Proline

Proline

SCHEMBL718906

O=C(O)C1CCCN1.O=C(O)[C@@H]1CCCN1

nearest known ligand 0.65

Full drug profile on Sugi Atlas →

Known targets — ChEMBL curated mechanism

SLC5A2

The experimentally established mechanism targets of Proline. The predicted profile below is derived independently by chemical similarity — agreement is a validation signal, a miss is honest.

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
BLM P54132 3/20 0.52
MEN1 O00255 2/20 0.52
KMT2A Q03164 2/20 0.52
NOS2 P35228 2/20 0.50
NOS3 P29474 1/20 0.50
NOS1 P29475 1/20 0.50
DPP4 P27487 4/20 0.48
DPP8 Q6V1X1 2/20 0.48
DPP9 Q86TI2 2/20 0.48
LMNA P02545 3/20 0.43
CYP2D6 P10635 2/20 0.43
TSHR P16473 2/20 0.43
ALOX15 P16050 1/20 0.43
CYP1A2 P05177 1/20 0.43
CYP2C19 P33261 1/20 0.43
RAB9A P51151 1/20 0.43
THRB P10828 1/20 0.43
PMP22 Q01453 1/20 0.43
SLC6A1 P30531 2/20 0.43
FAP Q12884 1/20 0.43

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
Proline SCHEMBL18875607 1.00
Proline SCHEMBL2939 1.00
Proline SCHEMBL6894672 1.00 BLM (0.52) BLMMEN1KMT2ANOS2NOS3
Proline SCHEMBL462226 1.00 BLM (0.52) BLMMEN1KMT2ANOS2NOS3
Proline SCHEMBL462225 1.00 BLM (0.52) BLMMEN1KMT2ANOS2NOS3
Proline SCHEMBL10141181 1.00
Proline SCHEMBL13248912 1.00
Proline SCHEMBL10141185 1.00
D-Proline SCHEMBL21462052 1.00 BLM (0.52) BLMMEN1KMT2ANOS2NOS3
Proline SCHEMBL6894675 1.00 BLM (0.52) BLMMEN1KMT2ANOS2NOS3

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-118146298-A Short peptide RQRG and application thereof in agriculture 北方民族大学 2024-06-07 CN disclosed
US-10724023-B2 Microorganisms expressing modified glucoamylase enzymes CARGILL, INCORPORATED (US) 2020-07-28 US disclosed
US-20200048623-A1 MODIFIED GLUCOAMYLASE ENZYMES AND YEAST STRAINS HAVING ENHANCED BIOPRODUCT PRODUCTION CARGILL, INCORPORATED (US) 2020-02-13 US disclosed
US-20190345471-A1 LEADER-MODIFIED GLUCOAMYLASE POLYPEPTIDES AND ENGINEERED YEAST STRAINS HAVING ENHANCED BIOPRODUCT PRODUCTION CARGILL, INCORPORATED (US) 2019-11-14 US disclosed
US-10364421-B2 Modified glucoamylase enzymes and yeast strains having enhanced bioproduct production CARGILL, INCORPORATED (US) 2019-07-30 US disclosed
US-10344288-B2 Glucoamylase-modified yeast strains and methods for bioproduct production CARGILL, INCORPORATED (US) 2019-07-09 US disclosed
EP-3494129-A1 LEADER-MODIFIED GLUCOAMYLASE POLYPEPTIDES AND ENGINEERED YEAST STRAINS HAVING ENHANCED BIOPRODUCT PRODUCTION Cargill, Incorporated (US) 2019-06-12 EP disclosed
US-20180094269-A1 GLUCOAMYLASE-MODIFIED YEAST STRAINS AND METHODS FOR BIOPRODUCT PRODUCTION CARGILL, INCORPORATED 2018-04-05 US disclosed
US-20180080014-A1 MODIFIED GLUCOAMYLASE ENZYMES AND YEAST STRAINS HAVING ENHANCED BIOPRODUCT PRODUCTION CARGILL, INCORPORATED 2018-03-22 US disclosed
WO-2018027131-A1 LEADER-MODIFIED GLUCOAMYLASE POLYPEPTIDES AND ENGINEERED YEAST STRAINS HAVING ENHANCED BIOPRODUCT PRODUCTION CARGILL, INCORPORATED (US) 2018-02-08 WO disclosed
US-8269037-B2 Absorption medium for removing acid gases which comprises amino acid and acid promoter BASF SE (DE) 2012-09-18 US disclosed
EP-2449488-A1 METHOD FOR NORMALIZATION IN METABOLOMICS ANALYSIS METHODS WITH ENDOGENOUS REFERENCE METABOLITES BIOCRATES Life Sciences AG (AT) 2012-05-09 EP disclosed
US-20120051989-A1 REMOVAL OF ACID GASES FROM A FLUID FLOW BY MEANS OF REDUCED COABSORPTION OF HYDROCARBONS AND OXYGEN BASF SE (DE) 2012-03-01 US disclosed
US-8034166-B2 Carbon dioxide absorbent requiring less regeneration energy BASF SE (DE) 2011-10-11 US disclosed
US-7964630-B2 Topical application agents against mimic and age-related wrinkles DSM IP ASSETS B.V. (NL) 2011-06-21 US disclosed
US-7927621-B2 Thioester-ester-amide copolymers ABBOTT CARDIOVASCULAR SYSTEMS INC. (US) 2011-04-19 US disclosed
US-7883200-B2 Electrophotographic ink jet printing on alkaline sized paper containing additive such as 2-pyrrolidone carboxylic acid; rapid drying; reduced bleeding and feathering FUJI XEROX CO., LTD. (JP) 2011-02-08 US disclosed
WO-2011000753-A1 METHOD FOR NORMALIZATION IN METABOLOMICS ANALYSIS METHODS WITH ENDOGENOUS REFERENCE METABOLITES BIOCRATES LIFE SCIENCES AG (AT) 2011-01-06 WO disclosed
US-20100186590-A1 ABSORPTION MEDIUM FOR REMOVING ACID GASES WHICH COMPRISES AMINO ACID AND ACID PROMOTER BASF SE (DE) 2010-07-29 US disclosed
US-6835808-B2 Synthetic oligopeptide heparin-neutralizing agents including basic amino acids and a N-heterocyclic end group; low turbidity; side effects reduction; in vitro diagnosis; calculate the blood clotting time; assaying clotting cascade DIAGNOSTICA-STAGO (FR) 2004-12-28 US disclosed