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[ CAS No. 106-22-9 ] {[proInfo.proName]}

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Chemical Structure| 106-22-9
Chemical Structure| 106-22-9
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Product Citations

Product Citations

Fryer, Emily ; Guha, Sujay ; Rogel-Hernandez, Lucero E , et al. DOI: PubMed ID:

Abstract: Throughout history, humans have relied on plants as a source of medication, flavoring, and food. Plants synthesize large chemical libraries and release many of these compounds into the rhizosphere and atmosphere where they affect animal and microbe behavior. To survive, nematodes must have evolved the sensory capacity to distinguish plant-made small molecules (SMs) that are harmful and must be avoided from those that are beneficial and should be sought. This ability to classify chemical cues as a function of their value is fundamental to olfaction, and represents a capacity shared by many animals, including humans. Here, we present an efficient platform based on multi-well plates, liquid handling instrumentation, low-cost optical scanners, and bespoke software that can efficiently determine the chemotaxis valence of single SMs in the model nematode, Caenorhabditis elegans. Using this integrated hardware-wetware-software platform, we screened 90 plant SMs and identified 37 that attracted or repelled wild-type animals, but had no effect on mutants defective in chemosensory transduction. Genetic dissection indicates that for at least 10 of these SMs, response valence emerges from the integration of opposing signals, arguing that olfactory valence is often determined by integrating chemosensory signals over multiple lines of information. This study establishes that C. elegans is an effective discovery engine for determining chemotaxis valence and for identifying natural products detected by the chemosensory nervous system.

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Product Details of [ 106-22-9 ]

CAS No. :106-22-9 MDL No. :MFCD00002935
Formula : C10H20O Boiling Point : No data available
Linear Structure Formula :(CH3)2CCH(CH2)2CHCH3(CH2)2OH InChI Key :QMVPMAAFGQKVCJ-UHFFFAOYSA-N
M.W : 156.27 Pubchem ID :8842
Synonyms :
(±)-Citronellol;(±)-β-Citronellol
Chemical Name :3,7-Dimethyloct-6-en-1-ol

Calculated chemistry of [ 106-22-9 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 11
Num. arom. heavy atoms : 0
Fraction Csp3 : 0.8
Num. rotatable bonds : 5
Num. H-bond acceptors : 1.0
Num. H-bond donors : 1.0
Molar Refractivity : 50.87
TPSA : 20.23 ?2

Pharmacokinetics

GI absorption : High
BBB permeant : Yes
P-gp substrate : No
CYP1A2 inhibitor : No
CYP2C19 inhibitor : No
CYP2C9 inhibitor : No
CYP2D6 inhibitor : No
CYP3A4 inhibitor : No
Log Kp (skin permeation) : -4.48 cm/s

Lipophilicity

Log Po/w (iLOGP) : 2.72
Log Po/w (XLOGP3) : 3.91
Log Po/w (WLOGP) : 2.75
Log Po/w (MLOGP) : 2.7
Log Po/w (SILICOS-IT) : 2.51
Consensus Log Po/w : 2.92

Druglikeness

Lipinski : 0.0
Ghose : None
Veber : 0.0
Egan : 0.0
Muegge : 2.0
Bioavailability Score : 0.55

Water Solubility

Log S (ESOL) : -2.94
Solubility : 0.179 mg/ml ; 0.00114 mol/l
Class : Soluble
Log S (Ali) : -4.03
Solubility : 0.0145 mg/ml ; 0.0000926 mol/l
Class : Moderately soluble
Log S (SILICOS-IT) : -2.21
Solubility : 0.964 mg/ml ; 0.00617 mol/l
Class : Soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 1.0 alert
Leadlikeness : 2.0
Synthetic accessibility : 2.61

Safety of [ 106-22-9 ]

Signal Word:Warning Class:
Precautionary Statements:P280-P305+P351+P338 UN#:
Hazard Statements:H315-H317-H319 Packing Group:
GHS Pictogram:

Application In Synthesis of [ 106-22-9 ]

* All experimental methods are cited from the reference, please refer to the original source for details. We do not guarantee the accuracy of the content in the reference.

  • Downstream synthetic route of [ 106-22-9 ]

[ 106-22-9 ] Synthesis Path-Downstream   1~2

  • 1
  • Muscat grape glycosides; mixture of [ No CAS ]
  • [ 78-70-6 ]
  • [ 106-22-9 ]
  • [ 106-25-2 ]
  • [ 98-55-5 ]
  • 2
  • Muscat grape glycosides; mixture of [ No CAS ]
  • [ 78-70-6 ]
  • [ 106-22-9 ]
  • [ 106-24-1 ]
  • [ 98-55-5 ]
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