SCHEMBL127179

SCHEMBL127179

Nc1ccn([C@H]2C[C@H](O)[C@@H](C(O)F)O2)c(=O)n1

nearest known ligand 0.50

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
POLB P06746 1/20 0.50
PDE3A Q14432 3/20 0.48
LMNA P02545 3/20 0.48
CACNA1F O60840 2/20 0.48
ALB P02768 2/20 0.48
MAPT P10636 2/20 0.48
CACNA1D Q01668 2/20 0.48
CACNA1S Q13698 2/20 0.48
CACNA1C Q13936 2/20 0.48
POLG P54098 2/20 0.48
PDE4D Q08499 1/20 0.45
SLC29A1 Q99808 1/20 0.45
THRB P10828 1/20 0.44
MTOR P42345 1/20 0.44
MDM2 Q00987 1/20 0.44
NCOA1 Q15788 1/20 0.44
NCOA3 Q9Y6Q9 1/20 0.44
NT5E P21589 1/20 0.44
P2RY2 P41231 3/20 0.41
P2RY4 P51582 3/20 0.41

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
SCHEMBL4201132 1.00 POLB (0.50) POLBPDE3ALMNACACNA1FALB
SCHEMBL28799641 0.91 POLB (0.53) POLBPDE3ALMNACACNA1FALB
SCHEMBL5666376 0.91 POLB (0.53) POLBPDE3ALMNACACNA1FALB
SCHEMBL7794947 0.89 POLB (0.51) POLBPDE3ALMNACACNA1FALB
SCHEMBL3449196 0.89 POLB (0.51) POLBPDE3ALMNACACNA1FALB
SCHEMBL51649 0.88 POLB (0.50) POLBPDE3ALMNACACNA1FALB
SCHEMBL3178721 0.88 POLB (0.50) POLBPDE3ALMNACACNA1FALB
SCHEMBL4199985 0.88 POLB (0.50) POLBPDE3ALMNACACNA1FALB
SCHEMBL13471863 0.88 POLB (0.50) POLBPDE3ALMNACACNA1FALB
SCHEMBL3896397 0.86 POLB (0.48) POLBPDE3ALMNACACNA1FALB

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 141 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-110234319-A The composition and its application method of benzamide and reactive compound 转化药物开发有限责任公司 2019-09-13 CN claimed
US-8470522-B2 Three-dimensional culture containing human articular chondrocytes with induced terminal differentiation changes and preparation process and uses of the same KAOHSIUNG MEDICAL UNIVERSITY (TW) 2013-06-25 US claimed
EP-2207786-A1 2 ' -FLU0R0-2 ' -DEOXYTETRAHYDROURIDINES AS CYTIDINE DEAMINASE INHIBITORS Eisai Inc. (US) 2010-07-21 EP claimed
US-20090137521-A1 Certain Compounds, Compositions and Methods TAIHO PHARMACEUTICAL CO., LTD. (JP) 2009-05-28 US claimed
WO-2009052287-A1 2 ' -FLU0R0-2 ' -DEOXYTETRAHYDROURIDINES AS CYTIDINE DEAMINASE INHIBITORS EISAL CORPORATION OF NORTH AMERICA (US) 2009-04-23 WO claimed
US-20080026362-A1 Three-dimensional culture containing human articular chondrocytes with induced terminal differentiation changes, and preparation process and uses of the same KAOHSIUNG MEDICAL UNIVERSITY (TW) 2008-01-31 US claimed
US-20060253263-A1 Method to optimize drug selection, dosing and evaluation and to help predict therapeutic response and toxicity from immunosuppressant therapy MESHKIN BRIAN J 2006-11-09 US claimed
EP-1156827-A2 TREATMENT OF NEOPLASTIC DISEASES BY RADIATION Halogenetics, Inc. (US) 2001-11-28 EP claimed
WO-2000051639-A9 TREATMENT OF NEOPLASTIC DISEASES BY RADIATION HALOGENETICS INC (US) 2001-10-25 WO claimed
WO-2000051639-A2 TREATMENT OF NEOPLASTIC DISEASES BY RADIATION HALOGENETICS, INC. (US) 2000-09-08 WO claimed
EP-0504279-B1 FERMENTATION PROCESS FOR THE PRODUCTION OF PYRIMIDINE DEOXYRIBONUCLEOSIDES CHEMGEN CORP (US) 1997-07-09 EP claimed
US-5213972-A Production of thymidine and deoxyuridine, intermediates for AZT CHEMGEN CORPORATION (US) 1993-05-25 US claimed
EP-0504279-A4 FERMENTATION PROCESS FOR THE PRODUCTION OF PYRIMIDINE DEOXYRIBONUCLEOSIDES 1993-02-17 EP claimed
EP-0504279-A1 FERMENTATION PROCESS FOR THE PRODUCTION OF PYRIMIDINE DEOXYRIBONUCLEOSIDES. CHEMGEN CORP (US) 1992-09-23 EP claimed
WO-1991009130-A1 FERMENTATION PROCESS FOR THE PRODUCTION OF PYRIMIDINE DEOXYRIBONUCLEOSIDES CHEMGEN CORPORATION (US) 1991-06-27 WO claimed
EP-0287128-A1 Antitumor agent RESEARCH CORPORATION TECHNOLOGIES, INC. (US) 1988-10-19 EP claimed
US-20260103746-A1 PROCESS FOR THE PRODUCTION OF CLOSED LINEAR DNA TYRIS THERAPEUTICS S L (ES) 2026-04-16 US disclosed
CN-112834678-B Method for detecting concentration of 11 antitumor drugs in serum 南京品生医学检验实验室有限公司 2025-01-14 CN disclosed
WO-1991009130-A1 FERMENTATION PROCESS FOR THE PRODUCTION OF PYRIMIDINE DEOXYRIBONUCLEOSIDES CHEMGEN CORPORATION (US) 1991-06-27 WO disclosed
EP-0287128-A1 Antitumor agent RESEARCH CORPORATION TECHNOLOGIES, INC. (US) 1988-10-19 EP 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 (2 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-20090137521-A1 Certain Compounds, Compositions and Methods DUT, TYMP, DPYD POLB 123/4885PDE3A 944/4885LMNA 1274/4885
US-20260103746-A1 PROCESS FOR THE PRODUCTION OF CLOSED LINEAR DNA POLM, POLL, POLB POLB 3/4885PDE3A 2760/4885LMNA 43/4885

“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.