U.S. Department of Health & Human Services Divider Arrow National Institutes of Health Divider Arrow NCATS

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Showing 2761 - 2770 of 13501 results

Status:
Investigational
Source:
NCT00811785: Phase 3 Interventional Completed Menkes Disease
(2009)
Source URL:

Class (Stereo):
CHEMICAL (ABSOLUTE)

Status:
Investigational
Source:
NCT03920982: Not Applicable Interventional Unknown status Acute Kidney Injury
(2019)
Source URL:

Class (Stereo):
CHEMICAL (ACHIRAL)

Status:
Investigational
Source:
NCT04263337: Phase 1 Interventional Enrolling by invitation Concussion, Brain
(2020)
Source URL:

Class (Stereo):
CHEMICAL (ACHIRAL)

Status:
Investigational
Source:
NCT01905228: Phase 1 Interventional Completed Solid Tumors
(2013)
Source URL:

Class (Stereo):
CHEMICAL (ACHIRAL)



CBL0137 (also known as Curaxin CBL0137) is a metabolically stable curaxin and belongs to the class of small molecules with anti-cancer activity. CBL0137 is in Phase I clinical trials to treat hematological malignancies and solid tumors. CBL0137 binds to Facilitates Chromatin Transcription (FACT) and sequesters the FACT complex on chromatin, which inhibits its activity. This prevents transcription of certain genes involved in cancer-associated signaling pathways; it specifically inhibits the transcription of both NF-kappa β and heat shock transcription factor 1 (HSF1) and simultaneously activates p53. In addition, CBL0137 was investigated in vitro and in models mice for pancreatic ductal adenocarcinoma (PDA) and the obtained data suggested testing of CBL0137 efficacy in Phase II trial in PDA patients alone and in combination with gemcitabine.
Status:
Investigational
Source:
NCT01664143: Phase 1 Interventional Completed Healthy Volunteer
(2012)
Source URL:

Class (Stereo):
CHEMICAL (ABSOLUTE)

Status:
Investigational
Source:
USAN:SCOPAFUNGIN [USAN]
Source URL:

Class (Stereo):
CHEMICAL (RACEMIC)

Scopafungin (also known as GE4800) is an inhibitor of oxidative phosphorylation in mitochondria. Scopafungin also inhibits, in vitro, a variety of pathogenic fungi, yeasts, and gram-positive bacteria.
Status:
Investigational
Source:
INN:metindizate
Source URL:

Class (Stereo):
CHEMICAL (MIXED)

Metindizate was developed as a spasmolytic agent. Information about the current use of this compound is not available.
Status:
Investigational
Source:
NCT01230749: Phase 2 Interventional Completed Diabetes Mellitus, Type 2
(2010)
Source URL:

Class (Stereo):
CHEMICAL (ACHIRAL)

JNJ-41443532 is a C-C motif chemokine receptor 2 antagonist. It is under development for the treatment of type 2 diabetes.
Status:
Investigational
Source:
NCT02193958: Phase 1/Phase 2 Interventional Completed AML
(2014)
Source URL:

Class (Stereo):
CHEMICAL (ACHIRAL)


Status:
Investigational
Source:
NCT01174927: Phase 1 Interventional Completed Opiate
(2010)
Source URL:

Class (Stereo):
CHEMICAL (ACHIRAL)

Diallylmelamine was tested in man as a gastric antisecretory agent. In these tests it was inactive. However, when this compound was administered to trained, unanesthetized dogs, it was surprisingly found to have pronounced and prolonged hypotensive activity. Diallylmelamine is an effective hypotensive agent in hypertensive dogs and rats, having a duration of action exceeding twenty-four hours from a single oral dose. It has limited efficacy in normotensive rats. Hypotensive activity of gradual onset is preceded by a latent period of up to two hours and becomes maximal six hours or more after dosing. This agent does not depress cardiac output or sympathetic vasoconstrictor activity.

Showing 2761 - 2770 of 13501 results