Benzoyl Peroxide

Benzoyl Peroxide

SCHEMBL2494185

O=C(O)c1ccccc1.O=C(OOC(=O)c1ccccc1)c1ccccc1

nearest known ligand 0.85

Full drug profile on Sugi Atlas →

Known targets — ChEMBL curated mechanism

CACNA1CCACNA1DCACNA1FCACNA1SDPP4HTR1BHTR1D

The experimentally established mechanism targets of Benzoyl Peroxide. 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
LMNA P02545 2/20 0.85
F2 P00734 1/20 0.85
TSHR P16473 5/20 0.70
DAO P14920 1/20 0.70
NAPRT Q6XQN6 1/20 0.70
CES2 O00748 2/20 0.58
CES1 P23141 2/20 0.58
SRD5A2 P31213 2/20 0.58
ALDH1A1 P00352 4/20 0.57
TDP1 Q9NUW8 3/20 0.57
HSD17B10 Q99714 1/20 0.57
TP53 P04637 2/20 0.52
KMT2A Q03164 3/20 0.48
MAPT P10636 2/20 0.48
MAPK1 P28482 1/20 0.48
HIF1A Q16665 1/20 0.48
POLB P06746 1/20 0.48
SLC6A2 P23975 1/20 0.48
SLC6A3 Q01959 1/20 0.48
SMN1; SMN2 Q16637 1/20 0.47

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
Benzoyl Peroxide SCHEMBL2929886 0.92 LMNA (1.00) LMNAF2TSHRDAONAPRT
Benzoyl Peroxide SCHEMBL9407293 0.92 LMNA (1.00) LMNAF2TSHRDAONAPRT
Benzoyl Peroxide SCHEMBL63 0.92 LMNA (1.00) LMNAF2TSHRDAONAPRT
Benzoyl Peroxide SCHEMBL3467853 0.92 LMNA (1.00) LMNAF2TSHRDAONAPRT
Benzoyl Peroxide SCHEMBL5312311 0.92 LMNA (1.00) LMNAF2TSHRDAONAPRT
Benzoyl Peroxide SCHEMBL4745654 0.90 LMNA (0.94) LMNAF2TSHRDAONAPRT
Benzoyl Peroxide SCHEMBL9463392 0.90 LMNA (0.94) LMNAF2TSHRDAONAPRT
Benzoyl Peroxide SCHEMBL178097 0.90 LMNA (0.94) LMNAF2TSHRDAONAPRT
SCHEMBL11512239 0.90 TSHR (0.67) LMNAF2TSHRDAONAPRT
Benzoyl Peroxide SCHEMBL7546726 0.90 LMNA (0.94) LMNAF2TSHRDAONAPRT

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 32 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-103724785-B A kind of low filling halogen-free expansion type flame-proof photovoltaic encapsulation material and preparation method thereof 杭州福斯特光伏材料股份有限公司 2016-08-17 CN claimed
US-20240076415-A1 MECHANICALLY INTERLOCKED MOLECULES-BASED MATERIALS FOR 3-D PRINTING TRUSTEES OF DARTMOUTH COLLEGE (US) 2024-03-07 US disclosed
US-20240002685-A1 THREE-DIMENSIONAL PRINTING WITH SUPRAMOLECULAR TEMPLATED HYDROGELS TRUSTEES OF DARTMOUTH COLLEGE (US) 2024-01-04 US disclosed
US-11845812-B2 Mechanically interlocked molecules-based materials for 3-D printing TRUSTEES OF DARTMOUTH COLLEGE (US) 2023-12-19 US disclosed
US-11814527-B2 Three-dimensional printing with supramolecular templated hydrogels TRUSTEES OF DARTMOUTH COLLEGE (US) 2023-11-14 US disclosed
CN-114432175-A Pet skin care agent 佛山市佛丹动物药业有限公司 2022-05-06 CN disclosed
WO-2021150819-A1 REDOX INITIATION SYSTEM FOR ACRYLIC ADHESIVES LORD CORPORATION (US) 2021-07-29 WO disclosed
US-20210171668-A1 MECHANICALLY INTERLOCKED MOLECULES-BASED MATERIALS FOR 3-D PRINTING TRUSTEES OF DARTMOUTH COLLEGE (US) 2021-06-10 US disclosed
US-10954315-B2 Mechanically interlocked molecules-based materials for 3-D printing TRUSTEES OF DARTMOUTH COLLEGE (US) 2021-03-23 US disclosed
US-10828399-B2 Three dimensional printing of supramolecular (hydro)gels THE TRUSTEES OF THE UNIVERSITY OF PENNSYLVANIA (US) 2020-11-10 US disclosed
CN-103636003-A Sealing film for solar cell and solar cell using same BRIDGESTONE CORP 2014-03-12 CN disclosed
WO-2014028209-A1 STABILIZING SHEAR-THINNING HYDROGELS THE TRUSTEES OF THE UNIVERSITY OF PENNSYLVANIA (US) 2014-02-20 WO disclosed
US-8030410-B2 Reacting anionic living end polymer that is end capped with steric hindering carbonyl-containing compound to produce polymer with homolytically cleaveable group; engineering plastics BRIDGESTONE CORPORATION (JP) 2011-10-04 US disclosed
US-7737218-B2 Method for generating free radical capable polymers using tin or silicon halide compounds BRIDGESTONE CORPORATION (JP) 2010-06-15 US disclosed
US-7560509-B2 Method of directing grafting by controlling the location of high vinyl segments in a polymer BRIDGESTONE CORPORATION (JP) 2009-07-14 US disclosed
US-7396887-B1 Insitu removal of chelator from anionic polymerization reactions BRIDGESTONE CORPORATION (JP) 2008-07-08 US disclosed
US-20080161495-A1 Method for Generating Free Radical Capable Polymers Using Tin or Silicon Halide Compounds BRIDGESTONE CORPORATION (JP) 2008-07-03 US disclosed
US-20080161484-A1 Method of Directing Grafting by Controlling the Location of High Vinyl Segments in a Polymer BRIDGESTONE CORPORATION (JP) 2008-07-03 US disclosed
US-20080161501-A1 Method for generating free radical capable polymers using carbonyl-containing compounds BRIDGESTONE CORPORATION (JP) 2008-07-03 US disclosed
US-20080161455-A1 INSITU REMOVAL OF CHELATOR FROM ANIONIC POLYMERIZATION REACTIONS BRIDGESTONE CORPORATION (JP) 2008-07-03 US disclosed