SCHEMBL2856760

SCHEMBL2856760

CCCCN(CCC)CCN

nearest known ligand 0.48

Predicted protein targets (top 12)

geneUniProtsupporting neighboursconfidence
LCK P06239 1/20 0.48
DNM1 Q05193 8/20 0.39
MEN1 O00255 1/20 0.39
KMT2A Q03164 1/20 0.39
ALDH1A1 P00352 1/20 0.39
TSHR P16473 1/20 0.39
EPHX1 P07099 1/20 0.39
MAPT P10636 1/20 0.38
CA12 O43570 1/20 0.34
CA1 P00915 1/20 0.34
CA9 Q16790 1/20 0.34
KDM5A P29375 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
SCHEMBL418559 0.95 LCK (0.46) LCKDNM1MEN1KMT2AALDH1A1
SCHEMBL5667065 0.95 LCK (0.46) LCKDNM1MEN1KMT2AALDH1A1
SCHEMBL12552468 0.92 LCK (0.50) LCKDNM1MEN1KMT2AALDH1A1
SCHEMBL18912879 0.92 LCK (0.44) LCKDNM1MEN1KMT2AALDH1A1
SCHEMBL7861470 0.92 LCK (0.44) LCKDNM1MEN1KMT2AALDH1A1
SCHEMBL18785200 0.90 DNM1 (0.48) LCKDNM1MEN1KMT2AALDH1A1
SCHEMBL13154393 0.90 LCK (0.48) LCKDNM1MEN1KMT2AALDH1A1
SCHEMBL26713010 0.90 DNM1 (0.46) LCKDNM1MEN1KMT2AALDH1A1
SCHEMBL3237514 0.90 DNM1 (0.46) LCKDNM1MEN1KMT2AALDH1A1
Bromide SCHEMBL10786110 0.90 DNM1 (0.43) LCKDNM1MEN1KMT2AALDH1A1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-0298096-A1 METHOD FOR STABILIZING CLAYISH FORMATIONS CECA S.A. (FR) 1989-01-11 EP claimed
WO-1988004680-A1 METHOD FOR STABILIZING CLAYISH FORMATIONS CECA S.A. (FR) 1988-06-30 WO claimed
EP-4406982-A2 PRODUCTION OF ISOBUTYLENE HOMO- OR COPOLYMER DERIVATIVES BASF SE (DE) 2024-07-31 EP disclosed
US-11306161-B2 Preparation of isobutene homo- or copolymer derivatives BASF SE (DE) 2022-04-19 US disclosed
EP-3170883-B1 CLEANING PRODUCT PROCTER & GAMBLE (US) 2021-08-11 EP disclosed
US-20200325253-A1 PREPARATION OF ISOBUTENE HOMO- OR COPOLYMER DERIVATIVES BASF SE (DE) 2020-10-15 US disclosed
US-10745496-B2 Preparation of isobutene homo- or copolymer derivatives BASF SE (DE) 2020-08-18 US disclosed
EP-3348629-A1 CLEANING PRODUCT The Procter & Gamble Company (US) 2018-07-18 EP disclosed
US-20170204075-A1 AMINOALCOHOL LIPIDOIDS AND USES THEREOF MASSACHUSETTS INSTITUTE OF TECHNOLOGY (US) 2017-07-20 US disclosed
US-9688791-B2 High-reactivity polyisobutylene having a high content of vinylidene double bonds in the side chains BASF SE (DE) 2017-06-27 US disclosed
EP-3019493-B1 MODIFIED BET-PROTEIN INHIBITING DIHYDROCHINOXALINONES AND DIHYDROPYRIDOPYRAZINONES Bayer Pharma AG (DE) 2017-06-14 EP disclosed
EP-0385039-A1 Synthesis of carbonyl compounds BP Chimie Société Anonyme (FR) 1990-09-05 EP disclosed
EP-0384086-A1 Synthesis of hydrocarbyl amines BP Chimie Société Anonyme (FR) 1990-08-29 EP disclosed
WO-1990009371-A1 SYNTHESIS OF HYDROCARBYL AMINES BP CHEMICALS LIMITED (GB) 1990-08-23 WO disclosed
EP-0298096-A1 METHOD FOR STABILIZING CLAYISH FORMATIONS CECA S.A. (FR) 1989-01-11 EP disclosed
WO-1988004680-A1 METHOD FOR STABILIZING CLAYISH FORMATIONS CECA S.A. (FR) 1988-06-30 WO disclosed
US-4169859-A POLYMERIC KETONE FROM ALPHA-OLEFIN AND ACYL HALIDE CATALYST, ASHLESS DETERGENTS ATLANTIC RICHFIELD COMPANY (US) 1979-10-02 US disclosed
US-4157339-A Phosphonamidic condensation reaction product ATLANTIC RICHFIELD COMPANY (US) 1979-06-05 US disclosed
US-4119552-A DISPERSANT, AMIDATION OF PHENOXYALKANOIC ACID, REACTION OF THE AMIDE WITH A BORON COMPOUND EDWIN COOPER AND COMPANY LIMITED (GB) 1978-10-10 US disclosed
US-4028414-A LUBE OIL DETERGENT ATLANTIC RICHFIELD COMPANY (US) 1977-06-07 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 (1 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-20170204075-A1 AMINOALCOHOL LIPIDOIDS AND USES THEREOF PHOSPHO1, PNMT, AASDHPPT LCK 3165/4885DNM1 640/4885MEN1 2403/4885

“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.