Foroxymithine

Details

Stereochemistry	ABSOLUTE
Molecular Formula	C22H37N7O11
Molecular Weight	575.5695
Optical Activity	UNSPECIFIED
Defined Stereocenters	4 / 4
E/Z Centers	0
Charge	0

SHOW SMILES / InChI

Structure Search

SMILES

CC(=O)N[C@@H](CCCN(O)C=O)C(=O)N[C@@H](CO)C(=O)N(O)CCC[C@@H]1NC(=O)[C@H](CCCN(O)C=O)NC1=O

InChI

InChIKey=IQMHGRIOYXVPSE-XSLAGTTESA-N

InChI=1S/C22H37N7O11/c1-14(33)23-15(5-2-8-27(38)12-31)19(34)26-18(11-30)22(37)29(40)10-4-7-17-21(36)24-16(20(35)25-17)6-3-9-28(39)13-32/h12-13,15-18,30,38-40H,2-11H2,1H3,(H,23,33)(H,24,36)(H,25,35)(H,26,34)/t15-,16-,17-,18-/m0/s1

HIDE SMILES / InChI

Molecular Formula	C22H37N7O11
Molecular Weight	575.5695
Charge	0
Count

Stereochemistry	ABSOLUTE
Additional Stereochemistry	No
Defined Stereocenters	4 / 4
E/Z Centers	0
Optical Activity	UNSPECIFIED

Approval Year

Substance Class	Chemical Created by `admin` on `Mon Mar 31 21:56:14 GMT 2025` Edited by `admin` on `Mon Mar 31 21:56:14 GMT 2025`
Record UNII	9QU4B47SMX
Record Status	`Validated (UNII)`
Record Version

Download

Name

Type

Language

L-Serinamide, N2-acetyl-N5-formyl-N5-hydroxy-L-ornithyl-N-[3-[(2S,5S)-5-[3-(formylhydroxyamino)propyl]-3,6-dioxo-2-piperazinyl]propyl]-N-hydroxy-

Preferred Name

English

Foroxymithine

Common Name

English

L-Serinamide, N2-acetyl-N5-formyl-N5-hydroxy-L-ornithyl-N-[3-[5-[3-(formylhydroxyamino)propyl]-3,6-dioxo-2-piperazinyl]propyl]-N-hydroxy-, (2S-cis)-

Systematic Name

English

N2-Acetyl-N5-formyl-N5-hydroxy-L-ornithyl-N-[3-[(2S,5S)-5-[3-(formylhydroxyamino)propyl]-3,6-dioxo-2-piperazinyl]propyl]-N-hydroxy-L-serinamid

Systematic Name

English

Code System Code Type Description

EPA CompTox

DTXSID50905233

Created by admin on Mon Mar 31 21:56:14 GMT 2025 , Edited by admin on Mon Mar 31 21:56:14 GMT 2025

PRIMARY

FDA UNII

9QU4B47SMX

Created by admin on Mon Mar 31 21:56:14 GMT 2025 , Edited by admin on Mon Mar 31 21:56:14 GMT 2025

PRIMARY

PUBCHEM

3035824

Created by admin on Mon Mar 31 21:56:14 GMT 2025 , Edited by admin on Mon Mar 31 21:56:14 GMT 2025

PRIMARY

CAS

100157-28-6

Created by admin on Mon Mar 31 21:56:14 GMT 2025 , Edited by admin on Mon Mar 31 21:56:14 GMT 2025

PRIMARY