SCHEMBL532839

SCHEMBL532839

Oc1ccc2c(c1)CCCN2

nearest known ligand 0.78

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
DRD2 P14416 3/20 0.78
DRD4 P21917 2/20 0.78
MAPT P10636 3/20 0.59
KDM4E B2RXH2 2/20 0.59
CA12 O43570 1/20 0.53
CA1 P00915 1/20 0.53
CA2 P00918 1/20 0.53
CA9 Q16790 1/20 0.53
GAA P10253 2/20 0.50
ALDH1A1 P00352 2/20 0.50
LMNA P02545 2/20 0.50
TP53 P04637 2/20 0.50
HTT P42858 2/20 0.50
THRB P10828 1/20 0.50
ALOX15 P16050 1/20 0.50
CASP1 P29466 1/20 0.50
CASP7 P55210 1/20 0.50
HSD17B10 Q99714 1/20 0.50
TDP1 Q9NUW8 1/20 0.50
DRD1 P21728 2/20 0.46

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
SCHEMBL29722558 1.00 DRD2 (0.78) DRD2DRD4MAPTKDM4ECA12
SCHEMBL6247150 0.94 DRD2 (0.75) DRD2DRD4MAPTKDM4ECA12
Bromide SCHEMBL3182004 0.92 DRD2 (0.72) DRD2DRD4MAPTKDM4ECA12
SCHEMBL59263 0.88 DRD2 (1.00) DRD2DRD4MAPTKDM4ECA12
Hydrochloric Acid SCHEMBL3900412 0.86 DRD2 (0.96) DRD2DRD4MAPTKDM4ECA12
SCHEMBL1119368 0.84 DRD2 (0.55) DRD2DRD4MAPTKDM4ECA12
Tert-Butyl Formate SCHEMBL27510897 0.82 DRD2 (0.54) DRD2DRD4MAPTKDM4ECA12
SCHEMBL6712764 0.81 DRD2 (0.85) DRD2DRD4MAPTKDM4ECA12
SCHEMBL1091532 0.80 MAPT (0.54) DRD2DRD4MAPTKDM4ECA12
SCHEMBL6807924 0.78 DRD2 (0.53) DRD2DRD4MAPTKDM4ECA12

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-119931978-A Application of monoamine oxidase as catalyst in preparation of quinoline nitrogen heterocyclic compound 河北工业大学 2025-05-06 CN claimed
CN-117986187-A Compound and acrylamide polymer with oil displacement effect as well as preparation methods and applications thereof 中国石油化工股份有限公司 2024-05-07 CN claimed
CN-115626889-B Organic chemical conversion method for oxidative dehydrogenation of nitrogen-containing heterocyclic compound 南京工业大学 2024-04-30 CN claimed
CN-116376858-A Application of monoamine oxidase from microorganism as catalyst in preparation of quinoline or quinoline derivative 浙江大学杭州国际科创中心 2023-07-04 CN claimed
CN-103524409-B Quinolines and preparation method thereof and application Shanghai Ren Li Pharmaceutical Technology Co., Ltd (CN) 2015-09-02 CN claimed
CN-103509005-B Quinazoline compound as well as preparation method and application thereof SUZHOU HAITE BIAO BIOLOG TECHNOLOGY CO LTD 2015-04-08 CN claimed
US-7101869-B2 2,4-diaminopyrimidine compounds useful as immunosuppressants PFIZER INC. (US) 2006-09-05 US claimed
EP-1242403-B1 2,4-DIAMINOPYRIMIDINE COMPOUNDS USFUL AS IMMUNOSUPPRESSANTS PFIZER PROD INC (US) 2006-01-04 EP claimed
US-20030191307-A1 2,4-Diaminopyrimidine compounds useful as immunosuppressants BLUMENKOPF TODD A (US) 2003-10-09 US claimed
EP-1242403-A1 2,4-DIAMINOPYRIMIDINE COMPOUNDS USFUL AS IMMUNOSUPPRESSANTS Pfizer Products Inc. (US) 2002-09-25 EP claimed
WO-2001040215-A1 2,4-DIAMINOPYRIMIDINE COMPOUNDS USFUL AS IMMUNOSUPPRESSANTS PFIZER PRODUCTS INC. (US) 2001-06-07 WO claimed
EP-0103797-B1 SUBSTITUTED BENZOXAZINE DERIVATIVES BAYER AG (DE) 1986-11-26 EP claimed
EP-0103797-A2 Substituted benzoxazine derivatives BAYER AG (DE) 1984-03-28 EP claimed
US-12624044-B2 SMARCA degraders and uses thereof KYMERA THERAPEUTICS, INC. (US) 2026-05-12 US disclosed
US-12551564-B2 IRAK degraders and uses thereof KYMERA THERAPEUTICS, INC. (US) 2026-02-17 US disclosed
CN-121108623-B EVA (ethylene-vinyl acetate copolymer) chemical foaming sole material with high whiteness and preparation method thereof 安踏(中国)有限公司 2026-02-03 CN disclosed
US-4088793-A NITROXIDE DERIVATIVES OF 1,2-DIHYDRO- AND 1,2,3,4-TETRAHYDRO- 6-ALKOXYQUINOLINES CANADA PACKERS LIMITED (CA) 1978-05-09 US disclosed
US-4055428-A COLO PHOTOGRAPHY, DIFFUSION TRANSFER SILVER HALIDE EMULSIONS FUJI PHOTO FILM CO., LTD. (JA) 1977-10-25 US disclosed
US-3997542-A 1-(Halogenated-acetyl)-1,2,3,4-tetrahydro-6-quinolinols and esters thereof STERLING DRUG INC. (US) 1976-12-14 US disclosed
US-3997542-A 1-(Halogenated-acetyl)-1,2,3,4-tetrahydro-6-quinolinols and esters thereof STERLING DRUG INC. (US) 1976-12-14 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 (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-20030191307-A1 2,4-Diaminopyrimidine compounds useful as immunosuppressants CCR1, AOC1, NOD1 DRD2 1796/4885DRD4 1511/4885MAPT 4588/4885
US-12551564-B2 IRAK degraders and uses thereof IRAK2, IRAK3, IRAK1 DRD2 1474/4885DRD4 2946/4885MAPT 4432/4885
US-12624044-B2 SMARCA degraders and uses thereof SMARCA1, SMARCC1, SMARCA2 DRD2 3826/4885DRD4 4069/4885MAPT 2169/4885

“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.