Cgc-11047

Cgc-11047

SCHEMBL427907

CCNCCCNCC=CCNCCCNCC.Cl.Cl.Cl.Cl

nearest known ligand 1.00 ✓ in ChEMBL — recovers established targets

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 Cgc-11047. The predicted profile below is derived independently by chemical similarity — agreement is a validation signal, a miss is honest.

Predicted protein targets (top 12)

geneUniProtsupporting neighboursconfidence
GLA known ✓ P06280 1/20 0.60
KDM1A O60341 5/20 1.00
CYP2C19 P33261 2/20 0.60
MEN1 O00255 1/20 0.60
KMT2A Q03164 1/20 0.60
CYP1A2 P05177 1/20 0.57
TSHR P16473 2/20 0.50
SAT1 P21673 3/20 0.44
SMOX Q9NWM0 1/20 0.36
TP53 P04637 1/20 0.35
ALDH1A1 P00352 1/20 0.33
PAOX Q6QHF9 2/20 0.32

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
Cgc-11047 SCHEMBL2359065 1.00 KDM1A (1.00) KDM1ACYP2C19MEN1GLAKMT2A
Cgc-11047 SCHEMBL427906 1.00 KDM1A (1.00) KDM1ACYP2C19MEN1GLAKMT2A
Cgc-11047 SCHEMBL2360444 0.97 KDM1A (1.00) KDM1ACYP2C19MEN1GLAKMT2A
Cgc-11047 SCHEMBL2359734 0.97 KDM1A (1.00) KDM1ACYP2C19MEN1GLAKMT2A
Cgc-11047 SCHEMBL2359741 0.97 KDM1A (1.00) KDM1ACYP2C19MEN1GLAKMT2A
Cgc-11047 SCHEMBL8640381 0.95 KDM1A (0.95) KDM1ACYP2C19MEN1GLAKMT2A
Cgc-11047 SCHEMBL8640375 0.95 KDM1A (0.95) KDM1ACYP2C19MEN1GLAKMT2A
SCHEMBL12085577 0.92 KDM1A (0.95) KDM1ACYP2C19MEN1GLAKMT2A
SCHEMBL13097481 0.92 KDM1A (0.95) KDM1ACYP2C19MEN1GLAKMT2A
Hydrochloric Acid SCHEMBL8639045 0.91 KDM1A (0.83) KDM1ACYP2C19MEN1GLAKMT2A

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-1937235-A2 METHODS FOR TREATING VIRAL INFECTIONS USING POLYAMINE ANALOGS Pathologica, LLC. (US) 2008-07-02 EP claimed
WO-2007035957-A2 METHODS FOR TREATING VIRAL INFECTIONS USING POLYAMINE ANALOGS PATHOLOGICA, LLC. (US) 2007-03-29 WO claimed
US-20050159493-A1 Methods for modulating macrophage proliferation using polyamine analogs THE REGENTS OF THE UNIVERSITY OF CALIFORNIA 2005-07-21 US claimed
JP-2001520990-A 2001-11-06 JP claimed
EP-1027040-A2 METHODS FOR MODULATING MACROPHAGE PROLIFERATION USING POLYAMINE ANALOGS The Regents of the University of California (US) 2000-08-16 EP claimed
WO-1999021542-A2 METHODS FOR MODULATING MACROPHAGE PROLIFERATION USING POLYAMINE ANALOGS THE REGENTS OF THE UNIVERSITY OF CALIFORNIA (US) 1999-05-06 WO claimed
EP-3228310-A1 METHYLGLYOXAL BIS(GUANYL-HYDRAZONE) FOR REGULATING OSTEOPONTIN IN A SUBJECT Pathologica LLC (US) 2017-10-11 EP disclosed
EP-2121586-B1 MGBG FOR THE REGULATION OF OSTEOPONTIN AND THE TREATMENT OF MULTIPLE SCLEROSIS PATHOLOGICA LLC (US) 2017-03-08 EP disclosed
EP-1937235-B1 METHODS FOR TREATING VIRAL INFECTIONS USING POLYAMINE ANALOGS PATHOLOGICA LLC (US) 2015-07-01 EP disclosed
US-20130102556-A1 Use of N1,N4-bis[3-(Ethylamino)Propyl]-2-Butene-1,4-Diamine Compounds in Combination with Epigenetic-Acting Pharmaceuticals for Enhanced Cancer Therapy THE JOHNS HOPKINS UNIVERSITY (US) 2013-04-25 US disclosed
US-20120219970-A1 METHODS FOR MODULATING MACROPHAGE PROLIFERATION IN OCULAR DISEASE USING POLYAMINE ANALOGS PATHOLOGICA LLC (US) 2012-08-30 US disclosed
US-8198334-B2 Vitreoretinopathy, diabetic retinopathy, nonexudative age related macular degeneration; small molecule amines PATHOLOGICA LLC (US) 2012-06-12 US disclosed
US-20120022166-A1 Methods for Modulating Macrophage Proliferation Using Polyamine Analogs THE REGENTS OF THE UNIVERSITY OF CALIFORNIA 2012-01-26 US disclosed
EP-0934249-A1 CONFORMATIONALLY RESTRICTED POLYAMINES AND THEIR USE AS ANTINEOPLASTIC AGENTS WISCONSIN ALUMNI RESEARCH FOUNDATION (US) 1999-08-11 EP disclosed
US-5889061-A ANTICANCER, ANTITUMOR AGENTS WISCONSIN ALUMNI RESEARCH FOUNDATION (US) 1999-03-30 US disclosed
EP-0686143-B1 UNSATURATE AMINO COMPOUNDS FOR USE AS ANTICANCER AND ANTIPROTOZOIC AGENT CIBA GEIGY AG (CH) 1998-08-12 EP disclosed
WO-1998017624-A1 CONFORMATIONALLY RESTRICTED POLYAMINES AND THEIR USE AS ANTINEOPLASTIC AGENTS WISCONSIN ALUMNI RESEARCH FOUNDATION (US) 1998-04-30 WO disclosed
US-5627215-A Unsaturate amino compounds for use as anticancer and antiprotozoic agent CIBA-GEIGY CORPORATION (US) 1997-05-06 US disclosed
EP-0686143-A1 UNSATURATE AMINO COMPOUNDS FOR USE AS ANTICANCER AND ANTIPROTOZOIC AGENT Novartis AG (CH) 1995-12-13 EP disclosed
WO-1995018091-A1 UNSATURATE AMINO COMPOUNDS FOR USE AS ANTICANCER AND ANTIPROTOZOIC AGENT CIBA-GEIGY AG (CH) 1995-07-06 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 (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-20130102556-A1 Use of N1,N4-bis[3-(Ethylamino)Propyl]-2-Butene-1,4-Diamine Compounds in Combination with Epigenetic-Acting Pharmaceuticals for Enhanced Cancer Therapy DNMT1, DNMT3L, TET1 GLA 2599/4885KDM1A 38/4885CYP2C19 3651/4885
US-20120022166-A1 Methods for Modulating Macrophage Proliferation Using Polyamine Analogs ARG1, MKI67, CSF1R GLA 833/4885KDM1A 259/4885CYP2C19 4826/4885
US-20050159493-A1 Methods for modulating macrophage proliferation using polyamine analogs ARG1, MKI67, CSF1R GLA 833/4885KDM1A 259/4885CYP2C19 4826/4885

“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.