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Merck
CN

SML1255

Nonyloxytryptamine oxalate

≥98% (HPLC)

Synonym(s):

5-(Nonyloxy)-1H-Indole-3-ethanamine ethanedioate, 5-(Nonyloxy)tryptamine oxalate, 5-Nonyloxytryptamine oxalate

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About This Item

Empirical Formula (Hill Notation):
C19H30N2O · C2H2O4
CAS Number:
157798-13-5
Molecular Weight:
392.49
UNSPSC Code:
12352116
PubChem Substance ID:
329825747
NACRES:
NA.77

Key Documents

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Product Name

Nonyloxytryptamine oxalate, ≥98% (HPLC)

SMILES string

CCCCCCCCCOC1=CC=C(NC=C2CCN)C2=C1.C

InChI

1S/C19H30N2O.CH4/c1-2-3-4-5-6-7-8-13-22-17-9-10-19-18(14-17)16(11-12-20)15-21-19;/h9-10,14-15,21H,2-8,11-13,20H2,1H3;1H4

InChI key

LXACPZFRJZIDDI-UHFFFAOYSA-N

assay

≥98% (HPLC)

form

powder

color

, white to yellow to light brown

solubility

DMSO: 2 mg/mL, clear (warmed)

storage temp.

room temp

Quality Level

100

Related Categories

Biochem/physiol Actions

Nonyloxytryptamine (5-nonyloxytryptamine) is a potent and selective 5-HT1B receptor agonist. Nonyloxytryptamine is a polysialic acid (PSA) mimick that triggers PSA-mediated functions. Nonyloxytryptamine enhances neurite outgrowth of cultured primary neurons, protects neurons from oxidative stress, enhanced Schwann cell proliferation, reduces migration of astrocytes and enhances myelination in vitro.
Nonyloxytryptamine is a potent and selective 5-HT1B receptor agonist; polysialic acid (PSA) mimick that triggers PSA-mediated functions.
Nonyloxytryptamine is known to possess antiproliferative and cytotoxic effect. It has been studied for its use in the treatment of breast cancer.

Storage Class

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

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Certificates of Analysis (COA)

Lot/Batch Number
0000173219
0000173219
0000112789
0000112788
0000081060

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Antiproliferative and cytotoxic activities of 5-(nonyloxy) tryptamine derivatives in breast cancer cells.
Tavares C D, et al.
Cancer Research, 74(19), 5462-5462 (2014)
Minjuan Wang et al.
International journal of molecular sciences, 21(19) (2020-09-30)
Because of the importance of the HNK-1 carbohydrate for preferential motor reinnervation after injury of the femoral nerve in mammals, we screened NIH Clinical Collection 1 and 2 Libraries and a Natural Product library comprising small organic compounds for identification

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