SCHEMBL202156

SCHEMBL202156

c1ccc2c(c1)ncc1nc[nH]c12

nearest known ligand 0.55

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
PDPK1 O15530 1/20 0.55
CA12 O43570 1/20 0.55
PARP1 P09874 1/20 0.55
ALOX15 P16050 1/20 0.55
SMN1; SMN2 Q16637 1/20 0.55
CA9 Q16790 1/20 0.55
TNKS2 Q9H2K2 1/20 0.55
KDM4E B2RXH2 3/20 0.45
GPR3 P46089 1/20 0.45
ALDH1A1 P00352 2/20 0.40
HPGD P15428 2/20 0.40
GABRA1 P14867 2/20 0.40
GABRG2 P18507 2/20 0.40
GABRB3 P28472 2/20 0.40
GABRA5 P31644 2/20 0.40
GABRA3 P34903 2/20 0.40
GABRA2 P47869 2/20 0.40
GABRA6 Q16445 2/20 0.40
HDAC6 Q9UBN7 1/20 0.40
PRNP P04156 1/20 0.40

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
SCHEMBL29508386 1.00 PDPK1 (0.55) PDPK1CA12PARP1ALOX15SMN1; SMN2
Ammonia Solution, Strong SCHEMBL4824906 0.98 PDPK1 (0.53) PDPK1CA12PARP1ALOX15SMN1; SMN2
SCHEMBL10427747 0.98 PDPK1 (0.53) PDPK1CA12PARP1ALOX15SMN1; SMN2
Hydrochloric Acid SCHEMBL4766699 0.98 PDPK1 (0.53) PDPK1CA12PARP1ALOX15SMN1; SMN2
Formic Acid SCHEMBL10727380 0.90 PDPK1 (0.50) PDPK1CA12PARP1ALOX15SMN1; SMN2
Formic Acid SCHEMBL10738924 0.88 PDPK1 (0.49) PDPK1CA12PARP1ALOX15SMN1; SMN2
Acetic Acid SCHEMBL10727228 0.88 SMN1; SMN2 (0.49) PDPK1CA12PARP1ALOX15SMN1; SMN2
Acetic Acid SCHEMBL10742452 0.87 SMN1; SMN2 (0.47) PDPK1CA12PARP1ALOX15SMN1; SMN2
Trifluoroacetic Acid SCHEMBL29627985 0.84 PARP1 (0.45) PDPK1CA12PARP1ALOX15SMN1; SMN2
Water SCHEMBL10734174 0.82 PDPK1 (0.40) PDPK1CA12PARP1ALOX15SMN1; SMN2

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 1245 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-4370515-A1 TRICYCLIC COMPOUNDS AS INHIBITORS OF KRAS Incyte Corporation (US) 2024-05-22 EP claimed
US-20230044248-A1 COMBINED INHIBITION OF PD-1, TGFBeta AND ATM TOGETHER WITH RADIOTHERAPY FOR THE TREATMENT OF CANCER ARES TRADING S.A. (CH) 2023-02-09 US claimed
WO-2023287896-A1 TRICYCLIC COMPOUNDS AS INHIBITORS OF KRAS INCYTE CORPORATION (US) 2023-01-19 WO claimed
EP-4051279-A1 COMBINED INHIBITION OF PD-1, TGFß AND ATM TOGETHER WITH RADIOTHERAPY FOR THE TREATMENT OF CANCER Ares Trading S.A. (CH) 2022-09-07 EP claimed
EP-3919076-A1 SYNTHETIC OLIGOSACCHARIDE VACCINES AGAINST STREPTOCOCCUS PNEUMONIAE WITH MICROPARTICLE ADJUVANT FORMULATIONS Max-Planck-Gesellschaft zur Förderung der Wissenschaften e.V. (DE) 2021-12-08 EP claimed
US-20210353614-A1 COMPOUNDS AND USES THEREOF TO TREAT TUMORS IN A SUBJECT MERCK PATENT GMBH (DE) 2021-11-18 US claimed
EP-3849615-A1 COMPOSITIONS FOR THE TREATMENT OF DISEASE WITH IMMUNE STIMULATORY CONJUGATES Silverback Therapeutics, Inc. (US) 2021-07-21 EP claimed
WO-2021084124-A1 COMBINED INHIBITION OF PD-1, TGFβ AND ATM TOGETHER WITH RADIOTHERAPY FOR THE TREATMENT OF CANCER ARES TRADING S.A. (CH) 2021-05-06 WO claimed
EP-3765019-A1 COMPOUNDS AND USES THEREOF TO TREAT TUMORS IN A SUBJECT Merck Patent GmbH (DE) 2021-01-20 EP claimed
US-10722591-B2 Cleavable conjugates of TLR7/8 agonist compounds, methods for preparation, and uses thereof DYNAVAX TECHNOLOGIES CORPORATION (US) 2020-07-28 US claimed
WO-2004011462-A1 PREPARATION OF 1H-IMIDAZO [4,5-C] QUINOLIN-4-AMINES VIA NOVEL 1H-IMIDAZO [4,5-C] QUINOLIN-4-CYANO AND 1H-IMIDAZO [4,5-C] QUINOLIN-4-CARBOXAMIDE INTERMEDIATES BIOGAL GYOGYSZERGYAR RT. (HU) 2004-02-05 WO claimed
EP-1177797-A9 NOVEL USE FUJISAWA PHARMACEUTICAL CO., LTD. (JP) 2002-05-15 EP claimed
EP-1177797-A1 NOVEL USE FUJISAWA PHARMACEUTICAL CO., LTD. (JP) 2002-02-06 EP claimed
EP-0575549-B1 PROCESS FOR IMIDAZO [4,5-c]QUINOLIN-4-AMINES MINNESOTA MINING & MFG (US) 1996-09-11 EP claimed
EP-0681570-A1 PROCESS FOR PREPARING QUINOLINE AMINES MINNESOTA MINING AND MANUFACTURING COMPANY (US) 1995-11-15 EP claimed
US-5395937-A Process for preparing quinoline amines MINNESOTA MINING AND MANUFACTURING COMPANY (US) 1995-03-07 US claimed
WO-1994017043-A1 PROCESS FOR PREPARING QUINOLINE AMINES MINNESOTA MINING AND MANUFACTURING COMPANY (US) 1994-08-04 WO claimed
EP-0575549-A1 PROCESS FOR IMIDAZO 4,5-c]QUINOLIN-4-AMINES. MINNESOTA MINING & MFG (US) 1993-12-29 EP claimed
US-5175296-A Reacting 1H-imidazolo(4,5-c)quinolin-5N-oxide with organic isocyanate; hydrolysis MINNESOTA MINING AND MANUFACTURING COMPANY (US) 1992-12-29 US claimed
WO-1992015581-A1 PROCESS FOR IMIDAZO[4,5-c]QUINOLIN-4-AMINES MINNESOTA MINING AND MANUFACTURING COMPANY (US) 1992-09-17 WO claimed

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-10722591-B2 Cleavable conjugates of TLR7/8 agonist compounds, methods for preparation, and uses thereof TLR7, TLR8, TLR9 PDPK1 1907/4885CA12 2101/4885PARP1 584/4885
US-20210353614-A1 COMPOUNDS AND USES THEREOF TO TREAT TUMORS IN A SUBJECT CD274, PDCD1, PDCD1LG2 PDPK1 152/4885CA12 213/4885PARP1 1076/4885
US-20230044248-A1 COMBINED INHIBITION OF PD-1, TGFBeta AND ATM TOGETHER WITH RADIOTHERAPY FOR THE TREATMENT OF CANCER ATM, PDCD1, CD274 PDPK1 50/4885CA12 4527/4885PARP1 100/4885

“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.