SCHEMBL225916

SCHEMBL225916

Cc1ccc2c(c1)Sc1cc(C)ccc1N2

nearest known ligand 0.59

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
▸ MAPT P10636 8/20 0.59
▸ NOX1 Q9Y5S8 7/20 0.59
▸ MEN1 O00255 6/20 0.59
▸ KMT2A Q03164 6/20 0.59
▸ GAA P10253 6/20 0.59
▸ TDP1 Q9NUW8 3/20 0.59
▸ NPC1 O15118 2/20 0.59
▸ RAB9A P51151 2/20 0.59
▸ SNCA P37840 7/20 0.55
▸ EPHX2 P34913 1/20 0.55
▸ ALOX15 P16050 3/20 0.53
▸ MAPK1 P28482 3/20 0.53
▸ HSD17B10 Q99714 2/20 0.53
▸ ALOX12 P18054 2/20 0.50
▸ LMNA P02545 1/20 0.47
▸ HTT P42858 1/20 0.47
▸ SMN1; SMN2 Q16637 1/20 0.47
▸ L3MBTL1 Q9Y468 1/20 0.47
▸ POLB P06746 2/20 0.47
▸ ALDH1A1 P00352 2/20 0.47

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
SCHEMBL29640485 1.00 MAPT (0.59) MAPTNOX1MEN1KMT2AGAA
SCHEMBL2756476 0.92 NOX1 (0.53) MAPTNOX1MEN1KMT2AGAA
SCHEMBL239549 0.90 NOX1 (0.65) MAPTNOX1MEN1KMT2AGAA
SCHEMBL9391898 0.88 SNCA (0.55) MAPTNOX1MEN1KMT2AGAA
SCHEMBL24255127 0.88 MAPT (0.50) MAPTNOX1MEN1KMT2AGAA
SCHEMBL17289246 0.85 SNCA (0.83) MAPTNOX1MEN1KMT2AGAA
SCHEMBL17949769 0.85 MAPT (0.48) MAPTNOX1MEN1KMT2AGAA
SCHEMBL31538892 0.85 SNCA (0.50) MAPTNOX1MEN1KMT2AGAA
SCHEMBL9980103 0.81 NOX1 (0.54) MAPTNOX1MEN1KMT2AGAA
SCHEMBL11381973 0.81 MAOA (0.59) MAPTNOX1MEN1KMT2AGAA

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-117567389-A Organic photoelectric material and synthesis method and application thereof 棓诺(苏州)新材料有限公司 2024-02-20 — — CN claimed
US-6210536-B1 DISTILLATION OF ACRYLIC OR METHACRYLIC ACID OR ESTER IN PRESENCE OF POLYMERIZATION INHIBITOR COMPRISING N,N*-DINITROSO PHENYLENEDIAMINE COMPOUND, A HYDROQUINONE OR HYDROQUINONE MONOMETHYL ETHER, PHENYLENEDIAMINE COMPOUND, PHENOTHIAZINE UNIROYAL CHEMICAL COMPANY, INC. 2001-04-03 — — US claimed
EP-0522709-B1 Polymerization inhibitors for acrylic acids and esters UNIROYAL CHEM CO INC (US) 1996-08-21 — — EP claimed
EP-0522709-A2 Polymerization inhibitors for acrylic acids and esters UNIROYAL CHEMICAL COMPANY, Inc. (US) 1993-01-13 — — EP claimed
EP-0334500-B1 VINYL AROMATIC COMPOSITONS STABILIZED AGAINST POLYMERIZATION UNIROYAL CHEMICAL COMPANY, Inc. (US) 1991-06-26 — — EP claimed
US-4915873-A PHENOTHIAZINE AND ARYL-SUBSTITUTED PHENYLENEDIAMINE UNIROYAL CHEMICAL COMPANY, INC. (US) 1990-04-10 — — US claimed
EP-0334500-A1 Vinyl aromatic compositons stabilized against polymerization UNIROYAL CHEMICAL COMPANY, Inc. (US) 1989-09-27 — — EP claimed
EP-0325059-A2 Polymerization inhibitor composition for vinyl aromatic compounds UNIROYAL CHEMICAL COMPANY, Inc. (US) 1989-07-26 — — EP claimed
US-4363745-A STERICALLY HINDERED PHENOL, BIS(A,A-DIMETHYLBENZYL) DIPHENYLAMINE AND A PHENOTHIAZINE COMPOUND STABILIZERS THE DOW CHEMICAL COMPANY (US) 1982-12-14 — — US claimed
US-4275173-A SYNERGISTIC COMBINATION OF A STERICALLY HINDERED PHENOL AND 4,4*-BIS/A,A-DIMETHYLBENZYL/DIPHENYL AMINE AND A PHENOTHIAZINE PROVIDE OXIDATION RESISTANCE THE DOW CHEMICAL COMPANY (US) 1981-06-23 — — US claimed
US-4265783-A SYNERGISTIC COMBINATION OF STERIC HINDERED PHENOL, 4,4*-BIS/A,A-DIMETHYL BENZYL/DIPHENYLAMINE AND A PHENOTHIAZINE THE DOW CHEMICAL COMPANY (US) 1981-05-05 — — US claimed
US-4010211-A 2,6-DI-TERT-BUTYL-P-CRESOL, DISUBSTITUTED DIPHENYLAMINE, PHENOTHIAZINE COMPOUND OLIN CORPORATION (US) 1977-03-01 — — US claimed
JP-1234405-A — — None — — JP disclosed
EP-4745659-A1 REFLECTING DEVICE, MANUFACTURING METHOD FOR REFLECTING DEVICE, AND VEHICLE BYD Company Limited (CN) 2026-05-20 — — EP disclosed
US-20260103652-A1 MACROMOLECULAR CORROSION (McIn) INHIBITORS: STRUCTURES, METHODS OF MAKING AND USING THE SAME POLNOX CORP (US) 2026-04-16 — — US disclosed
US-12492352-B2 Macromolecular corrosion (MCIN) inhibitors: structures, methods of making and using the same POLNOX CORPORATION (US) 2025-12-09 — — US disclosed
US-4363745-A STERICALLY HINDERED PHENOL, BIS(A,A-DIMETHYLBENZYL) DIPHENYLAMINE AND A PHENOTHIAZINE COMPOUND STABILIZERS THE DOW CHEMICAL COMPANY (US) 1982-12-14 — — US disclosed
US-4275173-A SYNERGISTIC COMBINATION OF A STERICALLY HINDERED PHENOL AND 4,4*-BIS/A,A-DIMETHYLBENZYL/DIPHENYL AMINE AND A PHENOTHIAZINE PROVIDE OXIDATION RESISTANCE THE DOW CHEMICAL COMPANY (US) 1981-06-23 — — US disclosed
US-4265783-A SYNERGISTIC COMBINATION OF STERIC HINDERED PHENOL, 4,4*-BIS/A,A-DIMETHYL BENZYL/DIPHENYLAMINE AND A PHENOTHIAZINE THE DOW CHEMICAL COMPANY (US) 1981-05-05 — — US disclosed
US-4010211-A 2,6-DI-TERT-BUTYL-P-CRESOL, DISUBSTITUTED DIPHENYLAMINE, PHENOTHIAZINE COMPOUND OLIN CORPORATION (US) 1977-03-01 — — 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 (2 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-12492352-B2 Macromolecular corrosion (MCIN) inhibitors: structures, methods of making and using the same MB, NCLN, CPN1 MAPT 2540/4885NOX1 606/4885MEN1 190/4885
US-20260103652-A1 MACROMOLECULAR CORROSION (McIn) INHIBITORS: STRUCTURES, METHODS OF MAKING AND USING THE SAME MPO, CYC1, CBR1 MAPT 4131/4885NOX1 9/4885MEN1 2382/4885

“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.

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