Hydrogen Peroxide

Hydrogen Peroxide

SCHEMBL6280050

CCc1ccc(C(C)C)cc1.OO

nearest known ligand 0.52

Full drug profile on Sugi Atlas →

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
L3MBTL1 Q9Y468 2/20 0.52
TSHR P16473 1/20 0.52
MAPK1 P28482 1/20 0.52
ATM Q13315 1/20 0.52
TDP1 Q9NUW8 1/20 0.52
IDO1 P14902 2/20 0.50
ALDH1A1 P00352 3/20 0.48
TP53 P04637 1/20 0.48
AKR1C3 P42330 1/20 0.47
AKR1C2 P52895 1/20 0.47
CYP2C9 P11712 2/20 0.45
CYP2C19 P33261 1/20 0.45
RXRA P19793 1/20 0.44
RXRB P28702 1/20 0.44
LPL P06858 1/20 0.44
LIPG Q9Y5X9 1/20 0.44
USP5 P45974 1/20 0.44
NPC1 O15118 2/20 0.43
RAB9A P51151 2/20 0.43
MEN1 O00255 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
SCHEMBL139408 0.95 L3MBTL1 (0.56) L3MBTL1TSHRMAPK1ATMTDP1
Isopropylbenzene SCHEMBL7651427 0.91 TP53 (0.56) L3MBTL1TSHRMAPK1ATMTDP1
Hydroquinone SCHEMBL27792140 0.89 ESR1 (0.55) L3MBTL1TSHRMAPK1ATMTDP1
Isopropylbenzene SCHEMBL11460058 0.88 TP53 (0.59) L3MBTL1TSHRMAPK1ATMTDP1
Isopropylbenzene SCHEMBL27664305 0.86 TP53 (0.64) L3MBTL1ALDH1A1TP53NPC1RAB9A
Dimethylamine SCHEMBL8528041 0.86 IDO1 (0.50) L3MBTL1TSHRMAPK1ATMTDP1
SCHEMBL21871202 0.84 L3MBTL1 (0.52) L3MBTL1TSHRMAPK1ATMTDP1
SCHEMBL19799400 0.84 L3MBTL1 (0.52) L3MBTL1TSHRMAPK1ATMTDP1
SCHEMBL26497194 0.84 L3MBTL1 (0.52) L3MBTL1TSHRMAPK1ATMTDP1
SCHEMBL23917847 0.83 ALDH1A1 (0.53) L3MBTL1ALDH1A1AKR1C3AKR1C2CYP2C9

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20160251289-A1 USE OF ALKANE SULFONIC ACID FOR PREPARING PHENOLIC ALCOHOL ARKEMA FRANCE (FR) 2016-09-01 US disclosed
US-6965056-B1 Removal of salts in the manufacture of phenolic compound SHELL OIL COMPANY (US) 2005-11-15 US disclosed
US-6720461-B2 ADDING WATER AND A DILUENT TO FORM A SEPARABLE CRUDE PHENOLIC BOTTOMS STREAM HAVING A COMBINED DENSITY LOWER THAN THE DENSITY OF THE BOTTOMS; SEPARATING OUT A HYDROCARBON PHASE AND A SALT-CONTAINING AQUEOUS PHASE; PHENOLS FROM PEROXIDES SHELL OIL COMPANY 2004-04-13 US disclosed
US-20010000260-A1 Removal of salts in the manufacture of phenolic compound SHELL OIL COMPANY 2001-04-12 US disclosed
EP-0028910-B1 IMPROVED PROCESS FOR PRODUCING PHENOLIC COMPOUNDS FROM ARALKYL HYDROPEROXIDES MITSUI PETROCHEMICAL INDUSTRIES, LTD. (JP) 1983-04-20 EP disclosed
US-4328377-A ACID CLEAVAGE OF ARYL HYDROPEROXIDES MITSUI PETROCHEMICAL INDUSTRIES LTD. (JP) 1982-05-04 US disclosed
EP-0028910-A1 Improved process for producing phenolic compounds from aralkyl hydroperoxides MITSUI PETROCHEMICAL INDUSTRIES, LTD. (JP) 1981-05-20 EP disclosed

Patent text — is the patent's own abstract consistent with the prediction?

For each of this compound's patents that has machine-readable text (2 of them — usually the abstract, not the full specification), we ask MedCPT which protein the text reads most about, and where the chemistry-predicted target lands among 4885 human targets. A high rank means the patent's own wording is consistent with the prediction — a weak, independent signal, not proof of activity.

PatentTitleText reads most aboutPredicted target · text-rank
US-20160251289-A1 USE OF ALKANE SULFONIC ACID FOR PREPARING PHENOLIC ALCOHOL ADH1C, ADH1A, ADH5 L3MBTL1 4365/4885TSHR 3275/4885MAPK1 640/4885
US-20010000260-A1 Removal of salts in the manufacture of phenolic compound SRMS, AGT, TYR L3MBTL1 1916/4885TSHR 3198/4885MAPK1 307/4885

“Text reads most about” is the patent abstract's nearest protein in MedCPT space (background-debiased). Only ~1.4% of patents have machine-readable text, so most compounds won't have this panel.