SCHEMBL1449334

SCHEMBL1449334

CC(C)(C)OC(=O)N1C[C@H](O)C[C@@H]1C(=O)OCc1ccccc1

nearest known ligand 0.53

Predicted protein targets (top 16)

geneUniProtsupporting neighboursconfidence
POLB P06746 2/20 0.53
CYP1A2 P05177 1/20 0.48
CYP3A4 P08684 1/20 0.48
CYP2C19 P33261 1/20 0.48
FKBP1A P62942 5/20 0.47
KLK7 P49862 1/20 0.45
CTSL P07711 1/20 0.45
ABCB1 P08183 1/20 0.43
PARP1 P09874 1/20 0.42
HTRA1 Q92743 1/20 0.42
HPGD P15428 1/20 0.42
RIPK1 Q13546 1/20 0.41
PDK1 Q15118 1/20 0.41
PDK2 Q15119 1/20 0.41
PDK3 Q15120 1/20 0.41
PDK4 Q16654 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
SCHEMBL1783541 1.00 POLB (0.53) POLBCYP1A2CYP3A4CYP2C19FKBP1A
SCHEMBL4847623 1.00 POLB (0.53) POLBCYP1A2CYP3A4CYP2C19FKBP1A
SCHEMBL9296386 1.00 POLB (0.53) POLBCYP1A2CYP3A4CYP2C19FKBP1A
SCHEMBL6783772 1.00 POLB (0.53) POLBCYP1A2CYP3A4CYP2C19FKBP1A
SCHEMBL17191527 1.00 POLB (0.53) POLBCYP1A2CYP3A4CYP2C19FKBP1A
SCHEMBL1448453 1.00 POLB (0.53) POLBCYP1A2CYP3A4CYP2C19FKBP1A
SCHEMBL1150829 1.00 POLB (0.53) POLBCYP1A2CYP3A4CYP2C19FKBP1A
SCHEMBL2709081 1.00 POLB (0.53) POLBCYP1A2CYP3A4CYP2C19FKBP1A
SCHEMBL21441908 0.91 FKBP1A (0.47) POLBFKBP1AKLK7CTSLABCB1
SCHEMBL21285649 0.91 FKBP1A (0.47) POLBFKBP1AKLK7CTSLABCB1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20250376443-A1 MASP-2 INHIBITORS AND METHODS OF USE OMEROS CORPORATION (US) 2025-12-11 US disclosed
US-20250368604-A1 MASP-2 INHIBITORS AND METHODS OF USE OMEROS CORPORATION (US) 2025-12-04 US disclosed
US-12486278-B2 MASP-2 inhibitors and methods of use OMEROS CORPORATION (US) 2025-12-02 US disclosed
US-20250129020-A1 MASP-2 INHIBITORS AND METHODS OF USE OMEROS CORPORATION (US) 2025-04-24 US disclosed
US-12195427-B2 MASP-2 inhibitors and methods of use OMEROS CORPORATION (US) 2025-01-14 US disclosed
EP-4405359-A2 MDM2 DEGRADERS AND USES THEREOF Kymera Therapeutics, Inc. (US) 2024-07-31 EP disclosed
US-20240092788-A1 MASP-2 INHIBITORS AND METHODS OF USE OMEROS CORPORATION (US) 2024-03-21 US disclosed
US-11807641-B2 MASP-2 inhibitors and methods of use OMEROS CORPORATION (US) 2023-11-07 US disclosed
WO-2023049790-A2 MDM2 DEGRADERS AND USES THEREOF KYMERA THERAPEUTICS, INC. (US) 2023-03-30 WO disclosed
US-11584714-B2 MASP-2 inhibitors and methods of use OMEROS CORPORATION (US) 2023-02-21 US disclosed
US-7598250-B2 Cyclic amine BACE-1 inhibitors having a heterocyclic substituent SCHERING CORPORATION (US) 2009-10-06 US disclosed
EP-1660443-B1 CYCLIC AMINE BACE-1 INHIBITORS HAVING A BENZAMIDE SUBSTITUENT SCHERING CORP (US) 2009-03-04 EP disclosed
EP-1660447-B1 CYCLIC AMINE BACE-1 INHIBITORS HAVING A HETEROCYCLIC SUBSTITUENT SCHERING CORP (US) 2008-07-30 EP disclosed
EP-1660447-A1 CYCLIC AMINE BASE-1 INHIBITORS HAVING A HETEROCYCLIC SUBSTITUENT SCHERING CORPORATION (US) 2006-05-31 EP disclosed
EP-1660443-A2 CYCLIC AMINE BACE-1 INHIBITORS HAVING A BENZAMIDE SUBSTITUENT SCHERING CORPORATION (US) 2006-05-31 EP disclosed
US-20050119227-A1 Cyclic amine bace-1 inhibitors having a benzamide substituent SCHERING CORPORATION 2005-06-02 US disclosed
WO-2005016876-A2 CYCLIC AMINE BACE-1 INHIBITORS HAVING A BENZAMIDE SUBSTITUENT SCHERING CORPORATION (US) 2005-02-24 WO disclosed
US-20050043290-A1 Cyclic amine BACE-1 inhibitors having a heterocyclic substituent SCHERING CORPORATION AND PHARMACOPEIA DRUG DISCOVERY INC. 2005-02-24 US disclosed
WO-2005014540-A1 CYCLIC AMINE BASE-1 INHIBITORS HAVING A HETEROCYCLIC SUBSTITUENT SCHERING CORPORATION (US) 2005-02-17 WO disclosed
US-5120859-A Anticoagulants GENENTECH, INC. (US) 1992-06-09 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 (10 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-11584714-B2 MASP-2 inhibitors and methods of use MASP2, METAP2, SPINT2 POLB 2031/4885CYP1A2 4233/4885CYP3A4 4677/4885
US-12486278-B2 MASP-2 inhibitors and methods of use MASP2, METAP2, SPINT2 POLB 2216/4885CYP1A2 4271/4885CYP3A4 4706/4885
US-11807641-B2 MASP-2 inhibitors and methods of use MASP2, METAP2, SPINT2 POLB 2216/4885CYP1A2 4271/4885CYP3A4 4706/4885
US-20050043290-A1 Cyclic amine BACE-1 inhibitors having a heterocyclic substituent BACE1, BACE2, PSEN1 POLB 1261/4885CYP1A2 1450/4885CYP3A4 1059/4885
US-20250368604-A1 MASP-2 INHIBITORS AND METHODS OF USE MASP2, METAP2, SPINT2 POLB 2031/4885CYP1A2 4233/4885CYP3A4 4677/4885
US-12195427-B2 MASP-2 inhibitors and methods of use MASP2, METAP2, SPINT2 POLB 2031/4885CYP1A2 4233/4885CYP3A4 4677/4885
US-20240092788-A1 MASP-2 INHIBITORS AND METHODS OF USE MASP2, METAP2, SPINT2 POLB 2216/4885CYP1A2 4271/4885CYP3A4 4706/4885
US-20050119227-A1 Cyclic amine bace-1 inhibitors having a benzamide substituent BACE1, BACE2, BCHE POLB 1206/4885CYP1A2 1837/4885CYP3A4 2043/4885
US-20250376443-A1 MASP-2 INHIBITORS AND METHODS OF USE MASP2, METAP2, SPINT2 POLB 1886/4885CYP1A2 4289/4885CYP3A4 4700/4885
US-20250129020-A1 MASP-2 INHIBITORS AND METHODS OF USE MASP2, METAP2, SPINT2 POLB 2031/4885CYP1A2 4233/4885CYP3A4 4677/4885

“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.