Thiolactams
4-Thiouridine, ∽98, MP Biomedicals™
CAS: 13957-31-8 Molecular Formula: C9H12N2O5S Molecular Weight (g/mol): 260.26 MDL Number: MFCD00006538 InChI Key: ZLOIGESWDJYCTF-XVFCMESISA-N Synonym: 4-thiouridine,thiouridine,uridine, 4-thio,1-beta-d-ribofuranosyl-4-thiouracil,1-2r,3r,4s,5r-3,4-dihydroxy-5-hydroxymethyl tetrahydrofuran-2-yl-4-thioxo-3,4-dihydropyrimidin-2 1h-one,1-beta-d-ribofuranosyl-4-thioxo-3,4-dihydropyrimidin-2 1h-one,s4u,thiouridine van,uridine,4-thio,4-thio-d-uridine PubChem CID: 3032615 ChEBI: CHEBI:20480 IUPAC Name: 1-[(2R,3R,4S,5R)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]-4-sulfanylidene-1,2,3,4-tetrahydropyrimidin-2-one SMILES: OC[C@H]1O[C@H]([C@H](O)[C@@H]1O)N1C=CC(=S)NC1=O
4-Thiouridine, 98+%
CAS: 13957-31-8 Molecular Formula: C9H12N2O5S Molecular Weight (g/mol): 260.26 MDL Number: MFCD00006538 InChI Key: ZLOIGESWDJYCTF-XVFCMESISA-N PubChem CID: 3032615 ChEBI: CHEBI:20480 SMILES: OC[C@H]1O[C@H]([C@H](O)[C@@H]1O)N1C=CC(=S)NC1=O
4-Thiouridine, MP Biomedicals™
CAS: 13957-31-8 Molecular Formula: C9H12N2O5S Molecular Weight (g/mol): 260.26 MDL Number: MFCD00006538 InChI Key: ZLOIGESWDJYCTF-XVFCMESISA-N Synonym: 4-thiouridine,thiouridine,uridine, 4-thio,1-beta-d-ribofuranosyl-4-thiouracil,1-2r,3r,4s,5r-3,4-dihydroxy-5-hydroxymethyl tetrahydrofuran-2-yl-4-thioxo-3,4-dihydropyrimidin-2 1h-one,1-beta-d-ribofuranosyl-4-thioxo-3,4-dihydropyrimidin-2 1h-one,s4u,thiouridine van,uridine,4-thio,4-thio-d-uridine PubChem CID: 3032615 ChEBI: CHEBI:20480 IUPAC Name: 1-[(2R,3R,4S,5R)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]-4-sulfanylidene-1,2,3,4-tetrahydropyrimidin-2-one SMILES: OC[C@H]1O[C@H]([C@H](O)[C@@H]1O)N1C=CC(=S)NC1=O
4-Thiouracil, 97%, Thermo Scientific Chemicals
CAS: 591-28-6 Molecular Formula: C4H4N2OS Molecular Weight (g/mol): 128.15 MDL Number: MFCD00090842 InChI Key: OVONXEQGWXGFJD-UHFFFAOYSA-N Synonym: 4-thiouracil,2-hydroxy-4 1h-pyrimidinethione,4-thioxo-3,4-dihydropyrimidin-2 1h-one,2-hydroxy-4-mercaptopyrimidine,uracil, 4-thio,4-mercaptopyrimidin-2-ol,4-sulfanylpyrimidin-2-ol,2-hydroxy-4-thiopyrimidine,2 1h-pyrimidinone, 3,4-dihydro-4-thioxo,2 1h-pyrimidinone, 4-mercapto-9ci PubChem CID: 2734394 IUPAC Name: 4-sulfanylidene-1,2,3,4-tetrahydropyrimidin-2-one SMILES: O=C1NC=CC(=S)N1
Thermo Scientific Chemicals 4-Thiouracil, 97%
CAS: 591-28-6 Molecular Formula: C4H4N2OS Molecular Weight (g/mol): 128.15 MDL Number: MFCD00090842 InChI Key: OVONXEQGWXGFJD-UHFFFAOYSA-N Synonym: 4-thiouracil,2-hydroxy-4 1h-pyrimidinethione,4-thioxo-3,4-dihydropyrimidin-2 1h-one,2-hydroxy-4-mercaptopyrimidine,uracil, 4-thio,4-mercaptopyrimidin-2-ol,4-sulfanylpyrimidin-2-ol,2-hydroxy-4-thiopyrimidine,2 1h-pyrimidinone, 3,4-dihydro-4-thioxo,2 1h-pyrimidinone, 4-mercapto-9ci PubChem CID: 2734394 IUPAC Name: 4-sulfanylidene-1H-pyrimidin-2-one SMILES: O=C1NC=CC(=S)N1
4-Thiouracil 97.0+%, TCI America™
CAS: 591-28-6 Molecular Formula: C4H4N2OS Molecular Weight (g/mol): 128.15 MDL Number: MFCD00090842 InChI Key: OVONXEQGWXGFJD-UHFFFAOYSA-N Synonym: 4-thiouracil,2-hydroxy-4 1h-pyrimidinethione,4-thioxo-3,4-dihydropyrimidin-2 1h-one,2-hydroxy-4-mercaptopyrimidine,uracil, 4-thio,4-mercaptopyrimidin-2-ol,4-sulfanylpyrimidin-2-ol,2-hydroxy-4-thiopyrimidine,2 1h-pyrimidinone, 3,4-dihydro-4-thioxo,2 1h-pyrimidinone, 4-mercapto-9ci PubChem CID: 2734394 IUPAC Name: 4-sulfanylidene-1,2,3,4-tetrahydropyrimidin-2-one SMILES: O=C1NC=CC(=S)N1
Sigma Aldrich 3-(Pyrrolidin-1-ylmethyl)aniline dihydrochloride
MilliporeSigma Sigma Organics products encompass a wide range of quality reagents, solvents, catalysts, and building blocks for organic synthesis. From benchtop discovery to process development and scale-up, Sigma Organics solutions are built to meet the needs of synthetic chemists.
Medchemexpress LLC 2-thiouridine | 20235-78-3 | MFCD03788697 | 99.7% | 260.27 g/mol | C9H12N2O5S | 1 ML
2-Thiouridine is a modified nucleoside provided as a ready-to-use 10 mM solution in DMSO for biochemical and virology research, used to study RNA base-pairing, nonenzymatic replication, and antiviral activity.
- Ready-to-use 10 mM solution in DMSO.
- Supplied volume 1 mL.
- Reported purity 99.7%.
- Molecular weight 260.27 g/mol.
- CAS number 20235-78-3.
- In-solution storage: -80°C (6 months) or -20°C (1 month).
Medchemexpress LLC 4-Thiouridine | 13957-31-8 | 99.98% | 260.27 | 25 MG
4-Thiouridine is a ribonucleoside analog, widely used in RNA analysis and (m)RNA labeling. It inhibits rRNA synthesis and causes a nucleolar stress response.
- Functions as a ribonucleoside analog.
- Utilized for RNA analysis and (m)RNA labeling.
- Labels and purifies nascent rRNA at concentrations of 0-10 μM without significantly affecting rRNA synthesis.
- Strongly inhibits the production and processing of rRNA at concentrations of ≥50 μM.
- Targets nucleoside antimetabolite/analog.
- Acts on the cell cycle/DNA damage pathway.
Medchemexpress LLC 4-Thiouracil | 591-28-6 | 99.98% | 128.15 | 10 G
4-Thiouracil is a thionucleobase with cytostatic properties. It can be utilized as biological photoprobes for detecting RNA structures and nucleic acid-nucleic acid contacts. Additionally, it functions as a potent ultraviolet A (UVA) photosensitizer, generating reactive oxygen species (O2). 4-Thiouracil shows promise for research in photocross linking, photodamage, and photodynamic therapy.
- Thionucleobase with cytostatic properties.
- Can be used as biological photoprobes to detect RNA structures and nucleic acid-nucleic acid contacts.
- Acts as a strong ultraviolet A (UVA) photosensitizer, providing a source of the reactive oxygen species of O2.
- Promising for research of photocross linking, photodamage, as well as photodynamic therapy.
Medchemexpress LLC Uridine,4-thio- | 13957-31-8 | 99.98% | 260.27 | 1 ML
4-Thiouridine is a ribonucleoside analog widely used in RNA analysis and (m)RNA labeling. It works by inhibiting rRNA synthesis, which leads to a nucleolar stress response. It is intended for research use only and is not sold to patients.
- Ribonucleoside analog
- Used in RNA analysis and mRNA labeling
- Inhibits rRNA synthesis
- Causes a nucleolar stress response
- High purity: 99.98%
- Labels and purifies nascent rRNA at 0-10 μM
- Strongly inhibits rRNA production and processing at ≥50 μM
Apexbio Technology LLC 2-Thiouracil 141-90-2 10mM (in 1mL DMSO)
2-Thiouracil (CAS 141-90-2) is a sulfur-containing derivative of uracil that functions as an inhibitor of thyroid hormone synthesis It exerts its antihyperthyroid effects by interfering with the enzymatic iodination of tyrosine residues within thyroglobulin thereby suppressing the production of triiodothyronine (T3) and thyroxine (T4) Due to its capacity to modulate thyroid function 2-Thiouracil is utilized in biomedical research to study thyroid hormone regulation and associated disorders as well as to model hypothyroid states in experimental settings
Medchemexpress LLC 4-Thiouracil | 591-28-6 | 99.98% | 128.15 | 100 MG
4-Thiouracil is a thionucleobase possessing cytostatic properties. It functions as a biological photoprobe for detecting RNA structures and nucleic acid-nucleic acid contacts. Additionally, it serves as a potent ultraviolet A (UVA) photosensitizer, generating reactive oxygen species (O2). 4-Thiouracil holds promise for research in photocrosslinking, photodamage, and photodynamic therapy.
- Thionucleobase with cytostatic properties.
- Can be used as biological photoprobes to detect RNA structures and nucleic acid-nucleic acid contacts.
- Acts as a strong UVA photosensitizer, providing a source of reactive oxygen species (O2).
- Promising for research in photocrosslinking, photodamage, and photodynamic therapy.
Apexbio Technology LLC 2-Thiouracil 141-90-2 5g
2-Thiouracil (CAS 141-90-2) is a sulfur-containing derivative of uracil that functions as an inhibitor of thyroid hormone synthesis It exerts its antihyperthyroid effects by interfering with the enzymatic iodination of tyrosine residues within thyroglobulin thereby suppressing the production of triiodothyronine (T3) and thyroxine (T4) Due to its capacity to modulate thyroid function 2-Thiouracil is utilized in biomedical research to study thyroid hormone regulation and associated disorders as well as to model hypothyroid states in experimental settings