SCHEMBL248043

SCHEMBL248043

N#Cc1ccc(Nc2nc(Cl)cc(Cl)n2)cc1

nearest known ligand 0.49

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
PDE4B Q07343 1/20 0.49
PDE4D Q08499 1/20 0.49
SYK P43405 1/20 0.49
CTSK P43235 2/20 0.47
CTSS P25774 1/20 0.47
ABCG2 Q9UNQ0 5/20 0.46
ABCB1 P08183 3/20 0.46
CTSL P07711 1/20 0.46
CTSB P07858 1/20 0.46
KCNH2 Q12809 2/20 0.44
SCN5A Q14524 1/20 0.44
SCN9A Q15858 1/20 0.44
IGF1R P08069 1/20 0.44
CYP2C19 P33261 4/20 0.44
CYP2C9 P11712 3/20 0.44
CYP3A4 P08684 2/20 0.44
ABCC3 O15438 1/20 0.44
ESR1 P03372 1/20 0.44
CYP1A2 P05177 1/20 0.44
PGR P06401 1/20 0.44

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
SCHEMBL13730341 0.89 JAK2 (0.53) PDE4BPDE4DSYKCTSKCTSS
Hydrochloric Acid SCHEMBL14880108 0.88 JAK2 (0.52) PDE4BPDE4DSYKCTSKCTSS
SCHEMBL21914834 0.85 CTSK (0.58) PDE4BPDE4DSYKCTSKCTSS
SCHEMBL1182188 0.84 NFKB1 (0.58) PDE4BPDE4DSYKCTSKCTSS
SCHEMBL13086645 0.82 PDE4B (0.45) PDE4BPDE4DSYKCTSKCTSS
SCHEMBL867999 0.81 KCNH2 (0.58) SYKABCG2KCNH2SCN5ASCN9A
SCHEMBL13851414 0.81 CYP2C19 (0.56) PDE4BPDE4DCTSKCTSSABCG2
SCHEMBL21915358 0.79 CTSK (0.54) SYKCTSKCTSSABCG2ABCB1
SCHEMBL20511301 0.79 TXN (0.63) PDE4BPDE4DSYKCTSKCTSS
SCHEMBL639631 0.79 ABCB1 (0.48) PDE4BPDE4DSYKCTSKCTSS

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-8598341-B2 Process for etravirine intermediate and polymorphs of etravirine HETERO RESEARCH FOUNDATION (IN) 2013-12-03 US claimed
EP-2584901-A1 A PROCESS FOR ETRA VIRINE INTERMEDIATE AND POLYMORPHS OF ETRAVIRINE Hetero Research Foundation (IN) 2013-05-01 EP claimed
US-20130096148-A1 PROCESS FOR ETRAVIRINE INTERMEDIATE AND POLYMORPHS OF ETRAVIRINE HETERO RESEARCH FOUNDATION (IN) 2013-04-18 US claimed
WO-2012001695-A1 A PROCESS FOR ETRA VIRINE INTERMEDIATE AND POLYMORPHS OF ETRAVIRINE HETERO RESEARCH FOUNDATION (IN) 2012-01-05 WO claimed
CN-110407756-B Preparation method of 4- [ (4, 6-dichloro-2-pyrimidinyl) amino ] benzonitrile 江西力田维康科技有限公司 2021-03-09 CN disclosed
CN-110407756-B Preparation method of 4- [ (4, 6-dichloro-2-pyrimidinyl) amino ] benzonitrile 江西力田维康科技有限公司 2021-03-09 CN 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
US-9006243-B2 HIV inhibiting 6-substituted pyrimidines JANSSEN R&D IRELAND (IE) 2015-04-14 US disclosed
US-9006243-B2 HIV inhibiting 6-substituted pyrimidines JANSSEN R&D IRELAND (IE) 2015-04-14 US disclosed
US-8809343-B2 Pyrimidine derivative, preparation method and use thereof FUDAN UNIVERSITY (CN) 2014-08-19 US disclosed
WO-2014068588-A2 PROCESS FOR THE SYNTHESIS OF ETRAVIRINE AND ITS INTERMEDIATES BIOPHORE INDIA PHARMACEUTICALS PVT. LTD. (IN) 2014-05-08 WO disclosed
US-20100121060-A1 HIV INHIBITING 2-(4-CYANOPHENYL)-6-HYDROXYLAMINOPYRIMIDINES JANSSEN SCIENCES IRELAND UC (IE) 2010-05-13 US disclosed
US-20100016317-A1 HIV INHIBITING 6-SUBSTITUTED PYRIMIDINES JANSSEN SCIENCES IRELAND UC (IE) 2010-01-21 US disclosed
US-20100016317-A1 HIV INHIBITING 6-SUBSTITUTED PYRIMIDINES JANSSEN SCIENCES IRELAND UC (IE) 2010-01-21 US disclosed
US-20090124644-A1 HIV INHIBITING 2-(4-CYANOPHENYLAMINO) PYRIMIDINE DERIVATIVES JANSSEN PHARMACEUTICA N.V. (BE) 2009-05-14 US disclosed
US-20080214588-A1 Hiv Inhibiting 2-(4-Cyanophenyl)-6-Hydroxylaminopyrimidines TIBOTEC BVBA (BE) 2008-09-04 US disclosed
WO-2008080964-A1 HIV INHIBITING 6-SUBSTITUTED PYRIMIDINES TIBOTEC PHARMACEUTICALS LTD. (IE) 2008-07-10 WO disclosed
EP-1858861-A1 HIV INHIBITING 2-(4-CYANOPHENYL)-6-HYDROXYLAMINOPYRIMIDINES Tibotec Pharmaceuticals Ltd. (IE) 2007-11-28 EP disclosed
WO-2006094930-A1 HIV INHIBITING 2-(4-CYANOPHENYL)-6-HYDROXYLAMINOPYRIMIDINES TIBOTEC PHARMACEUTICALS LTD. (IE) 2006-09-14 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 (6 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 PDE4B 2438/4885PDE4D 3258/4885SYK 4358/4885
US-20080214588-A1 Hiv Inhibiting 2-(4-Cyanophenyl)-6-Hydroxylaminopyrimidines RTF2, MCM6, SAMHD1 PDE4B 2998/4885PDE4D 3068/4885SYK 4673/4885
US-20100016317-A1 HIV INHIBITING 6-SUBSTITUTED PYRIMIDINES CCR5, CTR9, NR1H3 PDE4B 4442/4885PDE4D 4353/4885SYK 4347/4885
US-20130096148-A1 PROCESS FOR ETRAVIRINE INTERMEDIATE AND POLYMORPHS OF ETRAVIRINE CYP3A4, CYP3A5, CYP4B1 PDE4B 450/4885PDE4D 971/4885SYK 4555/4885
US-20100121060-A1 HIV INHIBITING 2-(4-CYANOPHENYL)-6-HYDROXYLAMINOPYRIMIDINES RTF2, MCM6, CDK6 PDE4B 3018/4885PDE4D 3088/4885SYK 4787/4885
US-20090124644-A1 HIV INHIBITING 2-(4-CYANOPHENYLAMINO) PYRIMIDINE DERIVATIVES NR4A3, NR4A1, NR4A2 PDE4B 1368/4885PDE4D 2146/4885SYK 2773/4885

“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.