SCHEMBL9939276

SCHEMBL9939276

O=C(O)c1ccc(Cl)cc1B(O)O

nearest known ligand 0.59

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
SMN1; SMN2 Q16637 2/20 0.59
TSHR P16473 2/20 0.59
CASP1 P29466 1/20 0.59
ALDH1A1 P00352 5/20 0.53
TP53 P04637 1/20 0.53
CA1 P00915 1/20 0.52
CA2 P00918 1/20 0.52
MYC P01106 2/20 0.50
F7 P08709 1/20 0.49
F3 P13726 1/20 0.49
KDM4E B2RXH2 4/20 0.47
MEN1 O00255 1/20 0.47
KMT2A Q03164 1/20 0.47
HSD17B10 Q99714 2/20 0.47
SRD5A2 P31213 1/20 0.47
NR4A1 P22736 1/20 0.46
ALOX15 P16050 1/20 0.45
GRIK1 P39086 2/20 0.44
RAB9A P51151 1/20 0.43
PTGES O14684 1/20 0.42

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
SCHEMBL9937971 0.86 ALDH1A1 (0.61) SMN1; SMN2TSHRCASP1ALDH1A1TP53
SCHEMBL13750063 0.84 TSHR (0.44) SMN1; SMN2TSHRCASP1ALDH1A1TP53
SCHEMBL29952852 0.82 KDM4E (0.51) SMN1; SMN2TSHRCASP1ALDH1A1KDM4E
SCHEMBL16971638 0.79 ABL1 (0.62) SMN1; SMN2CASP1ALDH1A1CA1CA2
SCHEMBL28674119 0.79 KDM4E (0.50) SMN1; SMN2TSHRALDH1A1TP53CA1
SCHEMBL2065197 0.78 CSNK2A1 (0.53) SMN1; SMN2ALDH1A1CA1CA2MYC
SCHEMBL1000440 0.76 ALDH1A1 (0.71) SMN1; SMN2TSHRCASP1ALDH1A1TP53
SCHEMBL9938748 0.76 KEAP1 (0.50) TSHRALDH1A1CA1CA2KDM4E
SCHEMBL12590922 0.75 ALDH1A1 (0.53) SMN1; SMN2TSHRALDH1A1MEN1KMT2A
SCHEMBL29950984 0.75 GABRA1 (0.43) SMN1; SMN2TSHRCASP1ALDH1A1KDM4E

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20250276007-A1 CARBAMOYLPHENYLBORONIC ACID-CONTAINING ACRYLIC MONOMERS AND USES THEREOF ALCON INC (CH) 2025-09-04 US disclosed
US-20250277076-A1 MUCOADHESIVE HYDROPHILIC COPOLYMERS AND USES THEREOF ALCON INC (CH) 2025-09-04 US disclosed
US-12398120-B2 Substituted hydantoinamides as ADAMTS7 antagonists BAYER AKTIENGESELLSCHAFT (DE) 2025-08-26 US disclosed
EP-4058448-B1 HYDANTOIN DERIVATIVES AS ADAMTS7 ANTAGONISTS FOR THE TREATMENT OF CARDIOVASCULAR DISEASES BAYER AG (DE) 2024-05-29 EP disclosed
US-20230027346-A1 SUBSTITUTED HYDANTOINAMIDES AS ADAMTS7 ANTAGONISTS BAYER AKTIENGESELLSCHAFT (DE) 2023-01-26 US disclosed
US-20220340893-A1 BI-FUNCTIONAL COMPLEXES AND METHODS FOR MAKING AND USING SUCH COMPLEXES NUEVOLUTION A/S (DK) 2022-10-27 US disclosed
EP-4058448-A1 SUBSTITUTED HYDANTOINAMIDES AS ADAMTS7 ANTAGONISTS Bayer Aktiengesellschaft (DE) 2022-09-21 EP disclosed
WO-2021094436-A1 SUBSTITUTED HYDANTOINAMIDES AS ADAMTS7 ANTAGONISTS BAYER AKTIENGESELLSCHAFT (DE) 2021-05-20 WO disclosed
EP-3822268-A1 SUBSTITUTED HYDANTOINAMIDES AS ADAMTS7 ANTAGONISTS Bayer Aktiengesellschaft (DE) 2021-05-19 EP disclosed
EP-2651917-A1 DIMERIC IAP INHIBITORS Novartis AG (CH) 2013-10-23 EP disclosed
US-20130266590-A1 DIMERIC IAP INHIBITORS NOVARTIS AG (CH) 2013-10-10 US disclosed
EP-2582680-A1 BIPHENYL SUBSTITUTED 1,3-DIHYDRO-BENZOIMIDAZOL-2-YLIDENEAMINE DERIVATIVES Novartis AG (CH) 2013-04-24 EP disclosed
US-20130090342-A1 BIPHENYL SUBSTITUTED 1,3-DIHYDRO-BENZOIMIDAZOL-2-YLIDENEAMINE DERIVATIVES NOVARTIS AG (CH) 2013-04-11 US disclosed
CN-102947274-A Biphenyl substituted 1, 3-dihydro-benzoimidazol-2-ylideneamine derivatives NOVARTIS AG 2013-02-27 CN disclosed
WO-2012080260-A1 DIMERIC IAP INHIBITORS NOVARTIS AG (CH) 2012-06-21 WO disclosed
WO-2011157787-A1 BIPHENYL SUBSTITUTED 1,3-DIHYDRO-BENZOIMIDAZOL-2-YLIDENEAMINE DERIVATIVES NOVARTIS AG (CH) 2011-12-22 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-20250276007-A1 CARBAMOYLPHENYLBORONIC ACID-CONTAINING ACRYLIC MONOMERS AND USES THEREOF ADCY6, ADCY1, ADCY7 SMN1; SMN2 4467/4885TSHR 2199/4885CASP1 3690/4885
US-20130266590-A1 DIMERIC IAP INHIBITORS XIAP, BIRC5, BIRC2 SMN1; SMN2 1323/4885TSHR 4621/4885CASP1 35/4885
US-20130090342-A1 BIPHENYL SUBSTITUTED 1,3-DIHYDRO-BENZOIMIDAZOL-2-YLIDENEAMINE DERIVATIVES IGF1R, IGFBP1, IGFBP2 SMN1; SMN2 552/4885TSHR 100/4885CASP1 1869/4885
US-12398120-B2 Substituted hydantoinamides as ADAMTS7 antagonists ADAMTS7, MMP7, ADAM17 SMN1; SMN2 3850/4885TSHR 1345/4885CASP1 840/4885
US-20250277076-A1 MUCOADHESIVE HYDROPHILIC COPOLYMERS AND USES THEREOF MUC1, TAS2R42, TAS2R41 SMN1; SMN2 4382/4885TSHR 921/4885CASP1 3000/4885
US-20230027346-A1 SUBSTITUTED HYDANTOINAMIDES AS ADAMTS7 ANTAGONISTS ADAMTS7, MMP7, ADAM17 SMN1; SMN2 3850/4885TSHR 1345/4885CASP1 840/4885

“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.