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Merck

852627

Sigma-Aldrich

2,6-二巯基嘌呤

别名:

2,6-二硫嘌呤, 2,6-嘌呤二硫酚, 二硫代黄嘌呤

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About This Item

经验公式(希尔记法):
C5H4N4S2
CAS号:
分子量:
184.24
EC號碼:
MDL號碼:
分類程式碼代碼:
12352100
PubChem物質ID:

mp

>350 °C (lit.)

SMILES 字串

Sc1nc(S)c2[nH]cnc2n1

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儲存類別代碼

11 - Combustible Solids

水污染物質分類(WGK)

WGK 3

閃點(°F)

Not applicable

閃點(°C)

Not applicable

個人防護裝備

Eyeshields, Gloves, type N95 (US)


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分析证书(COA)

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M C MacLeod et al.
Cancer research, 51(18), 4859-4864 (1991-09-25)
The chemotherapeutic agent 6-mercaptopurine was previously shown to inhibit the binding of 7r,8t-dihydroxy-9,10t-oxy-7,8,9,10-tetrahydro-benzo(a) pyrene (BPDE-I) to DNA in Chinese hamster ovary cells. Two compounds related to 6-mercaptopurine, 2,6-dithiopurine (DTP) and thiopurinol (TP), have been tested for inhibition of the binding
K Datta et al.
Toxicology, 125(1), 1-11 (1998-05-19)
2,6-Dithiopurine (DTP) has been proposed as a possible chemopreventive agent because of its ability to react with electrophiles. Acrolein, an electrophilic metabolite of cyclophosphamide (CP) involved in the toxicities of this anticancer drug, can be scavenged by DTP. The present
W G Qing et al.
Drug metabolism and disposition: the biological fate of chemicals, 23(8), 854-860 (1995-08-01)
2,6-Dithiopurine (DTP) has been proposed as a possible chemopreventive agent because of its facile reaction with the electrophilic ultimate carcinogen, benzo[a]pyrene diol epoxide, and other reactive electrophiles. Previous studies in mouse skin indicated almost complete inhibition of benzo[a]pyrene diol epoxide-induced
Stephen Boulware et al.
Toxicology and applied pharmacology, 263(2), 203-209 (2012-06-27)
Sulfur mustard [bis(2-chloroethyl)sulfide, SM] is a well-known DNA-damaging agent that has been used in chemical warfare since World War I, and is a weapon that could potentially be used in a terrorist attack on a civilian population. Dermal exposure to
W G Qing et al.
Chemical research in toxicology, 9(8), 1298-1304 (1996-12-01)
Purinethiols are a class of potential cancer chemopreventive agents that exhibit nucleophilic scavenging activity against the carcinogenic electrophile benzo[a]pyrene diol epoxide (BPDE). Of the purinethiols tested previously, 2,6-dithiopurine (DTP), exhibited the highest scavenging activity for BPDE when tested either in

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