SCHEMBL5809100

SCHEMBL5809100

CC1Cc2cc(Br)ccc2O1

nearest known ligand 0.60

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
PBRM1 Q86U86 1/20 0.60
TDP1 Q9NUW8 1/20 0.56
RAB9A P51151 4/20 0.47
NPC1 O15118 3/20 0.47
ADRA2A P08913 3/20 0.43
PNMT P11086 3/20 0.43
ADRA2B P18089 3/20 0.43
ADRA2C P18825 3/20 0.43
CASP3 P42574 1/20 0.42
SENP8 Q96LD8 1/20 0.42
SENP7 Q9BQF6 1/20 0.42
SENP6 Q9GZR1 1/20 0.42
AKR1B1 P15121 1/20 0.41
ALDH1A1 P00352 2/20 0.41
GAA P10253 1/20 0.41
SMN1; SMN2 Q16637 1/20 0.41
MAPT P10636 1/20 0.40
MAPK1 P28482 1/20 0.40
CYP11B2 P19099 2/20 0.39
AHR P35869 1/20 0.39

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
SCHEMBL15724660 1.00 PBRM1 (0.60) PBRM1TDP1RAB9ANPC1ADRA2A
SCHEMBL29891564 1.00 PBRM1 (0.60) PBRM1TDP1RAB9ANPC1ADRA2A
SCHEMBL18114486 0.85 PBRM1 (0.56) PBRM1TDP1RAB9ANPC1ADRA2A
SCHEMBL17233208 0.81 PBRM1 (0.49) PBRM1TDP1ADRA2APNMTADRA2B
SCHEMBL17321070 0.81 PBRM1 (0.49) PBRM1TDP1ADRA2APNMTADRA2B
SCHEMBL15667383 0.78 TDP1 (0.57) PBRM1TDP1RAB9ANPC1CASP3
SCHEMBL15667344 0.78 TDP1 (0.57) PBRM1TDP1RAB9ANPC1CASP3
SCHEMBL318360 0.78 TDP1 (0.57) PBRM1TDP1RAB9ANPC1CASP3
SCHEMBL15724650 0.77 TDP1 (0.56) PBRM1TDP1RAB9ANPC1CASP3
SCHEMBL5541364 0.77 TDP1 (0.60) PBRM1TDP1RAB9ANPC1CASP3

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-12478621-B2 Substituted aminoquinolones as dgkalpha inhibitors for immune activation DEUTSCHES KREBSFORSCHUNGSZENTRUM (DE) 2025-11-25 US disclosed
EP-4134364-B1 BROMODOMAIN INHIBITORS CELGENE QUANTICEL RES INC (US) 2025-07-30 EP disclosed
US-20240182490-A1 BROMODOMAIN INHIBITORS CELGENE QUANTICEL RESEARCH, INC. (US) 2024-06-06 US disclosed
US-11998539-B2 Substituted aminoquinolones as DGKalpha inhibitors for immune activation BAYER AKTIENGESELLSCHAFT (DE) 2024-06-04 US disclosed
US-11884680-B2 Bromodomain inhibitors CELGENE QUANTICEL RESEARCH, INC. (US) 2024-01-30 US disclosed
US-20230201186-A1 SUBSTITUTED AMINOQUINOLONES AS DGKALPHA INHIBITORS FOR IMMUNE ACTIVATION BAYER AKTIENGESELLSCHAFT (DE) 2023-06-29 US disclosed
US-20230148194-A1 SUBSTITUTED AMINOQUINOLONES AS DGKALPHA INHIBITORS FOR IMMUNE ACTIVATION BAYER AKTIENGESELLSCHAFT (DE) 2023-05-11 US disclosed
EP-4134364-A2 BROMODOMAIN INHIBITORS Celgene Quanticel Research, Inc. (US) 2023-02-15 EP disclosed
US-20220315601-A1 BROMODOMAIN INHIBITORS CELGENE QUANTICEL RESEARCH, INC. (US) 2022-10-06 US disclosed
EP-3640241-B1 BROMODOMAIN INHIBITORS CELGENE QUANTICEL RES INC (US) 2022-09-28 EP disclosed
US-6849649-B2 N-phenpropylcyclopentyl-substituted glutaramide derivatives as inhibitors of neutral endopeptidase PFIZER INC. (US) 2005-02-01 US disclosed
US-20040106611-A1 N-phenpropylcyclopentyl-substituted glutaramide derivatives as inhibitors of neutral endopeptidase PFIZER INC 2004-06-03 US disclosed
US-6660756-B2 N-phenpropylcyclopentyl-substituted glutaramide derivatives as inhibitors of neutral endopeptidase PFIZER INC. 2003-12-09 US disclosed
EP-0177448-B1 PROCESS FOR THE PREPARATION OF 1,2-BENZOXATHIIN DERIVATIVES CIBA-GEIGY AG (CH) 1989-05-03 EP disclosed
EP-0099339-B1 CONDENSED N-PHENYLSULFONYL-N'-PYRIMIDINYL AND TRIAZINYL UREA CIBA-GEIGY AG (CH) 1987-01-07 EP disclosed
US-4634465-A PRE- AND POSTEMERGENCE HERBICIDES CIBA-GEIGY CORPORATION (US) 1987-01-06 US disclosed
US-4603211-A Process for the preparation of 1,2-benzoxathiine derivatives CIBA-GEIGY CORPORATION (US) 1986-07-29 US disclosed
EP-0177448-A2 Process for the preparation of 1,2-benzoxathiin derivatives CIBA-GEIGY AG (CH) 1986-04-09 EP disclosed
US-4560771-A REACTING A DIHYDROBENZOFURAN DERIVATIVE WITH CHLOROSULFONIC ACID CIBA GEIGY CORPORATION (US) 1985-12-24 US disclosed
EP-0099339-A2 Condensed N-phenylsulfonyl-N'-pyrimidinyl and triazinyl urea CIBA-GEIGY AG (CH) 1984-01-25 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 (8 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-20230148194-A1 SUBSTITUTED AMINOQUINOLONES AS DGKALPHA INHIBITORS FOR IMMUNE ACTIVATION DGKK, DGKG, DGKA PBRM1 3409/4885TDP1 1336/4885RAB9A 599/4885
US-20240182490-A1 BROMODOMAIN INHIBITORS BRD3, EP300, BRPF3 PBRM1 144/4885TDP1 1684/4885RAB9A 3279/4885
US-12478621-B2 Substituted aminoquinolones as dgkalpha inhibitors for immune activation DGKK, DGKG, DGKA PBRM1 3409/4885TDP1 1336/4885RAB9A 599/4885
US-20220315601-A1 BROMODOMAIN INHIBITORS BRD3, EP300, BRPF3 PBRM1 144/4885TDP1 1684/4885RAB9A 3279/4885
US-11998539-B2 Substituted aminoquinolones as DGKalpha inhibitors for immune activation DGKK, DGKG, DGKA PBRM1 3409/4885TDP1 1336/4885RAB9A 599/4885
US-20040106611-A1 N-phenpropylcyclopentyl-substituted glutaramide derivatives as inhibitors of neutral endopeptidase PREP, ENGASE, ENPEP PBRM1 4454/4885TDP1 1854/4885RAB9A 3818/4885
US-20230201186-A1 SUBSTITUTED AMINOQUINOLONES AS DGKALPHA INHIBITORS FOR IMMUNE ACTIVATION DGKK, DGKG, DGKA PBRM1 3409/4885TDP1 1336/4885RAB9A 599/4885
US-11884680-B2 Bromodomain inhibitors BRD3, EP300, BRPF3 PBRM1 144/4885TDP1 1684/4885RAB9A 3279/4885

“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.