SCHEMBL6374113

SCHEMBL6374113

CC(=O)OC1C[C@@H](n2cc(F)c(=O)[nH]c2=O)O[C@H]1CO

nearest known ligand 0.67

Predicted protein targets (top 8)

geneUniProtsupporting neighboursconfidence
LMNA P02545 2/20 0.67
SMN1; SMN2 Q16637 2/20 0.67
RNASE1 P07998 1/20 0.59
SLC6A2 P23975 1/20 0.50
ALOX12 P18054 1/20 0.49
ADRA1A P35348 1/20 0.49
TK1 P04183 3/20 0.49
TK2 O00142 1/20 0.48

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
SCHEMBL6852678 1.00 LMNA (0.67) LMNASMN1; SMN2RNASE1SLC6A2ALOX12
SCHEMBL13026818 1.00 LMNA (0.67) LMNASMN1; SMN2RNASE1SLC6A2ALOX12
SCHEMBL16311910 0.91 LMNA (0.57) LMNASMN1; SMN2RNASE1TK1TK2
SCHEMBL24595722 0.89 LMNA (0.55) LMNASMN1; SMN2RNASE1SLC6A2TK1
SCHEMBL570200 0.89 LMNA (0.55) LMNASMN1; SMN2RNASE1TK1
SCHEMBL8329362 0.89 LMNA (0.55) LMNASMN1; SMN2RNASE1TK1
SCHEMBL6075436 0.88 RNASE1 (0.74) LMNARNASE1TK1
SCHEMBL31289437 0.88 RNASE1 (0.74) LMNARNASE1TK1
SCHEMBL265601 0.88 RNASE1 (0.74) LMNARNASE1TK1
SCHEMBL265600 0.88 RNASE1 (0.74) LMNARNASE1TK1

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 13 patents. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-4816570-A Biologically reversible phosphate and phosphonate protective groups THE BOARD OF REGENTS OF THE UNIVERSITY OF TEXAS SYSTEM (US) 1989-03-28 US claimed
JP-59093096-A None JP disclosed
US-8673885-B1 Compounds for the protection of sulfur containing linkers in nucleic acid synthesis DUFF ROBERT (US) 2014-03-18 US disclosed
US-20050090659-A1 Phospholepid derivatives of nucleosides as antitumaorl medicaments GANYMED 256 VERMOEGENSVERWALTUNGS GMBH (DE) 2005-04-28 US disclosed
US-6787525-B1 METHOD OF TREATING HIV INFECTIONS AND/OR CANCER DISEASES SCHOTT HERBERT (DE) 2004-09-07 US disclosed
EP-0331032-B1 2'-DEOXY-5-FLUOROURIDINE DERIVATIVES TAIHO PHARMACEUTICAL CO., LTD. (JP) 1993-04-28 EP disclosed
US-5032680-A Antitumor KURARAY CO., LTD. (JP) 1991-07-16 US disclosed
EP-0331032-A1 2'-Deoxy-5-fluorouridine derivatives TAIHO PHARMACEUTICAL CO., LTD. (JP) 1989-09-06 EP disclosed
US-4605645-A ANTITUMOR AGENTS TEIJIN LIMITED (JP) 1986-08-12 US disclosed
EP-0081386-B1 5-FLUORO-2'-DEOXYURIDINE DERIVATIVES AND A PROCESS FOR THE PREPARATION THEREOF TEIJIN LIMITED (JP) 1985-05-29 EP disclosed
JP-S5993096-A 5-FLUORO-2'-DEOXYURIDINE DERIVATIVE AND ITS PREPARATION TEIJIN LTD 1984-05-29 JP disclosed
EP-0081386-A1 5-Fluoro-2'-deoxyuridine derivatives and a process for the preparation thereof TEIJIN LIMITED (JP) 1983-06-15 EP disclosed
US-4056673-A VIRICIDE, ANTINEOPLASTIC HOFFMANN-LA ROCHE INC. (US) 1977-11-01 US 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 (1 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-20050090659-A1 Phospholepid derivatives of nucleosides as antitumaorl medicaments PHOSPHO1, TYMP, PNP LMNA 759/4885SMN1; SMN2 1063/4885RNASE1 23/4885

“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.