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Safety Information

SML3681

Sigma-Aldrich

ATM-3507

≥95% (HPLC)

Synonym(s):

ATM 3507, [3-​[[2,​3-​Dimethyl-​1-​[3-​(4-​methyl-​1-​piperazinyl)​propyl]​-​1H-​indol-​5-​yl]​oxy]​phenyl]​[4-​[2-​(4-​fluorophenyl)​ethyl]​-​1-​piperazinyl]​-methanone

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About This Item

Empirical Formula (Hill Notation):
C37H46FN5O2
CAS Number:
1861449-70-8
Molecular Weight:
611.79
MDL number:
MFCD31657327
UNSPSC Code:
12352200
NACRES:
NA.77
Pricing and availability is not currently available.

Quality Level

100

Assay

≥95% (HPLC)

form

powder

color

, Colorless to light brown

solubility

DMSO: 2 mg/mL, clear

storage temp.

-10 to -25°C

Biochem/physiol Actions

ATM-3507 is a potent anti-tropomyosin agent that disables Tpm3.1 containing actin filaments. It exhibits potent cytotoxic activity against multiple neuroblastoma cancer cell lines. ATM-3507 sensitizes cancer cells to anti-microtubule agents. ATM-3507 significantly prolonged mitotic arrest induced by anti-microtubule agent vinorelbine.
Potent anti-tropomyosin agent that disables Tpm3.1 containing actin filaments

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Regulatory Listings

Regulatory Listings are mainly provided for chemical products. Only limited information can be provided here for non-chemical products. No entry means none of the components are listed. It is the user’s obligation to ensure the safe and legal use of the product.

JAN Code

SML3681-VAR:
SML3681-BULK:
SML3681-25MG:
SML3681-5MG:

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Certificates of Analysis (COA)

Lot/Batch Number
0000269646
0000269645
0000261956
0000269646
0000269645

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Molecular integration of the anti-tropomyosin compound ATM-3507 into the coiled coil overlap region of the cancer-associated Tpm3.1
Scientific Reports, 9(1), 11262-11262 (2019)
Identification of Cancer-Targeted Tropomyosin Inhibitors and Their Synergy with Microtubule Drugs
Molecular Cancer Therapeutics, 16(8), 1555-1565 (2017)
Xing Xu et al.
British journal of cancer, 125(2), 265-276 (2021-05-14)
Anti-microtubule agents are widely used to treat ovarian cancers, but the efficacy is often compromised by drug resistance. We investigated co-targeting the actin/tropomyosin cytoskeleton and microtubules to increase treatment efficacy in ovarian cancers and potentially overcome resistance. The presence of

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