SCHEMBL1868979

SCHEMBL1868979

O=C1CCc2cccc(Br)c2C1

nearest known ligand 0.56

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
CYP2A6 P11509 1/20 0.52
PARP10 Q53GL7 1/20 0.41
PARP11 Q9NR21 1/20 0.41
PIM1 P11309 1/20 0.39
CSNK1A1 P48729 1/20 0.39
CDK5 Q00535 1/20 0.39
ROCK1 Q13464 1/20 0.39
DYRK1A Q13627 1/20 0.39
LRRK2 Q5S007 1/20 0.39
CLK4 Q9HAZ1 1/20 0.39
DYRK1B Q9Y463 1/20 0.39
CYP1A2 P05177 1/20 0.38
IL1RN P18510 2/20 0.37
ERAP2 Q6P179 2/20 0.37
ERAP1 Q9NZ08 2/20 0.37
TRPA1 O75762 1/20 0.37
ABHD6 Q9BV23 2/20 0.36
MEN1 O00255 1/20 0.36
KMT2A Q03164 1/20 0.36
CARM1 Q86X55 1/20 0.35

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
SCHEMBL14419537 0.89 MEN1 (0.40) CYP2A6PARP10PARP11PIM1CSNK1A1
SCHEMBL2066611 0.86 CYP2A6 (0.43) CYP2A6PARP10PARP11PIM1CSNK1A1
SCHEMBL1662187 0.84 CYP2A6 (0.52) CYP2A6PARP10PARP11PIM1CSNK1A1
SCHEMBL29385577 0.84 CYP2A6 (0.52) CYP2A6PARP10PARP11PIM1CSNK1A1
SCHEMBL29907208 0.83 CYP1A2 (0.52) CYP2A6PARP10PARP11PIM1CSNK1A1
SCHEMBL2327414 0.83 CYP1A2 (0.52) CYP2A6PARP10PARP11PIM1CSNK1A1
SCHEMBL206466 0.80 CYP2A6 (0.52) CYP2A6CYP1A2IL1RNERAP2ERAP1
SCHEMBL3976079 0.78
SCHEMBL7935846 0.78 CYP2A6 (0.46) CYP2A6CYP1A2MEN1KMT2ATRPV1
SCHEMBL5535806 0.78 CYP2A6 (0.54) CYP2A6CYP1A2IL1RNERAP2ERAP1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
JP-4244050-A None JP disclosed
US-20250250246-A1 METHOD FOR PRODUCING HETEROCYCLIDENE ACETAMIDE DERIVATIVE MOCHIDA PHARMACEUTICAL CO., LTD. (JP) 2025-08-07 US disclosed
US-12286414-B2 Method for producing heterocyclidene acetamide derivative MOCHIDA PHARMACEUTICAL CO., LTD. (JP) 2025-04-29 US disclosed
US-12209092-B2 Inhibitors of GLI1 as therapeutic agents NEW YORK UNIVERSITY (US) 2025-01-28 US disclosed
CN-115594669-B Parallel ring derivative and preparation method and medical application thereof 深圳信立泰药业股份有限公司 2024-11-05 CN disclosed
CN-118812481-A Process for producing heterocyclylacetamide derivative 持田制药株式会社 2024-10-22 CN disclosed
EP-4410989-A2 METHOD FOR PRODUCING HETEROCYCLIDENE ACETAMIDE DERIVATIVES Mochida Pharmaceutical Co., Ltd. (JP) 2024-08-07 EP disclosed
EP-4019485-B1 METHOD FOR PRODUCING HETEROCYCLIDENE ACETAMIDE DERIVATIVES MOCHIDA PHARM CO LTD (JP) 2024-08-07 EP disclosed
CN-114206847-B Process for producing heterocyclylacetamide derivative 持田制药株式会社 2024-07-16 CN disclosed
US-11834456-B2 11,13-modified saxitoxins for the treatment of pain SITEONE THERAPEUTICS, INC. (US) 2023-12-05 US disclosed
US-4968679-A DISORDERS OF CENTRAL NERVOUS SYSTEM, CARDIOVASCULAR SYSTEM OR INTESTINAL TRACT BAYER AKTIENGESELLSCHAFT (DE) 1990-11-06 US disclosed
CN-1046528-A As the new naphthalane base-3H-1 of antihyperglycemic agents, 2,3,5-oxygen thia diazole 2-oxide compound AMERICAN HOME PROD (US) 1990-10-31 CN disclosed
US-4966975-A Processes for the preparation of novel naphthalenylmethyl-3H-1,2,3,5-oxathiadiazole 2-oxides useful as antihyperglycemic agents AMERICAN HOME PRODUCT 1990-10-30 US disclosed
EP-0393941-A1 Naphthalene derivatives AMERICAN HOME PRODUCTS CORPORATION (US) 1990-10-24 EP disclosed
EP-0385658-A1 Ring-substituted 2-amino 1,2,3,4-tetra-hydronaphthalenes and 3-aminochromanes ELI LILLY AND COMPANY (US) 1990-09-05 EP disclosed
CN-1045099-A Ring-substituted 2-amino-1, 2, 3, 4-tetrahydronaphthalenes and 3-aminochromanes LILLY CO ELI (US) 1990-09-05 CN disclosed
US-4897405-A Novel naphthalenylalkyl-3H-1,2,3,5-oxathiadiazole 2-oxides useful as antihyperglycemic agents AMERICAN HOME PRODUCTS CORPORATION (US) 1990-01-30 US disclosed
US-4873262-A TREATMENT OF CENTRAL NERVOUS SYSTEM DISORDERS, CARDIIOVASCULAR SYSTEM OR INTESTINAL TRACT BAYER AKTIENGESELLSCHAFT (DE) 1989-10-10 US disclosed
CN-87101285-A 8-replaces-2-amino-1,2,3, the 4-tetrahydro-bitter edible plant 1988-08-17 CN disclosed
EP-0272534-A2 8-substituted 2-aminotetralins BAYER AG (DE) 1988-06-29 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 (4 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-12209092-B2 Inhibitors of GLI1 as therapeutic agents GLI1, GLI2, SHH CYP2A6 4734/4885PARP10 1758/4885PARP11 913/4885
US-11834456-B2 11,13-modified saxitoxins for the treatment of pain SCN11A, SCN10A, CACNA1A CYP2A6 2069/4885PARP10 3938/4885PARP11 4308/4885
US-12286414-B2 Method for producing heterocyclidene acetamide derivative COASY, NAAA, AADAC CYP2A6 217/4885PARP10 1626/4885PARP11 1282/4885
US-20250250246-A1 METHOD FOR PRODUCING HETEROCYCLIDENE ACETAMIDE DERIVATIVE COASY, NAAA, AADAC CYP2A6 217/4885PARP10 1626/4885PARP11 1282/4885

“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.