DIMETHYLAMINOPARTHENOLIDE

Details

Stereochemistry	ABSOLUTE
Molecular Formula	C17H27NO3
Molecular Weight	293.4012
Optical Activity	UNSPECIFIED
Defined Stereocenters	5 / 5
E/Z Centers	0
Charge	0

SHOW SMILES / InChI

Structure Search

SMILES

CN(C)C[C@@H]1[C@@H]2CCC(C)=CCC[C@@]3(C)O[C@@H]3[C@H]2OC1=O

InChI

InChIKey=UJNSFDHVIBGEJZ-CMRIBGNTSA-N

InChI=1S/C17H27NO3/c1-11-6-5-9-17(2)15(21-17)14-12(8-7-11)13(10-18(3)4)16(19)20-14/h6,12-15H,5,7-10H2,1-4H3/b11-6-/t12-,13+,14-,15+,17+/m0/s1

HIDE SMILES / InChI

Molecular Formula	C17H27NO3
Molecular Weight	293.4012
Charge	0
Count

Stereochemistry	ABSOLUTE
Additional Stereochemistry	No
Defined Stereocenters	5 / 5
E/Z Centers	0
Optical Activity	UNSPECIFIED

Approval Year

Targets

Primary Target	Pharmacology	Condition	Potency
reactive oxygen species biosynthetic process 41 Target ID: GO:1903409 Sources: https://www.ncbi.nlm.nih.gov/pubmed/30079458	Activator 1447
NF-kappa B signaling pathway 87 Target ID: map04064 Sources: https://www.ncbi.nlm.nih.gov/pubmed/30079458\|https://www.ncbi.nlm.nih.gov/pubmed/29531807\|https://www.ncbi.nlm.nih.gov/pubmed/28782644	Inhibitor 8504
60S ribosomal protein L10 2 Target ID: P27635 Gene ID: 6134.0 Gene Symbol: RPL10 Target Organism: Homo sapiens (Human) Sources: https://www.ncbi.nlm.nih.gov/pubmed/28388532	Binding Agent 1076

Substance Class	Chemical Created by `admin` on `Tue Apr 01 16:30:55 GMT 2025` Edited by `admin` on `Tue Apr 01 16:30:55 GMT 2025`
Record UNII	U41S5CG0SG
Record Status	`Validated (UNII)`
Record Version

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Name

Type

Language

LC-1

Preferred Name

English

DIMETHYLAMINOPARTHENOLIDE

Common Name

English

(1AR,4E,7AS,8S,10AS,10BR)-8-((DIMETHYLAMINO)METHYL)-2,3,6,7,7A,8,10A,10B-OCTAHYDRO-1A,5-DIMETHYLOXIRENO(9,10)CYCLODECA(1,2-B)FURAN-9(1AH)-ONE

Systematic Name

English

DMAPT

Common Name

English

NSC-734325

Code

English

OXIRENO(9,10)CYCLODECA(1,2-B)FURAN-9(1AH)-ONE, 8-((DIMETHYLAMINO)METHYL)-2,3,6,7,7A,8,10A,10B-OCTAHYDRO-1A,5-DIMETHYL-, (1AR,4E,7AS,8S,10AS,10BR)-

Systematic Name

English

Code System Code Type Description

FDA UNII

U41S5CG0SG

Created by admin on Tue Apr 01 16:30:55 GMT 2025 , Edited by admin on Tue Apr 01 16:30:55 GMT 2025

PRIMARY

NSC

734325

Created by admin on Tue Apr 01 16:30:55 GMT 2025 , Edited by admin on Tue Apr 01 16:30:55 GMT 2025

PRIMARY

CAS

870677-05-7

Created by admin on Tue Apr 01 16:30:55 GMT 2025 , Edited by admin on Tue Apr 01 16:30:55 GMT 2025

PRIMARY

PUBCHEM

129395999

Created by admin on Tue Apr 01 16:30:55 GMT 2025 , Edited by admin on Tue Apr 01 16:30:55 GMT 2025

PRIMARY

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NF-?B

TARGET -> INHIBITOR

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					U41S5CG0SG

DIMETHYLAMINOPARTHENOLIDE

ACTIVE MOIETY

Comments:

Class: Antineoplastic, Sesquiterpene, Small molecule; Mechanism of Action: Apoptosis stimulant, NF-kappa B inhibitor; Highest Development Phase: Suspended for Acute myeloid leukaemia; Most Recent Events: 31 Dec 2009 Suspended - Phase-I for Acute myeloid leukaemia in United Kingdom (PO), 28 Jan 2009 Phase I clinical trials in Acute myeloid leukaemia in United Kingdom (PO)


					U41S5CG0SG

DIMETHYLAMINOPARTHENOLIDE

ACTIVE MOIETY

Comments:

RESULTS: The 32-week trial showed that 40 mg/kg DMAPT alone significantly decreased the size of gross pancreatic cancers relative to placebo. No significant difference in gross tumor number was observed between the treatment groups and placebo with the exception of 50 mg/kg celecoxib with a higher tumor incidence this group also exhibited lower lymphotactin levels suggestive of decreased immune surveillance. Tumor invasion into adjacent organs and metastasis were not observed in the DMAPT/celecoxib treatment groups. Drug targets including prostaglandin E2, prostaglandin E2 metabolite and activated nuclear factor kappaB were significantly decreased.


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DIMETHYLAMINOPARTHENOLIDE

ACTIVE MOIETY

Comments:

Abstract #1718: Dimethylaminoparthenolide targets apoptotic machinery in glioblastoma through ROS generation and NF\#954-B inhibition