SCHEMBL6310987

SCHEMBL6310987

Oc1cccc(CN2CCCC2)c1

nearest known ligand 0.93

Predicted protein targets (top 18)

geneUniProtsupporting neighboursconfidence
PRMT6 Q96LA8 1/20 0.62
ALDH1A1 P00352 3/20 0.61
SMN1; SMN2 Q16637 2/20 0.61
TDP1 Q9NUW8 1/20 0.61
CYP2D6 P10635 2/20 0.58
CYP2C9 P11712 1/20 0.58
HIF1A Q16665 1/20 0.58
DRD2 P14416 2/20 0.57
DRD3 P35462 1/20 0.57
KDM4E B2RXH2 1/20 0.56
GAA P10253 1/20 0.56
BCL2L1 Q07817 1/20 0.54
HPGD P15428 1/20 0.53
ALOX15 P16050 1/20 0.53
HBB P68871 1/20 0.53
HSD17B10 Q99714 1/20 0.53
HRH3 Q9Y5N1 1/20 0.52
CYP2C19 P33261 1/20 0.52

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
SCHEMBL3154468 0.98 ALDH1A1 (0.64) PRMT6ALDH1A1SMN1; SMN2TDP1CYP2D6
SCHEMBL29966226 0.98 ALDH1A1 (0.64) PRMT6ALDH1A1SMN1; SMN2TDP1CYP2D6
SCHEMBL10367496 0.98 ALDH1A1 (0.64) PRMT6ALDH1A1SMN1; SMN2TDP1CYP2D6
SCHEMBL10370403 0.98 ALDH1A1 (0.64) PRMT6ALDH1A1SMN1; SMN2TDP1CYP2D6
SCHEMBL27650580 0.96 PRMT6 (0.58) PRMT6ALDH1A1SMN1; SMN2TDP1CYP2D6
SCHEMBL24556358 0.84 ALDH1A1 (0.59) ALDH1A1SMN1; SMN2TDP1DRD2DRD3
SCHEMBL10991095 0.84 MEN1 (0.66) ALDH1A1DRD2DRD3KDM4EBCL2L1
SCHEMBL10370696 0.84 MC4R (0.62) PRMT6ALDH1A1DRD2DRD3KDM4E
SCHEMBL30118939 0.84 NCF1 (0.66) ALDH1A1SMN1; SMN2CYP2D6CYP2C9DRD2
SCHEMBL1928790 0.84 NCF1 (0.66) ALDH1A1SMN1; SMN2CYP2D6CYP2C9DRD2

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-110724084-B Synthesis method of (S) -3-hydroxy-1-benzylpyrrolidine 苏州永健生物医药有限公司 2022-03-04 CN claimed
CN-110724084-A Synthesis method of (S) -3-hydroxy-1-benzylpyrrolidine 苏州永健生物医药有限公司 2020-01-24 CN claimed
US-20250216782-A1 MASKING PROCESS USING SWITCHABLE POLYMER TOKYO ELECTRON LTD (JP) 2025-07-03 US disclosed
US-20230149398-A1 TOPICAL PHARMACEUTICAL COMPOSITIONS COMPRISING IMIDAZO[1,2-B]PYRIDAZINE COMPOUNDS BENEVOLENTAI BIO LIMITED (GB) 2023-05-18 US disclosed
CN-110283118-B Preparation method of barnidipine key intermediate 贵州医科大学 2022-05-17 CN disclosed
CN-110724084-B Synthesis method of (S) -3-hydroxy-1-benzylpyrrolidine 苏州永健生物医药有限公司 2022-03-04 CN disclosed
CN-110724084-B Synthesis method of (S) -3-hydroxy-1-benzylpyrrolidine 苏州永健生物医药有限公司 2022-03-04 CN disclosed
CN-110724084-A Synthesis method of (S) -3-hydroxy-1-benzylpyrrolidine 苏州永健生物医药有限公司 2020-01-24 CN disclosed
CN-110724084-A Synthesis method of (S) -3-hydroxy-1-benzylpyrrolidine 苏州永健生物医药有限公司 2020-01-24 CN disclosed
CN-102471258-A 3-phenoxymethylpyrrolidine compounds THERAVANCE INC 2012-05-23 CN disclosed
US-6887905-B2 Treatment of depression or generalized anxiety disorder PFIZER INC (US) 2005-05-03 US disclosed
US-4954507-A 1-tertiary-alkyl-substituted naphthyridine carboxylic acid antibacterial agents BRISTOL-MYERS COMPANY (US) 1990-09-04 US disclosed
EP-0288519-A1 1-TERTIARY-ALKYL-SUBSTITUTED NAPHTHYRIDINE- AND QUINOLINE-CARBOXYLIC ACID ANTIBACTERIAL AGENTS Bristol-Myers Squibb Company (US) 1988-11-02 EP disclosed
EP-0266576-A2 1-Tert-alkyl-substituted naphthyridine and quinoline carboxylic acids as antibacterial agents Bristol-Myers Squibb Company (US) 1988-05-11 EP disclosed
WO-1988002627-A1 1-TERTIARY-ALKYL-SUBSTITUTED NAPHTHYRIDINE- AND QUINOLINE-CARBOXYLIC ACID ANTIBACTERIAL AGENTS BRISTOL-MYERS COMPANY (US) 1988-04-21 WO disclosed
US-4694008-A HISTAMINE H2-ANTAGONISTS SMITH KLINE & FRENCH LABORATORIES LIMITED (GB) 1987-09-15 US disclosed
EP-0180298-A2 Pyrimidine compounds SMITH KLINE & FRENCH LABORATORIES LIMITED (GB) 1986-05-07 EP disclosed
EP-0150073-A1 3,4-Disubstituted-1,2,5-oxadiazoles having histamine H2-receptor antagonist activity Bristol-Myers Squibb Company (US) 1985-07-31 EP disclosed
US-4507485-A 3,4-Disubstituted-1,2,5-oxadiazoles having histamine H2 -receptor antagonist activity BRISTOL-MYERS COMPANY (US) 1985-03-26 US disclosed
US-4433154-A ANTIHISTAMINES, ANTIULCER AGENTS SHIONOGI & COMPANY, LIMITED (JP) 1984-02-21 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 (1 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-20230149398-A1 TOPICAL PHARMACEUTICAL COMPOSITIONS COMPRISING IMIDAZO[1,2-B]PYRIDAZINE COMPOUNDS TNK2, TNIK, TNK1 PRMT6 3647/4885ALDH1A1 3027/4885SMN1; SMN2 1472/4885

“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.