SCHEMBL1506570

SCHEMBL1506570

COc1ccc(C2CCC(=O)CC2)cc1

nearest known ligand 0.58

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
ESR2 Q92731 2/20 0.58
ALDH1A1 P00352 4/20 0.53
SMN1; SMN2 Q16637 3/20 0.53
KMT2A Q03164 2/20 0.53
MEN1 O00255 1/20 0.53
MAPK1 P28482 1/20 0.53
PDE4A P27815 1/20 0.51
PDE4B Q07343 1/20 0.51
PDE4C Q08493 1/20 0.51
PDE4D Q08499 1/20 0.51
DDB1 Q16531 1/20 0.50
CRBN Q96SW2 1/20 0.50
DRD2 P14416 1/20 0.50
HRH3 Q9Y5N1 1/20 0.49
MAPT P10636 3/20 0.44
MAOA P21397 2/20 0.44
NPC1 O15118 2/20 0.44
RAB9A P51151 2/20 0.44
TP53 P04637 1/20 0.44
HPGD P15428 1/20 0.44

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
SCHEMBL12769099 0.90 ALDH1A1 (0.48) ESR2ALDH1A1SMN1; SMN2KMT2AMEN1
SCHEMBL2044506 0.89 ALDH1A1 (0.54) ESR2ALDH1A1SMN1; SMN2KMT2AMEN1
SCHEMBL27471526 0.89 ALDH1A1 (0.54) ESR2ALDH1A1SMN1; SMN2KMT2AMEN1
SCHEMBL2044509 0.89 ALDH1A1 (0.54) ESR2ALDH1A1SMN1; SMN2KMT2AMEN1
SCHEMBL3161832 0.84 PDE4A (0.52) ESR2ALDH1A1SMN1; SMN2KMT2AMEN1
SCHEMBL1515026 0.83 DRD2 (0.59) ALDH1A1SMN1; SMN2KMT2AMEN1MAPK1
SCHEMBL14403055 0.83 ESR2 (0.78) ESR2KMT2APDE4APDE4BPDE4C
SCHEMBL31019748 0.81 HRH3 (0.53) ESR2ALDH1A1SMN1; SMN2KMT2AMEN1
SCHEMBL4601394 0.80 TSHR (0.56) ESR2ALDH1A1SMN1; SMN2KMT2AMEN1
SCHEMBL4602856 0.80 HRH3 (0.56) ESR2SMN1; SMN2MAPK1CRBNHRH3

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-119409615-A 2- (Indol-3-yl) phenol compound and synthesis method thereof 湘潭大学 2025-02-11 CN claimed
CN-113296310-A Quantum dot light conversion layer and preparation method thereof 广东普加福光电科技有限公司 2021-08-24 CN claimed
CN-107619386-B Aromatic ring [ c ] carbazole derivative and synthesis method thereof 湘潭大学 2020-10-13 CN claimed
CN-107619386-A A kind of aromatic ring simultaneously [c] carbazole analog derivative and its synthetic method 湘潭大学 2018-01-23 CN claimed
US-20250281515-A1 CARBORANE COMPOUNDS, CARBORANE ANALOGS, AND METHODS OF USE THEREOF OHIO STATE INNOVATION FOUNDATION (US) 2025-09-11 US disclosed
US-20250270210-A1 BCL-2 Inhibitor BEIGENE, LTD. (KY) 2025-08-28 US disclosed
US-12286430-B2 Bcl-2 inhibitor BEIGENE, LTD. (KY) 2025-04-29 US disclosed
CN-119409615-A 2- (Indol-3-yl) phenol compound and synthesis method thereof 湘潭大学 2025-02-11 CN disclosed
US-20240376097-A1 BCL-2 Inhibitor BEIGENE LTD. (KY) 2024-11-14 US disclosed
EP-4460492-A1 COMPOUNDS CONTAINING A HYDROXYPHENYL MOIETY AND THEIR USE (INSERM) Institut National de la Santé et de la Recherche Médicale (FR) 2024-11-13 EP disclosed
CN-113347979-B Carborane compounds, carborane analogs, and methods of use thereof 俄亥俄州创新基金会 2024-08-16 CN disclosed
CN-116969936-A BCL-2 inhibitors 百济神州有限公司 2023-10-31 CN disclosed
US-20010056179-A1 Selective linear peptides with melanocortin-4 receptor (MC4-R) agonist activity HOFFMANN-LA ROCHE INC. 2001-12-27 US disclosed
WO-2001074844-A2 SELECTIVE LINEAR PEPTIDES WITH MELANOCORTIN-4 RECEPTOR (MC4-R) AGONIST ACTIVITY F. HOFFMANN-LA ROCHE AG (CH) 2001-10-11 WO disclosed
WO-2001060846-A1 CYCLIC HEXAPEPTIDE DERIVATIVES FUJISAWA PHARMACEUTICAL CO., LTD. (JP) 2001-08-23 WO disclosed
EP-0893424-A1 ALPHA,ALPHA-DIFLUOROBENZYL ETHER DERIVATIVES, LIQUID CRYSTAL COMPOSITIONS, AND LIQUID CRYSTAL DISPLAY DEVICES CHISSO CORPORATION (JP) 1999-01-27 EP disclosed
WO-1998031697-A1 ARYL C-GLYCOSIDE COMPOUNDS AND SULFATED ESTERS THEREOF SANKYO COMPANY, LIMITED (JP) 1998-07-23 WO disclosed
US-5712281-A Insecticidal substituted-2,4-diamino-5,6,7,8-tetrahydroquinazolines FMC CORPORATION (US) 1998-01-27 US disclosed
EP-0303398-B1 PREPARATION PROCESS OF 4-(4-HYDROXYPHENYL)-CYCLOHEXANOL MITSUI TOATSU CHEMICALS, Inc. (JP) 1991-12-11 EP disclosed
US-4894487-A Preparation process of 4-(4-hydroxyphenyl)-cyclohexanol MITSUI TOATSU CHEMICALS, INCORPORATED (JP) 1990-01-16 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 (5 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-20250270210-A1 BCL-2 Inhibitor BCL2, BCL2A1, BCL2L1 ESR2 1033/4885ALDH1A1 2918/4885SMN1; SMN2 1721/4885
US-20240376097-A1 BCL-2 Inhibitor BCL2, BCL2A1, BCL2L1 ESR2 1033/4885ALDH1A1 2918/4885SMN1; SMN2 1721/4885
US-12286430-B2 Bcl-2 inhibitor BCL2, BCL2A1, BCL2L1 ESR2 1033/4885ALDH1A1 2918/4885SMN1; SMN2 1721/4885
US-20250281515-A1 CARBORANE COMPOUNDS, CARBORANE ANALOGS, AND METHODS OF USE THEREOF ESR2, ESRRB, ESRRA ESR2 1/4885ALDH1A1 1094/4885SMN1; SMN2 788/4885
US-20010056179-A1 Selective linear peptides with melanocortin-4 receptor (MC4-R) agonist activity MC4R, MC3R, MC1R ESR2 1169/4885ALDH1A1 4684/4885SMN1; SMN2 2762/4885

“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.