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A4882

6-Thioguanine

≥98%, Guanine antimetabolite, powder

Synonym(s):

2-Amino-6-mercaptopurine, 2-Amino-6-purinethiol

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250 mg
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CLP 59,800
100 mg
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CLP 91,500
500 mg
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CLP 97,200
1 g
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CLP 172,000
5 g
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CLP 662,000

About This Item

Empirical Formula (Hill Notation):
C5H5N5S
CAS Number:
Molecular Weight:
167.19
NACRES:
NA.77
PubChem Substance ID:
UNSPSC Code:
12352202
EC Number:
205-827-2
MDL number:
Beilstein/REAXYS Number:
157765
Assay:
≥98%
Biological source:
synthetic (organic)
Form:
powder
Solubility:
1 M NaOH: 50 mg/mL, clear to hazy, colorless to light greenish-yellow
Storage temp.:
room temp

CLP 59,800


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Product Name

6-Thioguanine, ≥98%

biological source

synthetic (organic)

Quality Level

assay

≥98%

form

powder

mp

≥300 °C (lit.)

solubility

1 M NaOH: 50 mg/mL, clear to hazy, colorless to light greenish-yellow

storage temp.

room temp

SMILES string

NC1=Nc2nc[nH]c2C(=S)N1

InChI

1S/C5H5N5S/c6-5-9-3-2(4(11)10-5)7-1-8-3/h1H,(H4,6,7,8,9,10,11)

InChI key

WYWHKKSPHMUBEB-UHFFFAOYSA-N

Gene Information

General description

6-Thioguanine is a variant of guanine with hydrogen bonding at the N-7 of the purine ring. Its association with cytosine alters the dimension of the base stacking. 6-Thioguanine usage in treating inflammatory bowel disease (IBD) contributes to nodular regenerative hyperplasia (NRH) in the liver.

Application

6-Thioguanine has been used:
  • to induce autophagy and apoptosis in colorectal cancer cell lines HCT116
  • as a selection marker in the mutation and survival assay in chinese hamster lung fibroblasts culture V79
  • as a selection marker in clonogenic Lung metastasis assay of 4T1-luc cells

Biochem/physiol Actions

Antimetabolite used in the treatment of leukemias. Competes with hypoxanthine and guanine for the enzyme hypoxanthine-guanine phosphoribosyltransferase, which catalzyes a critical step in the generation of purine nucleotides.
Ribosylated and phosphorylated by the same pathway as natural purine bases; as the nucleotide, inhibits a variety of cellular processes involved in nucleic acid synthesis. Has a long history as an effective treatment of leukemia.

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This Item
A46601660000BP878
Tioguanine British Pharmacopoeia (BP) Reference Standard

BP878

Tioguanine

biological source

synthetic (organic)

biological source

synthetic (organic)

biological source

-

biological source

-

Quality Level

200

Quality Level

200

Quality Level

-

Quality Level

-

form

powder

form

lyophilized powder

form

-

form

powder

assay

≥98%

assay

~98%

assay

-

assay

-

storage temp.

room temp

storage temp.

room temp

storage temp.

-

storage temp.

2-8°C

solubility

1 M NaOH: 50 mg/mL, clear to hazy, colorless to light greenish-yellow

solubility

1 M NaOH: 50 mg/mL, clear to slightly hazy

solubility

-

solubility

-


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pictograms

Skull and crossbones

signalword

Danger

hcodes

Hazard Classifications

Acute Tox. 3 Oral

Storage Class

6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Faceshields, Gloves, type P2 (EN 143) respirator cartridges



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Related Content

Product Information Sheet


Delayed effects of accelerated heavy ions on the induction of HPRT mutations in V79 hamster cells
Blaha P, et al.
Mutation Research. Fundamental and Molecular Mechanisms of Mutagenesis, 803(46), 35-41 (2017)
Crystal and molecular structure of 6-thioguanine
Bugg CE and Thewalt U
Journal of the American Chemical Society, 92(25), 7441-7445 (1970)
Jen-Hwey Chiu et al.
Scientific reports, 10(1), 8060-8060 (2020-05-18)
Our previous study demonstrated that upregulation of multiple epidermal growth factor-like domains 11 (MEGF11) gene expression is involved in the mechanism by which recurrence of Triple Negative Breast Cancer (TNBC) occurs. Our aim was to elucidate the role of MEGF11



Global Trade Item Number

SKUGTIN
A4882-500MG04061833375075
A4882-1G04061826731680
A4882-5G04061833375082
A4882-250MG04061833375068
A4882-100MG04061833375051

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