SCHEMBL639631

SCHEMBL639631

N#Cc1ccc(Nc2nc(Cl)c(Br)c(Cl)n2)cc1

nearest known ligand 0.48

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
ABCB1 P08183 3/20 0.48
ABCG2 Q9UNQ0 3/20 0.48
ADORA1 P30542 3/20 0.48
KCNH2 Q12809 2/20 0.48
ABCC3 O15438 1/20 0.48
ESR1 P03372 1/20 0.48
CYP1A2 P05177 1/20 0.48
PGR P06401 1/20 0.48
CHRM2 P08172 1/20 0.48
CYP3A4 P08684 1/20 0.48
ADRA2A P08913 1/20 0.48
CYP2D6 P10635 1/20 0.48
CHRM1 P11229 1/20 0.48
CYP2C9 P11712 1/20 0.48
DRD1 P21728 1/20 0.48
PTGS1 P23219 1/20 0.48
SLC6A2 P23975 1/20 0.48
CYP2C19 P33261 1/20 0.48
ABCC1 P33527 1/20 0.48
OPRM1 P35372 1/20 0.48

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
SCHEMBL14880017 0.91 KCNH2 (0.56) ABCB1ABCG2ADORA1KCNH2ABCC3
SCHEMBL21914834 0.82 CTSK (0.58) ABCB1ABCG2ADORA1KCNH2ABCC3
SCHEMBL1182169 0.81 SYK (0.56) KCNH2CYP1A2CYP2D6CYP2C9CYP2C19
SCHEMBL12158629 0.81 ABCB1 (0.62) ABCB1ABCG2ADORA1KCNH2ABCC3
SCHEMBL1182188 0.81 NFKB1 (0.58) ABCB1ABCG2KCNH2CYP1A2CYP3A4
SCHEMBL1182388 0.81 CYP2C9 (0.53) ABCB1ABCG2ADORA1KCNH2ABCC3
SCHEMBL13681553 0.80 SYK (0.47) ABCB1ABCG2KCNH2SYKCTSK
SCHEMBL1182033 0.80 CYP2C9 (0.47) ABCB1ABCG2ADORA1KCNH2ABCC3
SCHEMBL1182516 0.80 KCNH2 (0.48) ABCB1ABCG2ADORA1KCNH2ABCC3
SCHEMBL248043 0.79 PDE4B (0.49) ABCB1ABCG2ADORA1KCNH2ABCC3

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-8003789-B2 HIV replication inhibiting pyrimidines JANSSEN PHARMACEUTICA, N.V. (BE) 2011-08-23 US claimed
US-20080176880-A1 Activity against strains having acquired resistance nonnucleoside reverse transcriptase inhibitors; human alpha1 acid glycoprotein nonbinding; such as 4-[[(5-bromo-4,6-dichloro)-2-pyrimidinyl]amino]-benzonitrile JANSSEN PHARMACEUTICA, N.V. (BE) 2008-07-24 US claimed
EP-2702045-B1 NOVEL PROCESS FOR THE PREPARATION OF ETRAVIRINE MYLAN LABORATORIES LTD (IN) 2017-10-18 EP disclosed
US-20150336900-A1 Process for the Synthesis of Etravirine and Its Intermediates BIOPHORE INDIA PHARMACEUTICALS PVT. LTD. (IN) 2015-11-26 US disclosed
US-20150336900-A1 Process for the Synthesis of Etravirine and Its Intermediates BIOPHORE INDIA PHARMACEUTICALS PVT. LTD. (IN) 2015-11-26 US disclosed
EP-1282607-B1 PRODRUGS OF HIV REPLICATION INHIBITING PYRIMIDINES JANSSEN PHARMACEUTICA NV (BE) 2015-11-11 EP disclosed
EP-2342186-B1 PROCESS FOR SYNTHESIS OF ETRAVIRINE EMCURE PHARMACEUTICALS LTD (IN) 2014-09-17 EP disclosed
WO-2014068588-A2 PROCESS FOR THE SYNTHESIS OF ETRAVIRINE AND ITS INTERMEDIATES BIOPHORE INDIA PHARMACEUTICALS PVT. LTD. (IN) 2014-05-08 WO disclosed
EP-2702045-A1 NOVEL PROCESS FOR THE PREPARATION OF ETRAVIRINE Mylan Laboratories, Limited (IN) 2014-03-05 EP disclosed
US-8653266-B2 Process for the production of etravirine MYLAN LABORATORIES LIMITED (IN) 2014-02-18 US disclosed
US-8530655-B2 HIV replication inhibiting pyrimidines JANSSEN PHARMACEUTICA NV (BE) 2013-09-10 US disclosed
US-20040039005-A1 Nitrogen compounds such as 4-((4-amino-5-bromo-6-(4-cyano-2,6-dimethylphenyloxy)-2 -pyrimidinyl)amino)benzonitrile, used as protease inhibitors for prophylaxis of viral diseases JANSSEN PHARMACEUTICA N.V. (BE) 2004-02-26 US disclosed
US-20030186990-A1 Prodrugs of hiv replication inhibiting pyrimidines JANSSEN PHARMACEUTICA, INC. 2003-10-02 US disclosed
US-20030114472-A1 Viricides JANSSEN PHARMACEUTICA, N.V. (BE) 2003-06-19 US disclosed
EP-1002795-B1 HIV Replication inhibiting pyrimidines JANSSEN PHARMACEUTICA NV (BE) 2003-03-05 EP disclosed
EP-1270560-A1 Hiv replication inhibiting pyrimidines JANSSEN PHARMACEUTICA N.V. (BE) 2003-01-02 EP disclosed
EP-1225874-A1 ANTIVIRAL COMPOSITIONS Janssen Pharmaceutica N.V. (BE) 2002-07-31 EP disclosed
WO-2001022938-A1 ANTIVIRAL COMPOSITIONS JANSSEN PHARMACEUTICA N.V. (BE) 2001-04-05 WO disclosed
EP-1002795-A1 HIV Replication inhibiting pyrimidines JANSSEN PHARMACEUTICA N.V. (BE) 2000-05-24 EP disclosed
WO-2000027825-A1 HIV REPLICATION INHIBITING PYRIMIDINES JANSSEN PHARMACEUTICA N.V. (BE) 2000-05-18 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 (5 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-20150336900-A1 Process for the Synthesis of Etravirine and Its Intermediates CYP3A4, CYP3A5, ERN1 ABCB1 331/4885ABCG2 1685/4885ADORA1 910/4885
US-20080176880-A1 Activity against strains having acquired resistance nonnucleoside reverse transcriptase inhibitors; human alpha1 acid glycoprotein nonbinding; such as 4-[[(5-bromo-4,6-dichloro)-2-pyrimidinyl]amino]-benzonitrile ABCC1, MGAT1, RRM2 ABCB1 35/4885ABCG2 85/4885ADORA1 131/4885
US-20030114472-A1 Viricides ZC3HAV1, ZC3HAV1L, POLR2H ABCB1 3198/4885ABCG2 2799/4885ADORA1 1551/4885
US-20030186990-A1 Prodrugs of hiv replication inhibiting pyrimidines CYP2S1, REV1, CYP1B1 ABCB1 530/4885ABCG2 1179/4885ADORA1 42/4885
US-20040039005-A1 Nitrogen compounds such as 4-((4-amino-5-bromo-6-(4-cyano-2,6-dimethylphenyloxy)-2 -pyrimidinyl)amino)benzonitrile, used as protease inhibitors for prophylaxis of viral diseases CPN1, CTRL, HPN ABCB1 2537/4885ABCG2 3070/4885ADORA1 2520/4885

“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.