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P6124

5-(4-Phenoxybutoxy)psoralen

≥98% (HPLC), voltage-gated potassium channel Kv1.3 inhibitor, solid

Sinonimo/i:

PAP-1

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A voi/SKUDisponibilitàPrezzo
5 mg
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244,00 €
207,40 €
25 mg
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782,00 €

Informazioni su questo articolo

Formula empirica (notazione di Hill):
C21H18O5
Numero CAS:
Peso molecolare:
350.36
UNSPSC Code:
12352200
PubChem Substance ID:
NACRES:
NA.77
MDL number:
Assay:
≥98% (HPLC)
Form:
solid
Storage condition:
protect from light

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Nome del prodotto

5-(4-Phenoxybutoxy)psoralen, ≥98% (HPLC), solid

assay

≥98% (HPLC)

form

solid

storage condition

protect from light

color

white

solubility

DMSO: 9 mg/mL

storage temp.

2-8°C

SMILES string

O=C1Oc2cc3occc3c(OCCCCOc4ccccc4)c2C=C1

InChI

1S/C21H18O5/c22-20-9-8-16-19(26-20)14-18-17(10-13-24-18)21(16)25-12-5-4-11-23-15-6-2-1-3-7-15/h1-3,6-10,13-14H,4-5,11-12H2

InChI key

KINMYBBFQRSVLL-UHFFFAOYSA-N

Biochem/physiol Actions

5-(4-Phenoxybutoxy)psoralen (PAP-1) is derived from 5-methoxypsoralen, a natural compound. PAP-1 show higher selectivity for Kv1.3 (voltage-gated potassium channels) than other Kv1 family members. Kv1.3 is predominant on cell membranes of activated effector memory T-cells. Inhibition of Kv1.3 results in membrane depolarization. In rat models, PAP-1 is known to delay the onset of diabetes. It might be used in the treatment of psoriasis and effector memory T cells mediated autoimmune diseases. Oral, intraperitoneal and topical administration of PAP-1 prevents allergic contact dermatitis induced by oxazolone.
Selective inhibitor of Kv1.3, voltage-gated K+ channel.
Selective inhibitor of Kv1.3, voltage-gated K+ channel. PAP-1 (EC50=2 nM) potently inhibits human T effector memory cell proliferation and delayed hypersensitivity. Effective orally or intraperitoneally. 5-(4-Phenoxybutoxy)psoralen has 23-fold selectivity for Kv1.3 over Kv1.5, and 33-125-fold selectivity over other Kv1 family channels.

Features and Benefits

This compound is featured on the Potassium Channels page of the Handbook of Receptor Classification and Signal Transduction. To browse other handbook pages, click here.

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Questo articolo
L4170654085C271
LDN-57444 ≥98% (HPLC)

Sigma-Aldrich

L4170

LDN-57444

TTNPB A synthetic stilbene analog of retinoic acid that acts as a potent retinoic acid receptor (RAR) agonist (EC50 = 21 nM, 4.0 nM, and 2.4 nM for RARα, RARβ, and RARγ, respectively).

Sigma-Aldrich

654085

TTNPB

CX546 ≥98% (HPLC), solid

Sigma-Aldrich

C271

CX546

form

solid

form

solid

form

solid

form

solid

assay

≥98% (HPLC)

assay

≥98% (HPLC)

assay

≥98% (HPLC)

assay

≥98% (HPLC)

Quality Level

100

Quality Level

100

Quality Level

100

Quality Level

100

storage temp.

2-8°C

storage temp.

2-8°C

storage temp.

2-8°C

storage temp.

2-8°C

storage condition

protect from light

storage condition

desiccated, protect from light

storage condition

OK to freeze, protect from light

storage condition

protect from light

solubility

DMSO: 9 mg/mL

solubility

DMSO: 16 mg/mL

solubility

DMSO: 5 mg/mL

solubility

DMSO: ≥10 mg/mL


pictograms

Health hazard

signalword

Danger

hcodes

Hazard Classifications

Resp. Sens. 1

Classe di stoccaggio

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Faceshields, Gloves



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