SCHEMBL497515

SCHEMBL497515

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

nearest known ligand 0.60

Predicted protein targets (top 11)

geneUniProtsupporting neighboursconfidence
ACE P12821 11/20 0.60
LMNA P02545 2/20 0.60
ABCB11 O95342 2/20 0.58
MEN1 O00255 2/20 0.56
KMT2A Q03164 2/20 0.56
USP2 O75604 1/20 0.56
CYP3A4 P08684 1/20 0.56
ALOX15 P16050 1/20 0.56
SMN1; SMN2 Q16637 2/20 0.56
PDE3A Q14432 1/20 0.53
REN P00797 1/20 0.52

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
SCHEMBL4669890 1.00 ACE (0.60) ACELMNAABCB11MEN1KMT2A
SCHEMBL28866775 1.00 ACE (0.60) ACELMNAABCB11MEN1KMT2A
SCHEMBL4669888 1.00 ACE (0.60) ACELMNAABCB11MEN1KMT2A
SCHEMBL3369452 1.00 ACE (0.60) ACELMNAABCB11MEN1KMT2A
SCHEMBL4669921 1.00 ACE (0.60) ACELMNAABCB11MEN1KMT2A
SCHEMBL3780597 1.00 ACE (0.60) ACELMNAABCB11MEN1KMT2A
SCHEMBL2897972 1.00 ACE (0.60) ACELMNAABCB11MEN1KMT2A
SCHEMBL1221172 1.00 ACE (0.60) ACELMNAABCB11MEN1KMT2A
Hydrochloric Acid SCHEMBL7264173 0.99 ACE (0.59) ACELMNAABCB11MEN1KMT2A
SCHEMBL11041388 0.99 ACE (0.59) ACELMNAABCB11MEN1KMT2A

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-118878432-A Method for preparing N- [1- (S) -ethoxycarbonyl-3-phenylpropyl ] -L-alanine by continuous flow method 浙江昌明药业有限公司 2024-11-01 CN claimed
CN-113549126-B Preparation method of ramipril 鲁南制药集团股份有限公司 2024-04-19 CN claimed
EP-3489215-B1 PROCESS FOR PRODUCING ORGANIC COMPOUND KANEKA CORP (JP) 2023-12-20 EP claimed
CN-113024632-B Preparation method of imidapril hydrochloride 山东中健康桥制药有限公司 2023-03-28 CN claimed
CN-109021064-B Preparation method of enalapril maleate 扬子江药业集团有限公司 2021-11-09 CN claimed
CN-113549126-A Preparation method of ramipril 鲁南制药集团股份有限公司 2021-10-26 CN claimed
CN-109689611-B Method for producing organic compound 株式会社钟化 2021-09-28 CN claimed
CN-105713068-B Method for preparing imidapril key intermediate and derivative thereof 湖南九典制药股份有限公司 2021-04-20 CN claimed
CN-108147973-B Preparation method of N- [1- (S) -ethoxycarbonyl-3-phenylpropyl ] -L-alanine 凯莱英医药集团(天津)股份有限公司 2021-04-06 CN claimed
US-10781193-B2 Process for producing organic compound KANEKA CORPORATION (JP) 2020-09-22 US claimed
US-5359086-A Process for preparing alkyl-L-alanyl-L-proline derivatives KRKA, PHARMACEUTICAL & CHEMICAL WORKS (SI) 1994-10-25 US claimed
EP-0281393-B1 METHOD FOR PRODUCING INDAN DERIVATIVES Takeda Chemical Industries, Ltd. (JP) 1993-08-04 EP claimed
EP-0215335-B1 PROCESS FOR PREPARING N-/1(S)-ETHOXYCARBONYL-3-PHENYLPROPYL/-L-ALANYL-L-PROLINE KANEGAFUCHI KAGAKU KOGYO KABUSHIKI KAISHA (JP) 1992-11-11 EP claimed
EP-0219651-B1 Inorganic acid salt of N-[1(S)-ethoxycarbonyl-3-phenylpropyl]-L-alanylchloride and process for preparing the same KANEGAFUCHI KAGAKU KOGYO KABUSHIKI KAISHA (JP) 1990-10-31 EP claimed
US-4835302-A Method for producing indan derivatives TAKEDA CHEMICAL INDUSTRIES, LTD. (JP) 1989-05-30 US claimed
EP-0281393-A2 Method for producing indan derivatives Takeda Chemical Industries, Ltd. (JP) 1988-09-07 EP claimed
US-4716235-A AMIDATION OF PROLINE KANEGAFUCHI KAGAKU KOGYO KABUSHIKI KAISHA (JP) 1987-12-29 US claimed
EP-0219651-A1 Inorganic acid salt of N-[1(S)-ethoxycarbonyl-3-phenylpropyl]-L-alanylchloride and process for preparing the same KANEGAFUCHI KAGAKU KOGYO KABUSHIKI KAISHA (JP) 1987-04-29 EP claimed
EP-0215335-A2 Process for preparing N-/1(S)-ethoxycarbonyl-3-phenylpropyl/-L-alanyl-L-proline KANEGAFUCHI KAGAKU KOGYO KABUSHIKI KAISHA (JP) 1987-03-25 EP claimed
EP-0050800-A1 Carboxyalkyl dipeptides, processes for their production and pharmaceutical compositions containing them SCHERING CORPORATION (US) 1982-05-05 EP claimed

Patent text — is the patent's own abstract consistent with the prediction?

For each of this compound's patents that has machine-readable text (1 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-10781193-B2 Process for producing organic compound TTL, DCLK1, CTH ACE 2636/4885LMNA 4879/4885ABCB11 3813/4885

“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.