Ciliobrevin A

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Names

[ CAS No. ]:
302803-72-1

[ Name ]:
Ciliobrevin A

[Synonym ]:
Ciliobrevin A
HPI-4

Chemical & Physical Properties

[ Molecular Formula ]:
C17H9Cl2N3O2

[ Molecular Weight ]:
358.17800

[ Exact Mass ]:
357.00700

[ PSA ]:
89.51000

[ LogP ]:
3.00128

[ Storage condition ]:
-20℃

Safety Information

[ Symbol ]:

GHS07, GHS09

[ Signal Word ]:
Warning

[ Hazard Statements ]:
H302-H410

[ Precautionary Statements ]:
P273-P501

[ RIDADR ]:
UN 3077 9 / PGIII

Articles

Effects of the dynein inhibitor ciliobrevin on the flagellar motility of sea urchin spermatozoa.

Cytoskeleton (Hoboken.) 72 , 182-92, (2015)

Ciliobrevin has recently been found to be a membrane-permeable inhibitor that is specific to AAA+ molecular motors such as cytoplasmic dyneins. In this study, we investigated how ciliobrevin inhibited...

The fate of the primary cilium during myofibroblast transition.

Mol. Biol. Cell 25(5) , 643-57, (2014)

Myofibroblasts, the culprit of organ fibrosis, can originate from mesenchymal and epithelial precursors through fibroblast-myofibroblast and epithelial-myofibroblast transition (EMyT). Because certain...

Polarity protein Par3 controls B-cell receptor dynamics and antigen extraction at the immune synapse.

Mol. Biol. Cell 26(7) , 1273-85, (2015)

B-cell receptor (BCR) engagement with surface-tethered antigens leads to the formation of an immune synapse, which facilitates antigen uptake for presentation to T-lymphocytes. Antigen internalization...


More Articles

Related Compounds

  • actinoplanone A
  • Thapsuine A
  • Apocynol A
  • (2S)-N-[(2S,5S,8S,11R,12S,15S,18S,21R)-5-[(3-bromo-4-methoxyphenyl)methyl]-2-[(2S)-butan-2-yl]-15-[3-(carbamoylamino)propyl]-21-hydroxy-4,11-dimethyl-3,6,9,13,16,22-hexaoxo-8-propan-2-yl-10-oxa-1,4,7,14,17-pentazabicyclo[16.3.1]docosan-12-yl]-2-(butanoyla
  • Pseudoanguillosporin A
  • Digitoside A
  • 1-[3-({[(9H-fluoren-9-yl)methoxy]carbonyl}amino)-2,2-dimethylpropanoyl]-3-methoxypiperidine-3-carboxylic acid
  • 1-[3-({[(9H-fluoren-9-yl)methoxy]carbonyl}amino)-4,4,4-trifluorobutanamido]cyclopropane-1-carboxylic acid
  • 1-[(3S)-3-({[(9H-fluoren-9-yl)methoxy]carbonyl}amino)pentanamido]-3-methylcyclohexane-1-carboxylic acid
  • 2-[(3S)-3-({[(9H-fluoren-9-yl)methoxy]carbonyl}amino)pentanoyl]-2-azabicyclo[2.2.2]octane-6-carboxylic acid
  • (1RS,2SR)-2-[(3S)-3-({[(9H-fluoren-9-yl)methoxy]carbonyl}amino)pentanamido]cyclohexane-1-carboxylic acid
  • 2-[(3S)-3-({[(9H-fluoren-9-yl)methoxy]carbonyl}amino)pentanamido]-5,5-dimethylhexanoic acid
  • 2-(3-{[(3S)-3-({[(9H-fluoren-9-yl)methoxy]carbonyl}amino)pentanamido]methyl}cyclopentyl)acetic acid
  • (2S,3R)-2-[(3S)-3-({[(9H-fluoren-9-yl)methoxy]carbonyl}amino)pentanamido]-3-methoxybutanoic acid
  • (2S)-2-[(3S)-3-({[(9H-fluoren-9-yl)methoxy]carbonyl}amino)butanamido]-3-methylbutanoic acid
  • 3-[(3S)-N-ethyl-3-({[(9H-fluoren-9-yl)methoxy]carbonyl}amino)butanamido]propanoic acid
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