SCHEMBL35966

SCHEMBL35966

O=Cc1ccc(-c2ccccc2-c2ccccc2)cc1

nearest known ligand 0.59

Predicted protein targets (top 18)

geneUniProtsupporting neighboursconfidence
ALDH1A1 P00352 5/20 0.59
CYP2A6 P11509 3/20 0.59
DRD1 P21728 3/20 0.56
DRD2 P14416 1/20 0.55
DRD4 P21917 1/20 0.55
DRD5 P21918 1/20 0.55
DRD3 P35462 1/20 0.55
PTGS2 P35354 1/20 0.47
NAT1 P18440 1/20 0.45
ELANE P08246 1/20 0.43
HSD17B10 Q99714 3/20 0.42
ALDH5A1 P51649 1/20 0.42
ABAT P80404 1/20 0.42
TP53 P04637 1/20 0.42
PTGS1 P23219 1/20 0.42
IP6K1 Q92551 1/20 0.41
HPGD P15428 1/20 0.41
BCL2L1 Q07817 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
Hydrogen Sulfide SCHEMBL27896687 0.98 ALDH1A1 (0.56) ALDH1A1CYP2A6DRD1DRD2DRD4
SCHEMBL1666926 0.95 DRD1 (0.60) ALDH1A1CYP2A6DRD1DRD2DRD4
SCHEMBL29733609 0.93 DRD1 (0.58) ALDH1A1CYP2A6DRD1DRD2DRD4
SCHEMBL29733602 0.93 DRD1 (0.58) ALDH1A1CYP2A6DRD1DRD2DRD4
SCHEMBL6032 0.87 ALDH1A1 (0.68) ALDH1A1CYP2A6DRD1DRD2DRD4
Benzene SCHEMBL28288569 0.87 ALDH1A1 (0.68) ALDH1A1CYP2A6DRD1DRD2DRD4
SCHEMBL5733969 0.87 ALDH1A1 (0.68) ALDH1A1CYP2A6DRD1DRD2DRD4
SCHEMBL10969109 0.87 ALDH1A1 (0.68) ALDH1A1CYP2A6DRD1DRD2DRD4
SCHEMBL5490742 0.87 ALDH1A1 (0.50) ALDH1A1CYP2A6DRD1DRD2DRD4
SCHEMBL29671482 0.87 ALDH1A1 (0.50) ALDH1A1CYP2A6DRD1DRD2DRD4

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-117164628-A Mercury ion ratio fluorescent probe based on hemicyanine and preparation and application thereof 贺州学院 2023-12-05 CN claimed
CN-122051301-A Preparation method and application of homogeneous vanadium battery conducting film modified in situ by covalent organic framework 浙江工业大学 2026-05-15 CN disclosed
US-20250357474-A1 SILICON NANOPARTICLE ELECTRODE COMPOSITIONS AND METHODS OF MAKING THE SAME ALLIANCE SUSTAINABLE ENERGY (US) 2025-11-20 US disclosed
CN-117164628-A Mercury ion ratio fluorescent probe based on hemicyanine and preparation and application thereof 贺州学院 2023-12-05 CN disclosed
CN-117164628-A Mercury ion ratio fluorescent probe based on hemicyanine and preparation and application thereof 贺州学院 2023-12-05 CN disclosed
CN-116093283-A Phthalocyanine-based covalent organic framework coated nano silicon composite material and preparation method thereof 宜春江理锂电新能源产业研究院 2023-05-09 CN disclosed
US-11459242-B2 Stabilized electrodes for ion batteries and methods of making the same ALLIANCE FOR SUSTAINABLE ENERGY, LLC (US) 2022-10-04 US disclosed
CN-112156758-B Porous material and preparation method and application thereof 清华大学 2021-08-31 CN disclosed
CN-112156758-A Porous material and preparation method and application thereof 清华大学 2021-01-01 CN disclosed
US-10626095-B2 Cyanotriazole compounds OTSUKA PHARMACEUTICAL CO., LTD. (JP) 2020-04-21 US disclosed
US-20160229816-A1 CYANOTRIAZOLE COMPOUNDS OTSUKA PHARMACEUTICAL CO., LTD. (JP) 2016-08-11 US disclosed
WO-2015008872-A1 CYANOTRIAZOLE COMPOUNDS OTSUKA PHARMACEUTICAL CO., LTD. (JP) 2015-01-22 WO disclosed
US-8513220-B2 Aromatic compounds having sphingosine-1-phosphonate (S1P) receptor activity ALLERGAN, INC. (US) 2013-08-20 US disclosed
EP-2569322-A1 AROMATIC COMPOUNDS HAVING SPHINGOSINE-1-PHOSPHONATE (S1P) RECEPTOR ACTIVITY Allergan, Inc. (US) 2013-03-20 EP disclosed
US-20130018019-A1 AROMATIC COMPOUNDS HAVING SPHINGOSINE-1-PHOSPHONATE (S1P) RECEPTOR ACTIVITY ALLERGAN, INC. (US) 2013-01-17 US disclosed
WO-2011143332-A1 AROMATIC COMPOUNDS HAVING SPHINGOSINE-1-PHOSPHONATE (S1P) RECEPTOR ACTIVITY ALLERGAN, INC. (US) 2011-11-17 WO disclosed
US-20110281822-A1 AROMATIC COMPOUNDS HAVING SPHINGOSINE-1-PHOSPHONATE (S1P) RECEPTOR ACTIVITY ALLERGAN, INC. (US) 2011-11-17 US disclosed
EP-1575964-B1 N-(BENZYL)AMINOALKYL CARBOXYLATE, PHOSPHINATES, PHOSPHONATES AND TETRAZOLES AS EDG RECEPTOR AGONISTS MERCK & CO INC (US) 2009-11-11 EP disclosed
US-7351725-B2 N-(benzyl)aminoalkylcarboxylates, phosphinates, phosphonates and tetrazoles as Edg receptor agonists MERCK & CO., INC. (US) 2008-04-01 US disclosed
US-7351725-B2 N-(benzyl)aminoalkylcarboxylates, phosphinates, phosphonates and tetrazoles as Edg receptor agonists MERCK & CO., INC. (US) 2008-04-01 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 (4 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-10626095-B2 Cyanotriazole compounds CS, PC, ACAT1 ALDH1A1 1611/4885CYP2A6 3084/4885DRD1 4556/4885
US-20130018019-A1 AROMATIC COMPOUNDS HAVING SPHINGOSINE-1-PHOSPHONATE (S1P) RECEPTOR ACTIVITY S1PR1, S1PR3, S1PR2 ALDH1A1 2617/4885CYP2A6 3025/4885DRD1 3624/4885
US-20110281822-A1 AROMATIC COMPOUNDS HAVING SPHINGOSINE-1-PHOSPHONATE (S1P) RECEPTOR ACTIVITY S1PR1, S1PR3, S1PR2 ALDH1A1 2617/4885CYP2A6 3025/4885DRD1 3624/4885
US-20160229816-A1 CYANOTRIAZOLE COMPOUNDS CS, PC, ACAT1 ALDH1A1 1611/4885CYP2A6 3084/4885DRD1 4556/4885

“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.