SCHEMBL3437129

SCHEMBL3437129

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

nearest known ligand 0.62

Predicted protein targets (top 14)

geneUniProtsupporting neighboursconfidence
LMNA P02545 5/20 0.62
SMN1; SMN2 Q16637 3/20 0.62
MAPT P10636 2/20 0.56
ESR1 P03372 1/20 0.56
ALB P02768 2/20 0.47
ALDH1A1 P00352 1/20 0.47
MAPK1 P28482 1/20 0.47
TSHR P16473 1/20 0.47
PMP22 Q01453 1/20 0.47
HBB P68871 1/20 0.47
ALOX12 P18054 1/20 0.44
ADRA1A P35348 1/20 0.44
TK1 P04183 2/20 0.43
PKM P14618 1/20 0.43

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
SCHEMBL26296051 1.00 LMNA (0.62) LMNASMN1; SMN2MAPTESR1ALB
SCHEMBL3437131 1.00 LMNA (0.62) LMNASMN1; SMN2MAPTESR1ALB
SCHEMBL21345305 1.00 LMNA (0.62) LMNASMN1; SMN2MAPTESR1ALB
SCHEMBL8104286 1.00 LMNA (0.62) LMNASMN1; SMN2MAPTESR1ALB
Phosphoric Acid SCHEMBL7906707 0.95 LMNA (0.57) LMNASMN1; SMN2MAPTESR1ALB
SCHEMBL21345988 0.87 LMNA (0.47) LMNASMN1; SMN2MAPTESR1ALB
SCHEMBL19657129 0.85 LMNA (0.48) LMNASMN1; SMN2ALBALDH1A1MAPK1
SCHEMBL23485 0.85 LMNA (0.58) LMNAALBALDH1A1TSHRPMP22
SCHEMBL14596607 0.85 LMNA (0.58) LMNAALBALDH1A1TSHRPMP22
SCHEMBL22992337 0.85 LMNA (0.58) LMNAALBALDH1A1TSHRPMP22

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-11021497-B2 Compositions and methods for synthesis of phosphorylated molecules THE REGENTS OF THE UNIVERSITY OF CALIFORNIA (US) 2021-06-01 US claimed
US-20200239500-A1 Compositions and Methods for Synthesis of Phosphorylated Molecules THE REGENTS OF THE UNIVERSITY OF CALIFORNIA 2020-07-30 US claimed
WO-2019195494-A1 COMPOSITIONS AND METHODS FOR SYNTHESIS OF PHOSPHORYLATED MOLECULES THE REGENTS OF THE UNIVERSITY OF CALIFORNIA (US) 2019-10-10 WO claimed
EP-3105243-B1 2',3'-DIDEOXY-5-FLUOROURIDINE DERIVATIVES, A PROCESS FOR THE MANUFACTURE THEREOF AND APPLICATION THEREOF ADAM MICKIEWICZ UNIV (PL) 2018-02-21 EP claimed
EP-3105243-A1 2',3'-DIDEOXY-5-FLUOROURIDINE DERIVATIVES, A PROCESS FOR THE MANUFACTURE THEREOF AND APPLICATION THEREOF Adam Mickiewicz University (PL) 2016-12-21 EP claimed
EP-3105242-A1 2',5'-DIDEOXY-5-FLUOROURIDINE DERIVATIVES HAVING CYTOTOXIC ACTIVITY, A PROCESS FOR THE MANUFACTURE THEREOF AND APPLICATION THEREOF Adam Mickiewicz University (PL) 2016-12-21 EP claimed
US-9388209-B2 2′, 3′-dideoxy-5-fluorouridine derivatives, a process for the manufacture thereof and application thereof ADAM MICKIEWICZ UNIVERSITY (PL) 2016-07-12 US claimed
US-20160152655-A1 2', 3'- DIDEOXY-5-FLUOROURIDINE DERIVATIVES, A PROCESS FOR THE MANUFACTURE THEREOF AND APPLICATION THEREOF ADAM MICKIEWICZ UNIVERSITY (PL) 2016-06-02 US claimed
WO-2015050467-A1 2',3'-DIDEOXY-5-FLUOROURIDINE DERIVATIVES, A PROCESS FOR THE MANUFACTURE THEREOF AND APPLICATION THEREOF ADAM MICKIEWICZ UNIVERSITY (PL) 2015-04-09 WO claimed
WO-2015041550-A1 2',5'-DIDEOXY-5-FLUOROURIDINE DERIVATIVES HAVING CYTOTOXIC ACTIVITY, A PROCESS FOR THE MANUFACTURE THEREOF AND APPLICATION THEREOF ADAM MICKIEWICZ UNIVERSITY (PL) 2015-03-26 WO claimed
US-7598230-B2 For the treatment of viral infections, microbial infections, and proliferative disorders; contain di- or triphosphate moeity mimetics, such as those containing boron anions BIOTA SCIENTIFIC MANAGEMENT PTY LTD (AU) 2009-10-06 US claimed
US-20070259832-A1 Nucleotide mimics and their prodrugs BIOTA SCIENTIFIC MANAGEMENT PTY LTD (AU) 2007-11-08 US claimed
EP-1485395-A2 NUCLEOTIDE MIMICS AND THEIR PRODRUGS Biota, Inc. (US) 2004-12-15 EP claimed
WO-2003072757-A9 NUCLEOTIDE MIMICS AND THEIR PRODRUGS BIOTA INC (US) 2004-10-21 WO claimed
US-20040059104-A1 Nucleotide mimics and their prodrugs BIOTA SCIENTIFIC MANAGEMENT PTY LTD (AU) 2004-03-25 US claimed
EP-1361227-A2 [5-carboxamide or 5-fluoro]-[2', 3'-unsaturated or 3'-modifield]-pyrimidine nucleosides Emory University (US) 2003-11-12 EP claimed
WO-2003072757-A2 NUCLEOTIDE MIMICS AND THEIR PRODRUGS BIOTA, INC. (US) 2003-09-04 WO claimed
US-11858953-B2 Compositions and methods for synthesis of phosphorylated molecules THE REGENTS OF THE UNIVERSITY OF CALIFORNIA (US) 2024-01-02 US disclosed
US-20040059104-A1 Nucleotide mimics and their prodrugs BIOTA SCIENTIFIC MANAGEMENT PTY LTD (AU) 2004-03-25 US disclosed
WO-2003072757-A2 NUCLEOTIDE MIMICS AND THEIR PRODRUGS BIOTA, INC. (US) 2003-09-04 WO 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 (6 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-20070259832-A1 Nucleotide mimics and their prodrugs NUDT14, ENTPD5, MTAP LMNA 3677/4885SMN1; SMN2 2496/4885MAPT 3539/4885
US-11858953-B2 Compositions and methods for synthesis of phosphorylated molecules PIK3CA, CHAMP1, TYMP LMNA 1794/4885SMN1; SMN2 3259/4885MAPT 1468/4885
US-20200239500-A1 Compositions and Methods for Synthesis of Phosphorylated Molecules PIK3CA, CHAMP1, TYMP LMNA 1794/4885SMN1; SMN2 3259/4885MAPT 1468/4885
US-11021497-B2 Compositions and methods for synthesis of phosphorylated molecules PIK3CA, CHAMP1, TYMP LMNA 1794/4885SMN1; SMN2 3259/4885MAPT 1468/4885
US-20160152655-A1 2', 3'- DIDEOXY-5-FLUOROURIDINE DERIVATIVES, A PROCESS FOR THE MANUFACTURE THEREOF AND APPLICATION THEREOF DUT, DCK, UGT1A8 LMNA 1428/4885SMN1; SMN2 3405/4885MAPT 4500/4885
US-20040059104-A1 Nucleotide mimics and their prodrugs NUDT14, ENTPD5, MTAP LMNA 3677/4885SMN1; SMN2 2496/4885MAPT 3539/4885

“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.