Dyrene

Dyrene

SCHEMBL2783938

Cl.Cl.Cl.Clc1nc(Cl)nc(Nc2ccccc2Cl)n1.Clc1nc(Cl)nc(Nc2ccccc2Cl)n1.Clc1nc(Cl)nc(Nc2ccccc2Cl)n1

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 Dyrene. 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
▸ HDAC3 known ✓ O15379 1/20 0.45
▸ HDAC1 known ✓ Q13547 1/20 0.45
▸ HDAC2 known ✓ Q92769 1/20 0.45
▸ HDAC6 known ✓ Q9UBN7 1/20 0.45
▸ ADRA2A known ✓ P08913 1/20 0.43
▸ ADRA2B known ✓ P18089 1/20 0.43
▸ ADRA2C known ✓ P18825 1/20 0.43
▸ FLT3 known ✓ P36888 1/20 0.43
▸ TSHR P16473 1/20 0.96
▸ NFKB1 P19838 2/20 0.57
▸ MAPT P10636 5/20 0.54
▸ KMT2A Q03164 5/20 0.54
▸ KDM4E B2RXH2 2/20 0.54
▸ ALDH1A1 P00352 2/20 0.54
▸ SMN1; SMN2 Q16637 2/20 0.54
▸ MEN1 O00255 1/20 0.52
▸ MAPK1 P28482 1/20 0.52
▸ IGF1R P08069 1/20 0.50
▸ NPSR1 Q6W5P4 2/20 0.48
▸ NPC1 O15118 2/20 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
Dyrene SCHEMBL8881784 1.00 TSHR (0.96) TSHRNFKB1MAPTKMT2AKDM4E
Dyrene SCHEMBL827164 1.00 TSHR (0.96) TSHRNFKB1MAPTKMT2AKDM4E
Dyrene SCHEMBL3326806 1.00 TSHR (0.96) TSHRNFKB1MAPTKMT2AKDM4E
Dyrene SCHEMBL29364667 0.98 TSHR (1.00) TSHRNFKB1MAPTKMT2AKDM4E
Dyrene SCHEMBL1903290 0.98 TSHR (1.00) TSHRNFKB1MAPTKMT2AKDM4E
Dyrene SCHEMBL6750152 0.98 TSHR (1.00) TSHRNFKB1MAPTKMT2AKDM4E
Dyrene SCHEMBL133054 0.98 TSHR (1.00) TSHRNFKB1MAPTKMT2AKDM4E
Dyrene SCHEMBL8166670 0.98 TSHR (1.00) TSHRNFKB1MAPTKMT2AKDM4E
Dyrene SCHEMBL13280 0.98 TSHR (1.00) TSHRNFKB1MAPTKMT2AKDM4E
Dyrene SCHEMBL5745643 0.96 TSHR (0.96) TSHRNFKB1MAPTKMT2AKDM4E

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-9700632-B2 Dendrimers, conjugates and methods thereof CENTRE FOR BIOSEPERATION TECHNOLOGY-VIT (IN) 2017-07-11 — — US claimed
US-20150238623-A1 Dendrimers, Conjugates and Methods Thereof CENTRE FOR BIOSEPARATION TECHNOLOGY-VIT (IN) 2015-08-27 — — US claimed
WO-2014041517-A2 DENDRIMERS, CONJUGATES AND METHODS THEREOF CENTRE FOR BIOSEPARATION TECHNOLOGY-VIT (IN) 2014-03-20 — — WO claimed
US-6806284-B1 Photosensitizers with ligand targeting properties for tumor therapy CERAM OPTEC INDUSTRIES, INC. 2004-10-19 — — US claimed
JP-56026925-A — — None — — JP disclosed
US-9700632-B2 Dendrimers, conjugates and methods thereof CENTRE FOR BIOSEPERATION TECHNOLOGY-VIT (IN) 2017-07-11 — — US disclosed
CN-105175409-A Triazine Derivatives and their Therapeutical Applications CALIFORNIA CAPITAL EQUITY LLC 2015-12-23 — — CN disclosed
US-20150238623-A1 Dendrimers, Conjugates and Methods Thereof CENTRE FOR BIOSEPARATION TECHNOLOGY-VIT (IN) 2015-08-27 — — US disclosed
CN-102573485-B triazine derivatives and their therapeutic use ABRAXIS BIOSCIENCE LLC 2014-11-26 — — CN disclosed
WO-2014041517-A2 DENDRIMERS, CONJUGATES AND METHODS THEREOF CENTRE FOR BIOSEPARATION TECHNOLOGY-VIT (IN) 2014-03-20 — — WO disclosed
EP-2562864-A1 Proton-conducting polymer Nippon Steel Chemical Co., Ltd. (JP) 2013-02-27 — — EP disclosed
US-8198387-B2 Proton-conducting compound and proton-conducting polymer NIPPON STEEL CHEMICAL CO., LTD. (JP) 2012-06-12 — — US disclosed
WO-1989007957-A1 CO2 INDICATOR FOR PLACEMENT OF TRACHEAL TUBES BRIGHAM AND WOMEN'S HOSPITAL (US) 1989-09-08 — — WO disclosed
EP-0316492-A1 Polymeric matrix for affinity chromatography and immobilization of ligands BIOPROBE INTERNATIONAL, INC. (US) 1989-05-24 — — EP disclosed
US-4753983-A Polymeric matrix for affinity chromatography and immobilization of ligands BIOPROBE INTERNATIONAL, INC. (US) 1988-06-28 — — US disclosed
EP-0184361-A2 Method of activating polymeric carrier BIOPROBE INTERNATIONAL, INC. (US) 1986-06-11 — — EP disclosed
JP-S5626925-A PRODUCTION OF EPOXY RESIN SUMITOMO CHEM CO LTD 1981-03-16 — — JP disclosed
US-4245107-A ANTIBIOTICS ASAHI KASEI KOGYO KABUSHIKI KAISHA (JP) 1981-01-13 — — US disclosed
US-4229573-A BACTERICIDES ASAHI KASEI KOGYO KABUSHIKI KAISHA (JP) 1980-10-21 — — US disclosed
US-4172197-A BACTERICIDES ASAHI KASEI KOGYO KABUSHIKI KAISHA (JP) 1979-10-23 — — 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 (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-20150238623-A1 Dendrimers, Conjugates and Methods Thereof PAICS, CD2BP2, CD44 HDAC3 1262/4885HDAC1 2287/4885HDAC2 1962/4885

“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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