SCHEMBL812920

SCHEMBL812920

O=C(O)CCN1CCCC1

nearest known ligand 0.71

Predicted protein targets (top 14)

geneUniProtsupporting neighboursconfidence
CYP1A2 P05177 1/20 0.71
MAPK1 P28482 1/20 0.71
SMN1; SMN2 Q16637 1/20 0.71
ALDH1A1 P00352 5/20 0.62
MAPT P10636 3/20 0.62
POLB P06746 2/20 0.62
GLA P06280 1/20 0.61
L3MBTL1 Q9Y468 1/20 0.60
KMT2A Q03164 5/20 0.52
GFER P55789 1/20 0.50
LMNA P02545 1/20 0.47
HSP90AA1 P07900 1/20 0.44
MEN1 O00255 1/20 0.43
HRH3 Q9Y5N1 1/20 0.42

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
SCHEMBL10939618 0.97 CYP1A2 (0.75) CYP1A2MAPK1SMN1; SMN2ALDH1A1MAPT
Hydrochloric Acid SCHEMBL1720619 0.97 CYP1A2 (0.68) CYP1A2MAPK1SMN1; SMN2ALDH1A1MAPT
SCHEMBL94068 0.97 CYP1A2 (0.75) CYP1A2MAPK1SMN1; SMN2ALDH1A1MAPT
SCHEMBL5313692 0.97 CYP1A2 (0.75) CYP1A2MAPK1SMN1; SMN2ALDH1A1MAPT
Hydrochloric Acid SCHEMBL1128098 0.95 CYP1A2 (0.72) CYP1A2MAPK1SMN1; SMN2ALDH1A1MAPT
SCHEMBL8202520 0.95 CYP1A2 (0.72) CYP1A2MAPK1SMN1; SMN2ALDH1A1MAPT
SCHEMBL3402164 0.95
Methylene Chloride SCHEMBL28294345 0.93 CYP1A2 (0.63) CYP1A2MAPK1SMN1; SMN2ALDH1A1MAPT
Ethylene SCHEMBL27789472 0.93 CYP1A2 (0.69) CYP1A2MAPK1SMN1; SMN2ALDH1A1MAPT
Hydrochloric Acid SCHEMBL23886232 0.92 GLA (0.65) CYP1A2MAPK1SMN1; SMN2ALDH1A1MAPT

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
WO-2017044411-A1 METHODS AND COMPOSITIONS FOR SOFT ANTICHOLINERGIC ZWITTERIONS BODOR LABORATORIES, INC. (US) 2017-03-16 WO claimed
WO-2017040307-A1 USE OF SELECTED ANTICHOLINERGIC ZWITTERIONS BODOR LABORATORIES, INC. (US) 2017-03-09 WO claimed
US-12624111-B2 Methods for treating metastatic colon cancer with leronlimab CYTODYN INC. (US) 2026-05-12 US disclosed
EP-4735418-A1 LIPID COMPOUNDS FOR GENE DELIVERY AND USE THEREOF Li, Bowen (CA) 2026-05-06 EP disclosed
EP-3814356-B1 TRIAZOLOTRIAZINE DERIVATIVES AS A2A RECEPTOR ANTAGONISTS ZHEJIANG VIMGREEN PHARMACEUTICALS LTD (CN) 2026-03-11 EP disclosed
US-20260060926-A1 NOVEL IONIZABLE LIPIDS AND LIPID NANOPARTICLES AND METHODS OF USING THE SAME SAIL BIOMEDICINES INC (US) 2026-03-05 US disclosed
EP-4581012-A2 NOVEL IONIZABLE LIPIDS AND LIPID NANOPARTICLES AND METHODS OF USING THE SAME Sail Biomedicines, Inc. (US) 2025-07-09 EP disclosed
US-20250213593-A1 Use of Derivatives based on Sarsasapogenin Structure and Pharmaceutical Compositions thereof BEIJING PHYTOVENT PHARMACEUTICAL TECHNOLOGY CO., LTD. (CN) 2025-07-03 US disclosed
US-20250205167-A1 NOVEL IONIZABLE LIPIDS AND LIPID NANOPARTICLES AND METHODS OF USING THE SAME SAIL BIOMEDICINES, INC. 2025-06-26 US disclosed
CN-118265692-B Carbon nucleus cationic lipid 厦门赛诺邦格生物科技股份有限公司 2025-06-13 CN disclosed
EP-4559896-A1 PH-SENSITIVE CATIONIC LIPID AND LIPID NANOPARTICLE National University Corporation Hokkaido University (JP) 2025-05-28 EP disclosed
CN-1010096-B CHARTREUSIN DERIVATIVE AND ITS SALT, ANTITUMOROUS PREPARATIONS CONTAINING THE SAME, AS WELL PROCESS FOR MAKING THE PREPARATION ISHIHARA SANGYO KAISHA (JP) 1990-10-24 CN disclosed
US-4927919-A ANTITUMOR AGENTS ISHIHARA SANGYO KAISHA, LTD. (JP) 1990-05-22 US disclosed
WO-1989009775-A1 N-HETEROCYCLIC PROPYLIDENE-1,1-BISPHOSPHONIC ACIDS, THEIR PRODUCTION AND A PHARMACEUTICAL COMPOSITION LEO PHARMACEUTICAL PRODUCTS LTD. A/S (LØVENS KEMIS (DK) 1989-10-19 WO disclosed
US-4760136-A Chartreusin derivatives and salts thereof ISHIHARA SANGYO KAISHA, LTD. (JP) 1988-07-26 US disclosed
US-4719176-A Enzyme-free diagnostic binding reagents KLOTZ IRVING M (US) 1988-01-12 US disclosed
EP-0110575-B1 1-AROYL-5-OXO-2-PYRROLIDINEPROPANOIC ACIDS AND RELATED ESTERS WARNER-LAMBERT COMPANY (US) 1987-05-20 EP disclosed
EP-0219852-A2 Chartreusin derivatives, salts thereof, antitumorous compositions containing the same, and processes for producing the same ISHIHARA SANGYO KAISHA, LTD. (JP) 1987-04-29 EP disclosed
CN-85103287-A Chartreusin (Chartreusin) derivative and its salt contain the anti-tumor compositions of these compounds, and the method for preparing these compounds 1987-02-04 CN disclosed
EP-0089926-A2 Pharmaceutical preparations of tetracycles containing nitrogen, and compounds of this type CIBA-GEIGY AG (CH) 1983-09-28 EP 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-20250205167-A1 NOVEL IONIZABLE LIPIDS AND LIPID NANOPARTICLES AND METHODS OF USING THE SAME PHOSPHO1, SGMS2, SGMS1 CYP1A2 4843/4885MAPK1 4424/4885SMN1; SMN2 2439/4885
US-12624111-B2 Methods for treating metastatic colon cancer with leronlimab CCR5, CCL2, CCR2 CYP1A2 2974/4885MAPK1 465/4885SMN1; SMN2 4160/4885
US-20260060926-A1 NOVEL IONIZABLE LIPIDS AND LIPID NANOPARTICLES AND METHODS OF USING THE SAME SGMS1, NPC1L1, SGMS2 CYP1A2 4683/4885MAPK1 1940/4885SMN1; SMN2 1074/4885
US-20250213593-A1 Use of Derivatives based on Sarsasapogenin Structure and Pharmaceutical Compositions thereof MAVS, NLN, TFAM CYP1A2 2086/4885MAPK1 3031/4885SMN1; SMN2 364/4885

“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.