Acetophenone

Acetophenone

SCHEMBL6573416

CC(=O)c1ccccc1.[NaH]

nearest known ligand 0.68

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Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
▸ MAPT P10636 4/20 0.68
▸ SMN1; SMN2 Q16637 2/20 0.68
▸ HPGD P15428 4/20 0.60
▸ ALDH1A1 P00352 2/20 0.60
▸ LMNA P02545 2/20 0.60
▸ CES2 O00748 3/20 0.59
▸ CES1 P23141 3/20 0.59
▸ RAB9A P51151 2/20 0.56
▸ NPC1 O15118 1/20 0.56
▸ TAAR1 Q96RJ0 1/20 0.56
▸ TSHR P16473 3/20 0.55
▸ DAO P14920 1/20 0.55
▸ NAPRT Q6XQN6 1/20 0.55
▸ KMT2A Q03164 3/20 0.52
▸ MEN1 O00255 1/20 0.52
▸ L3MBTL1 Q9Y468 2/20 0.50
▸ POLB P06746 2/20 0.50
▸ MAOB P27338 1/20 0.50
▸ CYP3A4 P08684 1/20 0.50
▸ PARP1 P09874 1/20 0.50

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
Acetophenone SCHEMBL16745259 0.97 — —
Acetophenone SCHEMBL30537005 0.97 — —
Acetophenone SCHEMBL30537000 0.97 — —
Acetophenone SCHEMBL1450855 0.97 — —
Acetophenone SCHEMBL737 0.97 — —
Acetophenone SCHEMBL719033 0.97 MAPT (0.71) MAPTSMN1; SMN2HPGDALDH1A1LMNA
Acetophenone SCHEMBL27462873 0.97 MAPT (0.71) MAPTSMN1; SMN2HPGDALDH1A1LMNA
Acetophenone SCHEMBL8054906 0.94 MAPT (0.68) MAPTSMN1; SMN2HPGDALDH1A1LMNA
Acetophenone SCHEMBL2517302 0.94 MAPT (0.68) MAPTSMN1; SMN2HPGDALDH1A1LMNA
Acetophenone SCHEMBL12475398 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 26 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
WO-1999023195-A1 MULTI-PURPOSE LIQUID AQUEOUS BLEACHING COMPOSITIONS THE PROCTER & GAMBLE COMPANY (US) 1999-05-14 — — WO claimed
EP-3426759-B1 PARTICLES INCLUDING ENZYME PROCTER & GAMBLE (US) 2023-07-26 — — EP disclosed
CN-108864173-B Process for converting substituted sodium arylsulfinates into aryltri-n-butyltin 天津师范大学 2020-07-21 — — CN disclosed
CN-105601929-B A method of improving protective film silicone pressure sensitive gluing agent stability 安徽明讯新材料科技股份有限公司 2018-07-31 — — CN disclosed
CN-105441017-B A method of improvement protective film silicone pressure sensitive gluing agent stability 安徽明讯新材料科技股份有限公司 2018-07-17 — — CN disclosed
US-9919300-B2 1-hexene production process SUMITOMO CHEMICAL COMPANY, LIMITED (JP) 2018-03-20 — — US disclosed
EP-2484685-B1 TRANSITION METAL COMPLEX, PREPARATION METHOD FOR SAID TRANSITION METAL COMPLEX, TRIMERIZATION CATALYST, PREPARATION METHOD FOR 1-HEXENE, PREPARATION METHOD FOR ETHYLENE POLYMER, SUBSTITUTED CYCLOPENTADIENE COMPOUND, AND PREPARATION METHOD FOR SAID SUBSTITUTED CYCLOPENTADIENE COMPOUND SUMITOMO CHEMICAL CO (JP) 2017-11-01 — — EP disclosed
US-20170036200-A1 1-HEXENE PRODUCTION PROCESS SUMITOMO CHEMICAL COMPANY, LIMITED (JP) 2017-02-09 — — US disclosed
US-20150105237-A1 CATALYTIC COMPONENT FOR TRIMERIZATION AND TRIMERIZATION CATALYST SUMITOMO CHEMICAL COMPANY, LIMITED (JP) 2015-04-16 — — US disclosed
US-20150105572-A1 TRANSITION METAL COMPLEX SUMITOMO CHEMICAL COMPANY, LIMITED (JP) 2015-04-16 — — US disclosed
EP-0970964-B1 Method for producing a titanium complex SUMITOMO CHEMICAL CO (JP) 2004-04-21 — — EP disclosed
CN-1140533-C Method for producing phosphabenzene compounds �����ɷ� 2004-03-03 — — CN disclosed
CN-1414969-A Catalyst for hydrosilylation reaction RHODIA CHIMIE SA (FR) 2003-04-30 — — CN disclosed
CN-1082508-C Heterocyclic azahexane derivatives with antiviral activity NOVARTIS AG (CH) 2002-04-10 — — CN disclosed
CN-1319587-A Heterocyclic azahexane derivatives with antiviral activity NOVARTIS AG (CH) 2001-10-31 — — CN disclosed
CN-1058002-C Method for treatment of mixture of hydroperoxide SUMITOMO CHEMICAL CO (JP) 2000-11-01 — — CN disclosed
EP-0970964-A2 Method for producing titanium complex SUMITOMO CHEMICAL COMPANY, LIMITED (JP) 2000-01-12 — — EP disclosed
CN-1216539-A Heterocyclic azahexane derivatives with antiviral activity NOVARTIS AG (CH) 1999-05-12 — — CN disclosed
CN-1128754-A Method for treatment of mixture of hydroperoxide SUMITOMO CHEMICAL CO (JP) 1996-08-14 — — CN disclosed
US-4880660-A Method for priming hard tissue MINNESOTA MINING AND MANUFACTURING COMPANY (US) 1989-11-14 — — US 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 (3 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-20170036200-A1 1-HEXENE PRODUCTION PROCESS AP1M1, HK1, CYC1 MAPT 3595/4885SMN1; SMN2 2268/4885HPGD 1006/4885
US-20150105572-A1 TRANSITION METAL COMPLEX AP1M1, AP3M1, EMC1 MAPT 2999/4885SMN1; SMN2 2723/4885HPGD 2180/4885
US-20150105237-A1 CATALYTIC COMPONENT FOR TRIMERIZATION AND TRIMERIZATION CATALYST AP1M1, AMY1A, AP3M1 MAPT 4270/4885SMN1; SMN2 2685/4885HPGD 1490/4885

“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.

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