Details
| Stereochemistry | ABSOLUTE |
| Molecular Formula | C9H13N3O3S |
| Molecular Weight | 243.283 |
| Optical Activity | UNSPECIFIED |
| Defined Stereocenters | 3 / 3 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
NC1=NC(=O)N(C=C1)[C@H]2C[C@H](O)[C@@H](CO)S2
InChI
InChIKey=MOMUJZRKXYLWMH-SHYZEUOFSA-N
InChI=1S/C9H13N3O3S/c10-7-1-2-12(9(15)11-7)8-3-5(14)6(4-13)16-8/h1-2,5-6,8,13-14H,3-4H2,(H2,10,11,15)/t5-,6+,8+/m0/s1
4-thio-2-deoxycytidine (TdCyd) is an orally bioavailable 4-thio modified 2-deoxycytidine analog, with potential antineoplastic activity. Upon administration of 4-thio-2-deoxycytidine (TdCyd), this cytidine analog is incorporated into DNA during replication and inhibits the activity of DNA methyltransferase 1 (DNMT1), which blocks DNA hypermethylation. This results in DNMT1 depletion, hypomethylation of DNA, and the reactivation of tumor suppressor genes that were silenced by hypermethylation; this results in antitumor activity and an inhibition of tumor cell proliferation. Data generated at Southern Research Institute and the NCI suggest a correlation between TdCyd activity in solid tumor xenograft models and decreased levels of DNMT1.
TdCyd offers an improvement over current DNA methyltransferase inhibitors by virtue of a higher incorporation rate into DNA at lower levels of cytotoxicity; treatment with TdCyd is anticipated to result in the inhibition of tumor growth due to DNMT1 depletion at oral doses that are well tolerated in extended dosing schedules.
Approval Year
Sample Use Guides
In Vivo Use Guide
Sources: https://www.ncbi.nlm.nih.gov/pubmed/24908436
Mice-bearing CCRF-CeM tumors (approximately 200 mg) were treated with either 9 mg/kg of TdCyd (i.p. qld × 9) or 5 mg/kg aza-TdCyd (i.p. qld × 9).
Route of Administration:
Intraperitoneal
In Vitro Use Guide
Sources: https://www.ncbi.nlm.nih.gov/pubmed/24908436
Leukemia lines (CCRF-CeM and KG1a) were sensitive to TdCyd and aza-TdCyd with IC50s below 1 uM. aza-TdCyd also decreased viability in the nCI-H23 lung carcinoma, HCt-116 colon carcinoma and IgrOV-1 ovarian carcinoma with IC50s of 4.5, 58 and 36 uM, respectively, whereas TdCyd had less than 50 % effect on viability in these cell lines at 100 uM.
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134111-30-1
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C121828
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10037425
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ACTIVE MOIETY