SCHEMBL5313640

SCHEMBL5313640

CC(=O)c1ncccc1Br

nearest known ligand 0.45

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
ALDH1A1 P00352 6/20 0.45
KDM4E B2RXH2 5/20 0.44
L3MBTL1 Q9Y468 3/20 0.44
MAPT P10636 2/20 0.44
CYP3A4 P08684 1/20 0.44
ALOX15 P16050 1/20 0.44
TSHR P16473 1/20 0.44
BLM P54132 1/20 0.44
AGER Q15109 1/20 0.44
NPSR1 Q6W5P4 1/20 0.44
TDP1 Q9NUW8 1/20 0.41
TLR7 Q9NYK1 1/20 0.40
MYC P01106 1/20 0.40
CYP1A2 P05177 1/20 0.39
EGLN2 Q96KS0 1/20 0.39
FTO Q9C0B1 1/20 0.39
PDE3B Q13370 1/20 0.39
PDE3A Q14432 1/20 0.39
HCRTR1 O43613 1/20 0.38
HCRTR2 O43614 1/20 0.38

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
SCHEMBL29543454 1.00 ALDH1A1 (0.45) ALDH1A1KDM4EL3MBTL1MAPTCYP3A4
SCHEMBL8866011 0.83 KDM4E (0.47) ALDH1A1KDM4EL3MBTL1MAPTCYP3A4
SCHEMBL398923 0.81 KDM4E (0.61) ALDH1A1KDM4EL3MBTL1MAPTCYP3A4
SCHEMBL720162 0.81 EGLN2 (0.51) ALDH1A1KDM4EL3MBTL1MAPTCYP3A4
SCHEMBL5700012 0.79 KDM4E (0.35) ALDH1A1KDM4EL3MBTL1MAPTCYP3A4
SCHEMBL518833 0.79 KDM4E (0.44) ALDH1A1KDM4EL3MBTL1MAPTCYP3A4
Hydrochloric Acid SCHEMBL27877482 0.79 KDM4E (0.59) ALDH1A1KDM4EL3MBTL1MAPTCYP3A4
SCHEMBL9956653 0.79 KDM4E (0.44) ALDH1A1KDM4EL3MBTL1MAPTCYP3A4
SCHEMBL20406114 0.79 PLK1 (0.45) ALDH1A1KDM4EL3MBTL1MAPTCYP3A4
SCHEMBL28177117 0.79 KDM4E (0.40) ALDH1A1KDM4EL3MBTL1MAPTCYP3A4

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-119613330-A 3-Bromopyridine derivative, continuous synthesis method and application thereof 苏州汉德创宏生化科技有限公司 2025-03-14 CN claimed
CN-110423234-A Thiosemicarbazone derivative of the segment containing indoles and its preparation method and application UNIV ZHENGZHOU 2019-11-08 CN claimed
WO-2026106912-A1 RAS INHIBITORS Revolution Medicines, Inc. (US) 2026-05-21 WO disclosed
US-12630566-B2 KRas G12D inhibitors Mirati Therapeutics, Inc. (US) 2026-05-19 US disclosed
US-12624053-B2 Ras inhibitors Revolution Medicines, Inc. (US) 2026-05-12 US disclosed
US-20260070930-A1 RAS INHIBITORS WILMINGTON TRUST, NATIONAL ASSOCIATION, AS ADMINISTRATIVE AGENT 2026-03-12 US disclosed
EP-4696316-A2 RAS INHIBITORS Revolution Medicines, Inc. (US) 2026-02-18 EP disclosed
EP-4695228-A1 SYNTHESIS OF RAS INHIBITORS Revolution Medicines, Inc. (US) 2026-02-18 EP disclosed
EP-4695233-A2 SYNTHESIS OF RAS INHIBITORS Revolution Medicines, Inc. (US) 2026-02-18 EP disclosed
US-20260042740-A1 RAS INHIBITORS REVOLUTION MEDICINES INC (US) 2026-02-12 US disclosed
EP-4054719-B1 RAS INHIBITORS REVOLUTION MEDICINES INC (US) 2026-02-11 EP disclosed
US-8546442-B2 Pyrazolopiperidine compounds as CCR1 receptor antagonists BOEHRINGER INGELHEIM INTERNATIONAL GMBH (DE) 2013-10-01 US disclosed
US-20120322790-A1 Pyrazolopiperidine Compounds As CCR1 Receptor Antagonists BOEHRINGER INGELHEIM INTERNATIONAL GMBH (DE) 2012-12-20 US disclosed
US-20120322790-A1 Pyrazolopiperidine Compounds As CCR1 Receptor Antagonists BOEHRINGER INGELHEIM INTERNATIONAL GMBH (DE) 2012-12-20 US disclosed
WO-2012087782-A1 PYRAZOLOPIPERIDINE COMPOUNDS AS CCR1 RECEPTOR ANTAGONISTS BOEHRINGER INGELHEIM INTERNATIONAL GMBH (DE) 2012-06-28 WO disclosed
US-7572927-B2 Method of producing an o-disubstituted aromatic compound, and method of producing a monosubstituted-monohaloaromatic compound FUJIFILM CORPORATION (JP) 2009-08-11 US disclosed
US-20080194816-A1 Method of producing an o-disubstituted aromatic compound, and method of producing a monosubstituted-monohaloaromatic compound FUJIFILM CORPORATION (JP) 2008-08-14 US disclosed
WO-2007065939-A1 SUBSTITUTED THIAZOLE DERIVATIVES AND THEIR USES AS TYROSINE KINASE INHIBITORS AB SCIENCE (FR) 2007-06-14 WO disclosed
CN-1297540-C Pyridylethanol (phenylethyl) amine derivatives as cholesterol biosynthesis inhibitors, process for their preparation and pharmaceutical compositions containing them LEK FARMACEVTSKA DRUZBA DD (SI) 2007-01-31 CN disclosed
CN-1284064-A 2,3-substituted indole compounds as cox-2 inhibitors PFIZER PHARMA (US) 2001-02-14 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 (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-20080194816-A1 Method of producing an o-disubstituted aromatic compound, and method of producing a monosubstituted-monohaloaromatic compound DDT, OXER1, OSTC ALDH1A1 1259/4885KDM4E 940/4885L3MBTL1 808/4885
US-20260070930-A1 RAS INHIBITORS KRAS, NRAS, RIN1 ALDH1A1 2609/4885KDM4E 3358/4885L3MBTL1 1851/4885
US-20260042740-A1 RAS INHIBITORS KRAS, NRAS, HRAS ALDH1A1 4551/4885KDM4E 1571/4885L3MBTL1 2146/4885
US-12624053-B2 Ras inhibitors KRAS, NRAS, HMGCR ALDH1A1 3405/4885KDM4E 2746/4885L3MBTL1 2718/4885
US-12630566-B2 KRas G12D inhibitors KRAS, NRAS, HRAS ALDH1A1 1816/4885KDM4E 2825/4885L3MBTL1 3074/4885
US-20120322790-A1 Pyrazolopiperidine Compounds As CCR1 Receptor Antagonists CCR1, CCR3, CCR4 ALDH1A1 719/4885KDM4E 4173/4885L3MBTL1 4332/4885

“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.