SCHEMBL77262

SCHEMBL77262

Cc1cccc(C(C)(C)C)n1

nearest known ligand 0.50

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
CCR1 P32246 1/20 0.50
CCR8 P51685 1/20 0.50
NOS3 P29474 1/20 0.46
NOS2 P35228 1/20 0.46
ALDH1A1 P00352 4/20 0.40
KDM4E B2RXH2 4/20 0.40
HPGD P15428 3/20 0.40
HSD17B10 Q99714 1/20 0.40
RAB9A P51151 4/20 0.38
MEN1 O00255 3/20 0.38
KMT2A Q03164 3/20 0.38
NPC1 O15118 3/20 0.36
GRM5 P41594 3/20 0.36
SMN1; SMN2 Q16637 3/20 0.36
HDAC6 Q9UBN7 2/20 0.36
CYP3A4 P08684 2/20 0.36
CYP2D6 P10635 2/20 0.36
CYP2C9 P11712 2/20 0.36
PKM P14618 2/20 0.36
CYP2C19 P33261 2/20 0.36

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
SCHEMBL29380771 1.00 CCR1 (0.50) CCR1CCR8NOS3NOS2ALDH1A1
SCHEMBL20348778 0.87 CCR1 (0.67) CCR1CCR8NOS3NOS2ALDH1A1
SCHEMBL958741 0.85 CCR1 (0.50) CCR1CCR8NOS3NOS2ALDH1A1
SCHEMBL13821747 0.85 CCR1 (0.50) CCR1CCR8NOS3NOS2ALDH1A1
SCHEMBL18471313 0.84 CCR1 (0.34) CCR1CCR8NOS3NOS2ALDH1A1
SCHEMBL42955 0.84 PGK1 (0.39) CCR1CCR8ALDH1A1KDM4EHPGD
SCHEMBL25458041 0.83 CCR1 (0.48) CCR1CCR8NOS3NOS2ALDH1A1
Iodide SCHEMBL2346492 0.81 PGK1 (0.38) CCR1CCR8ALDH1A1KDM4EHPGD
Hydrochloric Acid SCHEMBL30595152 0.81 PGK1 (0.38) CCR1CCR8ALDH1A1KDM4EHPGD
SCHEMBL12873766 0.81 NOS3 (0.48) CCR1CCR8NOS3NOS2ALDH1A1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-103122052-B A kind of soft section of crystallizable segmented copolymer of complete saturated hard section and preparation method thereof BEIJING UNIVERSITY OF CHEMICAL TECHNOLOGY (CN) 2015-12-09 CN claimed
US-8697820-B2 Process for preparing high-reactivity isobutene homo- or copolymers BASF SE (DE) 2014-04-15 US claimed
CN-103122052-A Segmented copolymer with fully-saturated soft segment and crystallizable hard segment and preparation method of segmented copolymer UNIV BEIJING CHEMICAL 2013-05-29 CN claimed
CN-101987877-B Cationic polymerization method of isotactic polymer UNIV BEIJING CHEMICAL 2012-10-17 CN claimed
EP-1172878-B1 Non-aqueous electrolytic solution and secondary battery containing same MITSUBISHI CHEM CORP (JP) 2011-06-22 EP claimed
US-6767671-B2 STABILITY; HEAT RESISTANCE MITSUBISHI CHEMICAL CORPORATION (JP) 2004-07-27 US claimed
US-20020025477-A1 Non-aqueous electrolytic solution and secondary battery containing same MITSUBISHI CHEMICAL CORPORATION (JP) 2002-02-28 US claimed
EP-1172878-A2 Non-aqueous electrolytic solution and secondary battery containing same MITSUBISHI CHEMICAL CORPORATION (JP) 2002-01-16 EP claimed
EP-4508101-B1 PROCESS FOR MANUFACTURING OF POLYISOBUTENE SUCCINIC ANHYDRIDES BASF SE (DE) 2026-03-25 EP disclosed
EP-4709518-A1 PROCESS FOR THE PREPARATION OF POLYISOBUTENE FROM OLEFINS FROM ISOBUTANOL OBTAINED FROM MIXED GUERBET REACTION OF ETHANOL AND METHANOL BASF SE (DE) 2026-03-18 EP disclosed
EP-4667447-A1 PROCESS FOR THE PREPARATION OF POLYISOBUTENE FROM BIO-BASED OLEFINS FROM PRIMARY ALCOHOL BASF SE (DE) 2025-12-24 EP disclosed
US-20250250382-A1 PROCESS FOR MANUFACTURING OF POLYISOBUTENE SUCCINIC ANHYDRIDES BASF SE (DE) 2025-08-07 US disclosed
US-20250250403-A1 PROCESS FOR MANUFACTURING OF POLYISOBUTENE SUCCINIC ANHYDRIDES BASF SE (DE) 2025-08-07 US disclosed
US-20250179224-A1 MEDIUM MOLECULAR POLYISOBUTENE WITH A CERTAIN DISTRIBUTION OF DOUBLE BOND ISOMERS BASF SE (DE) 2025-06-05 US disclosed
US-20040235939-A1 Synthesis of peloruside a and analogs thereof for use as antitumor agents UNIVERSITY OF TEXAS SYSTEM, THE 2004-11-25 US disclosed
WO-2004074249-A2 SYNTHESIS OF PELORUSIDE A AND ANALOGS THEREOF FOR USE AS ANTITUMOR AGENTS BOARD OF REGENTS, UNIVERSITY OF TEXAS SYSTEM (US) 2004-09-02 WO disclosed
US-6767671-B2 STABILITY; HEAT RESISTANCE MITSUBISHI CHEMICAL CORPORATION (JP) 2004-07-27 US disclosed
US-20040082578-A1 Arylindenopyridines and related therapeutic and prophylactic methods ORTHO-MCNEIL PHARMACEUTICAL, INC. 2004-04-29 US disclosed
US-20020025477-A1 Non-aqueous electrolytic solution and secondary battery containing same MITSUBISHI CHEMICAL CORPORATION (JP) 2002-02-28 US disclosed
EP-1172878-A2 Non-aqueous electrolytic solution and secondary battery containing same MITSUBISHI CHEMICAL CORPORATION (JP) 2002-01-16 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 (2 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-20040082578-A1 Arylindenopyridines and related therapeutic and prophylactic methods ADORA2A, ADORA1, PDE2A CCR1 488/4885CCR8 1576/4885NOS3 675/4885
US-20040235939-A1 Synthesis of peloruside a and analogs thereof for use as antitumor agents MAP4, MAPRE1, TUBA4A CCR1 4741/4885CCR8 4294/4885NOS3 4251/4885

“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.