Acetophenone

Acetophenone

SCHEMBL11042465

CC(=O)c1ccccc1.Cl

nearest known ligand 0.68

Full drug profile on Sugi Atlas →

Known targets — ChEMBL curated mechanism

ABL1ACEACHEACVR1ADRA1AADRA1BADRA1DADRA2AADRA2BADRA2CADRB1ADRB2ADRB3AGTR1ALKAVPR1AAVPR2BCHEBCRCA2CACNA1ACACNA1BCACNA1CCACNA1DCACNA1ECACNA1FCACNA1GCACNA1HCACNA1ICACNA1SCACNA2D1CACNA2D2CACNA2D3CACNA2D4CACNB1CACNB2CACNB3CACNB4CACNG1CACNG2CACNG3CACNG4CACNG5CACNG6CACNG7CACNG8CALCRLCASRCCR5CDK4CDK6CFBCHRM1CHRM2CHRM3CHRM4CHRM5CHRNA1CHRNA3CHRNA7CHRNB1CHRNB4CHRNDCHRNECHRNGCOXFA4COXFA4L2CRBNCSF1RCUL4ACYP19A1DDB1DPP4DRD1DRD2DRD3DRD4EDNRAEGFREML4ERBB2ERBB4ESR1ESR2FGFR1FGFR3FLT1FLT3FLT4GAAGABRA1GABRA2GABRA3GABRA4GABRA5GABRA6GABRB1GABRB2GABRB3GABRDGABREGABRG1GABRG2GABRG3GABRPGABRQGHSRGLAGNRHRGPD2GRIN1GRIN2AGRIN2BGRIN2CGRIN2DGRIN3AGRIN3BGSTP1HCN4HCRTR1HCRTR2HDAC1HDAC10HDAC11HDAC2HDAC3HDAC4HDAC5HDAC6HDAC7HDAC8HDAC9HRH1HRH2HRH3HSD11B1HSP90AA1HSP90AB1HTR1AHTR1BHTR1DHTR1EHTR1FHTR2AHTR2BHTR2CHTR3AHTR3BHTR3CHTR3DHTR3EHTR4HTR5AHTR6HTR7IMPDH1IMPDH2ITGA2BITGB3ITKJAK1JAK2KCNA1KCNA10KCNA2KCNA3KCNA4KCNA5KCNA6KCNA7KCNB1KCNB2KCNC1KCNC2KCNC3KCNC4KCND1KCND2KCND3KCNF1KCNG1KCNG2KCNG3KCNG4KCNH1KCNH2KCNH3KCNH4KCNH5KCNH6KCNH7KCNH8KCNJ2KCNJ3KCNJ5KCNK3KCNK9KCNQ1KCNQ2KCNQ3KCNQ4KCNQ5KCNS1KCNS2KCNS3KCNV1KCNV2KDRKITKLKB1LCKMMAOAMAOBMAPK14METMMP1MMP13MMP7MMP8MT-ND1MT-ND2MT-ND3MT-ND4MT-ND4LMT-ND5MT-ND6NDUFA1NDUFA10NDUFA11NDUFA12NDUFA13NDUFA2NDUFA3NDUFA5NDUFA6NDUFA7NDUFA8NDUFA9NDUFAB1NDUFAF1NDUFAF2NDUFAF3NDUFAF4NDUFB1NDUFB10NDUFB11NDUFB2NDUFB3NDUFB4NDUFB5NDUFB6NDUFB7NDUFB8NDUFB9NDUFC1NDUFC2NDUFS1NDUFS2NDUFS3NDUFS4NDUFS5NDUFS6NDUFS7NDUFS8NDUFV1NDUFV2NDUFV3NR3C1NS5ANTRK1NTRK2NTRK3ODC1OPRD1OPRK1OPRM1P2RY12PAHPARP1PDE3APDE3BPDE4APDE4BPDE4CPDE4DPDE5APDE7APDE7BPDE8APDE8BPDGFRAPDGFRBPIK3CAPIK3CDPNPPOLA1POLA2POLD1POLD2POLD3POLD4POLEPOLE2POLE3PPARGPRIM1PRIM2PRKCAPRKCBPRKCDPRKCEPRKCGPRKCHPRKCIPRKCQPRKCZPRKD1PRKD3PTGS1PTGS2RBX1RENRETROCK1ROCK2RPE65RRM1RRM2RRM2BS1PR1S1PR2S1PR3S1PR4S1PR5SCN10ASCN11ASCN1ASCN2ASCN3ASCN4ASCN5ASCN7ASCN8ASCN9ASCNN1ASCNN1BSCNN1GSIGMAR1SLC18A2SLC6A1SLC6A2SLC6A3SLC6A4SLC9A3SRCTACR1TOP1TOP2ATOP2BTTRTYMPdacAdacBdacCembAfolAftsIgyrAgyrBmrcAmrcBmrdAparCparEpolrplArplBrplCrplDrplErplFrplIrplJrplKrplLrplMrplNrplOrplPrplQrplRrplSrplTrplUrplVrplWrplXrplYrpmArpmBrpmCrpmDrpmErpmE2rpmFrpmGrpmG1rpmG2rpmG3rpmHrpmIrpmJrpsArpsBrpsCrpsDrpsErpsFrpsGrpsHrpsIrpsJrpsKrpsLrpsMrpsNrpsOrpsPrpsQrpsRrpsSrpsTrpsUykgMykgO

The experimentally established mechanism targets of Acetophenone. 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
MAOB known ✓ P27338 1/20 0.50
PARP1 known ✓ P09874 1/20 0.50
CA2 known ✓ P00918 1/20 0.50
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

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 SCHEMBL27600039 1.00 MAPT (0.68) MAPTSMN1; SMN2HPGDALDH1A1LMNA
Acetophenone SCHEMBL11354178 1.00 MAPT (0.68) MAPTSMN1; SMN2HPGDALDH1A1LMNA
Acetophenone SCHEMBL11683047 0.97 MAPT (0.65) MAPTSMN1; SMN2HPGDALDH1A1LMNA
Acetophenone SCHEMBL10706513 0.97 MAPT (0.65) MAPTSMN1; SMN2HPGDALDH1A1LMNA
Acetophenone SCHEMBL27865122 0.97 MAPT (0.65) MAPTSMN1; SMN2HPGDALDH1A1LMNA
Acetophenone SCHEMBL11683044 0.97 SMN1; SMN2 (0.65) MAPTSMN1; SMN2HPGDALDH1A1LMNA
Acetophenone SCHEMBL10707314 0.97 MAPT (0.65) MAPTSMN1; SMN2HPGDALDH1A1LMNA
Acetophenone SCHEMBL1450855 0.97
Acetophenone SCHEMBL16745259 0.97
Acetophenone SCHEMBL737 0.97

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-106852143-B Tricyclic triazolic compounds 埃斯蒂维制药股份公司 2019-07-16 CN claimed
CN-106478612-B 2- [4- (quinoxaline -2- base oxygroup) phenoxy group] amide derivatives and the preparation method and application thereof 湖南大学 2019-02-15 CN claimed
CN-106324794-B A kind of the chip automatic focusing device and its focus adjustment method of gene profile sequencing equipment 徐州工程学院 2018-10-23 CN claimed
CN-106217625-B A kind of multi-functional curing means of large-sized reinforced concrete profiled member and its method of work 徐州工程学院 2018-04-13 CN claimed
CN-107531615-A Indenyl compound, pharmaceutical composition and medical application thereof ADT制药有限责任公司 2018-01-02 CN claimed
CN-105263933-B A kind of simultaneously [1,2 a] benzazolyl compounds and preparation method thereof and the application in medicine of pyrazine 埃斯蒂维实验室股份有限公司 2017-12-22 CN claimed
CN-106999473-A Purposes of the sigma-receptor part in osteoarthritis 埃斯蒂文博士实验室股份有限公司 2017-08-01 CN claimed
CN-104507939-B tetrahydropyrazolopyrimidine compounds 卫材R&D管理有限公司 2017-07-25 CN claimed
CN-106852143-A Tricyclic triazolic compounds 埃斯蒂维实验室股份有限公司 2017-06-13 CN claimed
CN-105263933-A Pyrazino[1,2-a]indole compounds, their preparation and use in medicaments ESTEVE LABOR DR 2016-01-20 CN claimed
CN-104507939-A Tetrahydropyrazolopyrimidine compounds EISAI R&D MAN CO LTD 2015-04-08 CN claimed
CN-103228633-A Heterocyclic compounds as DGAT1 inhibitors PIRAMAL LIFE SCIENCES LTD 2013-07-31 CN claimed
CN-102007102-A Modulators of the histamine h3 receptor useful for the treatment of disorders related thereto ARENA PHARM INC 2011-04-06 CN claimed
CN-101553481-A Substituted sulfonamide derivatives GRUENENTHAL GMBH (DE) 2009-10-07 CN claimed
CN-1554649-A Metabotropic glutamate receptor antagonists for treating central nervous system diseases NPSҩ�����޹�˾ 2004-12-15 CN claimed
CN-1285820-A Metabotropic glutamate receptor antagonists for the treatment of central nervous system disorders NPS PHARMA INC (US) 2001-02-28 CN claimed
CN-1003013-B Synthesis of nitro acetophenone hydrochloride as intermediate of antidepressant Nomifenin 国家医药管理局天津药物研究院 1989-01-04 CN claimed
CN-113831218-B Method for preparing 4-fluorophenyl ethylene oxide 利尔化学股份有限公司 2023-11-28 CN disclosed
CN-86108706-A Synthesizing of alchol of antimelancholic ' Nomifensin ' intermediate nitro-acetophenone hydrochloride 1987-12-23 CN disclosed
EP-0043807-B1 1-(DIHYDROXYPHENYL)-2-AMINO-ETHANOL DERIVATIVES; PREPARATION, COMPOSITIONS AND INTERMEDIATES Aktiebolaget Draco (SE) 1984-05-30 EP disclosed