SCHEMBL749569

SCHEMBL749569

Brc1ccc2c(c1)CCCC2

nearest known ligand 0.54

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
PNMT P11086 2/20 0.54
ASIC3 Q9UHC3 1/20 0.54
TSHR P16473 1/20 0.46
TDP1 Q9NUW8 2/20 0.45
MAPT P10636 1/20 0.45
ALDH1A1 P00352 2/20 0.42
HSP90AA1 P07900 1/20 0.42
GAA P10253 1/20 0.42
KMT2A Q03164 1/20 0.42
ADRA2A P08913 2/20 0.42
ADRA2B P18089 2/20 0.42
ADRA2C P18825 2/20 0.42
METAP1 P53582 1/20 0.41
STS P08842 1/20 0.41
CTSL P07711 1/20 0.40
HSD17B3 P37058 1/20 0.40
PARP10 Q53GL7 2/20 0.39
L3MBTL1 Q9Y468 1/20 0.39
TDP2 O95551 1/20 0.39
PARP11 Q9NR21 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
SCHEMBL30406919 1.00 PNMT (0.54) PNMTASIC3TSHRTDP1MAPT
SCHEMBL22910024 0.97 PNMT (0.52) PNMTASIC3TSHRTDP1MAPT
SCHEMBL6192350 0.97 PNMT (0.52) PNMTASIC3TSHRTDP1MAPT
SCHEMBL21447111 0.97 PNMT (0.52) PNMTASIC3TSHRTDP1MAPT
SCHEMBL18746500 0.97 PNMT (0.52) PNMTASIC3TSHRTDP1MAPT
SCHEMBL18746707 0.97 PNMT (0.52) PNMTASIC3TSHRTDP1MAPT
SCHEMBL29576955 0.97 PNMT (0.52) PNMTASIC3TSHRTDP1MAPT
SCHEMBL1468326 0.95 PNMT (0.54) PNMTASIC3TSHRTDP1MAPT
Hydrochloric Acid SCHEMBL28759209 0.92 PNMT (0.52) PNMTASIC3TDP1MAPTALDH1A1
Ammonia Solution, Strong SCHEMBL4733194 0.92 PNMT (0.52) PNMTASIC3TSHRTDP1MAPT

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20250388565-A1 ESTROGEN RECEPTOR ALPHA DEGRADERS AND METHODS OF USE THEREOF RELAY THERAPEUTICS, INC. 2025-12-25 US disclosed
EP-4543871-A1 ESTROGEN RECEPTOR ALPHA DEGRADERS AND USE THEREOF Relay Therapeutics, Inc. (US) 2025-04-30 EP disclosed
CN-119751503-A Method for preparing aryl phosphonic acid dialkyl ester by one-pot method 苏州凯若利新材料科技有限公司 2025-04-04 CN disclosed
US-20240400499-A1 NOVEL AMINO ACID DERIVATIVES PEPTIDREAM INC (JP) 2024-12-05 US disclosed
US-20240208914-A1 AMINOCYCLOBUTANES AS MONOACYLGLYCEROL LIPASE MODULATORS JANSSEN PHARMACEUTICA NV (BE) 2024-06-27 US disclosed
CN-115335365-B Aminocyclobutane as monoacylglycerol lipase modulators 詹森药业有限公司 2024-06-18 CN disclosed
US-11919870-B2 Aminocyclobutanes as monoacylglycerol lipase modulators JANSSEN PHARMACEUTICA NV (BE) 2024-03-05 US disclosed
WO-2024044778-A2 NOVEL MODULATORS OF FSHR AND USES THEREOF CELMATIX INC. (US) 2024-02-29 WO disclosed
WO-2024006781-A1 ESTROGEN RECEPTOR ALPHA DEGRADERS AND USE THEREOF RELAY THERAPEUTICS, INC. (US) 2024-01-04 WO disclosed
US-20230331686-A1 AMINOCYCLOBUTANES AS MONOACYLGLYCEROL LIPASE MODULATORS JANSSEN PHARMACEUTICA NV (BE) 2023-10-19 US disclosed
WO-1999033821-A1 BENZOPYRAN AND BENZOTHIOPYRAN DERIVATIVES HAVING RETINOID ANTAGONIST-LIKE ACTIVITY ALLERGAN SALES, INC. (US) 1999-07-08 WO disclosed
WO-1998058922-A1 SYNTHESIS AND USE OF RETINOID COMPOUNDS HAVING NEGATIVE HORMONE AND/OR ANTAGONIST ACTIVITIES ALLERGAN SALES, INC. (US) 1998-12-30 WO disclosed
US-5723620-A Acetylenes disubstituted with a 5 substituted tetrahydronaphthyl group and with an aryl or heteroaryl groups having retinoid-like biological activity ALLERGAN (US) 1998-03-03 US disclosed
EP-0800517-A1 ACETYLENES DISUBSTITUTED WITH A 5 OR 8 SUBSTITUTED TETRAHYDRONAPHTHYL OR DIHYDRONAPHTHYL GROUP AND WITH AN ARYL OR HETEROARYL GROUPS HAVING RETINOID-LIKE BIOLOGICAL ACTIVITY Allergan (US) 1997-10-15 EP disclosed
US-5654469-A FOR TREATMENT OF SKIN DISORDERS ALLERGAN (US) 1997-08-05 US disclosed
US-5591858-A Acetylenes disubstituted with a 5 substituted tetrahydronaphthyl group and with an aryl or heteroaryl group having retinoid-like biological activity ALLERGAN 1997-01-07 US disclosed
US-5543534-A Acetylenes disubstituted with a 5 substituted tetrahydronaphthyl group and with an aryl or heteroaryl groups having retinoid-like biological activity ALLERGAN 1996-08-06 US disclosed
WO-1996020930-A1 ACETYLENES DISUBSTITUTED WITH A 5 OR 8 SUBSTITUTED TETRAHYDRONAPHTHYL OR DIHYDRONAPHTHYL GROUP AND WITH AN ARYL OR HETEROARYL GROUPS HAVING RETINOID-LIKE BIOLOGICAL ACTIVITY ALLERGAN (US) 1996-07-11 WO disclosed
US-5514825-A SYNTHETIC RETINOIDS ALLERGAN, INC. (US) 1996-05-07 US disclosed
US-4216105-A Compositions for the optical whitening of organic materials and use thereof HICKSON & WELCH LIMITED (GB) 1980-08-05 US 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 (5 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-11919870-B2 Aminocyclobutanes as monoacylglycerol lipase modulators MGLL, DAGLB, FAAH PNMT 2611/4885ASIC3 1434/4885TSHR 679/4885
US-20250388565-A1 ESTROGEN RECEPTOR ALPHA DEGRADERS AND METHODS OF USE THEREOF ESRRA, ESRRB, ESR2 PNMT 3489/4885ASIC3 2808/4885TSHR 68/4885
US-20230331686-A1 AMINOCYCLOBUTANES AS MONOACYLGLYCEROL LIPASE MODULATORS MGLL, DAGLB, FAAH PNMT 2611/4885ASIC3 1434/4885TSHR 679/4885
US-20240208914-A1 AMINOCYCLOBUTANES AS MONOACYLGLYCEROL LIPASE MODULATORS MGLL, DAGLB, FAAH PNMT 2611/4885ASIC3 1434/4885TSHR 679/4885
US-20240400499-A1 NOVEL AMINO ACID DERIVATIVES BCAT1, BCAT2, PELP1 PNMT 3623/4885ASIC3 3452/4885TSHR 2791/4885

“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.