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N1771

Sigma-Aldrich

nor-Binaltorphimine dihydrochloride

≥98% (TLC), solid, κ-opioid receptor antagonist

Sinônimo(s):

nor-BNI dihydrochloride

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About This Item

Fórmula empírica (Notação de Hill):
C40H43N3O6 · 2HCl
Número CAS:
113158-34-2
Peso molecular:
734.71
Número MDL:
MFCD00069374
Código UNSPSC:
12352200
ID de substância PubChem:
24278018
NACRES:
NA.77

product name

nor-Binaltorphimine dihydrochloride,

forma

solid

Nível de qualidade

200

temperatura de armazenamento

−20°C

cadeia de caracteres SMILES

Cl[H].Cl[H].Oc1ccc2C[C@H]3N(CC[C@@]45[C@@H](Oc1c24)c6[nH]c7[C@@H]8Oc9c(O)ccc%10C[C@H]%11N(CC[C@@]8(c9%10)[C@@]%11(O)Cc7c6C[C@@]35O)CC%12CC%12)CC%13CC%13

InChI

1S/C40H43N3O6.2ClH/c44-25-7-5-21-13-27-39(46)15-23-24-16-40(47)28-14-22-6-8-26(45)34-30(22)38(40,10-12-43(28)18-20-3-4-20)36(49-34)32(24)41-31(23)35-37(39,29(21)33(25)48-35)9-11-42(27)17-19-1-2-19;;/h5-8,19-20,27-28,35-36,41,44-47H,1-4,9-18H2;2*1H/t27-,28-,35+,36+,37+,38+,39-,40-;;/m1../s1

chave InChI

JOJPJLHRMGPDPV-LZQROVCBSA-N

Informações sobre genes

human ... OPRK1(4986)

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Ações bioquímicas/fisiológicas

Highly selective k-opioid receptor antagonist. nor-Binaltorphimine has antidepressant properties.

Características e benefícios

This compound is featured on the Opioid Receptors page of the Handbook of Receptor Classification and Signal Transduction. To browse other handbook pages, click here.

Código de classe de armazenamento

11 - Combustible Solids

Classe de risco de água (WGK)

WGK 3

Ponto de fulgor (°F)

Not applicable

Ponto de fulgor (°C)

Not applicable

Certificados de análise (COA)

Busque Certificados de análise (COA) digitando o Número do Lote do produto. Os números de lote e remessa podem ser encontrados no rótulo de um produto após a palavra “Lot” ou “Batch”.

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Sigma-Aldrich

E3888

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β-Estradiol ≥98%

Sigma-Aldrich

E8875

β-Estradiol

Central kappa-opioid receptor-mediated antidepressant-like effects of nor-Binaltorphimine: Behavioral and BDNF mRNA expression studies
Zhang H, et al.
European Journal of Pharmacology, 570(1-3), 89-96 (2007)
T K Eisenstein et al.
The Journal of pharmacology and experimental therapeutics, 275(3), 1484-1489 (1995-12-01)
An in vitro assay was used to compare the effect of opioids on antibody production by splenocytes from C3HeB/FeJ, C57BL/6J, C57BL/6ByJ and B6C3F1/J mice immunized with sheep red blood cells (SRBC). Spleen cells were removed from mice that had been
Yan Zhang et al.
Neuron, 99(5), 941-955 (2018-08-21)
The gate control theory proposes that Aβ mechanoreceptor inputs to spinal pain transmission T neurons are gated via feedforward inhibition, but it remains unclear how monosynaptic excitation is gated by disynaptic inhibitory inputs that arrive later. Here we report that
J G Wettstein et al.
Pharmacology, biochemistry, and behavior, 53(2), 411-416 (1996-02-01)
The antinociceptive effects of mu and kappa agonists were examined after the systemic administration of the opioid antagonists nor-binaltorphimine (nor-BNI) and naloxone in the late response or tonic nociceptive phase of the mouse formalin assay. Initially, SC morphine (ED50, 0.97
K W Kim et al.
Life sciences, 58(19), 1671-1679 (1996-01-01)
Receptor binding studies were performed to characterize the properties of subtypes of kappa opioid receptors in membrane preparations of human cerebral cortex. [3H]U69,593 ([3H]U69), a selective kappa 1-agonist, and [3H]diprenorphine ([3H]DIP), a non-selective opioid antagonist, in the presence of 1
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