drug design to identify peptide and substituted steroid compounds that can inhibit the activity of PBR and StAR via interaction with their cholesterol-binding domains. These approaches facilitated the identification of a number of inhibitory ligands that decrease steroid biosynthesis. |
Applicant(s) |
Samaritan Pharmaceuticals, Inc |
Patent ID |
WO2007057705 |
Title |
Tetracyclic Indole Derivatives As In Vivo Imaging Agents and Having Peripheralbenzodiazepine Receptor Affinity (Pbr). |
Abstract |
The present invention provides novel tetracyclic indole compounds of Formula (I) either as in vivo imaging agents or as therapeutic agents. A method for the preparation of the in vivo imaging agent compound is also provided by the invention, as well as a precursor for use in said method. Pharmaceutical compositions comprising the compounds of the invention are additionally provided. Where the pharmaceutical composition comprises a compound suitable for in vivo imaging, a kit is provided for the preparation of the pharmaceutical composition. In a further aspect, use of the compound for in vivo imaging or treatment of conditions associated with PBR is provided. |
Applicant(s) |
Hammersmith Imanet Ltd |
Patent ID |
WO2006068164 |
Title |
Tricyclic Compound and Use Thereof. |
Abstract |
Disclosed is a compound represented by the following general formula (I): (I) (wherein all the symbols are as defined in the description), a salt thereof, an N-oxide thereof, a solvate thereof, or a p. |
Applicant(s) |
Ono Pharmaceutical Co., Ltd |
Patent ID |
WO2000044384 |
Title |
Use of Pyridazino[4,5-B]Indole-1-Acetamide Derivatives for Preparing Medicines for Treating Diseases Related To The Dysfunction of Peripheral Benzodiazepin Receptors. |
Abstract |
The invention concerns the use of a compound of general formula (I) wherein: X represents a halogen atom; Y represents one or several atoms or groups selected among hydrogen, halogens and hydroxy, methyl, methoxy and nitro groups; R1 represents a C1-C4 alkyl group; R2 and R3 represent each a hydrogen atom or a C1-C4 alkyl group, or R2 and R3 together form with the nitrogen atom bearing them, a pyrrolidinyl, piperidinyl or morpholinyl group, for preparing a medicine for preventing or treating diseases and disorders related to the peripheral benzodiazepin receptor. |
Applicant(s) |
Sanofi Synthelabo |
Patent ID |
WO2010109007 |
Title |
Indole Derivatives. |
United States Patent and Trademark Office (USPTO) |
Patent ID |
US5998624 |
Title |
Haloisoquinoline Carboxamide. |
Representative Drug(s) |
D0I6CF |
Drug Info
|
Ki = 0.26 nM |
Click to Show More |
[1] |
2
|
D0EY2Q
|
Drug Info
|
Ki = 1.3 nM
|
[1] |
3
|
D0CL2E
|
Drug Info
|
Ki = 63 nM
|
[1] |
Patent ID |
US20130203754 |
Title |
2-Aryl Imidazo[1,2-A]Pyridine-3-Acetamide Derivatives, Preparation Methods and Uses Thereof. |
Representative Drug(s) |
D0EG4F |
Drug Info
|
Ki = 3 nM |
Click to Show More |
[1] |
2
|
D0PO3M
|
Drug Info
|
Ki = 7.2 nM
|
[1] |
3
|
D0MR8D
|
Drug Info
|
Ki = 9.3 nM
|
[1] |
4
|
D0K4UF
|
Drug Info
|
Ki = 11 nM
|
[1] |
5
|
D00EBN
|
Drug Info
|
Ki = 39 nM
|
[1] |
6
|
D06PPD
|
Drug Info
|
Ki = 49 nM
|
[1] |
Patent ID |
US20120189548 |
Title |
2-Arylpyrazolo[L,5-Alpha]Pyrimidin-3-Yl Acetamide Derivatives As Ligands for Translocator Protein (18 Kda). |
Representative Drug(s) |
D01LOJ |
Drug Info
|
Ki = 4.7 nM |
Click to Show More |
[1] |
2
|
D0LB3J
|
Drug Info
|
Ki = 7 nM
|
[1] |
Patent ID |
US20110142757 |
Title |
ANovel Compounds and Their Uses In Diagnosis. |
Representative Drug(s) |
D0KZ5O |
Drug Info
|
Ki = 12 nM |
Click to Show More |
[1] |
2
|
D0G5FS
|
Drug Info
|
Ki = 51 nM
|
[1] |
Patent ID |
US20110044898 |
Title |
Translocator Protein Ligands. |
Representative Drug(s) |
D04ESE |
Drug Info
|
Ki = 0.45 nM |
Click to Show More |
[1] |
2
|
D08RTY
|
Drug Info
|
Ki = 0.46 nM
|
[1] |
3
|
D07RWQ
|
Drug Info
|
Ki = 0.97 nM
|
[1] |
4
|
D0M9PB
|
Drug Info
|
Ki = 1.6 nM
|
[1] |
5
|
D09AKT
|
Drug Info
|
Ki = 2.4 nM
|
[1] |
6
|
D0P1TH
|
Drug Info
|
Ki = 2.6 nM
|
[1] |
7
|
D0K3MV
|
Drug Info
|
Ki = 11 nM
|
[1] |
Patent ID |
US20140301947 |
Title |
Methods To Predict Binding Affinity of Tspo Imaging Agents To Tspo. |
Representative Drug(s) |
D0FR9I |
Drug Info
|
IC50 = 0.92 nM; Ki = 2.8 nM |
Click to Show More |
[2] |
2
|
D0H2RG
|
Drug Info
|
Ki = 2.4 nM
|
[2] |
3
|
D01LOJ
|
Drug Info
|
Ki = 4.7 nM
|
[2] |
4
|
D08RNV
|
Drug Info
|
Ki = 8.6 nM
|
[2] |
5
|
D0HS8T
|
Drug Info
|
Ki = 16 nM
|
[2] |
6
|
D01KPW
|
Drug Info
|
Ki = 28 nM
|
[2] |
7
|
D01DWN
|
Drug Info
|
N.A.
|
[2] |
Patent ID |
US20090317328 |
Title |
Tricyclic Oxazepines As In Vivo Imaging Compounds. |
Representative Drug(s) |
D0K4VT |
Drug Info
|
N.A. |
[1] |
Patent ID |
US8338410 |
Title |
Neuroprotective Compounds and Pharmaceutical Compositions Comprising Them. |
Applicant(s) |
Biocodex |
Representative Drug(s) |
D07RRL |
Drug Info
|
N.A. |
Click to Show More |
[2] |
2
|
D0LE6B
|
Drug Info
|
N.A.
|
[2] |
Patent ID |
US20120244073 |
Title |
Aryloxyanilide Imaging Agents. |
Representative Drug(s) |
D01BXA |
Drug Info
|
N.A. |
Click to Show More |
[1] |
2
|
D03PTY
|
Drug Info
|
N.A.
|
[1] |
Patent ID |
US8541428 |
Title |
Heterocyclic Derivatives, Pharmaceutical Compositions and Methods of Use Thereof. |
Representative Drug(s) |
D06RNU |
Drug Info
|
Ki = 600 nM |
[1] |
Patent ID |
US8338488 |
Title |
Use of At Least One Oxime Derivative of 3,5-Seco-4-Nor-Cholestane As Antioxidants. |
Representative Drug(s) |
D09GSO |
Drug Info
|
Ki = 0.08 nM |
[2] |
Patent ID |
US20130177501 |
Title |
In Vivo Imaging Method of Mood Disorders. |
Representative Drug(s) |
D0L5EG |
Drug Info
|
Ki = 0.87 nM |
[2] |
Patent ID |
US20026372740 |
Title |
2-Aryl-8-Oxodihydropurine Derivative, Process for The Producing The Same, Medicinal Compositions Containing The Same, and Intermediates Thereof. |
Applicant(s) |
Dainippon Pharmaceutical Co., Ltd |
Representative Drug(s) |
D0RH7L |
Drug Info
|
N.A. |
[1] |
Patent ID |
US8110569 |
Title |
Enantiomerically Pure S-Etifoxine, Pharmaceutical Compositions Thereof and Methods of Their Use. |
Representative Drug(s) |
D0LE6B |
Drug Info
|
N.A. |
[2] |
Patent ID |
US6372740 |
Title |
2-Aryl-8-Oxodihydropurine Derivative, Process for The Producing The Same, Medicinal Compositions Containing The Same, and Intermediates Thereof. |
Representative Drug(s) |
D0N5LW |
Drug Info
|
N.A. |
[1] |
Patent ID |
US20110212025 |
Title |
Tspo-Targeting Compounds and Uses Thereof. |
Representative Drug(s) |
D05ZAV |
Drug Info
|
N.A. |
[1] |
Patent ID |
US20100029658 |
Title |
Heterocyclic Derivatives, Pharmaceutical Compositions and Methods of Use Thereof. |
Representative Drug(s) |
D0R2XX |
Drug Info
|
N.A. |
[1] |
Patent ID |
US20120039816 |
Title |
Use of 7-Chloro-N,N,5-Trimethyl-4-Oxo-3-Phenyl-3,5-Dihydro-4H-Pyridazino[4,5-B] Indole-1-Acetamide As A Biomarker of Peripheral Benzodiazepine Receptor Levels. |
Intellectual Property Office in India (IP India) |
Patent ID |
IN2012CH03232 |
Title |
Process for The Preparation of Etifoxine Hydrochloride. |
Applicant(s) |
Msn Laboratories Limited |
Representative Drug(s) |
D0LE6B |
Drug Info
|
N.A. |
[2] |