SCHEMBL4575275

SCHEMBL4575275

O=C(O)C1CCCCN1C(=O)OCC1c2ccccc2-c2ccccc21

nearest known ligand 0.53

Predicted protein targets (top 19)

geneUniProtsupporting neighboursconfidence
▸ ALDH1A1 P00352 1/20 0.53
▸ SMN1; SMN2 Q16637 1/20 0.53
▸ RAB9A P51151 1/20 0.47
▸ FABP5 Q01469 3/20 0.46
▸ FABP7 O15540 2/20 0.46
▸ ITGB3 P05106 1/20 0.43
▸ ITGB1 P05556 1/20 0.43
▸ ITGAV P06756 1/20 0.43
▸ ITGA5 P08648 1/20 0.43
▸ ITGA4 P13612 1/20 0.43
▸ LTA4H P09960 3/20 0.42
▸ CTSB P07858 1/20 0.42
▸ CTSS P25774 1/20 0.42
▸ CTSK P43235 1/20 0.42
▸ PREP P48147 2/20 0.42
▸ KMT2A Q03164 1/20 0.41
▸ FKBP1A P62942 2/20 0.41
▸ TSHR P16473 1/20 0.41
▸ F2 P00734 1/20 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
SCHEMBL119867 1.00 ALDH1A1 (0.53) ALDH1A1SMN1; SMN2RAB9AFABP5FABP7
SCHEMBL29402209 1.00 ALDH1A1 (0.53) ALDH1A1SMN1; SMN2RAB9AFABP5FABP7
SCHEMBL29383097 1.00 ALDH1A1 (0.53) ALDH1A1SMN1; SMN2RAB9AFABP5FABP7
SCHEMBL119365 1.00 ALDH1A1 (0.53) ALDH1A1SMN1; SMN2RAB9AFABP5FABP7
SCHEMBL30510359 1.00 ALDH1A1 (0.53) ALDH1A1SMN1; SMN2RAB9AFABP5FABP7
SCHEMBL29447672 1.00 ALDH1A1 (0.53) ALDH1A1SMN1; SMN2RAB9AFABP5FABP7
SCHEMBL17359219 0.99 ALDH1A1 (0.52) ALDH1A1SMN1; SMN2RAB9AFABP5FABP7
SCHEMBL30792899 0.99 ALDH1A1 (0.52) ALDH1A1SMN1; SMN2RAB9AFABP5FABP7
SCHEMBL27028706 0.99 ALDH1A1 (0.52) ALDH1A1SMN1; SMN2RAB9AFABP5FABP7
SCHEMBL119560 0.96 ALDH1A1 (0.58) ALDH1A1SMN1; SMN2RAB9AFABP5FABP7

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-117143179-B Synthesis method of thrombin chromogenic substrate S-2238 安徽峆一药业股份有限公司 2024-07-12 — — CN claimed
US-12371454-B2 Cyclic peptide compound having Kras inhibitory action CHUGAI SEIYAKU KABUSHIKI KAISHA (JP) 2025-07-29 — — US disclosed
US-20240400617-A1 CYCLIC PEPTIDE COMPOUND HAVING KRAS INHIBITORY ACTION CHUGAI SEIYAKU KABUSHIKI KAISHA (JP) 2024-12-05 — — US disclosed
CN-117143179-B Synthesis method of thrombin chromogenic substrate S-2238 安徽峆一药业股份有限公司 2024-07-12 — — CN disclosed
US-20240218021-A1 CYCLIN INHIBITORS CIRCLE PHARMA, INC. 2024-07-04 — — US disclosed
US-20240148821-A1 PHARMACEUTICAL USE OF CYCLIC PEPTIDE COMPOUND CHUGAI SEIYAKU KABUSHIKI KAISHA (JP) 2024-05-09 — — US disclosed
EP-4316503-A1 PHARMACEUTICAL USE OF CYCLIC PEPTIDE COMPOUND CHUGAI SEIYAKU KABUSHIKI KAISHA (JP) 2024-02-07 — — EP disclosed
CN-117143179-A Synthesis method of thrombin chromogenic substrate S-2238 安徽峆一药业股份有限公司 2023-12-01 — — CN disclosed
US-20230151060-A1 CYCLIC PEPTIDE COMPOUND HAVING KRAS INHIBITORY ACTION CHUGAI SEIYAKU KABUSHIKI KAISHA (JP) 2023-05-18 — — US disclosed
EP-3515880-B1 METHODS AND COMPOSITIONS FOR SYNTHESIS OF ENCODED LIBRARIES HITGEN INC (CN) 2023-05-10 — — EP disclosed
WO-1999003832-A1 PIPERIDINE OLIGOMERS AND COMBINATORIAL LIBRARIES THEREOF PHYTERA SYMBION APS (DK) 1999-01-28 — — WO disclosed
EP-0888303-A1 SYNTHETIC DERIVATIVES OF RAPAMYCIN AS MULTIMERIZING AGENTS FOR CHIMERIC PROTEINS WITH IMMUNOPHILIN-DERIVED DOMAINS ARIAD GENE THERAPEUTICS, INC. (US) 1999-01-07 — — EP disclosed
WO-1997031898-A1 SYNTHETIC DERIVATIVES OF RAPAMYCIN AS MULTIMERIZING AGENTS FOR CHIMERIC PROTEINS WITH IMMUNOPHILIN-DERIVED DOMAINS ARIAD GENE THERAPEUTICS, INC. (US) 1997-09-04 — — WO disclosed
EP-0502926-B1 ANTI-THROMBOTIC PEPTIDES AND PSEUDOPEPTIDES RHONE POULENC RORER INT (US) 1996-03-13 — — EP disclosed
US-5328900-A Anti-thrombotic peptide and pseudopeptide derivatives RHONE-POULENC RORER PHARMACEUTICALS INC. (US) 1994-07-12 — — US disclosed
EP-0502926-A1 ANTI-THROMBOTIC PEPTIDES AND PSEUDOPEPTIDES. RHONE POULENC RORER INT (US) 1992-09-16 — — EP disclosed
EP-0502926-A4 ANTI-THROMBOTIC PEPTIDES AND PSEUDOPEPTIDES. RHONE POULENC RORER INTERNAT H (US) 1992-07-13 — — EP disclosed
US-5064814-A Anti-thrombotic peptide and pseudopeptide derivatives RHONE-POULENC RORER PHARMACEUTICALS INC. (US) 1991-11-12 — — US disclosed
US-5053392-A Anticoagulants RHONE-POULENC RORER PHARMACEUTICALS INC. (US) 1991-10-01 — — US disclosed
WO-1991007976-A1 ANTI-THROMBOTIC PEPTIDES AND PSEUDOPEPTIDES RHONE-POULENC RORER INTERNATIONAL (HOLDINGS) INC. (US) 1991-06-13 — — 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 (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-20230151060-A1 CYCLIC PEPTIDE COMPOUND HAVING KRAS INHIBITORY ACTION KRAS, NRAS, HRAS ALDH1A1 4838/4885SMN1; SMN2 4201/4885RAB9A 65/4885
US-20240400617-A1 CYCLIC PEPTIDE COMPOUND HAVING KRAS INHIBITORY ACTION KRAS, NRAS, HRAS ALDH1A1 4838/4885SMN1; SMN2 4201/4885RAB9A 65/4885
US-20240218021-A1 CYCLIN INHIBITORS CCNI, CCNC, CDK2 ALDH1A1 2597/4885SMN1; SMN2 2812/4885RAB9A 3397/4885
US-20240148821-A1 PHARMACEUTICAL USE OF CYCLIC PEPTIDE COMPOUND VIP, IAPP, KRAS ALDH1A1 4861/4885SMN1; SMN2 4745/4885RAB9A 98/4885
US-12371454-B2 Cyclic peptide compound having Kras inhibitory action KRAS, NRAS, HRAS ALDH1A1 4838/4885SMN1; SMN2 4201/4885RAB9A 65/4885

“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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