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Acetic acid (3S,5R,8R,9R,10R,13R,14R)-4,4,8,10,14-pentamethyl-17-(2-methyl-5-oxo-tetrahydro-furan-2-yl)-hexadecahydro-cyclopenta[a]phenanthren-3-yl ester is a complex organic compound with a molecular formula of C28H46O4. It is a derivative of acetic acid, featuring a cyclopenta[a]phenanthren-3-yl ester group, which is a large, polycyclic aromatic hydrocarbon structure. The compound is characterized by its stereochemistry, with seven chiral centers (3S,5R,8R,9R,10R,13R,14R), indicating that it has a specific three-dimensional arrangement of atoms. The presence of a 2-methyl-5-oxo-tetrahydro-furan-2-yl group adds to the complexity of the molecule, contributing to its unique chemical properties. Acetic acid (3S,5R,8R,9R,10R,13R,14R)-4,4,8,10,14-pentamethyl-17-(2-methyl-5-oxo-tetrahydro-furan-2-yl)-hexadecahydro-cyclopenta[a]phenanthren-3-yl ester is likely to be found in specialized chemical research or pharmaceutical applications due to its intricate structure and potential biological activity.

4726-64-1

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4726-64-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 4726-64-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,7,2 and 6 respectively; the second part has 2 digits, 6 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 4726-64:
(6*4)+(5*7)+(4*2)+(3*6)+(2*6)+(1*4)=101
101 % 10 = 1
So 4726-64-1 is a valid CAS Registry Number.

4726-64-1Downstream Products

4726-64-1Relevant academic research and scientific papers

Newly synthesised oxime and lactone derivatives from: Dipterocarpus alatus dipterocarpol as anti-diabetic inhibitors: Experimental bioassay-based evidence and theoretical computation-based prediction

Bao, Nguyen Chi,Bui, Thanh Q.,Chi, Nguyen Linh,Dung, Nguyen Thi,Huynh, Lam K.,Nhung, Nguyen Thi Ai,Ninh, Pham Thi,Petrova, Anastasiya V.,Phuong Thao, Tran Thi,Quy, Phan Tu,Smirnova, Irina E.,Thi Thanh Hai, Nguyen,Van Loc, Tran,Van Sung, Tran

, p. 35765 - 35782 (2021/12/02)

Dipterocarpus alatus-derived products are expected to exhibit anti-diabetes properties. Natural dipterocarpol (1) was isolated from Dipterocarpus alatus collected in Quang Nam province, Vietnam; afterwards, 20 derivatives including 13 oxime esters (2 and 3a-3m) and 7 lactones (4, 5, 6a-6e) were semi-synthesised. Their inhibitory effects towards diabetes-related proteins were investigated experimentally (α-glucosidase) and computationally (3W37, 3AJ7, and PTP1B). Except for compound 2, the other 19 compounds (3a-3m, 4, 5, and 6a-6d) are reported for the first time, which were modified at positions C-3, C-24 and C-25 of the dipterocarpol via imidation, esterification, oxidative cleavage and lactonisation reactions. A framework based on docking-QSARIS combination was proposed to predict the inhibitory behaviour of the ligand-protein complexes. Enzyme assays revealed the most effective α-glucosidase inhibitors, which follow the order 5 (IC50 of 2.73 ± 0.05 μM) > 6c (IC50 of 4.62 ± 0.12 μM) > 6e (IC50 of 7.31 ± 0.11 μM), and the computation-based analysis confirmed this, i.e., 5 (mass: 416.2 aμ polarisability: 52.4 ?3; DS: -14.9 kcal mol-1) > 6c (mass: 490.1 aμ polarisability: 48.8 ?3; DS: -13.7 kcal mol-1) > 6e (mass: 549.2 aμ polarisability: 51.6 ?3; DS: -15.2 kcal mol-1). Further theoretical justifications predicted 5 and 6c as versatile anti-diabetic inhibitors. The experimental results encourage next stages for the development of anti-diabetic drugs and the computational strategy invites more relevant work for validation. This journal is

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