SCHEMBL244194

SCHEMBL244194

N#Cc1cc(N)n(-c2ccccc2)n1

nearest known ligand 0.56

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
▸ MAPK1 P28482 2/20 0.56
▸ CYP1A2 P05177 2/20 0.56
▸ CYP2C19 P33261 2/20 0.56
▸ SMN1; SMN2 Q16637 9/20 0.50
▸ RAB9A P51151 9/20 0.50
▸ ALDH1A1 P00352 6/20 0.50
▸ MEN1 O00255 2/20 0.50
▸ KMT2A Q03164 2/20 0.50
▸ TSHR P16473 1/20 0.50
▸ GFER P55789 1/20 0.50
▸ NPC1 O15118 7/20 0.47
▸ MAPT P10636 4/20 0.47
▸ KDM4E B2RXH2 3/20 0.47
▸ PKM P14618 2/20 0.47
▸ LMNA P02545 2/20 0.47
▸ STAT1 P42224 1/20 0.47
▸ TP53 P04637 1/20 0.47
▸ PTGS1 P23219 1/20 0.46
▸ HPGD P15428 2/20 0.46
▸ ALOX15 P16050 1/20 0.46

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
SCHEMBL28425661 0.86 CYP1A2 (0.47) MAPK1CYP1A2CYP2C19SMN1; SMN2RAB9A
SCHEMBL29083293 0.84 XDH (0.42) MAPK1CYP1A2CYP2C19SMN1; SMN2RAB9A
SCHEMBL28395393 0.83 MAPT (0.57) MAPK1CYP1A2CYP2C19SMN1; SMN2RAB9A
SCHEMBL28284102 0.83 LMNA (0.41) MAPK1CYP1A2CYP2C19SMN1; SMN2RAB9A
SCHEMBL28226658 0.83 PTGS2 (0.54) CYP1A2CYP2C19SMN1; SMN2RAB9AALDH1A1
SCHEMBL28226595 0.82 ALDH1A1 (0.42) MAPK1CYP1A2CYP2C19RAB9AALDH1A1
SCHEMBL28227459 0.82 ALDH1A1 (0.42) MAPK1CYP1A2CYP2C19SMN1; SMN2RAB9A
SCHEMBL537294 0.81 KDM4E (0.49) MAPK1CYP1A2CYP2C19RAB9AALDH1A1
SCHEMBL28400665 0.80 LMNA (0.65) SMN1; SMN2RAB9AALDH1A1MEN1KMT2A
SCHEMBL28227470 0.80 LOXL2 (0.42) MAPK1CYP1A2CYP2C19SMN1; SMN2RAB9A

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-115304607-B Pyrazolopyrimidine derivative and process for preparing same 华南农业大学 2023-06-27 — — CN disclosed
CN-115304607-A Process for preparing pyrazolopyrimidine derivatives 华南农业大学 2022-11-08 — — CN disclosed
CN-108203450-B Preparation method and application of amino phosphonate containing arylpyrazole compound 南京工业大学 2020-05-19 — — CN disclosed
CN-109575006-A A kind of diazole pyrazole amide analog derivative and its microwave attenuation materials method and application 中南民族大学 2019-04-05 — — CN disclosed
US-20170197939-A1 Tropomyosin-Related Kinase Inhibitors Containing Both A 1H-Pyrazole And A Pyrimidine Moiety PFIZER INC. (US) 2017-07-13 — — US disclosed
US-20170197939-A1 Tropomyosin-Related Kinase Inhibitors Containing Both A 1H-Pyrazole And A Pyrimidine Moiety PFIZER INC. (US) 2017-07-13 — — US disclosed
US-20170197939-A1 Tropomyosin-Related Kinase Inhibitors Containing Both A 1H-Pyrazole And A Pyrimidine Moiety PFIZER INC. (US) 2017-07-13 — — US disclosed
EP-3140298-A1 TROPOMYOSIN-RELATED KINASE INHIBITORS Pfizer Inc. (US) 2017-03-15 — — EP disclosed
EP-3131891-A1 TROPOMYOSIN-RELATED KINASE INHIBITORS CONTAINING BOTH A 1H-PYRAZOLE AND A PYRIMIDINE MOIETY Pfizer Inc. (US) 2017-02-22 — — EP disclosed
US-9328096-B2 Tropomyosin-related kinase inhibitors PFIZER INC. (US) 2016-05-03 — — US disclosed
US-20150322043-A1 TROPOMYOSIN-RELATED KINASE INHIBITORS PFIZER (US) 2015-11-12 — — US disclosed
US-20150322043-A1 TROPOMYOSIN-RELATED KINASE INHIBITORS PFIZER (US) 2015-11-12 — — US disclosed
WO-2015159175-A1 TROPOMYOSIN-RELATED KINASE INHIBITORS CONTAINING BOTH A 1H-PYRAZOLE AND A PYRIMIDINE MOIETY PFIZER INC. (US) 2015-10-22 — — WO disclosed
WO-2015159175-A1 TROPOMYOSIN-RELATED KINASE INHIBITORS CONTAINING BOTH A 1H-PYRAZOLE AND A PYRIMIDINE MOIETY PFIZER INC. (US) 2015-10-22 — — WO disclosed
EP-2443093-B1 PROCESS FOR THE PREPARATION OF PYRAZOLE DERIVATIVES BASF SE (DE) 2013-07-03 — — EP disclosed
US-8288563-B2 Process for the preparation of pyrazole derivatives BASF SE (DE) 2012-10-16 — — US disclosed
EP-2443093-A1 PROCESS FOR THE PREPARATION OF PYRAZOLE DERIVATIVES BASF SE (DE) 2012-04-25 — — EP disclosed
US-20120004421-A1 Process for the preparation of pyrazole derivatives BASF SE (DE) 2012-01-05 — — US disclosed
WO-2010105969-A1 PROCESS FOR THE PREPARATION OF PYRAZOLE DERIVATIVES BASF SE (DE) 2010-09-23 — — WO disclosed
CN-101675051-A Pyrazolopyrimidine analogs and their use as mtor kinase and pi3 kinase inhibitors WYETH CORP 2010-03-17 — — CN 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-20150322043-A1 TROPOMYOSIN-RELATED KINASE INHIBITORS TPM3, MUSK, TPM4 MAPK1 379/4885CYP1A2 3621/4885CYP2C19 4074/4885
US-20120004421-A1 Process for the preparation of pyrazole derivatives CBR3, CBR1, C1S MAPK1 782/4885CYP1A2 130/4885CYP2C19 251/4885
US-20170197939-A1 Tropomyosin-Related Kinase Inhibitors Containing Both A 1H-Pyrazole And A Pyrimidine Moiety TPM3, MUSK, TPM4 MAPK1 158/4885CYP1A2 2252/4885CYP2C19 2361/4885

“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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