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SML3236

Sigma-Aldrich

UNC10201652

≥98 mg/mL (HPLC)

Synonym(s):

4-(8-(piperazin-1-yl)-1,2,3,4-tetrahydro-[1,2,3]triazino[4′,5′:4,5]thieno[2,3-c]isoquinolin-5-yl)morpholine, 1,2,3,4-Tetrahydro-5-(4-morpholinyl)-8-(1-piperazinyl)[1,2,3]triazino[4′,5′:4,5]thieno[2,3-c]isoquinoline

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About This Item

Empirical Formula (Hill Notation):
C20H25N7OS
CAS Number:
372495-52-8
Molecular Weight:
411.52
UNSPSC Code:
12352107
NACRES:
NA.77
Pricing and availability is not currently available.

form

powder

Quality Level

100

concentration

≥98 mg/mL (HPLC)

color

white to beige

solubility

DMSO: 2 mg/mL, clear

storage temp.

2-8°C

SMILES string

C12=C(N3CCOCC3)N=C(SC4=C5N=NN=C4N6CCNCC6)C5=C1CCCC2

InChI key

ZPVQONCMKZBGTB-UHFFFAOYSA-N

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1 of 4

This Item
SML1741T7665SML0688
UNC10201652 ≥98 mg/mL (HPLC)

SML3236

UNC10201652

TH1020 ≥95% (HPLC)

SML1741

TH1020

Tyrphostin 51 ≥98%

T7665

Tyrphostin 51

PO1 ≥98% (HPLC)

SML0688

PO1

Quality Level

100

Quality Level

100

Quality Level

200

Quality Level

100

storage temp.

2-8°C

storage temp.

2-8°C

storage temp.

2-8°C

storage temp.

2-8°C

solubility

DMSO: 2 mg/mL, clear

solubility

DMSO: 3 mg/mL, clear (warmed)

solubility

DMSO: soluble 5 mg of Tyrphostin 51 in 0.1 ml of solvent, clear, orange to red

solubility

DMSO: 1 mg/mL, clear (warmed)

color

white to beige

color

white to beige

color

-

color

faintly pink to red

concentration

≥98 mg/mL (HPLC)

concentration

-

concentration

-

concentration

-

General description

UNC10201652 is a potent and substrate-dependent slow-binding inhibitor of bacterial β-glucuronidases (GUSs) in the gut.[1] UNC10201652 appears to target a catalytic intermediate. It alleviates irinotecan-induced gut damage in mouse models of cancer.

Biochem/physiol Actions

potent and selective slow binding inhibitor microbiome β-glucuronidase enzyme

Storage Class

11 - Combustible Solids

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

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    Aadra P Bhatt et al.
    Proceedings of the National Academy of Sciences of the United States of America, 117(13), 7374-7381 (2020-03-15)
    Irinotecan treats a range of solid tumors, but its effectiveness is severely limited by gastrointestinal (GI) tract toxicity caused by gut bacterial β-glucuronidase (GUS) enzymes. Targeted bacterial GUS inhibitors have been shown to partially alleviate irinotecan-induced GI tract damage and

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