U.S. Department of Health & Human Services Divider Arrow National Institutes of Health Divider Arrow NCATS

Details

Stereochemistry ABSOLUTE
Molecular Formula C12H14O35S8.8K.7H2O
Molecular Weight 1413.632
Optical Activity UNSPECIFIED
Defined Stereocenters 9 / 9
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of SUCROSOFATE POTASSIUM

SMILES

O.O.O.O.O.O.O.[K+].[K+].[K+].[K+].[K+].[K+].[K+].[K+].[O-]S(=O)(=O)OC[C@H]1O[C@@](COS([O-])(=O)=O)(O[C@H]2O[C@H](COS([O-])(=O)=O)[C@@H](OS([O-])(=O)=O)[C@H](OS([O-])(=O)=O)[C@H]2OS([O-])(=O)=O)[C@@H](OS([O-])(=O)=O)[C@@H]1OS([O-])(=O)=O

InChI

InChIKey=ZLYYTLMQNBUBHA-NGOJJLSFSA-F
InChI=1S/C12H22O35S8.8K.7H2O/c13-48(14,15)37-1-4-6(43-51(22,23)24)8(45-53(28,29)30)9(46-54(31,32)33)11(40-4)42-12(3-39-50(19,20)21)10(47-55(34,35)36)7(44-52(25,26)27)5(41-12)2-38-49(16,17)18;;;;;;;;;;;;;;;/h4-11H,1-3H2,(H,13,14,15)(H,16,17,18)(H,19,20,21)(H,22,23,24)(H,25,26,27)(H,28,29,30)(H,31,32,33)(H,34,35,36);;;;;;;;;7*1H2/q;8*+1;;;;;;;/p-8/t4-,5-,6-,7-,8+,9-,10+,11-,12+;;;;;;;;;;;;;;;/m1.............../s1

HIDE SMILES / InChI

Molecular Formula HO
Molecular Weight 17.0073
Charge -1
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Molecular Formula K
Molecular Weight 39.0983
Charge 1
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Molecular Formula C12H21O35S8
Molecular Weight 981.794
Charge -1
Count
Stereochemistry ABSOLUTE
Additional Stereochemistry No
Defined Stereocenters 9 / 9
E/Z Centers 0
Optical Activity UNSPECIFIED

Description
Curator's Comment: Description was created using several sources including http://www.drugbank.ca/drugs/DB01901; https://www.ncbi.nlm.nih.gov/pubmed/18540049; https://www.ncbi.nlm.nih.gov/pubmed/19686789; https://www.ncbi.nlm.nih.gov/pubmed/20053992

Sucrosofate (sucrose octasulfate) is a class of organic compounds known as disaccharide sulfates carrying one or more sulfate group on a sugar unit. It is used to encapsulate some anticancer drugs in liposomes allowing for highly active formulations against solid tumors and immunotargeting to cancer-overexpressing cell surface receptors. ONIVYDE (liposomal irinotecan) for intravenous use encapsulates an aqueous space containing irinotecan in a gelated or precipitated state as the sucrose octasulfate salt was initially approved by FDA in 1996 for treatment of pancreatic cancer. Sucrose octasulfate (SOS), a chemical analogue of heparin, has been demonstrated to activate fibroblast growth factors signalling pathways and SOS-mediated dimerization of FGF1 was observed. SOS can suppress thrombin generation in plasma that suggests a potential for oversulfated disaccharides in controlling heparin cofactor II -regulated thrombin generation.

Originator

Curator's Comment: Liposomal irinotecan - irinotecan sucrose octasulfate salt liposome injection

Approval Year

Conditions

Conditions

ConditionModalityTargetsHighest PhaseProduct
Primary
ONIVYDE

Approved Use

ONIVYDE is a topoisomerase inhibitor indicated, in combination with fluorouracil and leucovorin, for the treatment of patients with metastatict adenocarcinoma of pancreas after disease progression following gemcitabine-based therapy.

Launch Date

8.2304637E11
PubMed

PubMed

TitleDatePubMed
Structure and stability of an acidic fibroblast growth factor from Notophthalmus viridescens.
2002 Nov 29
Binding of sucrose octasulphate to the C-type lectin-like domain of the recombinant natural killer cell receptor NKR-P1A observed by NMR spectroscopy.
2002 Nov 4
Proteinases of common pathogenic bacteria degrade and inactivate the antibacterial peptide LL-37.
2002 Oct
Science review: The use of proton pump inhibitors for gastric acid suppression in critical illness.
2005 Feb
Therapeutic paint of cidofovir/sucralfate gel combination topically administered by spraying for treatment of orf virus infections.
2009 Jun
Topical use of sucralfate in epithelial wound healing: clinical evidences and molecular mechanisms of action.
2010 Jan
Development of a highly stable and targetable nanoliposomal formulation of topotecan.
2010 Jan 4
Patents

Sample Use Guides

In Vivo Use Guide
Curator's Comment: ONIVYDE is a sterile, white to slightly yellow opaque isotonic liposomal dispersion. Each 10 mL single-dose vial contains 43 mg irinotecan free base at a concentration of 4.3 mg/mL. The liposome is a unilamellar lipid bilayer vesicle, approximately 110 nm in diameter, which encapsulates an aqueous space containing irinotecan in a gelated or precipitated state as the sucrose octasulfate salt
Recommended dose of ONIVYDE is 70 mg/m^2 intravenous infusion over 90 minutes every two weeks. Recommended starting dose of ONIVYDE in patients homozygous for UGT1A1*28 is 50 mg/m^2 every two weeks.There is no recommended dose of ONIVYDE for patients with serum bilirubin above the upper limit of normal.
Route of Administration: Intravenous
In Vitro Use Guide
Unknown
Substance Class Chemical
Created
by admin
on Sat Dec 16 05:50:32 UTC 2023
Edited
by admin
on Sat Dec 16 05:50:32 UTC 2023
Record UNII
E6JGE99TEM
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
SUCROSOFATE POTASSIUM
USAN  
USAN  
Official Name English
AGENTM-01
Code English
AGENT-M-01
Code English
SUCROSE OCTAKIS(POTASSIUM SULFATE) HEPTAHYDRATE
Systematic Name English
AGENT M-01
Code English
SUCROSOFATE POTASSIUM [USAN]
Common Name English
POTASSIUM SUCROSE OCTASULFATE HEPTAHYDRATE
Systematic Name English
.ALPHA.-D-GLUCOPYRANOSIDE, 1,3,4,6-TETRA-O-SULFO-.BETA.-D-FRUCTOFURANOSYL, TETRAKIS(HYDROGEN SULFATE), OCTAPOTASSIUM SALT, HEPTAHYDRATE
Systematic Name English
Classification Tree Code System Code
NCI_THESAURUS C802
Created by admin on Sat Dec 16 05:50:33 UTC 2023 , Edited by admin on Sat Dec 16 05:50:33 UTC 2023
Code System Code Type Description
NCI_THESAURUS
C152445
Created by admin on Sat Dec 16 05:50:33 UTC 2023 , Edited by admin on Sat Dec 16 05:50:33 UTC 2023
PRIMARY
DRUG BANK
DBSALT002733
Created by admin on Sat Dec 16 05:50:33 UTC 2023 , Edited by admin on Sat Dec 16 05:50:33 UTC 2023
PRIMARY
FDA UNII
E6JGE99TEM
Created by admin on Sat Dec 16 05:50:33 UTC 2023 , Edited by admin on Sat Dec 16 05:50:33 UTC 2023
PRIMARY
ChEMBL
CHEMBL1235872
Created by admin on Sat Dec 16 05:50:33 UTC 2023 , Edited by admin on Sat Dec 16 05:50:33 UTC 2023
PRIMARY
PUBCHEM
23725031
Created by admin on Sat Dec 16 05:50:33 UTC 2023 , Edited by admin on Sat Dec 16 05:50:33 UTC 2023
PRIMARY
CAS
76578-81-9
Created by admin on Sat Dec 16 05:50:33 UTC 2023 , Edited by admin on Sat Dec 16 05:50:33 UTC 2023
PRIMARY
USAN
AA-100
Created by admin on Sat Dec 16 05:50:33 UTC 2023 , Edited by admin on Sat Dec 16 05:50:33 UTC 2023
PRIMARY
Related Record Type Details
ANHYDROUS->SOLVATE
PARENT -> SALT/SOLVATE
Related Record Type Details
ACTIVE MOIETY