SCHEMBL2805870

SCHEMBL2805870

O=C(O)C1CCC(=O)N1C(=O)O

nearest known ligand 0.56

Predicted protein targets (top 12)

geneUniProtsupporting neighboursconfidence
ACE P12821 6/20 0.56
ITGB1 P05556 2/20 0.37
ITGA5 P08648 2/20 0.37
ITGB3 P05106 1/20 0.34
ITGAV P06756 1/20 0.34
ITGA4 P13612 1/20 0.34
MEN1 O00255 1/20 0.33
KMT2A Q03164 1/20 0.33
L3MBTL1 Q9Y468 1/20 0.33
P2RX7 Q99572 2/20 0.31
MMP2 P08253 1/20 0.31
MMP9 P14780 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
SCHEMBL2715722 1.00 ACE (0.56) ACEITGB1ITGA5ITGB3ITGAV
SCHEMBL2712732 1.00 ACE (0.56) ACEITGB1ITGA5ITGB3ITGAV
SCHEMBL29880999 0.88 ACE (0.45) ACEITGB1ITGA5ITGB3ITGAV
SCHEMBL4709634 0.88 ACE (0.45) ACEITGB1ITGA5ITGB3ITGAV
SCHEMBL4709631 0.88 ACE (0.45) ACEITGB1ITGA5ITGB3ITGAV
SCHEMBL17979454 0.88 ACE (0.45) ACEITGB1ITGA5ITGB3ITGAV
SCHEMBL30317311 0.83 ACE (0.57) ACEITGB1ITGA5ITGB3ITGAV
SCHEMBL6899829 0.83 ACE (0.57) ACEITGB1ITGA5ITGB3ITGAV
SCHEMBL8213582 0.83 ACE (0.53) ACEITGB1ITGA5ITGB3ITGAV
SCHEMBL6899827 0.83 ACE (0.57) ACEITGB1ITGA5ITGB3ITGAV

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-114920771-A Novel synthesis process of intermediate of novel oral medicine for overactive bladder 苏州虞美景盛新药开发有限公司 2022-08-19 CN claimed
US-8968711-B2 Cosmetic or dermatological composition comprising a polymer bearing junction groups, and cosmetic treatment process L'OREAL (FR) 2015-03-03 US claimed
US-20100272660-A1 COSMETIC OR PHARMACEUTICAL COMPOSITION COMPRISING A POLYCONDENSATE, THE SAID POLYCONDENSATE AND METHOD OF COSMETIC TREATMENT L'OREAL (FR) 2010-10-28 US claimed
US-20100239509-A1 COSMETIC OR DERMATOLOGICAL COMPOSITION COMPRISING A POLYMER BEARING JUNCTION GROUPS, AND COSMETIC TREATMENT PROCESS L'OREAL (FR) 2010-09-23 US claimed
CN-114585637-B MASP-inhibitory compounds and uses thereof 拜耳公司 2025-04-15 CN disclosed
WO-2025076476-A2 MASP-2 INHIBITORS AND METHODS OF USE OMEROS CORPORATION (US) 2025-04-10 WO disclosed
US-20240228506-A1 RIPK1 INHIBITORS AND METHODS OF USE MERCK SHARP & DOHME LLC (US) 2024-07-11 US disclosed
WO-2024131827-A1 KRAS G12D INHIBITORS AND USES THEREOF 上海和誉生物医药科技有限公司 2024-06-27 WO disclosed
US-20240199647-A1 ANTI-VIRAL COMPOUNDS KATHOLIEKE UNIVERSITEIT LEUVEN (BE) 2024-06-20 US disclosed
CN-118215652-A Substituted hydroxymethyl pyrrolidines and medical uses thereof 阿托基公司 2024-06-18 CN disclosed
WO-2024123102-A1 NOVEL TRICYCLIC COMPOUND AS KRAS G12D INHIBITOR, AND USE THEREOF 에스케이바이오팜 주식회사 2024-06-13 WO disclosed
US-11993600-B2 Saturated spirocyclics as antiviral agents ENANTA PHARMACEUTICALS, INC. (US) 2024-05-28 US disclosed
US-20050059724-A1 Novel cyanopyrrolidides, process for their preparation and their use as medicaments AVENTIS PHARMA DEUTSCHLAND GMBH (DE) 2005-03-17 US disclosed
WO-2004052850-A2 METHODS AND COMPOUNDS PRODUCING DIPEPTIDYL PEPTIDASE IV INHIBITORS AND INTERMEDIATES THEREOF BRISTOL-MYERS SQUIBB COMPANY (US) 2004-06-24 WO disclosed
US-6653295-B2 Protease inhibitor; viricide BRISTOL-MYERS SQUIBB COMPANY 2003-11-25 US disclosed
US-20030064962-A1 Inhibitors of hepatitis C virus NS3 protease BRISTOL-MYERS SQUIBB COMPANY (FORMERLY D/B/A DUPONT PHARMACEUTICALS COMPANY) 2003-04-03 US disclosed
EP-1083897-A4 HIV INTEGRASE INHIBITORS MERCK & CO INC (US) 2003-01-02 EP disclosed
US-6306891-B1 INHIBITORS OF HIV INTEGRASE AND INHIBITORS OF HIV REPLICATION. THESE COMPOUNDS ARE USEFUL IN THE PREVENTION OR TREATMENT OF INFECTION BY HIV TREATMENT OF AIDS, EITHER AS COMPOUNDS, PHARMACEUTICALLY ACCEPTABLE SALTS MERCK & CO., INC. 2001-10-23 US disclosed
EP-1083897-A1 HIV INTEGRASE INHIBITORS Merck & Co., Inc. (US) 2001-03-21 EP disclosed
WO-1999062513-A1 HIV INTEGRASE INHIBITORS MERCK & CO., INC. (US) 1999-12-09 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 (7 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-11993600-B2 Saturated spirocyclics as antiviral agents ACE, ACE2, PKD1 ACE 1/4885ITGB1 4082/4885ITGA5 4047/4885
US-20240228506-A1 RIPK1 INHIBITORS AND METHODS OF USE RIPK1, RIPK2, RIPK3 ACE 3379/4885ITGB1 4515/4885ITGA5 4775/4885
US-20050059724-A1 Novel cyanopyrrolidides, process for their preparation and their use as medicaments CYP11B2, SLC5A2, CYP11B1 ACE 206/4885ITGB1 3655/4885ITGA5 3470/4885
US-20030064962-A1 Inhibitors of hepatitis C virus NS3 protease PRSS1, SERPINB1, SPINT2 ACE 42/4885ITGB1 3688/4885ITGA5 4249/4885
US-20100239509-A1 COSMETIC OR DERMATOLOGICAL COMPOSITION COMPRISING A POLYMER BEARING JUNCTION GROUPS, AND COSMETIC TREATMENT PROCESS CUTA, SUCLG1, KRT18 ACE 4847/4885ITGB1 4531/4885ITGA5 3623/4885
US-20100272660-A1 COSMETIC OR PHARMACEUTICAL COMPOSITION COMPRISING A POLYCONDENSATE, THE SAID POLYCONDENSATE AND METHOD OF COSMETIC TREATMENT ACMSD, CUTA, PCCA ACE 4664/4885ITGB1 2837/4885ITGA5 2767/4885
US-20240199647-A1 ANTI-VIRAL COMPOUNDS EIF2AK2, ZC3HAV1, HAVCR2 ACE 7/4885ITGB1 4432/4885ITGA5 4623/4885

“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.