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经验公式(希尔记法):
C22H25ClN2OS
化学文摘社编号:
分子量:
400.96
UNSPSC Code:
12352200
MDL number:
NACRES:
NA.21
Assay:
≥98% (HPLC)
Form:
powder
Quality Segment
assay
≥98% (HPLC)
form
powder
color
white to beige
solubility
DMSO: 2 mg/mL, clear
storage temp.
-10 to -25°C
SMILES string
S1c2c(cc(cc2)Cl)\C(=C/CCN4CCN(CC4)CCO)\c3c1cccc3
InChI key
WFPIAZLQTJBIFN-DVZOWYKESA-N
Biochem/physiol Actions
Oral and potent antagonist of D1/D2 dopamine receptors, α1-adrenergic receptors and 5-HT2 receptors.
Zuclopenthixol, a typical antipsychotic, is an oral and potent antagonist of D1/D2 dopamine receptors, α1-adrenergic receptors and 5-HT2 receptors. Zuclopenthixol is approved in some countries for treatment of schizophrenia and other psychoses. Zuclopenthixol is a cis isomer of neuroleptic clopenthixol.
Zuclopenthixol, a typical antipsychotic, is an oral and potent antagonist of D1/D2 dopamine receptors, α1-adrenergic receptors and 5-HT2 receptors. Zuclopenthixol is approved in some countries for treatment of schizophrenia and other psychoses. Zuclopenthixol is a cis isomer of neuroleptic clopenthixol.
signalword
Warning
hcodes
Hazard Classifications
Acute Tox. 4 Oral
存储类别
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
