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  3. Bupropion impurity 16

Bupropion impurity 16 is an impurity of Bupropion.

For research use only. We do not sell to patients.

Bupropion impurity 16

Bupropion impurity 16 Chemical Structure

CAS No. : 192374-15-5

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Description

Bupropion impurity 16 is an impurity of Bupropion.

Cellular Effect
Cell Line Type Value Description References
HEK293 IC50
>100 nM
Compound: (R,R)-5a
Inhibition of human SERT in HEK293 cells assessed as inhibition of [3H]serotonin uptake
Inhibition of human SERT in HEK293 cells assessed as inhibition of [3H]serotonin uptake
[PMID: 21319801]
HEK293 IC50
>100 μM
Compound: (2R,3R)-4a
Inhibition of [3H]serotonin reuptake at human SERT expressed in HEK293 cells after 90 mins by scintillation counting
Inhibition of [3H]serotonin reuptake at human SERT expressed in HEK293 cells after 90 mins by scintillation counting
[PMID: 20509659]
HEK293 IC50
1.6 μM
Compound: (R,R)-5a
Antagonist activity at human alpha3beta4 nAChR in HEK293 cells assessed as inhibition of carbamylcholine-induced radiolabeled Rb ion efflux
Antagonist activity at human alpha3beta4 nAChR in HEK293 cells assessed as inhibition of carbamylcholine-induced radiolabeled Rb ion efflux
[PMID: 21319801]
HEK293 IC50
12 μM
Compound: (R,R)-5a
Antagonist activity at human alpha4beta4 nAChR in HEK293 cells assessed as inhibition of carbamylcholine-induced radiolabeled Rb ion efflux
Antagonist activity at human alpha4beta4 nAChR in HEK293 cells assessed as inhibition of carbamylcholine-induced radiolabeled Rb ion efflux
[PMID: 21319801]
HEK293 IC50
1200 nM
Compound: (R,R)-5a
Inhibition of human NET in HEK293 cells assessed as inhibition of [3H]norepinephrine uptake
Inhibition of human NET in HEK293 cells assessed as inhibition of [3H]norepinephrine uptake
[PMID: 21319801]
HEK293 IC50
1600 nM
Compound: (R,R)-5a
Inhibition of human DAT in HEK293 cells assessed as inhibition of [3H]dopamine uptake
Inhibition of human DAT in HEK293 cells assessed as inhibition of [3H]dopamine uptake
[PMID: 21319801]
HEK293 IC50
17 μM
Compound: (R,R)-5a
Antagonist activity at human alpha4beta2 nAChR in HEK293 cells assessed as inhibition of carbamylcholine-induced radiolabeled Rb ion efflux
Antagonist activity at human alpha4beta2 nAChR in HEK293 cells assessed as inhibition of carbamylcholine-induced radiolabeled Rb ion efflux
[PMID: 21319801]
HEK293 IC50
241 nM
Compound: (2R,3R)-4a
Inhibition of [3H]norepinephrine reuptake at human NET expressed in HEK293 cells after 90 mins by scintillation counting
Inhibition of [3H]norepinephrine reuptake at human NET expressed in HEK293 cells after 90 mins by scintillation counting
[PMID: 20509659]
HEK293 IC50
630 nM
Compound: (2R,3R)-4a
Inhibition of [3H]dopamine reuptake at human DAT expressed in HEK293 cells after 90 mins by scintillation counting
Inhibition of [3H]dopamine reuptake at human DAT expressed in HEK293 cells after 90 mins by scintillation counting
[PMID: 20509659]
HEK293 IC50
9.4 μM
Compound: (R,R)-5a
Antagonist activity at human alpha1beta1 nAChR in HEK293 cells assessed as inhibition of carbamylcholine-induced radiolabeled Rb ion efflux
Antagonist activity at human alpha1beta1 nAChR in HEK293 cells assessed as inhibition of carbamylcholine-induced radiolabeled Rb ion efflux
[PMID: 21319801]
SH-SY5Y IC50
11 μM
Compound: (2R,3R)-4a
Antagonist activity at alpha3beta4 nicotinic receptor in human SH-SY5Y cells assessed as inhibition varbamylcholine-induced radiolabeled Rb+ influx at by liquid scintillation counting
Antagonist activity at alpha3beta4 nicotinic receptor in human SH-SY5Y cells assessed as inhibition varbamylcholine-induced radiolabeled Rb+ influx at by liquid scintillation counting
[PMID: 20509659]
TE-671 IC50
28 μM
Compound: (2R,3R)-4a
Antagonist activity at alpha-1-beta-1-gamma-delta nicotinic receptor in human TE671 cells assessed as inhibition varbamylcholine-induced radiolabeled Rb+ influx at by liquid scintillation counting
Antagonist activity at alpha-1-beta-1-gamma-delta nicotinic receptor in human TE671 cells assessed as inhibition varbamylcholine-induced radiolabeled Rb+ influx at by liquid scintillation counting
[PMID: 20509659]
Molecular Weight

255.74

Formula

C13H18ClNO2

CAS No.
SMILES

O[C@]1([C@@H](C)NC(C)(C)CO1)C2=CC(Cl)=CC=C2

Shipping

Room temperature in continental US; may vary elsewhere.

Storage

Please store the product under the recommended conditions in the Certificate of Analysis.

Purity & Documentation
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Bupropion impurity 16 Related Classifications

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Help & FAQs
  • Do most proteins show cross-species activity?

    Species cross-reactivity must be investigated individually for each product. Many human cytokines will produce a nice response in mouse cell lines, and many mouse proteins will show activity on human cells. Other proteins may have a lower specific activity when used in the opposite species.

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Product Name:
Bupropion impurity 16
Cat. No.:
HY-W701222
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