Monoamine Oxidase
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Monoamine oxidases (MAO) are a family of enzymes that catalyze the oxidation of monoamines. They are found bound to the outer membrane of mitochondria in most cell types in the body. They belong to the protein family of flavin-containing amine oxidoreductases. Monoamine oxidases catalyze the oxidative deamination of monoamines. Oxygen is used to remove an amine group from a molecule, resulting in the corresponding aldehyde and ammonia. Monoamine oxidases contain the covalently bound cofactor FAD and are, thus, classified as flavoproteins. Because of the vital role that MAOs play in the inactivation of neurotransmitters, MAO dysfunction is thought to be responsible for a number of psychiatric and neurological disorders. MAO-A inhibitors act as antidepressant and antianxiety agents, whereas MAO-B inhibitors are used alone or in combination to treat Alzheimer’sand Parkinson’s diseases.
Products Related to Monoamine Oxidase(100)
- GC31949PAT-1251 HydrochlorideCAS: 2098884-53-6Purity: >98%
PAT-1251 is a lysyl oxidase-like 2 (LOXL2; IC 50 =0.71μM) inhibitor.
- GC33573Rasagiline 13C3 mesylate racemic (AGN1135 13C3 racemic)CAS: 1216757-55-9Purity: >98%
Rasagiline 13C3 mesylate racemic (AGN1135 13C3 racemic) is a 13C-labeled Rasagiline mesylate racemic.
- GC33677Iproniazid phosphateCAS: 305-33-9Purity: >98.00%
Iproniazid phosphate is a non-selective, irreversible monoamine oxidase (MAO) inhibitor of the hydrazine class.
- GC33686(S)-Rasagiline (TVP1022)CAS: 185517-74-2Purity: >99.00%
(S)-Rasagiline (TVP1022) (TVP1022) is the relatively inactive S-enantiomer form of Rasagiline.
- GC33714Rasagiline (AGN1135)CAS: 136236-51-6Purity: >98.50%
Rasagiline (AGN1135) (R-AGN1135) is a highly potent selective irreversible mitochondrial monoamine oxidase (MAO) inhibitor with IC50s of 4.43nM and 412nM for rat brain MAO B and A activity, respectively.
- GC33718Brofaromine (CGP 11305A)CAS: 63638-91-5Purity: >98.50%
Brofaromine (CGP 11305A) (CGP 11305A) is a monoamine oxidase (MAO) inhibitor with IC50 of 0.2μM for MAO-A.
- GC33749SalsolidineCAS: 5784-74-7Purity: >98%
Salsolidine is a tetrahydroisoquinoline alkaloid, acts as a stereoselective competitive MAO A inhibitor.
- GC33983Amitraz (BTS-27419)CAS: 33089-61-1Purity: >98%
Amitraz (BTS-27419) is a non-systemic acaricide and insecticide, with alpha-adrenergic agonist activity, interaction with octopamine receptors of the central nervous system and inhibition of monoamine oxidases and prostaglandin synthesis.
- GC35006(S)-Rasagiline mesylateCAS: 202464-88-8Purity: >98%
(S)-Rasagiline (TVP1022) mesylate is the relatively inactive S-enantiomer form of Rasagiline mesylate.
- GC351927-Hydroxy-3,4-dihydro-2(1H)-quinolinoneCAS: 22246-18-0Purity: >99.50%
7-?Hydroxy-?3,?4-?dihydro-?2(1H)?-?quinolinone (3,4-Dihydro-7-hydroxy-2(1H)-quinolinone) is a weak MAO-A inhibitor, with an IC50 of 183 μM, and has no effect on MAO-B.
- GC36638Mofegiline hydrochlorideCAS: 120635-25-8Purity: >98%
Mofegiline hydrochloride (MDL72974A) is an orally active and selective enzyme-activated irreversible inhibitor of MAO-B, with marked selectivity on the MAO-B over MAO-A with IC50s of 3.6 nM (MAO-B) and 680 nM (MAO-A), respectively.
- GC38583PXS-5153A monohydrochloridePurity: >99.50%
PXS-5153A monohydrochloride is a potent, selective, orally active and fast-acting lysyl oxidase like 2/3 enzymatic (LOXL2/LOXL3) inhibitor, with an IC50 of <40 nM for LOXL2 across all mammalian species and an IC50 of 63 nM for human LOXL3.
| Catalog No. | Product Name | CAS No. | Purity | Structure |
|---|---|---|---|---|
| GC31021 | 2614W94 | 205187-35-5 | >98% | |
2614W94 is a selective, reversible inhibitor of monoamine oxidase-A with a competitive mechanism of inhibition and IC50 of 5 nM and Ki of 1.6 nM with serotonin as substrate. | ||||
| GC31024 | RS 8359 | 105365-76-2 | >98% | |
RS 8359 is a selective and reversible MAO-A inhibitor, with antidepressant activity. | ||||
| GC31094 | CR4056 | 1004997-71-0 | >98% | |
| GC31104 | Isocarboxazid | 59-63-2 | >98.50% | |
An inhibitor of MAO | ||||
| GC31155 | CX-157 | 205187-53-7 | >98% | |
CX-157 is a reversible inhibitor of monoamine oxidase-A (MAO-A) with an EC50 of 19.3?ng/mL. | ||||
| GC31252 | MAO-IN-1 | 124991-40-8 | >99.00% | |
MAO-IN-1 is a monoamine oxidase B (MAO B) inhibitor with an IC50 of 20 nM. | ||||
| GC31890 | PXS-5153A | 2125956-82-1 | >98% | |
PXS-5153A is a potent, selective, orally active and fast-acting lysyl oxidase like 2/3 enzymatic (LOXL2/LOXL3) inhibitor, with an IC50 of <40 nM for LOXL2 across all mammalian species and an IC50 of 63 nM for human LOXL3. | ||||
| GC31949 | PAT-1251 Hydrochloride | 2098884-53-6 | >98% | |
PAT-1251 is a lysyl oxidase-like 2 (LOXL2; IC 50 =0.71μM) inhibitor. | ||||
| GC32764 | GSK-LSD1 Dihydrochloride | 2102933-95-7 | >98.00% | |
An LSD1 inhibitor | ||||
| GC33573 | Rasagiline 13C3 mesylate racemic (AGN1135 13C3 racemic) | 1216757-55-9 | >98% | |
Rasagiline 13C3 mesylate racemic (AGN1135 13C3 racemic) is a 13C-labeled Rasagiline mesylate racemic. | ||||
| GC33677 | Iproniazid phosphate | 305-33-9 | >98.00% | |
Iproniazid phosphate is a non-selective, irreversible monoamine oxidase (MAO) inhibitor of the hydrazine class. | ||||
| GC33686 | (S)-Rasagiline (TVP1022) | 185517-74-2 | >99.00% | |
(S)-Rasagiline (TVP1022) (TVP1022) is the relatively inactive S-enantiomer form of Rasagiline. | ||||
| GC33714 | Rasagiline (AGN1135) | 136236-51-6 | >98.50% | |
Rasagiline (AGN1135) (R-AGN1135) is a highly potent selective irreversible mitochondrial monoamine oxidase (MAO) inhibitor with IC50s of 4.43nM and 412nM for rat brain MAO B and A activity, respectively. | ||||
| GC33718 | Brofaromine (CGP 11305A) | 63638-91-5 | >98.50% | |
Brofaromine (CGP 11305A) (CGP 11305A) is a monoamine oxidase (MAO) inhibitor with IC50 of 0.2μM for MAO-A. | ||||
| GC33749 | Salsolidine | 5784-74-7 | >98% | |
Salsolidine is a tetrahydroisoquinoline alkaloid, acts as a stereoselective competitive MAO A inhibitor. | ||||
| GC33983 | Amitraz (BTS-27419) | 33089-61-1 | >98% | |
Amitraz (BTS-27419) is a non-systemic acaricide and insecticide, with alpha-adrenergic agonist activity, interaction with octopamine receptors of the central nervous system and inhibition of monoamine oxidases and prostaglandin synthesis. | ||||
| GC34842 | Toloxatone | 29218-27-7 | >99.00% | |
An inhibitor of MAO-A | ||||
| GC35006 | (S)-Rasagiline mesylate | 202464-88-8 | >98% | |
(S)-Rasagiline (TVP1022) mesylate is the relatively inactive S-enantiomer form of Rasagiline mesylate. | ||||
| GC35192 | 7-Hydroxy-3,4-dihydro-2(1H)-quinolinone | 22246-18-0 | >99.50% | |
7-?Hydroxy-?3,?4-?dihydro-?2(1H)?-?quinolinone (3,4-Dihydro-7-hydroxy-2(1H)-quinolinone) is a weak MAO-A inhibitor, with an IC50 of 183 μM, and has no effect on MAO-B. | ||||
| GC36638 | Mofegiline hydrochloride | 120635-25-8 | >98% | |
Mofegiline hydrochloride (MDL72974A) is an orally active and selective enzyme-activated irreversible inhibitor of MAO-B, with marked selectivity on the MAO-B over MAO-A with IC50s of 3.6 nM (MAO-B) and 680 nM (MAO-A), respectively. | ||||
| GC36853 | Pargyline | 555-57-7 | >98.00% | |
Pargyline is an irreversible monoamine oxidase (MAO) inhibitor with Kis of 13 μM and 0.5 μM for MAO-A and MAO-B, respectively. | ||||
| GC37558 | Rosmarinic acid racemate | 537-15-5 | >98% | |
| GC38583 | PXS-5153A monohydrochloride | - | >99.50% | |
PXS-5153A monohydrochloride is a potent, selective, orally active and fast-acting lysyl oxidase like 2/3 enzymatic (LOXL2/LOXL3) inhibitor, with an IC50 of <40 nM for LOXL2 across all mammalian species and an IC50 of 63 nM for human LOXL3. | ||||
| GC39018 | Obtusin | 70588-05-5 | >98% | |
Obtusin, isolated from Cassia obtusifolia Linn seed, is a highly selective and competitive human monoamine oxidase-A (hMAO-A) inhibitor with an IC50 of 11.12 μM and a Ki of 6.15 μM. | ||||
