SCHEMBL640973

SCHEMBL640973

CC(C)C(CCCN)C(C)C

nearest known ligand 0.38

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
NFKB1 P19838 1/20 0.35
DNM1 Q05193 4/20 0.33
CA12 O43570 2/20 0.33
CA1 P00915 2/20 0.33
CA2 P00918 2/20 0.33
CA3 P07451 2/20 0.33
CA4 P22748 2/20 0.33
CA6 P23280 2/20 0.33
CA5A P35218 2/20 0.33
CA7 P43166 2/20 0.33
CA9 Q16790 2/20 0.33
CA14 Q9ULX7 2/20 0.33
CA5B Q9Y2D0 2/20 0.33
TSHR P16473 2/20 0.33
HTR2A P28223 1/20 0.33
HRH1 P35367 1/20 0.33
LMNA P02545 1/20 0.33
BLM P54132 1/20 0.33
TRPV1 Q8NER1 1/20 0.32
TRPA1 O75762 1/20 0.32

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
SCHEMBL504336 0.91 NFKB1 (0.41) NFKB1DNM1CA12CA1CA2
SCHEMBL9186569 0.86 TRPV1 (0.39) NFKB1HTR2AHRH1TRPV1TRPA1
SCHEMBL640718 0.80 GABRR1 (0.39) ALDH1A1
SCHEMBL14415093 0.79 NFKB1 (0.33) NFKB1DNM1CA12CA1CA2
SCHEMBL28411831 0.78
SCHEMBL565547 0.77 TRPV1 (0.40) NFKB1TSHRHTR2AHRH1TRPV1
SCHEMBL2268916 0.77
SCHEMBL30987407 0.76 LMNA (0.42) LMNATRPV1TRPA1
SCHEMBL19201004 0.75
SCHEMBL8557939 0.75

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-116120517-B Water-dispersible composite hydrophilic modified curing agent and preparation method thereof 万华化学(宁波)有限公司 2024-10-18 CN claimed
CN-116120517-A Water-dispersible composite hydrophilic modified curing agent and preparation method thereof 万华化学(宁波)有限公司 2023-05-16 CN claimed
US-7351339-B2 Using an auxiliary base to form a salt with the acid which is liquid at low enough temperature so that value product does not decompose during the removal of the liquid salt; e.g. acid catalyst removal; ionic liquids BASF AKTIENGESELLSCHAFT (DE) 2008-04-01 US claimed
US-20040073035-A1 Removal by salt formation BASF AKTIENGESELLSCHAFT (DE) 2004-04-15 US claimed
US-20260117080-A1 METAL OXIDE PARTICLES HAVING CORE/SHELL STRUCTURE HAVING UNIFORM PARTICLE SIZE DISTRIBUTION, AND METHOD FOR PRODUCING SAME NISSAN CHEMICAL CORPORATION (JP) 2026-04-30 US disclosed
US-12454526-B2 Method for producing pyrrole-imidazole (poly)amide KANEKA CORPORATION (JP) 2025-10-28 US disclosed
US-20250256980-A1 METAL OXIDE PARTICLE HAVING CORE-SHELL STRUCTURE AND METHOD FOR PRODUCING SAME NISSAN CHEMICAL CORPORATION (JP) 2025-08-14 US disclosed
US-12378127-B2 Silica sol having particle size distribution and production method therefor NISSAN CHEMICAL CORPORATION (JP) 2025-08-05 US disclosed
EP-4328182-B1 SILICA SOL HAVING PARTICLE SIZE DISTRIBUTION, AND METHOD FOR MANUFACTURING SAME NISSAN CHEMICAL CORP (JP) 2025-07-23 EP disclosed
US-12359039-B2 Metal oxide particle-containing composition with reduced occurrence of volatile aldehydes NISSAN CHEMICAL CORPORATION (JP) 2025-07-15 US disclosed
WO-2025127152-A1 METAL OXIDE PARTICLES HAVING IMPROVED HYDROPHOBICITY, HIGHLY CONCENTRATED METAL OXIDE SOL, AND METHODS FOR PRODUCING SAME 日産化学株式会社 2025-06-19 WO disclosed
US-20250197644-A1 ESTER-DISPERSED SILICA SOL AND PRODUCTION METHOD THEREFOR NISSAN CHEMICAL CORPORATION (JP) 2025-06-19 US disclosed
WO-1999016746-A1 AMINOALKYLPHENOL DERIVATIVES AND RELATED COMPOUNDS AVENTIS PHARMACEUTICALS INC. (US) 1999-04-08 WO disclosed
EP-0334455-B1 PROCESS FOR THE PRODUCTION OF KETO-DIESTERS SHELL INTERNATIONALE RESEARCHMAATSCHAPPIJ B.V. (NL) 1993-06-16 EP disclosed
US-4937315-A Transparent amorphous polyamide having high Tg from hindered aromatic diamine and branched chain aliphatic diamine RHONE-POULENC CHIMIE (FR) 1990-06-26 US disclosed
US-4937322-A Crystallized semiaromatic polyamides having high Tg and Tm less than 290 degree C. from hindered aromatic diamine and branched chain aliphatic diamine RHONE-POULENC CHIMIE (FR) 1990-06-26 US disclosed
EP-0347347-A1 Transparent amorphous polyamides with an elevated glass transition temperature RHONE-POULENC CHIMIE (FR) 1989-12-20 EP disclosed
EP-0347348-A1 Crystallised semi-aromatic polyamides with a melting point below 290o C RHONE-POULENC CHIMIE (FR) 1989-12-20 EP disclosed
EP-0334455-A1 Process for the production of keto-diesters SHELL INTERNATIONALE RESEARCHMAATSCHAPPIJ B.V. (NL) 1989-09-27 EP disclosed
US-4800231-A Keto-diesters production SHELL OIL COMPANY (US) 1989-01-24 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 (3 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-20260117080-A1 METAL OXIDE PARTICLES HAVING CORE/SHELL STRUCTURE HAVING UNIFORM PARTICLE SIZE DISTRIBUTION, AND METHOD FOR PRODUCING SAME CD63, SLC39A3, ZRANB2 NFKB1 2477/4885DNM1 2403/4885CA12 988/4885
US-20040073035-A1 Removal by salt formation ELOB, SNRPB2, REN NFKB1 485/4885DNM1 2471/4885CA12 60/4885
US-12454526-B2 Method for producing pyrrole-imidazole (poly)amide DDC, PAM, AADAC NFKB1 1491/4885DNM1 388/4885CA12 1186/4885

“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.