SCHEMBL601433

SCHEMBL601433

C#Cc1cn([C@H]2C[C@H](F)[C@@H](CO)O2)c(=O)[nH]c1=O

nearest known ligand 0.60

Predicted protein targets (top 12)

geneUniProtsupporting neighboursconfidence
LMNA P02545 2/20 0.56
SMN1; SMN2 Q16637 2/20 0.56
TK1 P04183 4/20 0.53
ALOX12 P18054 1/20 0.53
ADRA1A P35348 1/20 0.53
TK2 O00142 1/20 0.49
CYP1A2 P05177 1/20 0.48
CYP3A4 P08684 1/20 0.48
TSHR P16473 1/20 0.48
BLM P54132 1/20 0.48
PMP22 Q01453 1/20 0.48
NPSR1 Q6W5P4 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
SCHEMBL601434 1.00 LMNA (0.56) LMNASMN1; SMN2TK1ALOX12ADRA1A
SCHEMBL13944236 1.00 LMNA (0.56) LMNASMN1; SMN2TK1ALOX12ADRA1A
SCHEMBL610031 1.00 LMNA (0.56) LMNASMN1; SMN2TK1ALOX12ADRA1A
SCHEMBL13944238 0.88 LMNA (0.45) LMNASMN1; SMN2TK1ALOX12ADRA1A
SCHEMBL4169178 0.87 TK1 (0.53) LMNASMN1; SMN2TK1ALOX12ADRA1A
SCHEMBL6270422 0.87 TK1 (0.70) LMNASMN1; SMN2TK1ALOX12ADRA1A
SCHEMBL868882 0.87 TK1 (0.70) LMNASMN1; SMN2TK1ALOX12ADRA1A
SCHEMBL15740180 0.87 TK1 (0.70) LMNASMN1; SMN2TK1ALOX12ADRA1A
SCHEMBL18032569 0.87 TK1 (0.70) LMNASMN1; SMN2TK1ALOX12ADRA1A
SCHEMBL18032571 0.87 TK1 (0.70) LMNASMN1; SMN2TK1ALOX12ADRA1A

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-1027061-B1 IMINE-FORMING POLYSACCHARIDES, PREPARATION THEREOF AND THE USE THEREOF AS ADJUVANTS AND IMMUNOSTIMULANTS GALENICA PHARMACEUTICALS INC (US) 2005-05-25 EP claimed
US-20020150585-A1 Use of imine-forming polysaccharides as adjuvants and immunostimulants GALENICA PHARMACEUTICALS, INC. 2002-10-17 US claimed
US-20020042392-A1 Uracil reductase inactivators SMITHKLINE BEECHAM CORPORATION 2002-04-11 US claimed
US-6297223-B1 ADMINISTERING 5-SUBSTITUTED- OR 5,6-DIHYDRO-5-SUBSTITUTED-URACIL DERIVATIVE OR A PRODRUG THEREOF; IN CONJUNCTION WITH 5-FLUOROURACIL OR PRO-DRUG THEREOF. GLAXO WELLCOME INC. 2001-10-02 US claimed
US-6221852-B1 INACTIVATORS OF URACIL REDUCTASE. GLAXO WELLCOME INC. 2001-04-24 US claimed
EP-0356166-B1 Therapeutic nucleosides WELLCOME FOUND (GB) 1994-04-20 EP claimed
WO-1994005686-A1 ANOMERISATION PROCESS UNIVERSITY OF BIRMINGHAM (GB) 1994-03-17 WO claimed
US-5198539-A Viricides BURROUGHS WELLCOME CO. (US) 1993-03-30 US claimed
EP-0522128-A1 WATER-DISPERSIBLE TABLETS. WELLCOME FOUND (GB) 1993-01-13 EP claimed
US-5157114-A Treatment of HIV infections BURROUGHS WELLCOME CO. (US) 1992-10-20 US claimed
WO-1992013527-A1 WATER-DISPERSIBLE TABLETS THE WELLCOME FOUNDATION LIMITED (GB) 1992-08-20 WO claimed
EP-0356166-A2 Therapeutic nucleosides THE WELLCOME FOUNDATION LIMITED (GB) 1990-02-28 EP claimed
EP-2488182-B1 Treating neurotoxicity associated with combinations of 5-FU or its prodrugs and DPD inhibitors ELION ONCOLOGY LLC (US) 2017-07-19 EP disclosed
WO-2014089004-A1 METHODS FOR TREATING 5-FLUOROURACIL PRODRUG NON-RESPONSIVE CANCER PATIENTS ADHEREX TECHNOLOGIES, INC. (US) 2014-06-12 WO disclosed
US-8658618-B2 Methods for preventing or reducing neurotoxicity associated with administering DPD inhibitors in combination with 5-FU and 5-FU prodrugs ADHEREX TECHNOLOGIES, INC. (US) 2014-02-25 US disclosed
US-8541600-B2 11-aza, 11-thia and 11-oxa sterol compounds and compositions Harbor Therapeutics, Inc. (US) 2013-09-24 US disclosed
WO-1992013527-A1 WATER-DISPERSIBLE TABLETS THE WELLCOME FOUNDATION LIMITED (GB) 1992-08-20 WO disclosed
WO-1992004901-A1 URACIL REDUCTASE INACTIVATORS THE WELLCOME FOUNDATION LIMITED (GB) 1992-04-02 WO disclosed
WO-1992001452-A1 ENZYME INACTIVATORS THE WELLCOME FOUNDATION LIMITED (GB) 1992-02-06 WO disclosed
EP-0356166-A2 Therapeutic nucleosides THE WELLCOME FOUNDATION LIMITED (GB) 1990-02-28 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 (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-20020150585-A1 Use of imine-forming polysaccharides as adjuvants and immunostimulants TLR1, ICOS, TLR2 LMNA 4648/4885SMN1; SMN2 3571/4885TK1 1800/4885

“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.