SCHEMBL1220604

SCHEMBL1220604

COCC(CN1CCCCC1)OC

nearest known ligand 0.41

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
MEN1 O00255 1/20 0.41
KMT2A Q03164 1/20 0.41
KDM4E B2RXH2 1/20 0.39
POLB P06746 1/20 0.39
ATM Q13315 2/20 0.39
MAPT P10636 2/20 0.39
CYP2D6 P10635 3/20 0.36
CYP2C19 P33261 2/20 0.36
ALDH1A1 P00352 3/20 0.35
TDP1 Q9NUW8 1/20 0.35
TSHR P16473 1/20 0.34
HIF1A Q16665 1/20 0.34
DRD4 P21917 1/20 0.33
SLC6A2 P23975 1/20 0.33
CCKAR P32238 1/20 0.33
OPRM1 P35372 1/20 0.33
DRD3 P35462 1/20 0.33
SCN1A P35498 1/20 0.33
OPRK1 P41145 1/20 0.33
HTR2B P41595 1/20 0.33

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
SCHEMBL23706773 0.98 ATM (0.40) MEN1KMT2AKDM4EPOLBATM
SCHEMBL25480713 0.84 MEN1 (0.44) MEN1KMT2AKDM4EPOLBATM
SCHEMBL23706758 0.82 L3MBTL1 (0.37) MEN1KMT2AKDM4EALDH1A1DRD4
SCHEMBL20763691 0.82 KDM4E (0.41) MEN1KMT2AKDM4EPOLBMAPT
SCHEMBL11911641 0.81 MEN1 (0.43) MEN1KMT2AKDM4EPOLBATM
SCHEMBL23706755 0.80 SMN1; SMN2 (0.45) MEN1KMT2AKDM4EPOLBALDH1A1
SCHEMBL12083728 0.80 USP2 (0.45) KDM4EPOLBCYP2D6ALDH1A1TDP1
SCHEMBL23706764 0.79 KMT2A (0.44) MEN1KMT2AALDH1A1TSHRDRD4
SCHEMBL12349177 0.79 POLB (0.40) MEN1KMT2AKDM4EPOLBATM
SCHEMBL25135334 0.79 DRD2 (0.37) MEN1KMT2ASLC6A3

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20250262589-A1 AMINE COMPOSITION FOR CARBON DIOXIDE SEPARATION USE TOSOH CORPORATION (JP) 2025-08-21 US disclosed
EP-4494740-A1 AMINE COMPOSITION FOR CARBON DIOXIDE SEPARATION USE TOSOH CORPORATION (JP) 2025-01-22 EP disclosed
WO-2023204222-A1 AMINE COMPOSITION FOR CARBON DIOXIDE SEPARATION USE 東ソー株式会社 2023-10-26 WO disclosed
CN-114901383-A Composition for separating carbon dioxide and method for separating carbon dioxide 东曹株式会社 2022-08-12 CN disclosed
WO-2021153650-A1 COMPOSITION FOR CARBON DIOXIDE SEPARATION AND METHOD FOR SEPARATING CARBON DIOXIDE 東ソー株式会社 2021-08-05 WO disclosed
EP-1569937-B1 C-6 MODIFIED INDAZOLYLPYRROLOTRIAZINES BRISTOL MYERS SQUIBB CO (US) 2011-11-23 EP disclosed
US-20110039838-A1 PYRROLOTRIAZINE COMPOUNDS AS KINASE INHIBITORS BRISTOL-MYERS SQUIBB COMPANY 2011-02-17 US disclosed
US-7846931-B2 Pyrrolotriazine compounds as kinase inhibitors BRISTOL-MYERS SQUIBB COMPANY (US) 2010-12-07 US disclosed
EP-2058314-A1 Pyrrolotriazine compounds as kinase inhibitors Bristol-Myers Squibb Company (US) 2009-05-13 EP disclosed
EP-1699798-A4 DI-SUBSTITUTED PYRROLOTRIAZINE COMPOUNDS BRISTOL MYERS SQUIBB CO (US) 2009-03-11 EP disclosed
US-7064203-B2 Di-substituted pyrrolotriazine compounds BRISTOL MYERS SQUIBB COMPANY (US) 2006-06-20 US disclosed
US-20050222153-A1 C-6 modified indazolylpyrrolotriazines VITE GREGORY D 2005-10-06 US disclosed
US-20050197339-A1 Di-substituted pyrrolotrizine compounds BRISTOL-MYERS SQUIBB COMPANY 2005-09-08 US disclosed
EP-1569937-A2 C-6 MODIFIED INDAZOLYLPYRROLOTRIAZINES Bristol-Myers Squibb Company (US) 2005-09-07 EP disclosed
US-20050182058-A1 Pyrrolotriazine compounds as kinase inhibitors BRISTOL-MYERS SQUIBB COMPANY 2005-08-18 US disclosed
WO-2005066176-A1 PYRROLOTRIAZINE COMPOUNDS AS KINASE INHIBITORS BRISTOL-MYERS SQUIBB COMPANY (US) 2005-07-21 WO disclosed
WO-2005065266-A2 DI-SUBSTITUTED PYRROLOTRIAZINE COMPOUNDS BRISTOL-MYERS SQUIBB COMPANY (US) 2005-07-21 WO disclosed
US-6916815-B2 C-6 modified indazolylpyrrolotriazines BRISTOL-MYERS SQUIBB COMPANY (US) 2005-07-12 US disclosed
US-20040142931-A1 C-6 modified indazolylpyrrolotriazines BRISTOL-MYERS SQUIBB COMPANY 2004-07-22 US disclosed
WO-2004054514-A2 C-6 MODIFIED INDAZOLYLPYRROLOTRIAZINES BRISTOL-MYERS SQUIBB COMPANY (US) 2004-07-01 WO 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-20110039838-A1 PYRROLOTRIAZINE COMPOUNDS AS KINASE INHIBITORS ERBB2, ERBB4, ERBB3 MEN1 3024/4885KMT2A 1682/4885KDM4E 2206/4885
US-20050222153-A1 C-6 modified indazolylpyrrolotriazines ERBB2, ERBB4, EGFR MEN1 2849/4885KMT2A 2678/4885KDM4E 2779/4885
US-20050197339-A1 Di-substituted pyrrolotrizine compounds ERBB2, ERBB4, EGFR MEN1 2876/4885KMT2A 1877/4885KDM4E 1487/4885
US-20050182058-A1 Pyrrolotriazine compounds as kinase inhibitors ERBB2, ERBB4, ERBB3 MEN1 3024/4885KMT2A 1682/4885KDM4E 2206/4885
US-20040142931-A1 C-6 modified indazolylpyrrolotriazines ERBB2, ERBB4, EGFR MEN1 2283/4885KMT2A 2696/4885KDM4E 2902/4885

“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.