SCHEMBL1551571

SCHEMBL1551571

CN1CCN(c2ccc3[nH]c(-c4ccc(N)c(N)c4)nc3c2)CC1

nearest known ligand 0.58

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
ALDH1A1 P00352 5/20 0.58
SMN1; SMN2 Q16637 4/20 0.58
TOP1 P11387 3/20 0.58
TOP2A P11388 3/20 0.58
HPGD P15428 1/20 0.58
HSD17B10 Q99714 1/20 0.58
TERT O14746 4/20 0.55
MAPT P10636 4/20 0.53
MEN1 O00255 2/20 0.53
BLM P54132 2/20 0.53
KMT2A Q03164 2/20 0.53
RECQL P46063 2/20 0.53
SLCO2B1 O94956 1/20 0.53
GLA P06280 1/20 0.53
BCL2L1 Q07817 1/20 0.53
SLCO1B3 Q9NPD5 1/20 0.53
TDP1 Q9NUW8 1/20 0.53
SLCO1B1 Q9Y6L6 1/20 0.53
KDM4E B2RXH2 4/20 0.53
NPC1 O15118 1/20 0.53

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
SCHEMBL14669385 0.99 ALDH1A1 (0.57) ALDH1A1SMN1; SMN2TOP1TOP2AHPGD
SCHEMBL14892811 0.96 ALDH1A1 (0.54) ALDH1A1SMN1; SMN2TOP1TOP2AHPGD
SCHEMBL13528291 0.91 SMN1; SMN2 (0.57) ALDH1A1SMN1; SMN2TOP1TOP2AHPGD
SCHEMBL933054 0.91 ALDH1A1 (0.71) ALDH1A1SMN1; SMN2TOP1TOP2AHPGD
SCHEMBL14892248 0.87 ALDH1A1 (0.45) ALDH1A1SMN1; SMN2TOP1TOP2AHPGD
SCHEMBL6530109 0.86 ALDH1A1 (0.59) ALDH1A1SMN1; SMN2TOP1TOP2AHPGD
SCHEMBL14892180 0.86 TERT (0.54) ALDH1A1SMN1; SMN2TOP1TOP2AHPGD
SCHEMBL14665724 0.86 TERT (0.49) ALDH1A1SMN1; SMN2TOP1TOP2AHPGD
SCHEMBL2554887 0.86 LGMN (0.48) ALDH1A1SMN1; SMN2TOP1TOP2AHPGD
SCHEMBL14669422 0.86 PARP1 (0.44) ALDH1A1SMN1; SMN2TOP1TOP2AHPGD

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-1590332-B1 A PROCESS FOR THE SYNTHESIS OF BISBENZIMIDAZOLES AND THEIR DERIVATIVES. UNIV DELHI (IN) 2011-04-27 EP claimed
US-20210324198-A1 SILICON-SUBSTITUTED RHODAMINE DYES AND DYE CONJUGATES Life Technologies Corporation 2021-10-21 US disclosed
CN-106866635-B PLK1 inhibitor and preparation method and application thereof 深圳先进技术研究院 2020-06-05 CN disclosed
CN-106674209-B Programmed death receptor 1 gene inhibitor and preparation method and application thereof 深圳先进技术研究院 2020-03-06 CN disclosed
WO-2020033681-A2 SILICON-SUBSTITUTED RHODAMINE DYES AND DYE CONJUGATES Life Technologies Corporation (US) 2020-02-13 WO disclosed
US-RE46943-E1 Radioprotector compounds and methods PETER MACCALLUM CANCER INSTITUTE (AU) 2018-07-10 US disclosed
US-RE46943-E1 Radioprotector compounds and methods PETER MACCALLUM CANCER INSTITUTE (AU) 2018-07-10 US disclosed
US-RE46943-E1 Radioprotector compounds and methods PETER MACCALLUM CANCER INSTITUTE (AU) 2018-07-10 US disclosed
EP-2591795-B1 RNA targeting compounds and methods for making and using same UNIV NEW YORK STATE RES FOUND (US) 2018-02-28 EP disclosed
EP-2556058-B1 RADIOPROTECTOR COMPOUNDS AND METHODS PETER MACCALLUM CANCER INST (AU) 2017-06-14 EP disclosed
EP-2129388-B1 RNA TARGETING COMPOUNDS AND METHODS FOR MAKING AND USING SAME UNIV NEW YORK STATE RES FOUND 2012-09-12 EP disclosed
EP-1590332-B1 A PROCESS FOR THE SYNTHESIS OF BISBENZIMIDAZOLES AND THEIR DERIVATIVES. UNIV DELHI (IN) 2011-04-27 EP disclosed
EP-1590332-B1 A PROCESS FOR THE SYNTHESIS OF BISBENZIMIDAZOLES AND THEIR DERIVATIVES. UNIV DELHI (IN) 2011-04-27 EP disclosed
US-20080227213-A1 Comprising polymer backbone and two or more pendant RNA binding ligands; myotonic dystrophy RESEARCH FOUNDATION OF STATE UNIVERSITY OF NEW YORK, THE 2008-09-18 US disclosed
WO-2007045096-A1 OLIGOHETEROAROMATIC LUMINISCENT ASSEMBLIES AS HIGH-AFFINITY DNA SEQUENCE-DIRECTED LIGANDS UNIVERSITY OF SASKATCHEWAN (CA) 2007-04-26 WO disclosed
WO-2007016455-A2 COMPOSITIONS AND METHODS USING AMINOGLYCOSIDES TO BIND DNA AND RNA CLEMSON UNIVERSITY RESEARCH FOUNDATION (US) 2007-02-08 WO disclosed
EP-1590332-A1 A PROCESS FOR THE SYNTHESIS OF BISBENZIMIDAZOLES AND ITS DERIVATIONS University of Delhi (IN) 2005-11-02 EP disclosed
WO-2004063170-A1 A PROCESS FOR THE SYNTHESIS OF BISBENZIMIDAZOLES AND ITS DERIVATIONS UNIVERSITY OF DELHI (IN) 2004-07-29 WO disclosed
US-6548505-B1 Protecting biological materials from damage caused by radiation; side effect reduction during radiotherapy or chemotherapy; indole, benzimidazole, benzoxazole or benzothiazole compounds substituted with 4-alkylpiperazino PETER MACCALLUM CANCER INSTITUTE (AU) 2003-04-15 US disclosed
US-6194414-B1 CANCER THERAPY; PREVENT RADIATION DAMAGE THE INNER AND EASTERN HEALTH CARE NETWORK (AU) 2001-02-27 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-20210324198-A1 SILICON-SUBSTITUTED RHODAMINE DYES AND DYE CONJUGATES SRI, SI, IK ALDH1A1 1849/4885SMN1; SMN2 2012/4885TOP1 1255/4885

“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.