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900831

Sigma-Aldrich

3-(3-(But-3-yn-1-yl)-3H-diazirin-3-yl)propanoic acid

Synonym(s):

Carboxyl diazirine alkyne, Probe building block

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About This Item

Empirical Formula (Hill Notation):
C8H10N2O2
CAS Number:
1450754-37-6
Molecular Weight:
166.18
MDL number:
MFCD31433997
UNSPSC Code:
12352106
Pricing and availability is not currently available.

form

liquid

Quality Level

100

reaction suitability

reaction type: click chemistry

availability

available only in USA

storage temp.

−20°C

SMILES string

C#CCCC1(N=N1)CCC(O)=O

InChI

1S/C8H10N2O2/c1-2-3-5-8(9-10-8)6-4-7(11)12/h1H,3-6H2,(H,11,12)

InChI key

JRNSKSYASHYNCM-UHFFFAOYSA-N

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1 of 4

This Item
EHU152321EHU158371EHU121211
MISSION® esiRNA targeting human BORCS8-MEF2B

EHU147601

MISSION® esiRNA

MISSION® esiRNA targeting human NANOGNB

EHU152321

MISSION® esiRNA

MISSION® esiRNA targeting human TREH, PHLDB1

EHU158371

MISSION® esiRNA

MISSION® esiRNA targeting human BANF1

EHU121211

MISSION® esiRNA

esiRNA cDNA target sequence

CCAGGGAGCCATCTACACTGTGGAGTACGCCTGCAGCGCCGTGAAGAACCTGGTGGACAGCAGCGTCTACTTCCGCAGCGTGGAGGGTCTGCTCAAACAGGCCATCAGCATCCGGGACCATATGAATGCCAGTGCCCAGGGCCACAGCCCGGAGGAACCACCCCCGCCCTCCTCAGCCTGATCCTGGAAGAGACTCGGGGCCCCCCAGCCTCCGCCAACCCAGACAAAGATCATTCCACTCAGCCTGGGACGATGGGGAGGAAAAAAATCCAGATCTCCCGCATCCTGGACCAAAGGAATCGGCAGGTGACGTTCACCAAGCGGAAGTTCGGGCTGATGAAGAA

esiRNA cDNA target sequence

GCTATGCCTTGGGATCAAGATCCAGAACAATCAACTGGAAATTACAGTGAAGATGAACAAAATGGAAAGCAGAAATGGAGAGAAGAAGGAGAAGCAGGCAGAAAGAGAGAACGAGAAAAAGAAGAAAAAAACGAAAAGGAGCTGCAAGATGAACAGGAAAACAAAAGGAAAAGGGAAAATGAGAAACAGAAACAGTATCCCGAGAAAAGATTAGTCAGCAAATCCCTCATGCATACTCTCTGGGCAAAGTTTAAGTTAAACAGGTGCCCCACTATACAAGAGAGTCTATCACTGTCATTTGAATTTGACATGACACATAAACAGATAAGTCAATGGTTTTGTAAAACGAGGAAGAAATATAATAAAGAAATGTCCAAGAGAAAGCATAAGAAAAAACATATGAGATGGAGATCTCTGTGTTGCCAAGGCT

esiRNA cDNA target sequence

CTCCATCCCCTAGTTGCAGACTCATCACCATGGTTACCATAGTGACTGCTTCATTGCCATGGTTACATACTAATTGCTGCAGCTCTGTGGCCCAGCCCACTGCTTCAGCTGTGGGCCATCTGAGGGTACGTGCCATCATCTCTCCAGCCCAGGCCCCTGGGCATCTCATGCTGGGGGGAAGGGACTGAATACCTTTTTCCTTCCCCCTGCCTGTGTCTTCAGCCCTGATGCACAGGCTGCCAGCCCCCCAGTCCAGCCCTCTCCCTTCCACTGGTGCCTTGCTTAGAGCCAGAAGGGATGAAGCCGGGGGATCTATGGAACAGAGGAGGAGCGATGCAGTTGGGAGAGGAAGCTAGAAGGGTTATGGTTGGAGTTCTGTACAGTGTTGAGTTTCCGACAGGGAA

esiRNA cDNA target sequence

CTCTCCCTGGAGGCCTATCTCCCTCAGAACTGCGCGAGAAGCGAGACCTTAGAAGGCAGGGCTTCCCGCGAAGGACCGGAAAGGAGCGCCTACTAAGGACGCCGTCGAGGTCCGGGGCGCCTCAACTCTATAGCTCTAACTGGCTAGAAGTGCCCAACGTGGAATGTTTCTTTTTTAAAGGCGGCTCTTGAAGCGACCCGGAAGCGGAAGTGGAAGAAAGTTCTAGTGGCTTGAGGTATCCGCAGGAGCGGCCGGGTGGCGGGAGGAACCGTTACGGGAACTGAAGTTGCGGATTAAGCCTGATCAAGATGACAACCTCCCAAAAGCACCGAGACTTCGTGGCAGAGCCCATGGGGGAGAAGCCAGTGGGGAGCCTGGCTGGGATTGGTGAAGTCCTGGGCAAGAAG

product line

MISSION®

product line

MISSION®

product line

MISSION®

product line

MISSION®

Gene Information

human ... MEF2B(4207)

Gene Information

human ... NANOGNB(360030)

Gene Information

human ... TREH(11181), PHLDB1(23187)

Gene Information

human ... BANF1(8815)

Ensembl | human accession no.

ENSG00000064489

Ensembl | human accession no.

ENSG00000205857

Ensembl | human accession no.

ENSG00000019144

Ensembl | human accession no.

ENSG00000175334

storage temp.

−20°C

storage temp.

−20°C

storage temp.

−20°C

storage temp.

−20°C

NCBI accession no.

NM_001145785

NCBI accession no.

NM_001145465

NCBI accession no.

NM_001144758

NCBI accession no.

NM_001143985

Application

Used for chemical probe synthesis, this trifunctional building block contains a light-activated diazirine, alkyne tag, and carboxylic acid synthetic handle. When appended to a ligand or pharmacophore through its acid linker, this building block allows for UV light-induced covalent modification of a biological target with potential for downstream applications via the alkyne tag. Use alone or in parallel with other multi-functional building blocks to discover the optimal probe for your chemical biology experiments.

Other Notes

Design and Synthesis of Minimalist Terminal Alkyne-Containing Diazirine Photo-Crosslinkers and Their Incorporation into Kinase Inhibitors for Cell- and Tissue-Based Proteome Profiling

Fluorescein Derivatives as Bifunctional Molecules for the Simultaneous Inhibiting and Labeling of FTO Protein
Technology Spotlight: Trifuctional Probe Building Blocks

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pictograms

Flame
GHS02

signalword

Danger

hcodes

H242

Hazard Classifications

Self-react. C

Storage Class

5.2 - Organic peroxides and self-reacting hazardous materials

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

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