Ampyrone

Ampyrone

SCHEMBL1830291

Cc1c(N)c(=O)n(-c2ccccc2)n1C.Cl

nearest known ligand 0.96

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 Ampyrone. 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
BCHE known ✓ P06276 1/20 0.96
PTGS2 known ✓ P35354 1/20 0.96
HSP90AA1 known ✓ P07900 1/20 0.50
HSP90AB1 known ✓ P08238 1/20 0.50
GAA known ✓ P10253 1/20 0.50
ALOX15 P16050 2/20 0.62
ALDH1A1 P00352 2/20 0.62
LMNA P02545 2/20 0.60
ADORA3 P0DMS8 1/20 0.60
TSHR P16473 3/20 0.58
CYP1A2 P05177 2/20 0.58
THRB P10828 2/20 0.58
NAPRT Q6XQN6 1/20 0.58
KMT2A Q03164 2/20 0.55
KDM4E B2RXH2 4/20 0.55
CYP2D6 P10635 1/20 0.54
POLB P06746 1/20 0.53
MAPT P10636 3/20 0.50
TP53 P04637 1/20 0.50
MAPK1 P28482 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
Ampyrone SCHEMBL10746988 1.00 BCHE (0.96) BCHEPTGS2ALOX15ALDH1A1LMNA
Ampyrone SCHEMBL11674586 0.98 BCHE (1.00) BCHEPTGS2ALOX15ALDH1A1LMNA
Ampyrone SCHEMBL18159502 0.98 BCHE (1.00) BCHEPTGS2ALOX15ALDH1A1LMNA
Ampyrone SCHEMBL128544 0.98 BCHE (1.00) BCHEPTGS2ALOX15ALDH1A1LMNA
Ampyrone SCHEMBL28606780 0.90 BCHE (0.84) BCHEPTGS2ALOX15ALDH1A1LMNA
Ampyrone SCHEMBL3092850 0.90 BCHE (0.84) BCHEPTGS2ALOX15ALDH1A1LMNA
Ampyrone SCHEMBL10711697 0.89 BCHE (0.82) BCHEPTGS2ALOX15ALDH1A1LMNA
Ampyrone SCHEMBL4542675 0.88 BCHE (0.79) BCHEPTGS2ALOX15ALDH1A1LMNA
Ampyrone SCHEMBL28982549 0.88 BCHE (0.79) BCHEPTGS2ALOX15ALDH1A1LMNA
Ampyrone SCHEMBL8624284 0.88 BCHE (0.79) BCHEPTGS2ALOX15ALDH1A1LMNA

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-118717774-A Preparation method of small molecular compound GI-Y3 and application of small molecular compound GI-Y3 in preparation of anti-cell apoptosis drugs and inhibitors 温州医科大学附属第一医院 2024-10-01 CN claimed
CN-117625733-A Lactic acid detection freeze-dried reagent ball, preparation method and microfluidic detection chip 诺迈(苏州)科技有限公司 2024-03-01 CN claimed
CN-114200122-B Uric acid detection freeze-dried reagent ball, configuration method thereof and microfluidic detection chip 深圳市锦瑞生物科技股份有限公司 2023-09-15 CN claimed
CN-114200122-A Freeze-dried reagent ball for uric acid detection, configuration method thereof and microfluidic detection chip 深圳市锦瑞生物科技股份有限公司 2022-03-18 CN claimed
US-9574221-B2 Method for the determination of the concentration of vitamin B6 in a sample BÜHLMANN LABORATORIES AG (CH) 2017-02-21 US claimed
EP-2533053-B1 Method for the determination of the concentration of vitamin B6 in a sample BÜHLMANN LAB AG (CH) 2015-09-09 EP claimed
US-20140308691-A1 METHOD FOR THE DETERMINATION OF THE CONCENTRATION OF VITAMIN B6 IN A SAMPLE BUEHLMANN LABORATORIES AG (CH) 2014-10-16 US claimed
WO-2012168470-A1 METHOD FOR THE DETERMINATION OF THE CONCENTRATION OF VITAMIN B6 IN A SAMPLE BÜHLMANN LABORATORIES AG (CH) 2012-12-13 WO claimed
EP-2533053-A1 Method for the determination of the concentration of vitamin B6 in a sample Bühlmann Laboratories AG (CH) 2012-12-12 EP claimed
US-4283491-A ADDITION COPOLYMERS FOR IMPROVED STORAGE OR PEROXIDASE REAGENT EASTMAN KODAK COMPANY (US) 1981-08-11 US claimed
CN-118717774-A Preparation method of small molecular compound GI-Y3 and application of small molecular compound GI-Y3 in preparation of anti-cell apoptosis drugs and inhibitors 温州医科大学附属第一医院 2024-10-01 CN disclosed
CN-117625733-A Lactic acid detection freeze-dried reagent ball, preparation method and microfluidic detection chip 诺迈(苏州)科技有限公司 2024-03-01 CN disclosed
CN-114200122-B Uric acid detection freeze-dried reagent ball, configuration method thereof and microfluidic detection chip 深圳市锦瑞生物科技股份有限公司 2023-09-15 CN disclosed
CN-114200122-B Uric acid detection freeze-dried reagent ball, configuration method thereof and microfluidic detection chip 深圳市锦瑞生物科技股份有限公司 2023-09-15 CN disclosed
CN-114200122-A Freeze-dried reagent ball for uric acid detection, configuration method thereof and microfluidic detection chip 深圳市锦瑞生物科技股份有限公司 2022-03-18 CN disclosed
US-4166093-A REDUCTION OF DETECTABLE SPECIES MIGRATION IN ELEMENTS FOR THE ANALYSIS OF LIQUIDS EASTMAN KODAK COMPANY (US) 1979-08-28 US disclosed
US-4098574-A BUFFERED TRINDER'S REAGENT EASTMAN KODAK COMPANY (US) 1978-07-04 US disclosed
US-4066403-A DECOMPOSITION, PERMEABLE BARRIERS EASTMAN KODAK COMPANY (US) 1978-01-03 US disclosed
US-4042461-A HYDROPHOBIC CHROMATOGRAPHY EASTMAN KODAK COMPANY (US) 1977-08-16 US disclosed
US-3983005-A Integral element for the analysis of cholesterol EASTMAN KODAK COMPANY (US) 1976-09-28 US disclosed