SCHEMBL4297789

SCHEMBL4297789

O=C(O)CCC(=O)N1CCOCC1

nearest known ligand 0.58

Predicted protein targets (top 15)

geneUniProtsupporting neighboursconfidence
POLB P06746 2/20 0.58
TSHR P16473 2/20 0.58
LMNA P02545 1/20 0.58
FKBP1A P62942 2/20 0.56
ALDH1A1 P00352 1/20 0.56
L3MBTL1 Q9Y468 2/20 0.55
GLA P06280 2/20 0.53
RAB9A P51151 3/20 0.51
SMN1; SMN2 Q16637 3/20 0.51
NPC1 O15118 1/20 0.51
USP2 O75604 1/20 0.51
HSD17B10 Q99714 2/20 0.50
ALOX15 P16050 1/20 0.50
MEN1 O00255 1/20 0.46
KMT2A Q03164 1/20 0.46

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
SCHEMBL2952110 0.88 GLA (0.59) POLBTSHRLMNAFKBP1AALDH1A1
SCHEMBL2947983 0.88 GLA (0.64) POLBTSHRLMNAFKBP1AALDH1A1
SCHEMBL20885121 0.84 ALDH1A1 (0.56) LMNAALDH1A1SMN1; SMN2USP2HSD17B10
SCHEMBL9415751 0.82 GLA (0.67) POLBTSHRLMNAFKBP1AALDH1A1
SCHEMBL12888081 0.81 TSHR (0.61) POLBTSHRLMNAFKBP1AALDH1A1
SCHEMBL6233242 0.81 TSHR (0.56) POLBTSHRLMNAFKBP1AALDH1A1
SCHEMBL7347977 0.81 POLB (0.56) POLBTSHRLMNAFKBP1AALDH1A1
SCHEMBL3404224 0.80 L3MBTL1 (0.63) POLBTSHRLMNAFKBP1AALDH1A1
SCHEMBL7694058 0.80 GLA (0.65) POLBTSHRLMNAFKBP1AALDH1A1
SCHEMBL7380670 0.80 L3MBTL1 (0.57) POLBTSHRLMNAFKBP1AALDH1A1

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
WO-2025202864-A1 ENT1 INHIBITORS IN COMBINATION WITH ONCOLYTIC VIRUSES AND THEIR USE IN THE TREATMENT OF CANCER iTeos Belgium SA (BE) 2025-10-02 WO claimed
WO-2025126110-A1 ENT1 INHIBITORS IN COMBINATION WITH BISPECIFIC ANTIBODIES iTeos Belgium SA (BE) 2025-06-19 WO claimed
WO-2025104613-A1 ENT1 INHIBITORS IN COMBINATION WITH CHECKPOINT INHIBITORS iTeos Belgium SA (BE) 2025-05-22 WO claimed
CN-119143631-A Deprotection method for peptide compound or amide compound and resin removal method in solid phase reaction and method for producing peptide compound 中外制药株式会社 2024-12-17 CN claimed
CN-116535365-A Macrocyclic diamine derivatives and their combination with adenosine receptor antagonists as ENT inhibitors for the treatment of cancer ITEOS比利时公司 2023-08-04 CN claimed
US-20230203058-A1 MACROCYCLIC DIAMINE DERIVATIVES AS ENT INHIBITORS FOR THE TREATMENT OF CANCERS, AND COMBINATION THEREOF WITH ADENOSINE RECEPTOR ANTAGONISTS iTeos Belgium SA (BE) 2023-06-29 US claimed
EP-4132933-A1 MACROCYCLIC DIAMINE DERIVATIVES AS ENT INHIBITORS FOR THE TREATMENT OF CANCERS, AND COMBINATION THEREOF WITH ADENOSINE RECEPTOR ANTAGONISTS iTeos Belgium SA (BE) 2023-02-15 EP claimed
EP-0470702-B1 An optically active morpholino oxobutyric acid hydroxy binaphthalene derivative and its preparation TAKASAGO PERFUMERY CO LTD (JP) 1995-09-27 EP claimed
EP-0470702-A1 An optically active morpholino oxobutyric acid hydroxy binaphthalene derivative and its preparation Takasago International Corporation (JP) 1992-02-12 EP claimed
WO-2025202864-A1 ENT1 INHIBITORS IN COMBINATION WITH ONCOLYTIC VIRUSES AND THEIR USE IN THE TREATMENT OF CANCER iTeos Belgium SA (BE) 2025-10-02 WO disclosed
WO-2025126110-A1 ENT1 INHIBITORS IN COMBINATION WITH BISPECIFIC ANTIBODIES iTeos Belgium SA (BE) 2025-06-19 WO disclosed
WO-2025104613-A1 ENT1 INHIBITORS IN COMBINATION WITH CHECKPOINT INHIBITORS iTeos Belgium SA (BE) 2025-05-22 WO disclosed
CN-119143631-A Deprotection method for peptide compound or amide compound and resin removal method in solid phase reaction and method for producing peptide compound 中外制药株式会社 2024-12-17 CN disclosed
US-20240368183-A1 Macrocyclic Compounds Having ENT1 Inhibiting Activity iTeos Belgium SA (BE) 2024-11-07 US disclosed
EP-0470702-A1 An optically active morpholino oxobutyric acid hydroxy binaphthalene derivative and its preparation Takasago International Corporation (JP) 1992-02-12 EP disclosed
EP-0383635-A2 Peptides having renin inhibitory activity their preparation and use Sankyo Company Limited (JP) 1990-08-22 EP disclosed
US-4826815-A HYPOTENSIVE ABBOTT LABORATORIES (US) 1989-05-02 US disclosed
US-4349552-A TREATMENT OF CANCER FUJISAWA PHARMACEUTICAL COMPANY, LTD. (JP) 1982-09-14 US disclosed
EP-0010941-B1 5-FLUOROURACIL DERIVATIVES, PREPARATION THEREOF AND THEIR PHARMACEUTICAL COMPOSITIONS FUJISAWA PHARMACEUTICAL CO., LTD. (JP) 1982-05-12 EP disclosed
EP-0010941-A1 5-Fluorouracil derivatives, preparation thereof and their pharmaceutical compositions FUJISAWA PHARMACEUTICAL CO., LTD. (JP) 1980-05-14 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-20240368183-A1 Macrocyclic Compounds Having ENT1 Inhibiting Activity ENTPD5, ENTPD1, ENTPD8 POLB 2774/4885TSHR 2322/4885LMNA 2132/4885
US-20230203058-A1 MACROCYCLIC DIAMINE DERIVATIVES AS ENT INHIBITORS FOR THE TREATMENT OF CANCERS, AND COMBINATION THEREOF WITH ADENOSINE RECEPTOR ANTAGONISTS ENTPD1, SLC29A1, ENTPD5 POLB 1910/4885TSHR 778/4885LMNA 3959/4885

“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.