SCHEMBL699538

SCHEMBL699538

O=C(O)c1ccoc1C(=O)OC(=O)c1occc1C(=O)O

nearest known ligand 0.42

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
L3MBTL1 Q9Y468 3/20 0.41
TDP1 Q9NUW8 2/20 0.41
TP53 P04637 2/20 0.39
KMT2A Q03164 2/20 0.39
ALDH1A1 P00352 3/20 0.36
ALOX15 P16050 1/20 0.36
CYP1A2 P05177 1/20 0.36
NPC1 O15118 1/20 0.34
PKM P14618 1/20 0.34
RAB9A P51151 1/20 0.34
POLB P06746 2/20 0.33
ESR1 P03372 1/20 0.33
APEX1 P27695 1/20 0.33
MAPK1 P28482 1/20 0.33
ESR2 Q92731 1/20 0.33
SMN1; SMN2 Q16637 2/20 0.33
HSD17B10 Q99714 1/20 0.33
DAO P14920 1/20 0.32
KDM4E B2RXH2 1/20 0.31
CA12 O43570 1/20 0.31

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
SCHEMBL3605212 0.84 L3MBTL1 (0.45) L3MBTL1TDP1TP53KMT2AALDH1A1
SCHEMBL21049227 0.82 L3MBTL1 (0.41) L3MBTL1TDP1TP53KMT2AALDH1A1
SCHEMBL28257547 0.82 L3MBTL1 (0.45) L3MBTL1TDP1TP53KMT2AALDH1A1
SCHEMBL38507 0.82 L3MBTL1 (0.45) L3MBTL1TDP1TP53KMT2AALDH1A1
SCHEMBL31253429 0.81 L3MBTL1 (0.37) L3MBTL1TDP1TP53KMT2AALDH1A1
SCHEMBL28829681 0.80 L3MBTL1 (0.44) L3MBTL1TDP1TP53KMT2AALDH1A1
Hydrochloric Acid SCHEMBL4441902 0.80 L3MBTL1 (0.44) L3MBTL1TDP1TP53KMT2AALDH1A1
Bromide SCHEMBL28497865 0.80 L3MBTL1 (0.44) L3MBTL1TDP1TP53KMT2AALDH1A1
Bicarbonate SCHEMBL28887905 0.80 L3MBTL1 (0.44) L3MBTL1TDP1TP53KMT2AALDH1A1
Calcium SCHEMBL31344979 0.80 L3MBTL1 (0.44) L3MBTL1TDP1TP53KMT2AALDH1A1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-8653048-B2 Prodrugs based on gemcitabine structure and synthetic methods and applications thereof SANLUGEN PHARMATECH LTD. (CN) 2014-02-18 US claimed
US-20120088908-A1 Prodrugs Based on Gemcitabine Structure and Synthetic Methods and Applications Thereof SANLUGEN PHARMATECH LTD. (CN) 2012-04-12 US claimed
EP-2423215-A1 PRODRUGS BASED ON GEMCITABINE STRUCTURE AS WELL AS SYNTHETIC METHOD AND APPLICATION THEREOF Sanlugen Pharmatech Ltd. (CN) 2012-02-29 EP claimed
CN-116715836-A Polyester with antibacterial and antiviral functions and preparation method and application thereof 东华大学 2023-09-08 CN disclosed
US-8653048-B2 Prodrugs based on gemcitabine structure and synthetic methods and applications thereof SANLUGEN PHARMATECH LTD. (CN) 2014-02-18 US disclosed
US-20120088908-A1 Prodrugs Based on Gemcitabine Structure and Synthetic Methods and Applications Thereof SANLUGEN PHARMATECH LTD. (CN) 2012-04-12 US disclosed
EP-2423215-A1 PRODRUGS BASED ON GEMCITABINE STRUCTURE AS WELL AS SYNTHETIC METHOD AND APPLICATION THEREOF Sanlugen Pharmatech Ltd. (CN) 2012-02-29 EP disclosed
US-5770340-A USING ELECTROGRAPHIC PRINTING PLATE HAVING ELECTROCONDUCTIVE SUPPORT WITH PHOTOCONDUCTIVE LAYER CONTAINING INORGANIC PHOTOCONDUCTOR, SPECIFIC SENSITIZING DYE AND BINDER, ALSO WITH BACKING HAVING LOW ELECTRICAL RESISTANCE FUJI PHOTO FILM CO., LTD. (JP) 1998-06-23 US disclosed
US-5677098-A USING CYANINE DYE FUJI PHOTO FILM CO., LTD. (JP) 1997-10-14 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-20120088908-A1 Prodrugs Based on Gemcitabine Structure and Synthetic Methods and Applications Thereof TYMP, DCTD, GLS2 L3MBTL1 497/4885TDP1 1766/4885TP53 254/4885

“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.