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 SCHEMBL10141185 1.00 — —
Proline SCHEMBL7792 1.00 — —
Proline SCHEMBL458825 1.00 BLM (0.52) BLMMEN1KMT2ANOS2NOS3
Proline SCHEMBL18875607 1.00 — —
Proline SCHEMBL146827 1.00 BLM (0.52) BLMMEN1KMT2ANOS2NOS3
Proline SCHEMBL10141181 1.00 — —
Proline SCHEMBL6894672 1.00 BLM (0.52) BLMMEN1KMT2ANOS2NOS3
Proline SCHEMBL6894675 1.00 BLM (0.52) BLMMEN1KMT2ANOS2NOS3
D-Proline SCHEMBL21462052 1.00 BLM (0.52) BLMMEN1KMT2ANOS2NOS3
Proline SCHEMBL13248912 1.00 — —

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
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