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MMTC - 95%, high purity , CAS No.1210-56-6

  • ≥95%
Item Number
M338135
Grouped product items
SKUSizeAvailabilityPrice Qty
M338135-1mg
1mg
Available within 8-12 weeks(?)
Production requires sourcing of materials. We appreciate your patience and understanding.
$60.90
M338135-5mg
5mg
Available within 8-12 weeks(?)
Production requires sourcing of materials. We appreciate your patience and understanding.
$236.90
M338135-10mg
10mg
Available within 8-12 weeks(?)
Production requires sourcing of materials. We appreciate your patience and understanding.
$425.90
M338135-25mg
25mg
Available within 8-12 weeks(?)
Production requires sourcing of materials. We appreciate your patience and understanding.
$958.90
M338135-50mg
50mg
Available within 8-12 weeks(?)
Production requires sourcing of materials. We appreciate your patience and understanding.
$1,724.90
M338135-100mg
100mg
Available within 8-12 weeks(?)
Production requires sourcing of materials. We appreciate your patience and understanding.
$3,104.90

an analog of pinolin found to increase the concentration of plasma aldosterone and inhibit the uptake of seratonin.

Basic Description

SynonymsAdrenoglomerulotropin|1210-56-6|MMTC|6-methoxy-1-methyl-2,3,4,9-tetrahydro-1H-pyrido[3,4-b]indole|1-Methyl-6-methoxy-1,2,3,4-tetrahydro-beta-carboline|6-Methoxytetrahydroharman|6-MEO-THH|1-Methyl-6-methoxy-1,2,3,4-tetrahydro-2-carboline|CHEMBL221811|U18P8
Specifications & Purity≥95%
Storage TempStore at -20°C,Desiccated
Shipped InIce chest + Ice pads
Product Description

MMTC is endogenous to the rat brain and to human urine. It is an analog of pinolin, another endogenous beta-carboline. Beta-carbolines have been found to increase the activity of plasma renin, increase the concentration of plasma aldosterone, and inhibi

Associated Targets

ACHE Tclin Acetylcholinesterase 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

ALDH1A1 Tchem Retinal dehydrogenase 1 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

HTR2B Tclin 5-hydroxytryptamine receptor 2B 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

MAPT Tclin Microtubule-associated protein tau 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

BCHE Tclin Cholinesterase 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

Names and Identifiers

IUPAC Name 6-methoxy-1-methyl-2,3,4,9-tetrahydro-1H-pyrido[3,4-b]indole
INCHI InChI=1S/C13H16N2O/c1-8-13-10(5-6-14-8)11-7-9(16-2)3-4-12(11)15-13/h3-4,7-8,14-15H,5-6H2,1-2H3
InChi Key RDUORFDQRFHYBF-UHFFFAOYSA-N
Canonical SMILES CC1C2=C(CCN1)C3=C(N2)C=CC(=C3)OC
Isomeric SMILES CC1C2=C(CCN1)C3=C(N2)C=CC(=C3)OC
PubChem CID 71028
Molecular Weight 216.28

Certificates

Certificate of Analysis(COA)

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Chemical and Physical Properties

SolubilitySoluble in water (5 mg/mL), DMSO (7 mg/mL and ethanol (4 mg/mL)

Related Documents

Solution Calculators