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36912-00-2

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36912-00-2 Usage

Description

(3aS)-1,2,3,3aβ,5aβ,7,10b,10cβ-Octahydro-3a,10bα-dimethyl-7β-isopropyl-4H,9H-furo[2',3',4':4,5]naphtho[2,1-c]pyran-4,9-dione is a diterpene lactone that is isolated from the Podocarpus latifolius plant. It has been demonstrated to exhibit inhibitory activity against activator protein 1 (AP-1), which is a transcription factor that plays a role in cell proliferation, differentiation, and apoptosis.

Uses

Used in Pharmaceutical Industry:
(3aS)-1,2,3,3aβ,5aβ,7,10b,10cβ-Octahydro-3a,10bα-dimethyl-7β-isopropyl-4H,9H-furo[2',3',4':4,5]naphtho[2,1-c]pyran-4,9-dione is used as a potential therapeutic agent for various diseases due to its inhibitory activity against activator protein 1 (AP-1). This activity suggests that it may have applications in treating conditions related to cell proliferation and differentiation, such as cancer.
Used in Research Applications:
In the field of research, (3aS)-1,2,3,3aβ,5aβ,7,10b,10cβ-Octahydro-3a,10bα-dimethyl-7β-isopropyl-4H,9H-furo[2',3',4':4,5]naphtho[2,1-c]pyran-4,9-dione can be used as a tool compound to study the role of activator protein 1 (AP-1) in cellular processes. This may lead to a better understanding of the underlying mechanisms of various diseases and the development of new therapeutic strategies.
Used in Drug Discovery:
The inhibitory activity of (3aS)-1,2,3,3aβ,5aβ,7,10b,10cβ-Octahydro-3a,10bα-dimethyl-7β-isopropyl-4H,9H-furo[2',3',4':4,5]naphtho[2,1-c]pyran-4,9-dione against activator protein 1 (AP-1) makes it a valuable compound in drug discovery efforts. It can be used as a starting point for the development of new drugs targeting AP-1, which may have potential applications in treating a range of diseases, including cancer and other conditions related to cell proliferation and differentiation.

Check Digit Verification of cas no

The CAS Registry Mumber 36912-00-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,6,9,1 and 2 respectively; the second part has 2 digits, 0 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 36912-00:
(7*3)+(6*6)+(5*9)+(4*1)+(3*2)+(2*0)+(1*0)=112
112 % 10 = 2
So 36912-00-2 is a valid CAS Registry Number.
InChI:InChI=1/C19H24O4/c1-10(2)15-11-8-13-16-18(3,12(11)9-14(20)23-15)6-5-7-19(16,4)17(21)22-13/h8-10,13,15-16H,5-7H2,1-4H3/t13-,15-,16-,18-,19+/m1/s1

36912-00-2SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name nagilactone F

1.2 Other means of identification

Product number -
Other names NAGILACTONE F

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:36912-00-2 SDS

36912-00-2Upstream product

36912-00-2Downstream Products

36912-00-2Relevant articles and documents

Hayashi et al.

, p. 3311,3312,3314 (1979)

Total synthesis of nagilactone F, a biologically active norditerpenoid dilactone isolated from Podocarpus nagi

Hayashi,Matsumoto,Nishizawa,et al.

, p. 3428 - 3433 (1982)

-

Total synthesis of oidiodendrolides and related norditerpene dilactones from a common precursor: Metabolites CJ-14,445, LL-Z1271γ, oidiolactones A, B, C, and D, and nagilactone F

Hanessian, Stephen,Boyer, Nicolas,Reddy, Gone Jayapal,Deschenes-Simard, Benoit

supporting information; experimental part, p. 4640 - 4643 (2009/12/09)

An efficient, high-yielding strategy has been developed for the asymmetric total synthesis of seven norditerpenoid dilactones known for their diverse biological properties. The three key steps employed to obtain a tricyclic lactone intermediate involved a

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