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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
Structure of ISOPROPYL .BETA.-D-THIOGALACTOPYRANOSIDE

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

HIDE SMILES / InChI

Molecular Formula C9H18O5S
Molecular Weight 238.301
Charge 0
Count
Stereochemistry ABSOLUTE
Additional Stereochemistry No
Defined Stereocenters 5 / 5
E/Z Centers 0
Optical Activity UNSPECIFIED

Description
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

Sources: Chemische Berichte (1956), 89, 2215-19.

Approval Year

Targets

Targets

Primary TargetPharmacologyConditionPotency
Target ID: P03023
Gene ID: 945007.0
Gene Symbol: lacI
Target Organism: Escherichia coli (strain K12)
Conditions

Conditions

ConditionModalityTargetsHighest PhaseProduct
PubMed

PubMed

TitleDatePubMed
Patents

Patents

Sample Use Guides

In Vivo Use Guide
Unknown
Route of Administration: Unknown
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.
Substance Class Chemical
Created
by admin
on Sat Dec 16 09:06:12 GMT 2023
Edited
by admin
on Sat Dec 16 09:06:12 GMT 2023
Record UNII
X73VV2246B
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
ISOPROPYL .BETA.-D-THIOGALACTOPYRANOSIDE
Common Name English
ISOPROPYL THIO-.BETA.-D-GALACTOSIDE
Common Name English
IPTG
MI  
Common Name English
ISOPROPYL .BETA.-THIOGALACTOPYRANOSIDE
Common Name English
.BETA.-D-GALACTOPYRANOSIDE, 1-METHYLETHYL 1-THIO-
Systematic Name English
1-METHYLETHYL 1-THIO-.BETA.-D-GALACTOPYRANOSIDE
Systematic Name English
ISOPROPYL .BETA.-THIOGALACTOSIDE
Common Name English
ISOPROPYL BETA-D-1-THIOGALACTOPYRANOSIDE
Common Name English
ISOPROPYL THIOGALACTOSIDE
Common Name English
THIOISOPROPYL .BETA.-D-GALACTOPYRANOSIDE
Common Name English
IPTG [MI]
Common Name English
Code System Code Type Description
PUBCHEM
656894
Created by 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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FDA UNII
X73VV2246B
Created by 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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CAS
367-93-1
Created by 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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SMS_ID
100000151880
Created by 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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ECHA (EC/EINECS)
206-703-0
Created by 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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WIKIPEDIA
Isopropyl thiogalactoside
Created by 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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MERCK INDEX
m6396
Created by admin on Sat Dec 16 09:06:13 GMT 2023 , Edited by admin on Sat Dec 16 09:06:13 GMT 2023
PRIMARY Merck Index
CHEBI
61448
Created by 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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EVMPD
SUB126300
Created by 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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EPA CompTox
DTXSID6041052
Created by 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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DRUG BANK
DB01862
Created by 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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