SCHEMBL3836129

SCHEMBL3836129

CCC[C@H](NC(C)C(=O)O)C(=O)O

nearest known ligand 0.45

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
CHRM1 P11229 1/20 0.44
AKR1A1 P14550 1/20 0.44
CHRM3 P20309 1/20 0.44
HTR2A P28223 1/20 0.44
HTR2C P28335 1/20 0.44
ADRA1A P35348 1/20 0.44
HRH1 P35367 1/20 0.44
DRD3 P35462 1/20 0.44
SLC6A3 Q01959 1/20 0.44
HDAC1 Q13547 1/20 0.44
HDAC2 Q92769 1/20 0.44
TDP1 Q9NUW8 1/20 0.44
ACE P12821 4/20 0.40
FPR2 P25090 1/20 0.39
MME P08473 2/20 0.39
FAAH O00519 1/20 0.38
FOLH1 Q04609 2/20 0.36
NAALAD2 Q9Y3Q0 2/20 0.36
ALDH1A1 P00352 1/20 0.36
CPA1 P15085 1/20 0.36

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
SCHEMBL5940872 1.00 CHRM1 (0.44) CHRM1AKR1A1CHRM3HTR2AHTR2C
SCHEMBL27767453 1.00 CHRM1 (0.44) CHRM1AKR1A1CHRM3HTR2AHTR2C
SCHEMBL15375770 1.00 CHRM1 (0.44) CHRM1AKR1A1CHRM3HTR2AHTR2C
SCHEMBL3836127 1.00 CHRM1 (0.44) CHRM1AKR1A1CHRM3HTR2AHTR2C
SCHEMBL715422 0.88 CHRM1 (0.41) CHRM1AKR1A1CHRM3HTR2AHTR2C
SCHEMBL10735795 0.86 CHRM1 (0.52) CHRM1AKR1A1CHRM3HTR2AHTR2C
SCHEMBL9363858 0.86 CHRM1 (0.40) CHRM1AKR1A1CHRM3HTR2AHTR2C
SCHEMBL9737506 0.86 CHRM1 (0.40) CHRM1AKR1A1CHRM3HTR2AHTR2C
SCHEMBL16750050 0.84 CHRM1 (0.46) CHRM1AKR1A1CHRM3HTR2AHTR2C
SCHEMBL5131687 0.84 CHRM1 (0.46) CHRM1AKR1A1CHRM3HTR2AHTR2C

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20250388940-A1 ENGINEERED IMINE REDUCTASES AND METHODS FOR THE REDUCTIVE AMINATION OF KETONE AND AMINE COMPOUNDS CODEXIS, INC. (US) 2025-12-25 US disclosed
US-20250346870-A1 ENGINEERED IMINE REDUCTASES AND METHODS FOR THE REDUCTIVE AMINATION OF KETONE AND AMINE COMPOUNDS CODEXIS INC (US) 2025-11-13 US disclosed
US-20250304924-A1 ENGINEERED IMINE REDUCTASES AND METHODS FOR THE REDUCTIVE AMINATION OF KETONE AND AMINE COMPOUNDS CODEXIS INC (US) 2025-10-02 US disclosed
US-12421532-B2 Polynucleotides encoding engineered imine reductases CODEXIS, INC. (US) 2025-09-23 US disclosed
US-12378533-B2 Engineered imine reductases and methods for the reductive amination of ketone and amine compounds CODEXIS, INC. (US) 2025-08-05 US disclosed
US-12312609-B2 Engineered imine reductases and methods for the reductive amination of ketone and amine compounds CODEXIS, INC. (US) 2025-05-27 US disclosed
US-20250137019-A1 ENGINEERED IMINE REDUCTASES AND METHODS FOR THE REDUCTIVE AMINATION OF KETONE AND AMINE COMPOUNDS CODEXIS INC (US) 2025-05-01 US disclosed
US-12215368-B2 Engineered imine reductases and methods for the reductive amination of ketone and amine compounds CODEXIS, INC. (US) 2025-02-04 US disclosed
US-20240254457-A1 ENGINEERED IMINE REDUCTASES AND METHODS FOR THE REDUCTIVE AMINATION OF KETONE AND AMINE COMPOUNDS CODEXIS, INC. (US) 2024-08-01 US disclosed
US-20240228982-A9 ENGINEERED IMINE REDUCTASES AND METHODS FOR THE REDUCTIVE AMINATION OF KETONE AND AMINE COMPOUNDS INNOVATUS LIFE SCIENCES LENDING FUND I, LP, AS COLLATERAL AGENT 2024-07-11 US disclosed
EP-1380590-A1 Method for synthesis of perindopril and its pharmaceutically acceptable salts Les Laboratoires Servier (FR) 2004-01-14 EP disclosed
EP-1371659-A1 Method for synthesis of perindopril and its pharmaceutically acceptable salts [2003/26] Les Laboratoires Servier (FR) 2003-12-17 EP disclosed
EP-1367063-A1 Method for synthesis of perindopril and its pharmaceutically acceptable salts Les Laboratoires Servier (FR) 2003-12-03 EP disclosed
EP-1367062-A1 Method for synthesis of perindopril and its pharmaceutically acceptable salts Les Laboratoires Servier (FR) 2003-12-03 EP disclosed
EP-1367061-A1 Method for synthesis of perindopril and its pharmaceutically acceptable salts Les Laboratoires Servier (FR) 2003-12-03 EP disclosed
EP-1362845-A2 New process for the synthesis of N-((S)-1-carboxybutyl)-(S)-alanine esters and their use in the synthesis of perindopril Les Laboratoires Servier (FR) 2003-11-19 EP disclosed
EP-1362864-A1 Method for synthesis of perindopril and its pharmaceutically acceptable salts Les Laboratoires Servier (FR) 2003-11-19 EP disclosed
EP-1362845-A2 New process for the synthesis of N-((S)-1-carboxybutyl)-(S)-alanine esters and their use in the synthesis of perindopril Les Laboratoires Servier (FR) 2003-11-19 EP disclosed
EP-1321471-A1 Method for synthesis of perindopril and its pharmaceutically acceptable salts LES LABORATOIRES SERVIER (FR) 2003-06-25 EP disclosed
EP-1256590-A1 Method for synthesis of (2S,3aS,7aS)-1-(S)-alanyl-octahydro-1H-indole-2- carboxylic acid derivatives and use in the synthesis of perindopril Les Laboratoires Servier S.A. (FR) 2002-11-13 EP 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 (4 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-20250346870-A1 ENGINEERED IMINE REDUCTASES AND METHODS FOR THE REDUCTIVE AMINATION OF KETONE AND AMINE COMPOUNDS AKR1C4, AKR7A2, AKR1C2 CHRM1 3942/4885AKR1A1 7/4885CHRM3 3814/4885
US-20250388940-A1 ENGINEERED IMINE REDUCTASES AND METHODS FOR THE REDUCTIVE AMINATION OF KETONE AND AMINE COMPOUNDS DCXR, PDXK, XDH CHRM1 1958/4885AKR1A1 35/4885CHRM3 2481/4885
US-12378533-B2 Engineered imine reductases and methods for the reductive amination of ketone and amine compounds AKR1C4, AKR7A2, AKR1C2 CHRM1 3942/4885AKR1A1 7/4885CHRM3 3814/4885
US-20240228982-A9 ENGINEERED IMINE REDUCTASES AND METHODS FOR THE REDUCTIVE AMINATION OF KETONE AND AMINE COMPOUNDS AKR1C4, AKR7A2, AKR1C2 CHRM1 3942/4885AKR1A1 7/4885CHRM3 3814/4885

“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.