SCHEMBL979351

SCHEMBL979351

O=C(O)c1ccc(Cl)cc1Cc1ccccc1

nearest known ligand 0.62

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
HPGD P15428 2/20 0.62
HSD17B10 Q99714 2/20 0.62
MEN1 O00255 2/20 0.62
KMT2A Q03164 2/20 0.62
CYP3A4 P08684 1/20 0.62
ALOX15 P16050 1/20 0.62
HIF1A Q16665 1/20 0.62
PTPN1 P18031 3/20 0.53
PTPN2 P17706 1/20 0.53
PTPN6 P29350 1/20 0.53
TSHR P16473 2/20 0.52
CASP1 P29466 1/20 0.52
SMN1; SMN2 Q16637 1/20 0.52
MRGPRX4 Q96LA9 1/20 0.49
DCLRE1B Q9H816 1/20 0.48
HNF4A P41235 1/20 0.47
ALDH1A1 P00352 2/20 0.47
TP53 P04637 1/20 0.47
NR4A1 P22736 1/20 0.46
PTGER1 P34995 2/20 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
SCHEMBL11464005 0.90 CYP3A4 (0.62) HPGDHSD17B10MEN1KMT2ACYP3A4
SCHEMBL28838076 0.87 MEN1 (0.58) HPGDHSD17B10MEN1KMT2ACYP3A4
SCHEMBL11537482 0.87 CYP3A4 (0.58) HPGDHSD17B10MEN1KMT2ACYP3A4
SCHEMBL6772376 0.82 TSHR (0.69) HSD17B10PTPN1PTPN2PTPN6TSHR
SCHEMBL8961442 0.82 PTPN1 (0.65) PTPN1PTPN2PTPN6TSHRHNF4A
SCHEMBL9440497 0.81 PTPN1 (0.55) MEN1KMT2APTPN1PTPN2PTPN6
SCHEMBL6441850 0.81 PTPN1 (0.62) ALOX15PTPN1PTPN2PTPN6TSHR
SCHEMBL4905340 0.81 TSHR (0.72) HPGDHSD17B10MEN1KMT2ACYP3A4
SCHEMBL310681 0.81 PTPN1 (0.58) MEN1KMT2APTPN1PTPN2PTPN6
SCHEMBL3442800 0.80 MEN1 (0.58) HPGDHSD17B10MEN1KMT2ACYP3A4

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-115646505-B Method for preparing aminomethylbenzoic acid by catalytic oxidation of nano-carrier 天和药业股份有限公司 2023-12-15 CN disclosed
CN-115646505-A Method for preparing aminomethylbenzoic acid by catalytic oxidation of nano-carrier 天和药业股份有限公司 2023-01-31 CN disclosed
US-8063098-B2 GlyT1 receptor antagonists HOFFMANN-LA ROCHE INC. (US) 2011-11-22 US disclosed
US-20110021540-A1 Bis-(Sulfonylamino) Derivatives in Therapy 066 ASTRAZENECA AB (SE) 2011-01-27 US disclosed
CN-101910121-A Bis (sulfonylamino) derivatives 066 in therapy ASTRAZENECA AB 2010-12-08 CN disclosed
EP-2217566-A1 BIS-(SULFONYLAMINO) DERIVATIVES IN THERAPY 066 AstraZeneca AB (SE) 2010-08-18 EP disclosed
US-20100048531-A1 GlyT1 RECEPTOR ANTAGONISTS HOFFMANN-LA ROCHE, INC. 2010-02-25 US disclosed
US-20090281138-A1 Bis-(Sulfonylamino) Derivatives in Therapy 066 ASTRAZENECA AB (SE) 2009-11-12 US disclosed
WO-2009064250-A1 BIS-(SULFONYLAMINO) DERIVATIVES IN THERAPY 065 ASTRAZENECA AB (SE) 2009-05-22 WO disclosed
WO-2009064251-A1 BIS-(SULFONYLAMINO) DERIVATIVES IN THERAPY 066 ASTRAZENECA AB (SE) 2009-05-22 WO disclosed
US-4431823-A SEDATIVES HOFFMANN-LA ROCHE INC. (US) 1984-02-14 US disclosed
US-4428879-A SEDATIVES, TRANQUILIZERS HOFFMANN-LA ROCHE INC. (US) 1984-01-31 US disclosed
US-4428878-A SEDATIVES, TRANQUILIZERS HOFFMANN-LA ROCHE INC. (US) 1984-01-31 US disclosed
EP-0094668-A2 Pyrrole (3,4-d)(2)benzazepine derivatives F. HOFFMANN-LA ROCHE & CO. Aktiengesellschaft (CH) 1983-11-23 EP disclosed
US-4409390-A 3-(2-AMINOETHYL)-4-(2-HYDROXYBENZYL-PHENYL) PYRROLE INTERMEDIATE HOFFMANN-LA ROCHE INC. (US) 1983-10-11 US disclosed
US-4405518-A SEDATIVES HOFFMANN-LA ROCHE INC. (US) 1983-09-20 US disclosed
US-4379765-A SEDATIVES, ANXIETY HOFFMANN-LA ROCHE INC. (US) 1983-04-12 US disclosed
US-4354973-A SEDATIVES AND ANXIOLYTICS HOFFMANN-LA ROCHE INC. (US) 1982-10-19 US disclosed
EP-0045519-A2 Pyrrolo-(3,4-d)-benzapines, process and intermediates for their preparation and pharmaceutical compositions containing them F. HOFFMANN-LA ROCHE & CO. Aktiengesellschaft (CH) 1982-02-10 EP disclosed
EP-0045521-A1 Pyrazolobenzazepines, process for their preparation and pharmaceutical compositions containing them F. HOFFMANN-LA ROCHE & CO. Aktiengesellschaft (CH) 1982-02-10 EP 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-20090281138-A1 Bis-(Sulfonylamino) Derivatives in Therapy 066 CYP2D6, PTGER1, CYP2B6 HPGD 232/4885HSD17B10 709/4885MEN1 2317/4885
US-20100048531-A1 GlyT1 RECEPTOR ANTAGONISTS GLRA1, GLRA2, GRIA1 HPGD 2184/4885HSD17B10 1205/4885MEN1 1701/4885
US-20110021540-A1 Bis-(Sulfonylamino) Derivatives in Therapy 066 CYP2D6, PTGER1, CYP2B6 HPGD 232/4885HSD17B10 709/4885MEN1 2317/4885

“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.