SCHEMBL8655892

SCHEMBL8655892

COc1ccccc1CC(P)C1CCCCC1

nearest known ligand 0.54

Predicted protein targets (top 10)

geneUniProtsupporting neighboursconfidence
▸ LMNA P02545 1/20 0.48
▸ MEN1 O00255 1/20 0.46
▸ KMT2A Q03164 1/20 0.46
▸ TAAR1 Q96RJ0 1/20 0.44
▸ ALDH1A1 P00352 3/20 0.43
▸ POLB P06746 1/20 0.43
▸ HRH3 Q9Y5N1 3/20 0.42
▸ HPGD P15428 2/20 0.42
▸ SMN1; SMN2 Q16637 1/20 0.41
▸ GAA P10253 1/20 0.41

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
SCHEMBL14874433 0.77 POLB (0.47) LMNAMEN1KMT2AALDH1A1POLB
SCHEMBL11310166 0.74 LMNA (0.42) LMNAMEN1KMT2AALDH1A1HPGD
SCHEMBL7975883 0.74 POLB (0.47) LMNAMEN1KMT2AALDH1A1POLB
SCHEMBL1042297 0.72 EPHX2 (0.49) HPGDSMN1; SMN2
SCHEMBL27091860 0.72 MEN1 (0.65) LMNAMEN1KMT2AALDH1A1POLB
SCHEMBL7446651 0.70 CYP2D6 (0.50) LMNAMEN1KMT2ATAAR1HRH3
SCHEMBL31029938 0.70 LMNA (0.48) LMNAMEN1KMT2ATAAR1ALDH1A1
SCHEMBL11020973 0.70 LMNA (0.48) LMNAMEN1KMT2ATAAR1ALDH1A1
SCHEMBL12204085 0.70 ALDH1A1 (0.76) LMNAMEN1KMT2AALDH1A1POLB
SCHEMBL585112 0.70 IDO1 (0.50) MEN1KMT2ATAAR1ALDH1A1HRH3

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 8 patents. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-9896451-B2 Method for producing endo-9-azabicyclo[3.3.1]nonan-3-ol derivative NIPPON SODA CO., LTD. (JP) 2018-02-20 — — US disclosed
US-20160200726-A1 METHOD FOR PRODUCING ENDO-9-AZABICYCLO[3.3.1]NONAN-3-OL DERIVATIVE NIPPON SODA CO., LTD. (JP) 2016-07-14 — — US disclosed
EP-3042902-A1 METHOD FOR PRODUCING ENDO-9-AZABICYCLO[3.3.1]NONANE-3-OL DERIVATIVE Nippon Soda Co., Ltd. (JP) 2016-07-13 — — EP disclosed
US-5756863-A Process for preparing optically active cyclohexanol derivatives TAKASAGO INTERNATIONAL CORPORATION (JP) 1998-05-26 — — US disclosed
EP-0768288-A2 Process for preparing optically active cyclohexanol derivatives Takasago International Corporation (JP) 1997-04-16 — — EP disclosed
US-RE29990-E Processes for stereospecifically preparing chiral 2-substituted-4-hydroxy-2-cyclopenten-1-one WISCONSIN ALUMNI RESEARCH FOUNDATION (US) 1979-05-08 — — US disclosed
US-4057851-A PROSTAGLANDIN INTERMEDIATES WISCONSIN ALUMNI RESEARCH FOUNDATION (US) 1977-11-08 — — US disclosed
US-3968141-A Processes for stereospecifically preparing chiral 2-substituted-4-hydroxy-2-cyclopenten-1-one WISCONSIN ALUMNI RESEARCH FOUNDATION (US) 1976-07-06 — — 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-20160200726-A1 METHOD FOR PRODUCING ENDO-9-AZABICYCLO[3.3.1]NONAN-3-OL DERIVATIVE CYP8B1, CYP2C9, HAAO LMNA 4766/4885MEN1 2476/4885KMT2A 3635/4885

“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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