Valine

Valine

SCHEMBL4582565

CC(C)[C@H](N)C(=O)O.c1ccccc1

nearest known ligand 0.88

Full drug profile on Sugi Atlas →

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
SLC7A5 Q01650 2/20 0.88
SLC1A2 P43004 5/20 0.44
SLC1A3 P43003 4/20 0.44
SLC1A1 P43005 4/20 0.44
TP53 P04637 1/20 0.40
DPP4 P27487 1/20 0.38
FAP Q12884 1/20 0.38
DPP8 Q6V1X1 1/20 0.38
DPP9 Q86TI2 1/20 0.38
DPP7 Q9UHL4 1/20 0.38
SLC15A1 P46059 1/20 0.38
NR1I2 O75469 1/20 0.38
PTGS1 P23219 1/20 0.38
ADRA1A P35348 1/20 0.38
LAP3 P28838 1/20 0.38
LMNA P02545 1/20 0.38
BLM P54132 1/20 0.38
TDP1 Q9NUW8 1/20 0.38
ACHE P22303 1/20 0.37
MEN1 O00255 1/20 0.36

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
Valine SCHEMBL28052598 1.00 SLC7A5 (0.88) SLC7A5SLC1A2SLC1A3SLC1A1TP53
Valine SCHEMBL27817390 0.95 SLC7A5 (0.79) SLC7A5SLC1A2SLC1A3SLC1A1TP53
Valine SCHEMBL27597271 0.95 SLC7A5 (0.79) SLC7A5SLC1A2SLC1A3SLC1A1TP53
Valine SCHEMBL31618928 0.94
Valine SCHEMBL1813972 0.94 SLC7A5 (1.00) SLC7A5SLC1A2SLC1A3SLC1A1TP53
Valine SCHEMBL2785563 0.94 SLC7A5 (1.00) SLC7A5SLC1A2SLC1A3SLC1A1TP53
Valine SCHEMBL41225 0.94 SLC7A5 (1.00) SLC7A5SLC1A2SLC1A3SLC1A1TP53
Valine SCHEMBL8516 0.94
Valine SCHEMBL288203 0.94 SLC7A5 (1.00) SLC7A5SLC1A2SLC1A3SLC1A1TP53
Valine SCHEMBL30540418 0.94

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
EP-1941415-A2 SYSTEM AND METHOD OF COMPUTING AND RENDERING THE NATURE OF POLYATOMIC MOLECULES AND POLYATOMIC MOLECULAR IONS Blacklight Power, Inc. (US) 2008-07-09 EP claimed
WO-2007053486-A2 SYSTEM AND METHOD OF COMPUTING AND RENDERING THE NATURE OF POLYATOMIC MOLECULES AND POLYATOMIC MOLECULAR IONS BLACKLIGHT POWER, INC. (US) 2007-05-10 WO claimed
WO-2007051078-A2 SYSTEM AND METHOD OF COMPUTING AND RENDERING THE NATURE OF POLYATOMIC MOLECULES AND POLYATOMIC MOLECULAR IONS BLACKLIGHT POWER, INC. (US) 2007-05-03 WO claimed
EP-1169287-B1 METHOD FOR THE OXIDATION OF BENZENE AND/OR TOLUENE TO PHENOL AND/OR CRESOLS GEN ELECTRIC (US) 2004-10-27 EP disclosed
US-6388145-B1 USING ZEOLITE OXIDATION CATALYST GENERAL ELECTRIC COMPANY 2002-05-14 US disclosed
US-20020042544-A1 METHOD FOR THE OXIDATION OF BENZENE AND/OR TOLUENE TO PHENOL AND/OR CRESOLS SABIC GLOBAL TECHNOLOGIES B.V. (NL) 2002-04-11 US disclosed
EP-1169287-A1 METHOD FOR THE OXIDATION OF BENZENE AND/OR TOLUENE TO PHENOL AND/OR CRESOLS GENERAL ELECTRIC COMPANY (US) 2002-01-09 EP disclosed
CN-1282331-A Herbicides 3-(benzazol-4-yl) pyrimidine-dione-derivatives BASF AG (DE) 2001-01-31 CN disclosed
WO-2000059852-A1 METHOD FOR THE OXIDATION OF BENZENE AND/OR TOLUENE TO PHENOL AND/OR CRESOLS GENERAL ELECTRIC COMPANY (US) 2000-10-12 WO disclosed
US-6013674-A INDENONE AMIDE DERIVATIVES, USEFUL FOR FOR THE INHIBITION OF LEUKOCYTE ADHERENCE TO ENDOTHELIAL CELLS; USEFUL IN THE TREATMENT OF INFLAMMATORY DISEASES, AS ARTHRITIS, ASTHAMA, PSORIASIS, RESPIRATORY DISTRESS SYNDROME, STROKE AND ULCER ELI LILLY AND COMPANY (US) 2000-01-11 US disclosed
EP-0882706-A1 Cell adhesion inhibitors ELI LILLY AND COMPANY (US) 1998-12-09 EP disclosed
US-4550094-A POLYMERIZATION COORDINATION CATALYST CONTAINING SILICON COMPOUND WITH A TRANSITION METAL, ORGANOMAGNESIUM AND HALOGEN COMPOUNDS SUMITOMO CHEMICAL COMPANY, LIMITED (JP) 1985-10-29 US disclosed
US-4398035-A INTERMEDIATE FOR FLURBIPROFEN THE UPJOHN COMPANY (US) 1983-08-09 US disclosed
US-4324904-A COMPOUND USEFUL IN MAKING FLURBIPROFEN THE UPJOHN COMPANY (US) 1982-04-13 US disclosed
EP-0032620-A1 Process for preparing therapeutic 2-arylpropionic acids and esters, and novel arylmethylmalonate esters THE UPJOHN COMPANY (US) 1981-07-29 EP disclosed
US-4266069-A Processes for the preparation of hydratropic acids and esters THE UPJOHN COMPANY (US) 1981-05-05 US disclosed