SCHEMBL7148935

SCHEMBL7148935

N#C[C@@H]1O[C@H](COC(=O)c2ccccc2)[C@@H](OC(=O)c2ccccc2)[C@H]1OC(=O)c1ccccc1

nearest known ligand 0.52

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
▸ USP2 O75604 2/20 0.52
▸ POLB P06746 2/20 0.52
▸ MEN1 O00255 1/20 0.52
▸ KMT2A Q03164 1/20 0.52
▸ PTPN1 P18031 4/20 0.47
▸ CA1 P00915 2/20 0.45
▸ CA2 P00918 2/20 0.45
▸ CA9 Q16790 1/20 0.45
▸ ALDH1A1 P00352 2/20 0.44
▸ F11 P03951 1/20 0.43
▸ LGALS9 O00182 1/20 0.43
▸ LGALS1 P09382 1/20 0.43
▸ LGALS3 P17931 1/20 0.43
▸ LGALS7; LGALS7B P47929 1/20 0.43
▸ GAPDH P04406 2/20 0.42
▸ PTPN2 P17706 1/20 0.42
▸ PTPN11 Q06124 1/20 0.42
▸ TSHR P16473 1/20 0.41
▸ MAPT P10636 1/20 0.41
▸ MAPK1 P28482 2/20 0.41

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
SCHEMBL24941146 1.00 USP2 (0.52) USP2POLBMEN1KMT2APTPN1
SCHEMBL10865013 1.00 USP2 (0.52) USP2POLBMEN1KMT2APTPN1
SCHEMBL7213369 1.00 USP2 (0.52) USP2POLBMEN1KMT2APTPN1
SCHEMBL10864836 1.00 USP2 (0.52) USP2POLBMEN1KMT2APTPN1
SCHEMBL14553315 0.89 POLB (0.44) USP2POLBMEN1KMT2APTPN1
SCHEMBL20927140 0.87 USP2 (0.52) USP2POLBMEN1KMT2APTPN1
SCHEMBL21650361 0.86 USP2 (0.51) USP2POLBMEN1KMT2APTPN1
SCHEMBL21650362 0.84 USP2 (0.49) USP2POLBMEN1KMT2APTPN1
SCHEMBL11318512 0.83 ALDH1A1 (0.50) USP2POLBMEN1KMT2APTPN1
SCHEMBL21650360 0.82 USP2 (0.50) USP2POLBMEN1KMT2APTPN1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-0171171-B1 A PROCESS FOR PREPARING 2-BETA-D-RIBOFURANOSYLSELENAZOLE-4-CARBOXAMIDE WARNER-LAMBERT COMPANY (US) 1990-04-25 — — EP claimed
US-4619996-A Process for preparing 2-β-D-ribofuranosylselenazole-4-carboxamide WARNER-LAMBERT COMPANY (US) 1986-10-28 — — US claimed
EP-0171171-A1 A process for preparing 2-beta-D-ribofuranosylselenazole-4-carboxamide WARNER-LAMBERT COMPANY (US) 1986-02-12 — — EP claimed
US-20230302030-A1 COMPOUNDS, PHARMACEUTICAL COMPOSITIONS AND USE THEREOF AS INHIBITORS OF RAN GTPase CENTRE HOSPITALIER DE L'UNIVERSITE DE MONTREAL (CA) 2023-09-28 — — US disclosed
US-11667663-B2 Cyclic dinucleotides as anticancer agents BRISTOL-MYERS SQUIBB COMPANY (US) 2023-06-06 — — US disclosed
US-11660311-B2 Cyclic dinucleotides as anticancer agents BRISTOL-MYERS SQUIBB COMPANY (US) 2023-05-30 — — US disclosed
US-11660311-B2 Cyclic dinucleotides as anticancer agents BRISTOL-MYERS SQUIBB COMPANY (US) 2023-05-30 — — US disclosed
US-20230033360-A1 COMPOUNDS AS CD73 INHIBITORS BIOARDIS LLC 2023-02-02 — — US disclosed
EP-4055026-A1 COMPOUNDS AS CD73 INHIBITORS Bioardis LLC (US) 2022-09-14 — — EP disclosed
CN-114945578-A Compounds as CD73 inhibitors 博奥阿迪斯生物科技公司 2022-08-26 — — CN disclosed
US-20220117995-A1 CYCLIC DINUCLEOTIDES AS ANTICANCER AGENTS BRISTOL MYERS SQUIBB CO (US) 2022-04-21 — — US disclosed
EP-0171171-A1 A process for preparing 2-beta-D-ribofuranosylselenazole-4-carboxamide WARNER-LAMBERT COMPANY (US) 1986-02-12 — — EP disclosed
EP-0171171-A1 A process for preparing 2-beta-D-ribofuranosylselenazole-4-carboxamide WARNER-LAMBERT COMPANY (US) 1986-02-12 — — EP disclosed
US-4544741-A Azole dinucleotide compounds and methods for their production BRIGHAM YOUNG UNIVERSITY, PROVO, UT., A NONPROFIT CORP. OF UT 1985-10-01 — — US disclosed
US-4531001-A 2-β-D-ribofuranosylselenazole-4-carboxamide compounds BRIGHAM YOUNG UNIVERSITY (US) 1985-07-23 — — US disclosed
US-4451648-A VIRICIDE BY MULTI-STEP PROCESS THE UNITED STATES OF AMERICA AS REPRESENTED BY THE DEPARTMENT OF HEALTH AND HUMAN SERVICES (US) 1984-05-29 — — US disclosed
EP-0090405-A1 Novel azole dinucleotide compounds and methods for their production BRIGHAM YOUNG UNIVERSITY (US) 1983-10-05 — — EP disclosed
EP-0089678-A1 Novel 2-beta-D-ribofuranosylselenazole-4-carboxamide compounds and methods for their production BRIGHAM YOUNG UNIVERSITY (US) 1983-09-28 — — EP disclosed
EP-0072977-A1 Process for the production of 2-beta-D-ribofuranosylthiazole-4-carboxamide Starks Associates, Incorporated (US) 1983-03-02 — — EP disclosed
EP-0072977-A1 Process for the production of 2-beta-D-ribofuranosylthiazole-4-carboxamide Starks Associates, Incorporated (US) 1983-03-02 — — 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 (5 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-20230033360-A1 COMPOUNDS AS CD73 INHIBITORS ENTPD5, ENTPD1, NT5E USP2 4174/4885POLB 1585/4885MEN1 2427/4885
US-20230302030-A1 COMPOUNDS, PHARMACEUTICAL COMPOSITIONS AND USE THEREOF AS INHIBITORS OF RAN GTPase RAN, RANBP1, GDI2 USP2 4401/4885POLB 1318/4885MEN1 1886/4885
US-11660311-B2 Cyclic dinucleotides as anticancer agents DPYD, CD38, DUT USP2 4165/4885POLB 31/4885MEN1 1929/4885
US-11667663-B2 Cyclic dinucleotides as anticancer agents DPYD, NTPCR, DUT USP2 3819/4885POLB 40/4885MEN1 2234/4885
US-20220117995-A1 CYCLIC DINUCLEOTIDES AS ANTICANCER AGENTS DPYD, CD38, DUT USP2 4165/4885POLB 31/4885MEN1 1929/4885

“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.

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