SCHEMBL497669

SCHEMBL497669

CC(N)(CCCO)C(=O)O

nearest known ligand 0.59

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
ARG2 P78540 5/20 0.59
ARG1 P05089 4/20 0.59
GGT1 P19440 1/20 0.54
BLM P54132 2/20 0.38
CYP4F2 P78329 2/20 0.38
CYP4A11 Q02928 2/20 0.38
GPR84 Q9NQS5 1/20 0.37
FFAR1 O14842 1/20 0.37
FFAR4 Q5NUL3 1/20 0.37
MEN1 O00255 2/20 0.35
ALDH1A1 P00352 2/20 0.35
CYP1A2 P05177 2/20 0.35
KMT2A Q03164 2/20 0.35
TDP1 Q9NUW8 2/20 0.35
KDM4E B2RXH2 1/20 0.35
USP2 O75604 1/20 0.35
EGFR P00533 1/20 0.35
FYN P06241 1/20 0.35
POLB P06746 1/20 0.35
CYP3A4 P08684 1/20 0.35

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
SCHEMBL28391632 1.00 ARG2 (0.59) ARG2ARG1GGT1BLMCYP4F2
SCHEMBL28396676 1.00 ARG2 (0.59) ARG2ARG1GGT1BLMCYP4F2
SCHEMBL498228 0.98 ARG2 (0.62) ARG2ARG1GGT1BLMCYP4F2
SCHEMBL21498188 0.96 ARG2 (0.60) ARG2ARG1GGT1BLMCYP4F2
SCHEMBL8688802 0.87 ARG2 (0.72) ARG2ARG1GGT1BLMFFAR1
SCHEMBL13774924 0.85
SCHEMBL9615913 0.85
SCHEMBL8687592 0.82 GGT1 (0.65) ARG2ARG1GGT1BLMMEN1
SCHEMBL18124758 0.81 ARG1 (0.59) ARG2ARG1GGT1BLMMEN1
SCHEMBL162337 0.81 ARG1 (0.59) ARG2ARG1GGT1BLMMEN1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-111138335-B Preparation method of optically active 2-methylproline 山东四环药业股份有限公司 2021-10-01 CN claimed
CN-111138335-A Preparation method of optically active 2-methylproline 山东四环药业股份有限公司 2020-05-12 CN claimed
US-20220340893-A1 BI-FUNCTIONAL COMPLEXES AND METHODS FOR MAKING AND USING SUCH COMPLEXES NUEVOLUTION A/S (DK) 2022-10-27 US disclosed
CN-111138335-B Preparation method of optically active 2-methylproline 山东四环药业股份有限公司 2021-10-01 CN disclosed
CN-111138335-B Preparation method of optically active 2-methylproline 山东四环药业股份有限公司 2021-10-01 CN disclosed
CN-111138335-A Preparation method of optically active 2-methylproline 山东四环药业股份有限公司 2020-05-12 CN disclosed
CN-111138335-A Preparation method of optically active 2-methylproline 山东四环药业股份有限公司 2020-05-12 CN disclosed
US-20190315785-A1 PHOSPHONATE ANALOGS OF HIV INHIBITOR COMPOUNDS GILEAD SCIENCES, INC. 2019-10-17 US disclosed
US-20180086784-A1 Phosphonate analogs of HIV inhibitor compounds GILEAD SCIENCES, INC. 2018-03-29 US disclosed
US-20170210770-A1 PHOSPHONATE ANALOGS OF HIV INHIBITOR COMPOUNDS GILEAD SCIENCES, INC. 2017-07-27 US disclosed
US-9629789-B2 Rosacea treatments using polymetal complexes OBAGI MEDICAL PRODUCTS, INC. (US) 2017-04-25 US disclosed
US-5536750-A ANTITUMOR MERCK & CO., INC. (US) 1996-07-16 US disclosed
EP-0719274-A1 METHOD FOR DOSING THERAPEUTIC COMPOUNDS GILEAD SCIENCES, INC. (US) 1996-07-03 EP disclosed
EP-0719273-A1 NUCLEOTIDE ANALOGS GILEAD SCIENCES, INC. (US) 1996-07-03 EP disclosed
EP-0668856-A4 INHIBITORS OF FARNESYL-PROTEIN TRANSFERASE. MERCK & CO INC (US) 1995-11-22 EP disclosed
EP-0668856-A1 INHIBITORS OF FARNESYL-PROTEIN TRANSFERASE MERCK & CO. INC. (US) 1995-08-30 EP disclosed
WO-1995007920-A1 NUCLEOTIDE ANALOGS GILEAD SCIENCES, INC. (US) 1995-03-23 WO disclosed
WO-1995007919-A1 METHOD FOR DOSING THERAPEUTIC COMPOUNDS GILEAD SCIENCES, INC. (US) 1995-03-23 WO disclosed
US-5326773-A Prodrug enzyme inhibitors MERCK & CO., INC. (US) 1994-07-05 US disclosed
WO-1994010137-A1 INHIBITORS OF FARNESYL-PROTEIN TRANSFERASE MERCK & CO., INC. (US) 1994-05-11 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 (3 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-20190315785-A1 PHOSPHONATE ANALOGS OF HIV INHIBITOR COMPOUNDS PIK3CA, TYMP, ITPA ARG2 4411/4885ARG1 4390/4885GGT1 1221/4885
US-20180086784-A1 Phosphonate analogs of HIV inhibitor compounds PIK3CA, TYMP, ITPA ARG2 4411/4885ARG1 4390/4885GGT1 1221/4885
US-20170210770-A1 PHOSPHONATE ANALOGS OF HIV INHIBITOR COMPOUNDS PIK3CA, TYMP, ITPA ARG2 4411/4885ARG1 4390/4885GGT1 1221/4885

“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.