Glycerin

Glycerin

SCHEMBL8015455

CC(CCC(N)=O)C(N)=O.OCC(O)CO

nearest known ligand 0.39

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Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
DPP4 P27487 1/20 0.39
DPP8 Q6V1X1 1/20 0.39
DPP9 Q86TI2 1/20 0.39
ALOX15 P16050 1/20 0.38
BLM P54132 1/20 0.38
PMP22 Q01453 1/20 0.38
KMT2A Q03164 1/20 0.38
ALDH1A1 P00352 2/20 0.36
LMNA P02545 1/20 0.36
CYP1A2 P05177 1/20 0.34
THRB P10828 1/20 0.31
TSHR P16473 1/20 0.31
GABRP O00591 2/20 0.30
GABRD O14764 2/20 0.30
GABRA1 P14867 2/20 0.30
GABRB1 P18505 2/20 0.30
GABRG2 P18507 2/20 0.30
GABRB3 P28472 2/20 0.30
GABRA5 P31644 2/20 0.30
GABRA3 P34903 2/20 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
SCHEMBL15774679 0.87 ALOX15 (0.46) DPP4DPP8DPP9ALOX15BLM
SCHEMBL487784 0.87 ALOX15 (0.46) DPP4DPP8DPP9ALOX15BLM
SCHEMBL14895150 0.87 ALOX15 (0.46) DPP4DPP8DPP9ALOX15BLM
SCHEMBL15155212 0.78
SCHEMBL28023797 0.78
SCHEMBL11137912 0.76 LTA4H (0.41) DPP4DPP8DPP9ALOX15BLM
Isobutyramide SCHEMBL6027666 0.75 LMNA (0.50) KMT2AALDH1A1LMNATHRBTSHR
SCHEMBL1679787 0.74 LTA4H (0.48) DPP4DPP8DPP9ALOX15BLM
SCHEMBL18554189 0.74 LMNA (0.36) ALDH1A1LMNATHRBTSHRGABRR1
SCHEMBL22593906 0.74 LMNA (0.36) ALDH1A1LMNATHRBTSHRGABRR1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-6077955-A CONTACTING AN AQUEOUS PRODUCT MIXTURE CONTAINING A W-NITRILOCARBOXYLIC ACID AMMONIUM SALT WITH HYDROGEN AND A HYDROGENATION CATALYST, WHEREBY THE SALT IS CONVERTED DIRECTLY TO THE CORRESPONDING LACTAM WITHOUT ISOLATION OF INTERMEDIATES E. I. DU PONT DE NEMOURS AND COMPANY (US) 2000-06-20 US disclosed
US-6066490-A MICROORGANISMS THAT PRODUCES A HYDROLASE ENZYME THAT DEMONSTRATES PREFERENTIAL ACTIVITY E. I. DU PONT DE NEMOURS & COMPANY (US) 2000-05-23 US disclosed
US-5936114-A Preparation of lactams from aliphatic α, ω-dinitriles E. I. DU PONT DE NEMOURS AND COMPANY (US) 1999-08-10 US disclosed
US-5922589-A ISOLATED COMAMONAS TESTOSTERONI 5-MGAM-4D WITH NITRILE HYDRATASE AND AMIDASE ACTIVITIES; FOR HIGH YIELD WITH HIGH REGIOSELECTIVITY AND BY PRODUCT INHIBITION E. I. DU PONT DE NEMOURS AND COMPANY (US) 1999-07-13 US disclosed
EP-0901468-A1 PREPARATION OF LACTAMS FROM ALIPHATIC $g(a),$g(v)-DINITRILES E.I. DU PONT DE NEMOURS AND COMPANY (US) 1999-03-17 EP disclosed
US-5858736-A CONTACTING DINITRILE IN AQUEOUS MIXTURE WITH ENZYME CATALYST HAVING ALIPHATIC NITRILASE ACTIVITY OR COMBINATION OF NITRILE HYDRATASE AND AMIDASE ACTIVITY, CONTACTING PRODUCT WITH HYDROGEN AND HYDROGENATION CATALYST TO PRODUCE LACTAM E. I. DU PONT DE NEMOURS AND COMPANY (US) 1999-01-12 US disclosed
US-5814508-A TREATING A WHOLE CELL CATALYST TO SELECT FOR A REGIOSELECTIVE NITRILASE ACTIVITY OR A NITRILE HYDRATASE ACTIVITY; CATALYTIC CONVERSION OF ALPHA-OMEGA DINITRILES E. I. DU PONT DE NEMOURS AND COMPANY (US) 1998-09-29 US disclosed
WO-1997044318-A1 PREPARATION OF LACTAMS FROM ALIPHATIC α,φ-DINITRILES E.I. DU PONT DE NEMOURS AND COMPANY (US) 1997-11-27 WO disclosed