SCHEMBL4990259

SCHEMBL4990259

CCOC(=O)[C@H](CCc1ccccc1)N(C(=O)O)[C@@H](C)C(=O)OC(=O)[C@H](C)N(C(=O)O)[C@@H](CCc1ccccc1)C(=O)OCC

nearest known ligand 0.48

Predicted protein targets (top 13)

geneUniProtsupporting neighboursconfidence
SMN1; SMN2 Q16637 2/20 0.48
LMNA P02545 3/20 0.42
L3MBTL1 Q9Y468 3/20 0.42
ALDH1A1 P00352 1/20 0.42
POLB P06746 1/20 0.42
HSD17B10 Q99714 1/20 0.42
ACE P12821 10/20 0.41
MAPT P10636 1/20 0.41
MEN1 O00255 1/20 0.41
KMT2A Q03164 1/20 0.41
ABCB11 O95342 1/20 0.40
TSHR P16473 1/20 0.40
MMP8 P22894 1/20 0.39

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
SCHEMBL28259387 0.94 SMN1; SMN2 (0.49) SMN1; SMN2LMNAL3MBTL1ALDH1A1POLB
SCHEMBL1994865 0.85 SMN1; SMN2 (0.44) SMN1; SMN2LMNAL3MBTL1ALDH1A1POLB
SCHEMBL1994862 0.85 SMN1; SMN2 (0.44) SMN1; SMN2LMNAL3MBTL1ALDH1A1POLB
SCHEMBL8261408 0.84 SMN1; SMN2 (0.50) SMN1; SMN2LMNAL3MBTL1ALDH1A1POLB
Hydrochloric Acid SCHEMBL5593739 0.81 SMN1; SMN2 (0.44) SMN1; SMN2LMNAL3MBTL1ALDH1A1POLB
SCHEMBL6656395 0.81 SMN1; SMN2 (0.44) SMN1; SMN2LMNAL3MBTL1ALDH1A1POLB
SCHEMBL6656396 0.81 SMN1; SMN2 (0.44) SMN1; SMN2LMNAL3MBTL1ALDH1A1POLB
SCHEMBL5967532 0.80 L3MBTL1 (0.50) SMN1; SMN2LMNAL3MBTL1ALDH1A1POLB
SCHEMBL6672953 0.79 SMN1; SMN2 (0.48) SMN1; SMN2LMNAL3MBTL1ALDH1A1POLB
SCHEMBL10834757 0.79 SMN1; SMN2 (0.50) SMN1; SMN2LMNAL3MBTL1ALDH1A1POLB

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 15 patents. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20080171885-A1 Process for Preparation of Highly Pure Trandolapril LUPIN LIMITED (IN) 2008-07-17 US claimed
EP-1866327-A1 IMPROVED PROCESS FOR PREPARATION OF HIGHLY PURE TRANDOLAPRIL Lupin Ltd. (IN) 2007-12-19 EP claimed
WO-2006085332-A1 IMPROVED PROCESS FOR PREPARATION OF HIGHLY PURE TRANDOLAPRIL LUPIN LIMITED (IN) 2006-08-17 WO claimed
EP-0967221-A1 PROCESS FOR PREPARING PHARMACOLOGICALLY ACCEPTABLE SALTS OF N-(1(S)-ETHOXYCARBONYL-3-PHENYLPROPYL)-L-ALANYL AMINO ACIDS KANEKA CORPORATION (JP) 1999-12-29 EP claimed
US-5359086-A Process for preparing alkyl-L-alanyl-L-proline derivatives KRKA, PHARMACEUTICAL & CHEMICAL WORKS (SI) 1994-10-25 US claimed
US-20080171885-A1 Process for Preparation of Highly Pure Trandolapril LUPIN LIMITED (IN) 2008-07-17 US disclosed
EP-1866327-A1 IMPROVED PROCESS FOR PREPARATION OF HIGHLY PURE TRANDOLAPRIL Lupin Ltd. (IN) 2007-12-19 EP disclosed
US-20070093664-A1 Process for the production of lisinopril ECZACIBASI-ZENTIVA KIMYASAL URUNLER SANAYI VE TICARET A.S. (TR) 2007-04-26 US disclosed
WO-2006085332-A1 IMPROVED PROCESS FOR PREPARATION OF HIGHLY PURE TRANDOLAPRIL LUPIN LIMITED (IN) 2006-08-17 WO disclosed
EP-1513868-B1 PROCESS FOR THE PRODUCTION OF LISINOPRIL EOS ECZACIBASI OZGUN KIMYASAL (TR) 2006-08-09 EP disclosed
EP-1513868-A1 PROCESS FOR THE PRODUCTION OF LISINOPRIL EOS Eczacibasi Ozgun Kimyasal Urunler Sanayi Ve Ti Caret A.S. (TR) 2005-03-16 EP disclosed
WO-2004000874-A1 PROCESS FOR THE PRODUCTION OF LISINOPRIL EOS ECZACIBASI OZGUN KIMYASAL URUNLER SANYI VE TI CARET A.S. (TR) 2003-12-31 WO disclosed
EP-0967221-A1 PROCESS FOR PREPARING PHARMACOLOGICALLY ACCEPTABLE SALTS OF N-(1(S)-ETHOXYCARBONYL-3-PHENYLPROPYL)-L-ALANYL AMINO ACIDS KANEKA CORPORATION (JP) 1999-12-29 EP disclosed
US-5359086-A Process for preparing alkyl-L-alanyl-L-proline derivatives KRKA, PHARMACEUTICAL & CHEMICAL WORKS (SI) 1994-10-25 US disclosed
US-5359086-A Process for preparing alkyl-L-alanyl-L-proline derivatives KRKA, PHARMACEUTICAL & CHEMICAL WORKS (SI) 1994-10-25 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 (2 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-20070093664-A1 Process for the production of lisinopril ACE, LOX, AGT SMN1; SMN2 2164/4885LMNA 222/4885L3MBTL1 114/4885
US-20080171885-A1 Process for Preparation of Highly Pure Trandolapril TPH1, HTR1A, HTR3A SMN1; SMN2 3548/4885LMNA 693/4885L3MBTL1 1669/4885

“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.