Details
Stereochemistry | ABSOLUTE |
Molecular Formula | C9H18O5S |
Molecular Weight | 238.301 |
Optical Activity | UNSPECIFIED |
Defined Stereocenters | 5 / 5 |
E/Z Centers | 0 |
Charge | 0 |
SHOW SMILES / InChI
SMILES
CC(C)S[C@@H]1O[C@H](CO)[C@H](O)[C@H](O)[C@H]1O
InChI
InChIKey=BPHPUYQFMNQIOC-NXRLNHOXSA-N
InChI=1S/C9H18O5S/c1-4(2)15-9-8(13)7(12)6(11)5(3-10)14-9/h4-13H,3H2,1-2H3/t5-,6+,7+,8-,9+/m1/s1
DescriptionSources: https://www.drugbank.ca/drugs/DB01862Curator's Comment: The description was created based on several sources, including
https://www.ncbi.nlm.nih.gov/pubmed/24269673 | https://www.ncbi.nlm.nih.gov/pubmed/10659857 | https://www.ncbi.nlm.nih.gov/pubmed/22723426
Sources: https://www.drugbank.ca/drugs/DB01862
Curator's Comment: The description was created based on several sources, including
https://www.ncbi.nlm.nih.gov/pubmed/24269673 | https://www.ncbi.nlm.nih.gov/pubmed/10659857 | https://www.ncbi.nlm.nih.gov/pubmed/22723426
Isopropyl β-D-1-thiogalactopyranoside (IPTG) is a molecular biology reagent that induces β-galactosidase activity in many bacteria. This compound is a molecular mimic of allolactose, a lactose metabolite that triggers transcription of the lac operon, and it is therefore used to induce protein expression where the gene is under the control of the lac operator. Like allolactose, IPTG binds to the lac repressor and releases the tetrameric repressor from the lac operator in an allosteric manner, thereby allowing the transcription of genes in the lac operon, such as the gene coding for beta-galactosidase, a hydrolase enzyme that catalyzes the hydrolysis of β-galactosides into monosaccharides. But unlike allolactose, the sulfur atom creates a chemical bond which is non-hydrolyzable by the cell, preventing the cell from metabolizing or degrading the inducer.
Originator
Approval Year
Targets
Primary Target | Pharmacology | Condition | Potency |
---|---|---|---|
Target ID: P03023 Gene ID: 945007.0 Gene Symbol: lacI Target Organism: Escherichia coli (strain K12) Sources: https://www.ncbi.nlm.nih.gov/pubmed/22723426 |
Conditions
Condition | Modality | Targets | Highest Phase | Product |
---|---|---|---|---|
Sample Use Guides
In Vitro Use Guide
Sources: https://www.ncbi.nlm.nih.gov/pubmed/10659857
E. coli strain JM2.300 were used for activity evaluation. All cells were grown in LB medium (Difco) with 100 mkg/ml ampicillin plus inducers (Isopropyl β-D-1-thiogalactopyranoside ). Plasmids (pTAK117 and pTAK102) were constructed using basic molecular cloning techniques. pTAK117 (initially in the low state), and pTAK102 (as a control) were grown in thirteen (10^-6-10^-2 M) different concentrations of IPTG for 17 h to steady state, which is diluted twice (at 6 and 12.5 h), into a fresh medium with the same IPTG concentration. However, the induction of pTAK102 control has a familiar sigmoidal shape. In contrast, the pTAK117 toggle follows the induction curve of pTAK102, up to an IPTG concentration of 40 μM, at which point it crosses the bifurcation and exhibits a quasidiscontinuous jump to a high expression state.
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656894
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X73VV2246B
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367-93-1
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100000151880
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206-703-0
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Isopropyl thiogalactoside
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m6396
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61448
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SUB126300
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DTXSID6041052
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DB01862
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admin on Sat Dec 16 09:06:13 GMT 2023 , Edited by admin on Sat Dec 16 09:06:13 GMT 2023
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SUBSTANCE RECORD