SCHEMBL126194

SCHEMBL126194

CCN1CCN(CC(=O)O)CC1

nearest known ligand 0.75

Predicted protein targets (top 11)

geneUniProtsupporting neighboursconfidence
HSD17B10 Q99714 1/20 0.52
MEN1 O00255 1/20 0.48
KMT2A Q03164 1/20 0.48
KDM4E B2RXH2 2/20 0.44
SMN1; SMN2 Q16637 1/20 0.43
ALDH1A1 P00352 3/20 0.43
LMNA P02545 2/20 0.43
HSD11B1 P28845 2/20 0.43
S1PR1 P21453 1/20 0.42
MAPT P10636 1/20 0.42
GAA P10253 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
SCHEMBL15468170 1.00 HSD17B10 (0.52) HSD17B10MEN1KMT2AKDM4ESMN1; SMN2
SCHEMBL5517050 1.00 HSD17B10 (0.52) HSD17B10MEN1KMT2AKDM4ESMN1; SMN2
SCHEMBL21547377 1.00 HSD17B10 (0.52) HSD17B10MEN1KMT2AKDM4ESMN1; SMN2
SCHEMBL12344760 1.00 HSD17B10 (0.52) HSD17B10MEN1KMT2AKDM4ESMN1; SMN2
SCHEMBL16645332 1.00 HSD17B10 (0.52) HSD17B10MEN1KMT2AKDM4ESMN1; SMN2
Bromide SCHEMBL2542868 0.98 HSD17B10 (0.50) HSD17B10MEN1KMT2AKDM4ESMN1; SMN2
Hydrochloric Acid SCHEMBL1375642 0.98 HSD17B10 (0.50) HSD17B10MEN1KMT2AKDM4ESMN1; SMN2
SCHEMBL16645317 0.93 HSD17B10 (0.47) HSD17B10MEN1KMT2AKDM4ESMN1; SMN2
SCHEMBL29299530 0.91 HSD17B10 (0.45) HSD17B10MEN1KMT2AKDM4EALDH1A1
SCHEMBL20686921 0.91 HSD17B10 (0.45) HSD17B10MEN1KMT2AKDM4EALDH1A1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-7271195-B2 Carbonyl compounds as inhibitors of histone deacetylase for the treatment of disease KALYPSYS, INC. (US) 2007-09-18 US claimed
EP-1635800-A2 CARBONYL COMPOUNDS AS INHIBITORS OF HISTONE DEACETYLASE FOR THE TREATMENT OF DISEASE Kalypsys, Inc. (US) 2006-03-22 EP claimed
US-20050026907-A1 Carbonyl compounds as inhibitors of histone deacetylase for the treatment of disease KALYPSYS, INC. (US) 2005-02-03 US claimed
WO-2004110418-A2 CARBONYL COMPOUNDS AS INHIBITORS OF HISTONE DEACETYLASE FOR THE TREATMENT OF DISEASE KALYPSYS, INC. (US) 2004-12-23 WO claimed
CN-118084892-A Compounds useful as HPK1 inhibitors 深圳福沃药业有限公司 2024-05-28 CN disclosed
EP-3954679-A2 AMIDE COMPOUNDS FOR THE TREATMENT OF HIV INFECTIONS Gilead Sciences, Inc. (US) 2022-02-16 EP disclosed
US-11161856-B2 Spirocycle compounds and methods of making and using same H. LUNDBECK A/S (DK) 2021-11-02 US disclosed
EP-3409667-B1 AMIDE COMPOUNDS FOR THE TREATMENT OF HIV INFECTIONS GILEAD SCIENCES INC (US) 2021-07-21 EP disclosed
US-11034718-B2 C-3 novel triterpenone with C-17 reverse amide derivatives as HIV inhibitors HETERO LABS LIMITED (IN) 2021-06-15 US disclosed
US-11034718-B2 C-3 novel triterpenone with C-17 reverse amide derivatives as HIV inhibitors HETERO LABS LIMITED (IN) 2021-06-15 US disclosed
US-20210009555-A1 THERAPEUTIC COMPOUNDS GILEAD SCIENCES, INC. 2021-01-14 US disclosed
WO-2020154683-A1 METHODS OF TREATING DISEASE WITH MAGL INHIBITORS LUNDBECK LA JOLLA RESEARCH CENTER, INC. (US) 2020-07-30 WO disclosed
US-20060030554-A1 Novel sulfonamides as inhibitors of histone deacetylase for the treatment of disease KALYPSYS, INC. 2006-02-09 US disclosed
WO-2005123089-A2 MULTICYCLIC SULFONAMIDE COMPOUNDS AS INHIBITORS OF HISTONE DEACETYLASE FOR THE TREATMENT OF DISEASE KALYPSYS, INC. (US) 2005-12-29 WO disclosed
WO-2005120515-A2 NOVEL SULFONAMIDES AS INHIBITORS OF HISTONE DEACETYLASE FOR THE TREATMENT OF DISEASE KALYPSYS, INC. (US) 2005-12-22 WO disclosed
WO-2005110987-A1 PIPERIDINE DERIVATIVES AS NK1 AND NK3 ANTAGONISTS PFIZER PRODUCTS INC. (US) 2005-11-24 WO disclosed
US-20050256164-A1 NK1 and NK3 antagonists PFIZER INC 2005-11-17 US disclosed
US-20050026907-A1 Carbonyl compounds as inhibitors of histone deacetylase for the treatment of disease KALYPSYS, INC. (US) 2005-02-03 US disclosed
WO-2004110418-A2 CARBONYL COMPOUNDS AS INHIBITORS OF HISTONE DEACETYLASE FOR THE TREATMENT OF DISEASE KALYPSYS, INC. (US) 2004-12-23 WO disclosed
US-5532255-A Adhesion receptor antagonists MERCK PATENT GESELLSCHAFT MIT BESCHRANKTER HAFTUNG (DE) 1996-07-02 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 (6 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-11034718-B2 C-3 novel triterpenone with C-17 reverse amide derivatives as HIV inhibitors IL17A, CDK17, CCR3 HSD17B10 90/4885MEN1 4501/4885KMT2A 3663/4885
US-20050256164-A1 NK1 and NK3 antagonists TAC3, TACR1, TACR2 HSD17B10 4616/4885MEN1 786/4885KMT2A 1384/4885
US-20210009555-A1 THERAPEUTIC COMPOUNDS HAVCR2, SARS1, RPL35 HSD17B10 967/4885MEN1 2845/4885KMT2A 4689/4885
US-11161856-B2 Spirocycle compounds and methods of making and using same OPRL1, MGLL, VKORC1L1 HSD17B10 670/4885MEN1 1235/4885KMT2A 4106/4885
US-20050026907-A1 Carbonyl compounds as inhibitors of histone deacetylase for the treatment of disease HDAC6, HDAC5, HDAC1 HSD17B10 626/4885MEN1 4045/4885KMT2A 64/4885
US-20060030554-A1 Novel sulfonamides as inhibitors of histone deacetylase for the treatment of disease HDAC6, HDAC3, HDAC5 HSD17B10 812/4885MEN1 4446/4885KMT2A 50/4885

“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.