3?-Hydroxydesoxyartemether

Details

Stereochemistry	ABSOLUTE
Molecular Formula	C16H26O5
Molecular Weight	298.3746
Optical Activity	( + )
Defined Stereocenters	9 / 9
E/Z Centers	0
Charge	0

SHOW SMILES / InChI

Structure Search

SMILES

CO[C@H]1O[C@@H]2O[C@]3(C)O[C@@]24[C@@H](C[C@H]3O)[C@H](C)CC[C@H]4[C@H]1C

InChI

InChIKey=NYMSZZKRBMNKGP-HPHKUEEDSA-N

InChI=1S/C16H26O5/c1-8-5-6-10-9(2)13(18-4)19-14-16(10)11(8)7-12(17)15(3,20-14)21-16/h8-14,17H,5-7H2,1-4H3/t8-,9-,10+,11+,12-,13+,14-,15-,16+/m1/s1

HIDE SMILES / InChI

Molecular Formula	C16H26O5
Molecular Weight	298.3746
Charge	0
Count

Stereochemistry	ABSOLUTE
Additional Stereochemistry	No
Defined Stereocenters	9 / 9
E/Z Centers	0
Optical Activity	UNSPECIFIED

Approval Year

Substance Class	Chemical Created by `admin` on `Wed Apr 02 17:19:25 GMT 2025` Edited by `admin` on `Wed Apr 02 17:19:25 GMT 2025`
Record UNII	JD8A9QT3HQ
Record Status	`Validated (UNII)`
Record Version

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Name

Type

Language

3-alfa-Hydroxydesoxy Artemether

Preferred Name

English

3?-Hydroxydesoxyartemether

Common Name

English

(2S,3R,3aS,6R,6aS,8R,9S,10aR,10bR)-Decahydro-2-methoxy-3,6,9-trimethyl-10aH-9,10b-epoxypyrano[4,3,2-jk][2]benzoxepin-8-ol

Systematic Name

English

10aH-9,10b-Epoxypyrano[4,3,2-jk][2]benzoxepin-8-ol, decahydro-2-methoxy-3,6,9-trimethyl-, [2S-(2?,3?,3a?,6?,6a?,8?,9?,10a?,10b?)]-

Systematic Name

English

10aH-9,10b-Epoxypyrano[4,3,2-jk][2]benzoxepin-8-ol, decahydro-2-methoxy-3,6,9-trimethyl-, (2S,3R,3aS,6R,6aS,8R,9S,10aR,10bR)-

Systematic Name

English

Code System Code Type Description

CAS

174097-70-2

Created by admin on Wed Apr 02 17:19:25 GMT 2025 , Edited by admin on Wed Apr 02 17:19:25 GMT 2025

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EPA CompTox

DTXSID20857755

Created by admin on Wed Apr 02 17:19:25 GMT 2025 , Edited by admin on Wed Apr 02 17:19:25 GMT 2025

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PUBCHEM

21604123

Created by admin on Wed Apr 02 17:19:25 GMT 2025 , Edited by admin on Wed Apr 02 17:19:25 GMT 2025

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FDA UNII

JD8A9QT3HQ

Created by admin on Wed Apr 02 17:19:25 GMT 2025 , Edited by admin on Wed Apr 02 17:19:25 GMT 2025

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