SCHEMBL1001820

SCHEMBL1001820

CCCCCCC(I)CC

nearest known ligand 0.48

Predicted protein targets (top 14)

geneUniProtsupporting neighboursconfidence
TSHR P16473 1/20 0.44
THRB P10828 1/20 0.44
LMNA P02545 1/20 0.44
DNM1 Q05193 2/20 0.43
OPRM1 P35372 1/20 0.42
GPR84 Q9NQS5 3/20 0.39
FDPS P14324 3/20 0.39
SPHK1 Q9NYA1 1/20 0.39
FFAR1 O14842 1/20 0.39
MAPT P10636 1/20 0.38
LCK P06239 1/20 0.38
PPARD Q03181 1/20 0.38
ZDHHC20 Q5W0Z9 1/20 0.38
ZDHHC2 Q9UIJ5 1/20 0.38

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
SCHEMBL18107258 1.00 TSHR (0.44) TSHRTHRBLMNADNM1OPRM1
SCHEMBL10600001 1.00 TSHR (0.44) TSHRTHRBLMNADNM1OPRM1
SCHEMBL1000844 1.00 TSHR (0.44) TSHRTHRBLMNADNM1OPRM1
SCHEMBL18107314 1.00 TSHR (0.44) TSHRTHRBLMNADNM1OPRM1
SCHEMBL14964587 1.00 TSHR (0.44) TSHRTHRBLMNADNM1OPRM1
SCHEMBL9457340 1.00 TSHR (0.44) TSHRTHRBLMNADNM1OPRM1
SCHEMBL20957527 1.00 TSHR (0.44) TSHRTHRBLMNADNM1OPRM1
SCHEMBL21493266 1.00 TSHR (0.44) TSHRTHRBLMNADNM1OPRM1
SCHEMBL20957524 1.00 TSHR (0.44) TSHRTHRBLMNADNM1OPRM1
SCHEMBL18107351 1.00 TSHR (0.44) TSHRTHRBLMNADNM1OPRM1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-12391645-B2 N-isopropyl tryptamines and method of making monoalkylated and dialkylated tryptamine analogs CAAMTECH, INC. (US) 2025-08-19 US disclosed
US-20250250675-A1 METHOD OF DEPOSITING METAL FILMS APPLIED MATERIALS, INC. (US) 2025-08-07 US disclosed
US-20250197352-A1 N-ISOPROPYL TRYPTAMINES AND METHOD OF MAKING MONOALKYLATED AND DIALKYLATED TRYPTAMINE ANALOGS CAAMTECH, INC. 2025-06-19 US disclosed
US-12281387-B2 Method of depositing metal films APPLIED MATERIALS, INC. (US) 2025-04-22 US disclosed
EP-4525861-A2 N-ISOPROPYL TRYPTAMINES AND METHOD OF MAKING MONOALKYLATED AND DIALKYLATED TRYPTAMINE ANALOGS Caamtech, Inc. (US) 2025-03-26 EP disclosed
CN-111954848-B Photosensitive resin composition, cured product, insulating material, resin material for solder resist, and resist member DIC株式会社 2024-05-03 CN disclosed
WO-2023225679-A2 N-ISOPROPYL TRYPTAMINES AND METHOD OF MAKING MONOALKYLATED AND DIALKYLATED TRYPTAMINE ANALOGS CAAMTECH, INC. (US) 2023-11-23 WO disclosed
US-20230227975-A1 METHOD OF DEPOSITING METAL FILMS APPLIED MATERIALS, INC. (US) 2023-07-20 US disclosed
WO-2023129499-A1 METHOD OF DEPOSITING METAL FILMS APPLIED MATERIALS, INC. (US) 2023-07-06 WO disclosed
CN-109153653-B Novel compound, photocurable composition, cured product thereof, printing ink, and printed matter using the printing ink DIC株式会社 2022-06-28 CN disclosed
CN-109153653-A New compound, Photocurable composition, its solidfied material, printing ink and the printed article for having used the printing ink DIC株式会社 2019-01-04 CN disclosed
US-9738738-B2 Polymers functionalized with activated nitrogen heterocycles containing a pendant functional group BRIDGESTONE CORPORATION (JP) 2017-08-22 US disclosed
US-20160289355-A1 POLYMERS FUNCTIONALIZED WITH ACTIVATED NITROGEN HETEROCYCLES CONTAINING A PENDANT FUNCTIONAL GROUP BRIDGESTONE CORPORATION (JP) 2016-10-06 US disclosed
US-20110274925-A1 POLY (N - ALKYLCARBAZOLE) COLUMNAR STRUCTURE AND METHOD FOR PRODUCING THE SAME NATIONAL UNIVERSITY CORPORATION CHIBA UNIVERSITY (JP) 2011-11-10 US disclosed
US-20110017958-A1 ORGANIC TRANSPARENT ELECTROCONDUCTIVE MATERIAL, INK FOR FORMING ORGANIC TRANSPARENT ELECTROCONDUCTIVE MATERIAL, AND METHODS FOR PRODUCING THEM NATIONAL UNIVERSITY CORPORATION CHIBA UNIVERSITY (JP) 2011-01-27 US disclosed
EP-1957644-B1 ENZYMATIC ENCODING METHODS FOR EFFICIENT SYNTHESIS OF LARGE LIBRARIES NUEVOLUTION AS (DK) 2010-12-01 EP disclosed
EP-0442635-B1 Novel initiators for cationic polymerization MINNESOTA MINING & MFG (US) 1995-11-08 EP disclosed
US-5124417-A Comprising an organic onium cation and a nonnucleophilic, partially-fluorinated hydrocarbylsulfonato metallate; high-molecular-weight polymers from epoxides, tetrahydrofurans, oxazolines, vinyls, lactones, etc. MINNESOTA MINING AND MANUFACTURING COMPANY (US) 1992-06-23 US disclosed
US-5084586-A Polymerization catalysts MINNESOTA MINING AND MANUFACTURING COMPANY (US) 1992-01-28 US disclosed
EP-0442635-A1 Novel initiators for cationic polymerization MINNESOTA MINING AND MANUFACTURING COMPANY (US) 1991-08-21 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 (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-12281387-B2 Method of depositing metal films TPO, TSNAX, C5 TSHR 295/4885THRB 997/4885LMNA 3280/4885
US-12391645-B2 N-isopropyl tryptamines and method of making monoalkylated and dialkylated tryptamine analogs INMT, SLC6A4, HNMT TSHR 724/4885THRB 892/4885LMNA 2055/4885
US-20230227975-A1 METHOD OF DEPOSITING METAL FILMS TPO, TSNAX, C5 TSHR 295/4885THRB 997/4885LMNA 3280/4885
US-20250250675-A1 METHOD OF DEPOSITING METAL FILMS TPO, TSNAX, C5 TSHR 295/4885THRB 997/4885LMNA 3280/4885
US-20250197352-A1 N-ISOPROPYL TRYPTAMINES AND METHOD OF MAKING MONOALKYLATED AND DIALKYLATED TRYPTAMINE ANALOGS INMT, SLC6A4, HNMT TSHR 731/4885THRB 854/4885LMNA 2052/4885

“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.