Skip to Content
Merck
All Photos(1)

Documents

N1771

Sigma-Aldrich

nor-Binaltorphimine dihydrochloride

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

Synonym(s):

nor-BNI dihydrochloride

Sign Into View Organizational & Contract Pricing
All Photos(1)

About This Item

Empirical Formula (Hill Notation):
C40H43N3O6 · 2HCl
CAS Number:
113158-34-2
Molecular Weight:
734.71
MDL number:
MFCD00069374
UNSPSC Code:
12352200
PubChem Substance ID:
24278018
NACRES:
NA.77

product name

nor-Binaltorphimine dihydrochloride,

form

solid

Quality Level

200

storage temp.

−20°C

SMILES string

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

InChI key

JOJPJLHRMGPDPV-LZQROVCBSA-N

Gene Information

human ... OPRK1(4986)

Looking for similar products? Visit Product Comparison Guide

Biochem/physiol Actions

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

Features and Benefits

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.

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

Customers Also Viewed

Slide 1 of 2

1 of 2

[D-Pen2,5]-Enkephalin hydrate ≥95% (HPLC)

Sigma-Aldrich

E3888

[D-Pen2,5]-Enkephalin hydrate

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
View All Related Papers

Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.

Contact Technical Service