SCHEMBL5747307

SCHEMBL5747307

O=C(O)[C@H]1C[C@H]2CCCC[C@H]2N1

nearest known ligand 0.52

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
▸ CYP2D6 P10635 3/20 0.52
▸ LMNA P02545 2/20 0.52
▸ BLM P54132 2/20 0.52
▸ ALOX15 P16050 2/20 0.52
▸ CYP1A2 P05177 2/20 0.52
▸ CYP2C19 P33261 2/20 0.52
▸ TSHR P16473 1/20 0.52
▸ RAB9A P51151 1/20 0.52
▸ MEN1 O00255 1/20 0.52
▸ THRB P10828 1/20 0.52
▸ PMP22 Q01453 1/20 0.52
▸ KMT2A Q03164 1/20 0.52
▸ CTSC P53634 4/20 0.36
▸ PRMT5 O14744 1/20 0.35
▸ WDR77 Q9BQA1 1/20 0.35
▸ L3MBTL1 Q9Y468 1/20 0.34
▸ SLC1A2 P43004 2/20 0.33
▸ SLC1A1 P43005 2/20 0.33
▸ SLC1A3 P43003 1/20 0.33
▸ GRIK1 P39086 1/20 0.32

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
SCHEMBL8244065 1.00 CYP2D6 (0.52) CYP2D6LMNABLMALOX15CYP1A2
SCHEMBL14605825 1.00 CYP2D6 (0.52) CYP2D6LMNABLMALOX15CYP1A2
SCHEMBL5435908 1.00 CYP2D6 (0.52) CYP2D6LMNABLMALOX15CYP1A2
SCHEMBL5429033 1.00 CYP2D6 (0.52) CYP2D6LMNABLMALOX15CYP1A2
SCHEMBL1414979 1.00 CYP2D6 (0.52) CYP2D6LMNABLMALOX15CYP1A2
SCHEMBL5748972 1.00 CYP2D6 (0.52) CYP2D6LMNABLMALOX15CYP1A2
SCHEMBL3330154 1.00 CYP2D6 (0.52) CYP2D6LMNABLMALOX15CYP1A2
SCHEMBL5747937 1.00 CYP2D6 (0.52) CYP2D6LMNABLMALOX15CYP1A2
SCHEMBL22418410 1.00 CYP2D6 (0.52) CYP2D6LMNABLMALOX15CYP1A2
SCHEMBL14052951 1.00 CYP2D6 (0.52) CYP2D6LMNABLMALOX15CYP1A2

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-11793855-B2 TFPI inhibitors and methods of use TAKEDA PHARMACEUTICAL COMPANY LIMITED (JP) 2023-10-24 — — US disclosed
US-11793855-B2 TFPI inhibitors and methods of use TAKEDA PHARMACEUTICAL COMPANY LIMITED (JP) 2023-10-24 — — US disclosed
US-10800816-B2 TFPI inhibitors and methods of use Baxalta GmbH (CH) 2020-10-13 — — US disclosed
US-20190134147-A1 TFPI INHIBITORS AND METHODS OF USE Baxalta GmbH (CH) 2019-05-09 — — US disclosed
EP-2827883-B1 TFPI INHIBITORS AND METHODS OF USE Baxalta GmbH (CH) 2019-05-08 — — EP disclosed
US-10201586-B2 TFPI inhibitors and methods of use Baxalta GmbH (CH) 2019-02-12 — — US disclosed
US-20180155399-A1 TFPI INHIBITORS AND METHODS OF USE Baxalta GmbH (CH) 2018-06-07 — — US disclosed
US-20180155399-A1 TFPI INHIBITORS AND METHODS OF USE Baxalta GmbH (CH) 2018-06-07 — — US disclosed
US-9873720-B2 TFPI inhibitors and methods of use Baxalta GmbH (CH) 2018-01-23 — — US disclosed
US-9873720-B2 TFPI inhibitors and methods of use Baxalta GmbH (CH) 2018-01-23 — — US disclosed
US-20120028901-A1 TFPI INHIBITORS AND METHODS OF USE BAXTER INTERNATIONAL INC. (US) 2012-02-02 — — US disclosed
US-20120028901-A1 TFPI INHIBITORS AND METHODS OF USE BAXTER INTERNATIONAL INC. (US) 2012-02-02 — — US disclosed
US-7521566-B2 Process for preparation of perindopril and salts thereof LES LABORATOIRES SERVIER (FR) 2009-04-21 — — US disclosed
US-7521566-B2 Process for preparation of perindopril and salts thereof LES LABORATOIRES SERVIER (FR) 2009-04-21 — — US disclosed
US-7456296-B2 Method for preparation of crystalline perindopril erbumine LUPIN LTD (IN) 2008-11-25 — — US disclosed
EP-1603558-B1 PROCESS FOR PREPARATION OF PERINDOPRIL AND SALTS THEREOF SERVIER S A LAB (FR) 2008-05-21 — — EP disclosed
US-20070149604-A1 Reacting perindopril in a solvent selected from N,N-dimethylformamide, dimethoxymethane, 2,2-dimethoxypropane and 1,2-dimethoxyethane with tert-butylamine, crystallization; stereospecific LUPIN LTD. (IN) 2007-06-28 — — US disclosed
EP-1615885-A1 B -FUSED BICYCLIC PROLINE DERIVATIVES AND THEIR USE FOR TREATING ARTHRITIC CONDITIONS Warner-Lambert Company LLC (US) 2006-01-18 — — EP disclosed
US-20050143427-A1 [B]-fused bicyclic proline derivatives and their use for treating arthritic conditions BARVIAN NICOLE C (US) 2005-06-30 — — US disclosed
WO-2004092132-A1 [B]-FUSED BICYCLIC PROLINE DERIVATIVES AND THEIR USE FOR TREATING ARTHRITIC CONDITIONS WARNER-LAMBERT COMPANY LLC (US) 2004-10-28 — — 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 (8 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-20120028901-A1 TFPI INHIBITORS AND METHODS OF USE TFPI, TFPI2, F3 CYP2D6 3856/4885LMNA 1445/4885BLM 4480/4885
US-20180155399-A1 TFPI INHIBITORS AND METHODS OF USE TFPI, TFPI2, F13B CYP2D6 3769/4885LMNA 1505/4885BLM 4444/4885
US-20050143427-A1 [B]-fused bicyclic proline derivatives and their use for treating arthritic conditions PRAP1, PRR12, PPIB CYP2D6 4004/4885LMNA 1576/4885BLM 3792/4885
US-10201586-B2 TFPI inhibitors and methods of use TFPI, TFPI2, F3 CYP2D6 3870/4885LMNA 1466/4885BLM 4503/4885
US-20070149604-A1 Reacting perindopril in a solvent selected from N,N-dimethylformamide, dimethoxymethane, 2,2-dimethoxypropane and 1,2-dimethoxyethane with tert-butylamine, crystallization; stereospecific REN, AGTR2, AGTR1 CYP2D6 40/4885LMNA 1430/4885BLM 2602/4885
US-11793855-B2 TFPI inhibitors and methods of use TFPI, TFPI2, F3 CYP2D6 3870/4885LMNA 1466/4885BLM 4503/4885
US-10800816-B2 TFPI inhibitors and methods of use TFPI, TFPI2, F13B CYP2D6 3769/4885LMNA 1505/4885BLM 4444/4885
US-20190134147-A1 TFPI INHIBITORS AND METHODS OF USE TFPI, TFPI2, F3 CYP2D6 3870/4885LMNA 1466/4885BLM 4503/4885

“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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