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Details

Stereochemistry ABSOLUTE
Molecular Formula C27H49N3O8P.Na.H2O
Molecular Weight 615.6721
Optical Activity UNSPECIFIED
Defined Stereocenters 4 / 4
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of CYTARABINE OCFOSFATE HYDRATE

SMILES

O.[Na+].CCCCCCCCCCCCCCCCCCOP([O-])(=O)OC[C@H]1O[C@H]([C@@H](O)[C@@H]1O)N2C=CC(N)=NC2=O

InChI

InChIKey=NSFFYSQTVOCNLX-JKIHJDPOSA-M
InChI=1S/C27H50N3O8P.Na.H2O/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15-16-17-20-36-39(34,35)37-21-22-24(31)25(32)26(38-22)30-19-18-23(28)29-27(30)33;;/h18-19,22,24-26,31-32H,2-17,20-21H2,1H3,(H,34,35)(H2,28,29,33);;1H2/q;+1;/p-1/t22-,24-,25+,26-;;/m1../s1

HIDE SMILES / InChI

Molecular Formula Na
Molecular Weight 22.9898
Charge 1
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Molecular Formula C27H50N3O8P
Molecular Weight 575.675
Charge 0
Count
Stereochemistry ABSOLUTE
Additional Stereochemistry No
Defined Stereocenters 4 / 4
E/Z Centers 0
Optical Activity UNSPECIFIED

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

Cytarabine ocfosfate (commercial name: Starasid) is a prodrug having stearyl group attached to phosphoric acid at 5' position of arabinose moiety of cytosine arabinoside (Ara-C). This drug is given orally. The mode of action is in the inhibition of DNA synthesis after conversion to Ara-CTP as in Ara-C. The drug is metabolized in the liver, producing the intermediate metabolite, C-C3PCA which is converted to Ara-C gradually. This property results in the maintenance of relatively long time the blood Ara-C levels. This was proved to be active clinically against acute leukemia and MDS.

Approval Year

TargetsConditions

Conditions

ConditionModalityTargetsHighest PhaseProduct
Primary
Starasid

Approved Use

cytarabine ocfosfate is used clinically in Japan for the treatment of leukemia or myelodysplastic syndrome.

Launch Date

1992
Primary
Starasid

Approved Use

cytarabine ocfosfate is used clinically in Japan for the treatment of leukemia or myelodysplastic syndrome.

Launch Date

1992
PubMed

PubMed

TitleDatePubMed
[A new antileukemic drug, cytarabine ocfosfate].
1993 Sep
Response to cytarabine ocfosfate (YNK01) in a patient with chronic lymphocytic leukemia refractory to treatment with chlorambucil/prednisone, fludarabine, and prednimustine/mitoxantrone.
1996 Oct
[Late phase II study of YNK-01 (an oral prodrug of cytarabine) for hepatocellular carcinoma].
1998 Oct
Patents

Sample Use Guides

For adult acute non-lymphatic leukemia: In general, for adults, take 2-6 capsules (100-300mg of the active ingredient anhydride) in 1-3 divided doses a day after meal. For myelodysplastic syndrome: In general, for adults, take 2-4 capsules (100-200mg of the active ingredient anhydride) in 1-3 divided doses a day after meal, for 2 to 3 weeks every day, then discontinue the medication for 2-3 weeks and repeat this schedule. The dosage may be adjusted according to your disease or symptoms.Strictly follow the instructions.
Route of Administration: Oral
In Vitro Use Guide
Unknown
Substance Class Chemical
Created
by admin
on Sat Dec 16 05:27:09 GMT 2023
Edited
by admin
on Sat Dec 16 05:27:09 GMT 2023
Record UNII
93Q159SRNN
Record Status Validated (UNII)
Record Version
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Name Type Language
CYTARABINE OCFOSFATE HYDRATE
JAN  
Common Name English
CYTARABINE OCFOSFATE HYDRATE [JAN]
Common Name English
2(1H)-PYRIMIDINONE, 4-AMINO-1-(5-O-(HYDROXY(OCTADECYLOXY)PHOSPHINYL)-.BETA.-D-ARABINOFURANOSYL)-, MONOSODIUM SALT, MONOHYDRATE
Common Name English
Code System Code Type Description
CAS
116459-64-4
Created by admin on Sat Dec 16 05:27:10 GMT 2023 , Edited by admin on Sat Dec 16 05:27:10 GMT 2023
PRIMARY
FDA UNII
93Q159SRNN
Created by admin on Sat Dec 16 05:27:10 GMT 2023 , Edited by admin on Sat Dec 16 05:27:10 GMT 2023
PRIMARY
PUBCHEM
23663412
Created by admin on Sat Dec 16 05:27:10 GMT 2023 , Edited by admin on Sat Dec 16 05:27:10 GMT 2023
PRIMARY
EPA CompTox
DTXSID70151396
Created by admin on Sat Dec 16 05:27:10 GMT 2023 , Edited by admin on Sat Dec 16 05:27:10 GMT 2023
PRIMARY
Related Record Type Details
ANHYDROUS->SOLVATE