Hydrogen Peroxide

Hydrogen Peroxide

SCHEMBL3127404

CCCCCCCCCCCCS.OO

nearest known ligand 0.53

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Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
TSHR P16473 6/20 0.53
THRB P10828 1/20 0.53
KMT2A Q03164 3/20 0.47
ALDH1A1 P00352 3/20 0.47
LMNA P02545 2/20 0.47
HSD17B10 Q99714 2/20 0.47
MEN1 O00255 2/20 0.47
MAPT P10636 1/20 0.46
GPR84 Q9NQS5 7/20 0.46
PPARG P37231 7/20 0.46
PPARD Q03181 7/20 0.46
PPARA Q07869 7/20 0.46
HDAC11 Q96DB2 5/20 0.46
PTPN1 P18031 3/20 0.46
TLR2 O60603 2/20 0.46
TDP1 Q9NUW8 2/20 0.46
FABP4 P15090 2/20 0.46
SLC22A6 Q4U2R8 1/20 0.46
SLC22A8 Q8TCC7 1/20 0.46
ESR1 P03372 1/20 0.46

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
Methyl Alcohol SCHEMBL28278054 0.93 TSHR (0.53) TSHRTHRBKMT2AALDH1A1LMNA
Methyl Alcohol SCHEMBL27924806 0.93 TSHR (0.53) TSHRTHRBKMT2AALDH1A1LMNA
Methyl Alcohol SCHEMBL28011697 0.93 TSHR (0.53) TSHRTHRBKMT2AALDH1A1LMNA
SCHEMBL51303 0.93 TSHR (0.61) TSHRTHRBKMT2AALDH1A1LMNA
SCHEMBL20943436 0.93 TSHR (0.61) TSHRTHRBKMT2AALDH1A1LMNA
SCHEMBL23668483 0.93 TSHR (0.61) TSHRTHRBKMT2AALDH1A1LMNA
SCHEMBL28162 0.93
SCHEMBL21048444 0.93 TSHR (0.61) TSHRTHRBKMT2AALDH1A1LMNA
SCHEMBL2734278 0.93 TSHR (0.61) TSHRTHRBKMT2AALDH1A1LMNA
SCHEMBL7616706 0.93 TSHR (0.61) TSHRTHRBKMT2AALDH1A1LMNA

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20100322890-A1 Pathogen eradication composition EDWARDS JOHN LEE 2010-12-23 US disclosed
EP-1195393-B1 Process for preparing ethylene interpolymers and ethylene interpolymers obtained therefrom WESTLAKE LONGVIEW CORP (US) 2010-04-07 EP disclosed
EP-1195392-B1 Process for preparing ethylene interpolymers and ethylene interpolymers obtained therefrom EASTMAN CHEM CO (US) 2006-07-19 EP disclosed
US-6608156-B1 And optionally carbon monoxide; high pressure, free radical initiator; melting peak temperatures (Tm) equal to or greater than 50 degrees C.; olefin hetero monomer is allyl; vinyl ethylene carbonate, 3,4-diacetoxy-1-butene, 3-butene-1,2-diol EASTMAN CHEMICAL COMPANY 2003-08-19 US disclosed
US-6608157-B1 And optionally carbon monoxide; high pressure, free radicalinitiator; melting peak temperatures (Tm) equal to or greaterthan 50 degrees C.; olefin hetero monomer is allyl; vinylethylene carbonate, 3,4-diacetoxy-1-butene, EASTMAN CHEMICAL COMPANY 2003-08-19 US disclosed
US-6472491-B1 PREPARING INTERPOLYMERS COMPRISING ETHYLENE AND AT LEAST TWO MONOMER UNITS SELECTED FROM HETEROATOM SUBSTITUTED OLEFIN MONOMER UNITS DERIVED FROM A COMPOUND WITH HETEROATOMS SELECTED FROM OXYGEN, NITROGEN, AND SULFUR, WHICH ARE BOUND TO EASTMAN CHEMICAL COMPANY 2002-10-29 US disclosed
EP-1195392-A2 Process for preparing ethylene interpolymers and ethylene interpolymers obtained therefrom EASTMAN CHEMICAL COMPANY (US) 2002-04-10 EP disclosed
EP-1195393-A2 Process for preparing ethylene interpolymers and ethylene interpolymers obtained therefrom EASTMAN CHEMICAL COMPANY (US) 2002-04-10 EP disclosed
US-6106853-A TREATING GASES OR VAPOR POLLUTANTS AND NEUTRALIZATION BROMINE COMPOUDS, CHLORINE COMPOUNDS, ALCOHOL OR ACETIC ACID COX JAMES P (US) 2000-08-22 US disclosed
WO-1994014524-A1 DEVOLATILIZING AND STABILIZING VAPOROUS POLLUTANTS COX JAMES P (US) 1994-07-07 WO disclosed