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Merck
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Documenti fondamentali

222909

Sigma-Aldrich

N-Phenylthiourea

97%

Sinonimo/i:

1-Phenyl-2-thiourea, PTU, Phenylthiocarbamide

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About This Item

Formula condensata:
C6H5NHCSNH2
Numero CAS:
Peso molecolare:
152.22
Beilstein:
907309
Numero CE:
Numero MDL:
Codice UNSPSC:
12352100
ID PubChem:

Saggio

97%

Punto di fusione

145-150 °C (lit.)

Stringa SMILE

NC(=S)Nc1ccccc1

InChI

1S/C7H8N2S/c8-7(10)9-6-4-2-1-3-5-6/h1-5H,(H3,8,9,10)
FULZLIGZKMKICU-UHFFFAOYSA-N

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Pittogrammi

Skull and crossbones

Avvertenze

Danger

Indicazioni di pericolo

Classi di pericolo

Acute Tox. 1 Oral - Skin Sens. 1

Codice della classe di stoccaggio

6.1B - Non-combustible acute toxic Cat. 1 and 2 / very toxic hazardous materials

Classe di pericolosità dell'acqua (WGK)

WGK 3

Punto d’infiammabilità (°F)

Not applicable

Punto d’infiammabilità (°C)

Not applicable

Dispositivi di protezione individuale

Eyeshields, Faceshields, Gloves, type P3 (EN 143) respirator cartridges


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Anna A Brozyna et al.
International journal of cancer, 123(6), 1448-1456 (2008-06-21)
Melanin pigment displays strong photo- and radioprotective properties, suggesting that inhibition melanogenesis could increase sensitivity of melanoma to ionizing radiation. We tested this concept in human melanoma cells cultured in either Ham's F10 medium to maintain amelanotic phenotype or DMEM
Xiangguo Shi et al.
Blood, 125(19), 2974-2984 (2015-03-18)
Isocitrate dehydrogenase 1 mutation (IDH1-R132H) was recently identified in acute myeloid leukemia with normal cytogenetics. The mutant enzyme is thought to convert α-ketoglutarate to the pathogenic 2-hydroxyglutarate (2-HG) that affects DNA methylation via inhibition of ten-eleven translocation 2. However, the
Marco Venturin et al.
Journal of medical genetics, 51(7), 436-443 (2014-04-09)
Cardiovascular malformations have a higher incidence in patients with NF1 microdeletion syndrome compared to NF1 patients with intragenic mutation, presumably owing to haploinsufficiency of one or more genes included in the deletion interval and involved in heart development. In order
Thomas Grau et al.
Antimicrobial agents and chemotherapy, 56(2), 1142-1145 (2011-11-23)
Ethionamide (ETH) is a second-line drug for the treatment of tuberculosis. As a prodrug, ETH has to be activated by EthA. ethA is controlled by its repressor EthR. 2-Phenylethyl-butyrate (2-PEB) inhibits EthR binding, enhances expression of EthA, and thereby enhances
Laila Gannoun-Zaki et al.
Antimicrobial agents and chemotherapy, 57(1), 629-632 (2012-11-02)
The mechanism by which the antitubercular drug isoxyl (ISO) inhibits mycolic acid biosynthesis has not yet been reported. We found that point mutations in either the HadA or HadC component of the type II fatty acid synthase (FAS-II) are associated

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