Salbostatin

[H][C@@]1(CO[C@H](CO)[C@@H](O)[C@@H]1O)N[C@H]2C=C(CO)[C@@H](O)[C@H](O)[C@H]2O

InChIKey=OCTNNXHKAOLDJL-BMGYQPLYSA-N

InChI=1S/C13H23NO8/c15-2-5-1-6(10(18)13(21)9(5)17)14-7-4-22-8(3-16)12(20)11(7)19/h1,6-21H,2-4H2/t6-,7-,8+,9+,10-,11+,12+,13-/m0/s1

Stereochemistry	ABSOLUTE
Additional Stereochemistry	No
Defined Stereocenters	8 / 8
E/Z Centers	0
Optical Activity	UNSPECIFIED

Substance Class	Chemical Created by `admin` on `Sat Dec 16 19:51:14 GMT 2023` Edited by `admin` on `Sat Dec 16 19:51:14 GMT 2023`
Record UNII	YQ57B9ZL48
Record Status	`Validated (UNII)`
Record Version

Name

Type

Language

Salbostatin

Common Name

English

D-Glucitol, 1,5-anhydro-2-deoxy-2-[[4,5,6-trihydroxy-3-(hydroxymethyl)-2-cyclohexen-1-yl]amino]-, [1S-(1α,4α,5β,6α)]-

Systematic Name

English

D-Glucitol, 1,5-anhydro-2-deoxy-2-[[(1S,4R,5S,6S)-4,5,6-trihydroxy-3-(hydroxymethyl)-2-cyclohexen-1-yl]amino]-

Systematic Name

English

1,5-Anhydro-2-deoxy-2-[[(1S,4R,5S,6S)-4,5,6-trihydroxy-3-(hydroxymethyl)-2-cyclohexen-1-yl]amino]-D-glucitol

Systematic Name

English

Code System Code Type Description

PUBCHEM

9818549

Created by admin on Sat Dec 16 19:51:14 GMT 2023 , Edited by admin on Sat Dec 16 19:51:14 GMT 2023

PRIMARY

WIKIPEDIA

Salbostatin

Created by admin on Sat Dec 16 19:51:14 GMT 2023 , Edited by admin on Sat Dec 16 19:51:14 GMT 2023

PRIMARY

CAS

128826-89-1

Created by admin on Sat Dec 16 19:51:14 GMT 2023 , Edited by admin on Sat Dec 16 19:51:14 GMT 2023

NON-SPECIFIC STEREOCHEMISTRY

FDA UNII

YQ57B9ZL48

Created by admin on Sat Dec 16 19:51:14 GMT 2023 , Edited by admin on Sat Dec 16 19:51:14 GMT 2023

PRIMARY