Dapi

Dapi

SCHEMBL3492008

Cl.Cl.N=C(N)c1ccc(-c2cc3ccc(C(=N)N)cc3[nH]2)cc1.O

nearest known ligand 0.94

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 Dapi. The predicted profile below is derived independently by chemical similarity — agreement is a validation signal, a miss is honest.

Predicted protein targets (top 19)

geneUniProtsupporting neighboursconfidence
PRMT5 O14744 1/20 0.79
PRMT3 O60678 1/20 0.79
CARM1 Q86X55 1/20 0.79
EHMT2 Q96KQ7 1/20 0.79
PRMT6 Q96LA8 1/20 0.79
PRMT1 Q99873 1/20 0.79
WDR77 Q9BQA1 1/20 0.79
PRMT8 Q9NR22 1/20 0.79
PRMT7 Q9NVM4 1/20 0.79
F2 P00734 2/20 0.60
ASIC3 Q9UHC3 2/20 0.54
CASP3 P42574 1/20 0.51
SENP8 Q96LD8 1/20 0.51
SENP7 Q9BQF6 1/20 0.51
SENP6 Q9GZR1 1/20 0.51
F10 P00742 1/20 0.51
PLG P00747 1/20 0.51
PLAU P00749 1/20 0.51
PRSS1 P07477 1/20 0.51

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
Dapi SCHEMBL15966967 1.00 PRMT5 (0.79) PRMT5PRMT3CARM1EHMT2PRMT6
Dapi SCHEMBL2464378 0.98 PRMT5 (0.81) PRMT5PRMT3CARM1EHMT2PRMT6
Dapi SCHEMBL30442885 0.98 PRMT5 (0.81) PRMT5PRMT3CARM1EHMT2PRMT6
Dapi SCHEMBL94350 0.98 PRMT5 (0.81) PRMT5PRMT3CARM1EHMT2PRMT6
Dapi SCHEMBL29350295 0.97 PRMT5 (0.83) PRMT5PRMT3CARM1EHMT2PRMT6
Dapi SCHEMBL28176609 0.97 PRMT5 (0.83) PRMT5PRMT3CARM1EHMT2PRMT6
Dapi SCHEMBL235865 0.97 PRMT5 (0.83) PRMT5PRMT3CARM1EHMT2PRMT6
SCHEMBL29428907 0.95 PRMT5 (0.81) PRMT5PRMT3CARM1EHMT2PRMT6
SCHEMBL14854556 0.95 PRMT5 (0.81) PRMT5PRMT3CARM1EHMT2PRMT6
Dapi SCHEMBL1609032 0.94 PRMT5 (0.79) PRMT5PRMT3CARM1EHMT2PRMT6

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20210222226-A1 METHODS OF MEASURING ENZYME ACTIVITY IN COATING COMPOSTIONS BASF SE (DE) 2021-07-22 US claimed
EP-3814518-A1 METHODS OF MEASURING ENZYME ACTIVITY IN COATING COMPOSITIONS BASF SE (DE) 2021-05-05 EP claimed
CN-112513287-A Method for measuring enzyme activity in coating compositions 巴斯夫欧洲公司 2021-03-16 CN claimed
US-5403744-A Colorimetric analysis using metachromatic dye, pH indicator dye, polyelectrolytes with anionic sites to bind with dyes; for testing urine, blood MILES INC. (US) 1995-04-04 US claimed
US-20220160705-A1 METHODS FOR CONTROLLING PROSTAGLANDIN-MEDIATED BIOLOGICAL PROCESSES CORNELL UNIVERSITY 2022-05-26 US disclosed
US-20210222226-A1 METHODS OF MEASURING ENZYME ACTIVITY IN COATING COMPOSTIONS BASF SE (DE) 2021-07-22 US disclosed
EP-3814518-A1 METHODS OF MEASURING ENZYME ACTIVITY IN COATING COMPOSITIONS BASF SE (DE) 2021-05-05 EP disclosed
CN-112513287-A Method for measuring enzyme activity in coating compositions 巴斯夫欧洲公司 2021-03-16 CN disclosed
WO-2020191227-A1 METHODS FOR CONTROLLING PROSTAGLANDIN-MEDIATED BIOLOGICAL PROCESSES CORNELL UNIVERSITY (US) 2020-09-24 WO disclosed
EP-3034093-B1 COMPOSITIONS AND METHODS OF TREATING TUMORS UNIV PENNSYLVANIA (US) 2019-03-13 EP disclosed
US-9901608-B2 Composition and method for enhancing alcohol metabolism Gangneung-Wonju National University Industry Academy Cooperation Group (KR) 2018-02-27 US disclosed
EP-2363410-B1 Isoforms of MUC1 MINERVA BIOTECHNOLOGIES CORP (US) 2017-10-11 EP disclosed
WO-1999021574-A9 ENHANCEMENT OF MORPHOGEN ACTIVITY CREATIVE BIOMOLECULES INC (US) 1999-08-12 WO disclosed
WO-1999021574-A2 ENHANCEMENT OF MORPHOGEN ACTIVITY CREATIVE BIOMOLECULES, INC. (US) 1999-05-06 WO disclosed
EP-0558740-B1 PROBE COMPOSITION FOR GENOME IDENTIFICATION AND METHODS VYSIS INC (US) 1998-08-05 EP disclosed
US-5789161-A Methods for genome identification using direct label probe composition AMOCO CORPORATION (US) 1998-08-04 US disclosed
US-5403744-A Colorimetric analysis using metachromatic dye, pH indicator dye, polyelectrolytes with anionic sites to bind with dyes; for testing urine, blood MILES INC. (US) 1995-04-04 US disclosed
EP-0611966-A1 Method, composition and device for measuring the ionic strength or specific gravity of a test sample Bayer Corporation (US) 1994-08-24 EP disclosed
EP-0558740-A1 PROBE COMPOSITION FOR GENOME IDENTIFICATION AND METHODS VYSIS, Inc. (US) 1993-09-08 EP disclosed
WO-1993006245-A1 PROBE COMPOSITION FOR GENOME IDENTIFICATION AND METHODS AMOCO CORPORATION (US) 1993-04-01 WO 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 (1 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-20220160705-A1 METHODS FOR CONTROLLING PROSTAGLANDIN-MEDIATED BIOLOGICAL PROCESSES PTGES, PTGS1, PTGES2 PRMT5 3685/4885PRMT3 3403/4885CARM1 4738/4885

“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.