SCHEMBL552932

SCHEMBL552932

Brc1ccc2c(c1)CNCC2

nearest known ligand 1.00 ✓ in ChEMBL — recovers established targets

Predicted protein targets (top 12)

geneUniProtsupporting neighboursconfidence
PNMT P11086 6/20 1.00
ASIC3 Q9UHC3 1/20 0.85
ADRA2A P08913 2/20 0.60
ADRA2B P18089 2/20 0.60
ADRA2C P18825 2/20 0.60
DRD2 P14416 1/20 0.56
DRD3 P35462 1/20 0.56
CD44 P16070 1/20 0.54
MAOB P27338 1/20 0.54
HTR2A P28223 1/20 0.51
HTR2C P28335 1/20 0.51
HTR2B P41595 1/20 0.51

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
SCHEMBL29473102 1.00 PNMT (1.00) PNMTASIC3ADRA2AADRA2BADRA2C
Hydrochloric Acid SCHEMBL29528420 0.98 PNMT (0.96) PNMTASIC3ADRA2AADRA2BADRA2C
Hydrochloric Acid SCHEMBL1266299 0.98 PNMT (0.96) PNMTASIC3ADRA2AADRA2BADRA2C
SCHEMBL505055 0.92 ASIC3 (1.00) PNMTASIC3ADRA2AADRA2BADRA2C
Hydrochloric Acid SCHEMBL1017313 0.90 ASIC3 (0.96) PNMTASIC3ADRA2AADRA2BADRA2C
SCHEMBL1849383 0.88 PNMT (0.79) PNMTASIC3ADRA2AADRA2BADRA2C
SCHEMBL29573611 0.88 PNMT (0.79) PNMTASIC3ADRA2AADRA2BADRA2C
SCHEMBL1264341 0.87 PNMT (0.77) PNMTASIC3ADRA2AADRA2BADRA2C
Hydrochloric Acid SCHEMBL21753269 0.85 PNMT (0.74) PNMTASIC3ADRA2AADRA2BADRA2C
SCHEMBL329957 0.82 PNMT (0.69) PNMTASIC3ADRA2AADRA2BADRA2C

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-110294758-B 2-substituted 5, 6-dihydropyrazolo [5, 1-alpha ] isoquinoline, derivatives and synthesis method thereof 湘潭大学 2021-10-22 CN claimed
CN-109293569-B Method for preparing formamide derivative through amine transfer reaction without participation of catalyst 湘潭大学 2021-08-06 CN claimed
CN-107827817-B Method for synthesizing formamide derivative through molybdenum catalytic formylation reaction 湘潭大学 2020-03-13 CN claimed
CN-107827816-B Method for synthesizing formamide derivative through graphene oxide catalytic formylation reaction 湘潭大学 2020-01-10 CN claimed
CN-107892670-B Method for synthesizing formamide derivative through cobalt-catalyzed formylation reaction 湘潭大学 2019-12-13 CN claimed
CN-110294758-A 2- replaces 5,6- dihydro-pyrazolo [5,1- α] isoquinolin, derivative and its synthetic method 湘潭大学 2019-10-01 CN claimed
WO-2026106389-A1 NMT INHIBITOR AND USE THEREOF 주식회사 이노보테라퓨틱스 2026-05-21 WO disclosed
US-20260092053-A1 KHK INHIBITORS GILEAD SCIENCES INC (US) 2026-04-02 US disclosed
US-20260092059-A1 Broad Spectrum Antiviral Compositions and Methods EVRYS BIO, LLC (US) 2026-04-02 US disclosed
EP-4712969-A1 CYCLIN INHIBITORS Circle Pharma, Inc. (US) 2026-03-25 EP disclosed
US-20260062443-A1 PHARMACEUTICAL COMPOUNDS FOR THE TREATMENT OF COMPLEMENT MEDIATED DISORDERS ALEXION PHARMA INC (US) 2026-03-05 US disclosed
EP-4681774-A2 KHK INHIBITORS Gilead Sciences, Inc. (US) 2026-01-21 EP disclosed
EP-4676476-A1 INHIBITORS OF TDP-43 AND TAU AGGREGATION Aquinnah Pharmaceuticals, Inc. (US) 2026-01-14 EP disclosed
EP-0832069-A1 BIPHENYL-2-CARBOXYLIC ACID-TETRAHYDRO-ISOQUINOLIN-6-YL AMIDE DERIVATIVES, THEIR PREPARATION AND THEIR USE AS INHIBITORS OF MICROSOMAL TRIGLYCERIDE TRANSFER PROTEIN AND/OR APOLIPOPROTEIN B (Apo B) SECRETION PFIZER INC. (US) 1998-04-01 EP disclosed
EP-0828754-A1 DIPEPTIDES WHICH PROMOTE RELEASE OF GROWTH HORMONE PFIZER INC. (US) 1998-03-18 EP disclosed
WO-1998006699-A1 TETRAHYDROISOQUINOLINE DERIVATIVES AND THEIR PHARMACEUTICAL USE SMITHKLINE BEECHAM PLC (GB) 1998-02-19 WO disclosed
WO-1997043262-A1 TETRAHYDROISOQUINOLINE DERIVATIVES AS MODULATORS OF DOPAMINE D3 RECEPTORS SMITHKLINE BEECHAM P.L.C. (GB) 1997-11-20 WO disclosed
WO-1996040640-A1 BIPHENYL-2-CARBOXYLIC ACID-TETRAHYDRO-ISOQUINOLIN-6-YL AMIDE DERIVATIVES, THEIR PREPARATION AND THEIR USE AS INHIBITORS OF MICROSOMAL TRIGLYCERIDE TRANSFER PROTEIN AND/OR APOLIPOPROTEIN B (Apo B) SECRETION PFIZER INC. (US) 1996-12-19 WO disclosed
WO-1996038471-A1 DIPEPTIDES WHICH PROMOTE RELEASE OF GROWTH HORMONE PFIZER INC. (US) 1996-12-05 WO disclosed
WO-1996035713-A1 DIPEPTIDES WHICH PROMOTE RELEASE OF GROWTH HORMONE PFIZER, INC. (US) 1996-11-14 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-20260092059-A1 Broad Spectrum Antiviral Compositions and Methods IRF3, ZC3HAV1, ZC3HAV1L PNMT 3725/4885ASIC3 4127/4885ADRA2A 3048/4885
US-20260062443-A1 PHARMACEUTICAL COMPOUNDS FOR THE TREATMENT OF COMPLEMENT MEDIATED DISORDERS C9, SSB, C1S PNMT 4716/4885ASIC3 2850/4885ADRA2A 2304/4885
US-20260092053-A1 KHK INHIBITORS KHK, SLC5A2, HK1 PNMT 4766/4885ASIC3 2433/4885ADRA2A 1434/4885

“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.