SCHEMBL6175355

SCHEMBL6175355

COc1ccc(N)c(OCc2ccccc2)n1

nearest known ligand 0.46

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
L3MBTL1 Q9Y468 2/20 0.46
ALDH1A1 P00352 3/20 0.45
MGMT P16455 4/20 0.44
CDK1 P06493 2/20 0.44
CCNB1 P14635 2/20 0.44
CCNA2 P20248 2/20 0.44
CDK2 P24941 2/20 0.44
CCNA1 P78396 2/20 0.44
NUDT1 P36639 1/20 0.43
ATP4A P20648 1/20 0.43
ATP4B P51164 1/20 0.43
LMNA P02545 3/20 0.43
TSHR P16473 3/20 0.43
CYP3A4 P08684 2/20 0.43
MPO P05164 1/20 0.43
TPO P07202 1/20 0.43
EPX P11678 1/20 0.43
CYP1A2 P05177 1/20 0.43
CYP2D6 P10635 1/20 0.43
CYP2C9 P11712 1/20 0.43

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
SCHEMBL30271317 1.00 L3MBTL1 (0.46) L3MBTL1ALDH1A1MGMTCDK1CCNB1
SCHEMBL30026947 0.89 MGMT (0.48) L3MBTL1MGMTCDK1CCNB1CCNA2
SCHEMBL20595507 0.89 MGMT (0.48) L3MBTL1MGMTCDK1CCNB1CCNA2
Hydrochloric Acid SCHEMBL25369331 0.87 MGMT (0.47) L3MBTL1MGMTCDK1CCNB1CCNA2
SCHEMBL26329102 0.80 CYP1A2 (0.46) L3MBTL1ALDH1A1NUDT1LMNATSHR
SCHEMBL26089894 0.76 MCL1 (0.40) L3MBTL1ALDH1A1MGMTCDK1CCNB1
SCHEMBL31375611 0.76 MAOB (0.53) L3MBTL1ALDH1A1NUDT1LMNATSHR
SCHEMBL17459263 0.76 MAOB (0.53) L3MBTL1ALDH1A1NUDT1LMNATSHR
SCHEMBL4651410 0.76 LMNA (0.47) L3MBTL1ALDH1A1MGMTCDK1CCNB1
SCHEMBL6175892 0.76 PIN1 (0.59) MGMTPIN1MAPTRAB9AMAPK1

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 10 patents. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20250034110-A1 LPAR1 ANTAGONISTS AND USES THEREOF Pipeline Therapeutics, Inc. 2025-01-30 US disclosed
CN-118043041-A LPAR1 antagonists and uses thereof 康蒂内乌姆医疗公司 2024-05-14 CN disclosed
WO-2023014908-A1 LPAR1 ANTAGONISTS AND USES THEREOF Pipeline Therapeutics, Inc. (US) 2023-02-09 WO disclosed
US-20100160346-A1 NEUROLOGICALLY ACTIVE COMPOUNDS PRANA BIOTECHNOLOGY LIMITED (AU) 2010-06-24 US disclosed
US-7692011-B2 8-hydroxy and 8-mercapto quinazolinones PRANA BIOTECHNOLOGY LIMITED (AU) 2010-04-06 US disclosed
EP-1392280-A4 ARYLSULFONAMIDE ETHERS, AND METHODS OF USE THEREOF WARNER LAMBERT CO (US) 2005-11-30 EP disclosed
US-6875765-B2 Arylsulfonamide ethers, and methods of use thereof WARNER-LAMBERT COMPANY (US) 2005-04-05 US disclosed
EP-1392280-A2 ARYLSULFONAMIDE ETHERS, AND METHODS OF USE THEREOF Abbott GmbH & Co. KG (DE) 2004-03-03 EP disclosed
US-20030096826-A1 Arylsulfonamide ethers, and methods of use thereof WARNER-LAMBERT COMPANY 2003-05-22 US disclosed
WO-2002089749-A2 ARYLSULFONAMIDE ETHERS, AND METHODS OF USE THEREOF ABBOTT GMBH & CO.KG (DE) 2002-11-14 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 (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-20030096826-A1 Arylsulfonamide ethers, and methods of use thereof CASP1, IRAK1, STS L3MBTL1 2397/4885ALDH1A1 1294/4885MGMT 1122/4885
US-20250034110-A1 LPAR1 ANTAGONISTS AND USES THEREOF LPAR1, LPAR2, LPAR3 L3MBTL1 980/4885ALDH1A1 1523/4885MGMT 4876/4885
US-20100160346-A1 NEUROLOGICALLY ACTIVE COMPOUNDS ACHE, PSEN1, PSEN2 L3MBTL1 2272/4885ALDH1A1 703/4885MGMT 3640/4885

“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.