SCHEMBL1008583

SCHEMBL1008583

O=C(O)/C=C/C1CCCCC1

nearest known ligand 0.61

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
HTT P42858 2/20 0.47
SMN1; SMN2 Q16637 2/20 0.47
NPC1 O15118 1/20 0.47
GAA P10253 1/20 0.47
GRIN1 Q05586 1/20 0.39
GRIN2B Q13224 1/20 0.39
TSHR P16473 2/20 0.38
TP53 P04637 2/20 0.38
EGLN1 Q9GZT9 1/20 0.38
EGLN3 Q9H6Z9 1/20 0.38
MEN1 O00255 1/20 0.37
MITF O75030 1/20 0.37
LMNA P02545 1/20 0.37
CYP3A4 P08684 1/20 0.37
MAPT P10636 1/20 0.37
ALOX15 P16050 1/20 0.37
KMT2A Q03164 1/20 0.37
NPSR1 Q6W5P4 1/20 0.37
NLRP1 Q9C000 1/20 0.37
GPR55 Q9Y2T6 1/20 0.37

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
SCHEMBL1151112 1.00 HTT (0.47) HTTSMN1; SMN2NPC1GAAGRIN1
SCHEMBL17263955 1.00 HTT (0.47) HTTSMN1; SMN2NPC1GAAGRIN1
SCHEMBL221714 1.00 HTT (0.47) HTTSMN1; SMN2NPC1GAAGRIN1
SCHEMBL11845850 1.00 HTT (0.47) HTTSMN1; SMN2NPC1GAAGRIN1
SCHEMBL9063561 1.00 HTT (0.47) HTTSMN1; SMN2NPC1GAAGRIN1
SCHEMBL4599663 1.00 HTT (0.47) HTTSMN1; SMN2NPC1GAAGRIN1
SCHEMBL23749603 1.00 HTT (0.47) HTTSMN1; SMN2NPC1GAAGRIN1
SCHEMBL1151110 1.00 HTT (0.47) HTTSMN1; SMN2NPC1GAAGRIN1
SCHEMBL9743609 1.00 HTT (0.47) HTTSMN1; SMN2NPC1GAAGRIN1
SCHEMBL15290579 1.00 HTT (0.47) HTTSMN1; SMN2NPC1GAAGRIN1

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-120132832-A Double-function catalyst for synthesizing saturated acid ester by unsaturated acid or/and anhydride esterification-hydrogenation coupling reaction and application thereof 上海师范大学 2025-06-13 CN claimed
CN-120132832-A Double-function catalyst for synthesizing saturated acid ester by unsaturated acid or/and anhydride esterification-hydrogenation coupling reaction and application thereof 上海师范大学 2025-06-13 CN disclosed
CN-119790041-A Alpha, beta-unsaturated amide compounds, preparation method, pharmaceutical composition and application thereof 中国科学院上海药物研究所 2025-04-08 CN disclosed
US-20240308931-A1 LIGAND-CONTROLLED DIVERGENT DEHYDROGENATIVE REACTIONS OF ALIPHATIC ACIDS THE SCRIPPS RESEARCH INSTITUTE 2024-09-19 US disclosed
EP-4370490-A1 LIGAND-CONTROLLED DIVERGENT DEHYDROGENATIVE REACTIONS OF ALIPHATIC ACIDS The Scripps Research Institute (US) 2024-05-22 EP disclosed
CN-117402123-A Alpha, beta-unsaturated amide compounds, preparation method, pharmaceutical composition and application thereof 中国科学院上海药物研究所 2024-01-16 CN disclosed
WO-2024008166-A1 α,β-UNSATURATED AMIDE COMPOUND, AND PREPARATION METHOD THEREFOR, AND PHARMACEUTICAL COMPOSITION AND USE THEREOF 中国科学院上海药物研究所 2024-01-11 WO disclosed
US-11820165-B2 Printed object DAI NIPPON TORYO CO., LTD. (JP) 2023-11-21 US disclosed
CN-116891409-A Photoactive compound, photoresist composition comprising the same, and pattern forming method 罗门哈斯电子材料有限责任公司 2023-10-17 CN disclosed
US-20230314934-A1 PHOTOACTIVE COMPOUNDS, PHOTORESIST COMPOSITIONS INCLUDING THE SAME, AND PATTERN FORMATION METHODS U.S. BANK TRUST COMPANY, NATIONAL ASSOCIATION, AS NOTES COLLATERAL AGENT 2023-10-05 US disclosed
US-5490945-A OIL CONTAINING CARBOXYLIC MODIFIED POLYOLEFIN THE LUBRIZOL CORPORATION (US) 1996-02-13 US disclosed
WO-1995029148-A1 O-ACYL-4-PHENYL-CYCLOHEXANOLS, THEIR SALTS, MEDICAMENTS CONTAINING SUCH COMPOUNDS AND THEIR USE, AS WELL AS A METHOD OF PREPARING THEM DR. KARL THOMAE GMBH (DE) 1995-11-02 WO disclosed
EP-0596047-A1 LUBRICATING COMPOSITIONS AND CONCENTRATES THE LUBRIZOL CORPORATION (US) 1994-05-11 EP disclosed
EP-0596048-A1 LUBRICATING COMPOSITIONS AND CONCENTRATES THE LUBRIZOL CORPORATION (US) 1994-05-11 EP disclosed
WO-1993023505-A1 LUBRICATING COMPOSITIONS AND CONCENTRATES THE LUBRIZOL CORPORATION (US) 1993-11-25 WO disclosed
WO-1993023504-A1 LUBRICATING COMPOSITIONS AND CONCENTRATES THE LUBRIZOL CORPORATION (US) 1993-11-25 WO disclosed
US-5135833-A Low temperature-fixing toner comprising a binder resin containing 5-10% tetrahydrofuran-insoluble matter having a specific molecular weight profile; offset resistance; antisoilants CANON KABUSHIKI KAISHA (JP) 1992-08-04 US disclosed
US-4161476-A α-Halo-2-oxo-1-azetidinemethane-carboxylic acid compounds CIBA-GEIGY CORPORATION (US) 1979-07-17 US disclosed
US-4052408-A OXYACETIC ACID COMPOUNDS AND PROCESS FOR THEIR MANUFACTURE CIBA-GEIGY CORPORATION (US) 1977-10-04 US disclosed
US-3975429-A Cyclopropanemethyl esters of cinnamic acid and derivatives thereof ZOECON CORPORATION (US) 1976-08-17 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 (2 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-20240308931-A1 LIGAND-CONTROLLED DIVERGENT DEHYDROGENATIVE REACTIONS OF ALIPHATIC ACIDS PPARD, PPARA, PDCD1LG2 HTT 3977/4885SMN1; SMN2 3416/4885NPC1 3920/4885
US-20230314934-A1 PHOTOACTIVE COMPOUNDS, PHOTORESIST COMPOSITIONS INCLUDING THE SAME, AND PATTERN FORMATION METHODS CRY1, CBR3, C1S HTT 3650/4885SMN1; SMN2 4834/4885NPC1 2740/4885

“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.