SCHEMBL8420717

SCHEMBL8420717

CC(C)(C)CCC(=O)C(=O)O

nearest known ligand 0.46

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
OR51E2 Q9H255 2/20 0.46
MAPK1 P28482 1/20 0.46
SLC13A3 Q8WWT9 1/20 0.46
EGLN1 Q9GZT9 1/20 0.46
HAO1 Q9UJM8 1/20 0.32
NAALAD2 Q9Y3Q0 1/20 0.32
FFAR1 O14842 1/20 0.32
CPT2 P23786 1/20 0.32
TDP1 Q9NUW8 1/20 0.32
HMGCR P04035 1/20 0.32
CHRM1 P11229 1/20 0.32
TBXA2R P21731 1/20 0.32
ADRA1A P35348 1/20 0.32
TSHR P16473 2/20 0.32
ALDH1A1 P00352 1/20 0.32
CYP2D6 P10635 1/20 0.31
CYP2C19 P33261 1/20 0.31
HIF1A Q16665 1/20 0.31
CES2 O00748 1/20 0.30
CES1 P23141 1/20 0.30

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
SCHEMBL8873751 0.97 OR51E2 (0.43) OR51E2MAPK1SLC13A3EGLN1HAO1
SCHEMBL1233703 0.82 OR51E2 (0.40) OR51E2MAPK1SLC13A3EGLN1HAO1
SCHEMBL25670656 0.78 CES1 (0.46) TSHRALDH1A1CES2CES1
SCHEMBL120318 0.77
SCHEMBL1462669 0.76 CES2 (0.63) TSHRALDH1A1CES2CES1
SCHEMBL28316613 0.76 FAAH (0.36)
SCHEMBL8873753 0.76 CA4 (0.36)
Hydrochloric Acid SCHEMBL2180509 0.74 NAALAD2 (0.48) EGLN1NAALAD2FFAR1CPT2TDP1
SCHEMBL22396500 0.74 NAALAD2 (0.48) EGLN1NAALAD2FFAR1CPT2TDP1
Ammonia Solution, Strong SCHEMBL8995890 0.74 NAALAD2 (0.48) EGLN1NAALAD2FFAR1CPT2TDP1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-9376694-B2 Method for preparing optically active amino acid using cosubstrate shuttling of transaminase INDUSTRY-ACADEMIC COOPERATION FOUNDATION, YONSEI UNIVERSITY (KR) 2016-06-28 US claimed
US-20150284750-A1 METHOD FOR PREPARING OPTICALLY ACTIVE AMINO ACID USING COSUBSTRATE SHUTTLING OF TRANSAMINASE INDUSTRY-ACADEMIC COOPERATION FOUNDATION, YONSEI UNIVERSITY (KR) 2015-10-08 US claimed
US-5854035-A Enzyme with leuDH activity, nucleotide sequence coding therefor and process for the prepartion of the enzyme DEGUSSA AG (DE) 1998-12-29 US claimed
EP-0792933-A2 Enzyme having LeuDH activity, nucleotide sequence coding therefor and process for the preparation of this enzyme Degussa Aktiengesellschaft (DE) 1997-09-03 EP claimed
EP-4684030-A2 METHOD OF DEPROTECTING AT LEAST ONE D-AMINO ACID AND/OR D-AMINO ACID DERIVATIVE PROTECTED FUNCTIONAL GROUP Martin-Luther-Universität Halle-Wittenberg (DE) 2026-01-28 EP disclosed
WO-2024227957-A2 METHOD OF DEPROTECTING AT LEAST ONE D-AMINO ACID AND/OR D-AMINO ACID DERIVATIVE PROTECTED FUNCTIONAL GROUP Martin-Luther-Universität Halle-Wittenberg (DE) 2024-11-07 WO disclosed
US-11701371-B2 ENPP1 inhibitors and their use for the treatment of cancer THE BOARD OF TRUSTEES OF THE LELAND STANFORD JUNIOR UNIVERSITY (US) 2023-07-18 US disclosed
US-11701371-B2 ENPP1 inhibitors and their use for the treatment of cancer THE BOARD OF TRUSTEES OF THE LELAND STANFORD JUNIOR UNIVERSITY (US) 2023-07-18 US disclosed
US-20210369747-A1 ENPP1 Inhibitors and Their Use for the Treatment of Cancer THE BOARD OF TRUSTEES OF THE LELAND STANFORD JUNIOR UNIVERSITY 2021-12-02 US disclosed
US-9376694-B2 Method for preparing optically active amino acid using cosubstrate shuttling of transaminase INDUSTRY-ACADEMIC COOPERATION FOUNDATION, YONSEI UNIVERSITY (KR) 2016-06-28 US disclosed
US-20150284750-A1 METHOD FOR PREPARING OPTICALLY ACTIVE AMINO ACID USING COSUBSTRATE SHUTTLING OF TRANSAMINASE INDUSTRY-ACADEMIC COOPERATION FOUNDATION, YONSEI UNIVERSITY (KR) 2015-10-08 US disclosed
EP-0692538-B1 Process for producing optically active L-amino acids DEGUSSA (DE) 1999-09-22 EP disclosed
US-5854035-A Enzyme with leuDH activity, nucleotide sequence coding therefor and process for the prepartion of the enzyme DEGUSSA AG (DE) 1998-12-29 US disclosed
EP-0792933-A2 Enzyme having LeuDH activity, nucleotide sequence coding therefor and process for the preparation of this enzyme Degussa Aktiengesellschaft (DE) 1997-09-03 EP disclosed
EP-0692478-A1 Process for the preparation of optically active 4 substituted (S)-2-oxazolidinone, optically active (S)-aminoalcohols and utilization of there compounds Degussa Aktiengesellschaft (DE) 1996-01-17 EP disclosed
EP-0692538-A2 Process for producing optically active L-amino acids, novel optically active L-aminoacids with bulky side-chains and their use Degussa Aktiengesellschaft (DE) 1996-01-17 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 (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-11701371-B2 ENPP1 inhibitors and their use for the treatment of cancer ENPP1, ENPP3, ENTPD1 OR51E2 4592/4885MAPK1 818/4885SLC13A3 3062/4885
US-20210369747-A1 ENPP1 Inhibitors and Their Use for the Treatment of Cancer ENPP1, ENPP3, ENTPD1 OR51E2 4592/4885MAPK1 818/4885SLC13A3 3062/4885

“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.