SCHEMBL28378385

SCHEMBL28378385

O=c1[nH]c(=O)n([C@H]2C[C@H](O)[C@@H](COP(=O)(O)OP(=O)(O)O)O2)cc1F

nearest known ligand 0.69

Predicted protein targets (top 4)

geneUniProtsupporting neighboursconfidence
LMNA P02545 1/20 0.66
SMN1; SMN2 Q16637 1/20 0.66
POLB P06746 1/20 0.63
TYMS P04818 4/20 0.60

Click a target to see other patent compounds predicted against it — the reverse direction, in place.

Similar compounds — the chemically nearest patent molecules

Nearest neighbours by Morgan-fingerprint cosine across the patent-compound collection, with each neighbour's top predicted target and the predicted targets it shares with this molecule.

Compoundsimilaritytop predictedshared targets
SCHEMBL17117799 0.98 LMNA (0.64) LMNASMN1; SMN2POLBTYMS
SCHEMBL2132784 0.98 LMNA (0.64) LMNASMN1; SMN2POLBTYMS
SCHEMBL152962 0.98 LMNA (0.64) LMNASMN1; SMN2POLBTYMS
5-Fluorodeoxyuridylate SCHEMBL6107 0.92 LMNA (0.71) LMNASMN1; SMN2TYMS
5-Fluorodeoxyuridylate SCHEMBL21901970 0.92 LMNA (0.71) LMNASMN1; SMN2TYMS
5-Fluorodeoxyuridylate SCHEMBL17117772 0.92 LMNA (0.71) LMNASMN1; SMN2TYMS
5-Fluorodeoxyuridylate SCHEMBL973436 0.92 LMNA (0.71) LMNASMN1; SMN2TYMS
5-Fluorodeoxyuridylate SCHEMBL15189164 0.92 LMNA (0.71) LMNASMN1; SMN2TYMS
SCHEMBL24220694 0.91 LMNA (0.65) LMNASMN1; SMN2POLBTYMS
SCHEMBL19389362 0.91 LMNA (0.68) LMNASMN1; SMN2POLBTYMS

Similarity is cosine over the 2,048-bit Morgan fingerprint (≈ Tanimoto). Identical fingerprints score 1.00.

Patent provenance — the patents this molecule appears in, and who filed them

Claimed or disclosed in 12 patents. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-12419893-B2 Methods and compositions for maximizing the prevention and/or reduction of various maladies and drug side-effects using uridine TOSK, INC. (US) 2025-09-23 US disclosed
WO-2024187069-A1 ENGINEERING ENTEROBACTERIA TO SITE-SPECIFICALLY ACTIVATE THE ANTICANCER PRODRUG 5-FLUOROCYTOSINE FOR TREATING COLON CANCER UNIVERSITY OF FLORIDA RESEARCH FOUNDATION, INCORPORATED (US) 2024-09-12 WO disclosed
EP-3538151-B1 HUMAN PLASMA-LIKE MEDIUM WHITEHEAD INST BIOMEDICAL RES (US) 2024-06-26 EP disclosed
CN-117903229-A Fluorouridine derivatives, application thereof in preparation of anticancer drugs/prodrugs, drugs/prodrugs and preparation method 中国科学院微生物研究所 2024-04-19 CN disclosed
US-11925658-B2 Phosphoramidate derivatives of 5-fluoro-2′—deoxyuridine for use in the treatment of cancer NuCana plc (GB) 2024-03-12 US disclosed
US-20230165886-A1 PHOSPHORAMIDATE DERIVATIVES OF 5 - FLUORO - 2' - DEOXYURIDINE FOR USE IN THE TREATMENT OF CANCER NuCana plc (GB) 2023-06-01 US disclosed
US-20230051644-A1 HUMAN PLASMA-LIKE MEDIUM WHITEHEAD INSTITUTE FOR BIOMEDICAL RESEARCH 2023-02-16 US disclosed
US-11559542-B2 Phosphoramidate derivatives of 5-fluoro-2′-deoxyuridine for use in the treatment of cancer NuCana plc (GB) 2023-01-24 US disclosed
CN-110840907-B Free radical sensitive uracil ProTide prodrug and pharmaceutical application thereof 南京医科大学 2022-11-25 CN disclosed
US-11453858-B2 Human plasma-like medium WHITEHEAD INSTITUTE FOR BIOMEDICAL RESEARCH (US) 2022-09-27 US disclosed
US-20220023330-A1 PHOSPHORAMIDATE DERIVATIVES OF 5 - FLUORO - 2` - DEOXYURIDINE FOR USE IN THE TREATMENT OF CANCER NuCana plc (GB) 2022-01-27 US disclosed
CN-110840907-A Free radical sensitive uracil ProTide prodrug and pharmaceutical application thereof 南京医科大学 2020-02-28 CN disclosed

Patent text — is the patent's own abstract consistent with the prediction?

For each of this compound's patents that has machine-readable text (5 of them — usually the abstract, not the full specification), we ask MedCPT which protein the text reads most about, and where the chemistry-predicted target lands among 4885 human targets. A high rank means the patent's own wording is consistent with the prediction — a weak, independent signal, not proof of activity.

PatentTitleText reads most aboutPredicted target · text-rank
US-20230165886-A1 PHOSPHORAMIDATE DERIVATIVES OF 5 - FLUORO - 2' - DEOXYURIDINE FOR USE IN THE TREATMENT OF CANCER SLC29A2, SLC29A1, TYMP LMNA 3712/4885SMN1; SMN2 2708/4885POLB 479/4885
US-11559542-B2 Phosphoramidate derivatives of 5-fluoro-2′-deoxyuridine for use in the treatment of cancer SLC29A2, SLC29A1, TYMP LMNA 3671/4885SMN1; SMN2 2657/4885POLB 474/4885
US-20220023330-A1 PHOSPHORAMIDATE DERIVATIVES OF 5 - FLUORO - 2` - DEOXYURIDINE FOR USE IN THE TREATMENT OF CANCER SLC29A2, SLC29A1, TYMP LMNA 3621/4885SMN1; SMN2 2660/4885POLB 469/4885
US-12419893-B2 Methods and compositions for maximizing the prevention and/or reduction of various maladies and drug side-effects using uridine UMPS, UNG, UGDH LMNA 2375/4885SMN1; SMN2 308/4885POLB 329/4885
US-11925658-B2 Phosphoramidate derivatives of 5-fluoro-2′—deoxyuridine for use in the treatment of cancer SLC29A2, SLC29A1, TYMP LMNA 3653/4885SMN1; SMN2 2652/4885POLB 492/4885

“Text reads most about” is the patent abstract's nearest protein in MedCPT space (background-debiased). Only ~1.4% of patents have machine-readable text, so most compounds won't have this panel.