SCHEMBL352059

SCHEMBL352059

CC(C)=CCCC(C)=CCN

nearest known ligand 0.68

Predicted protein targets (top 11)

geneUniProtsupporting neighboursconfidence
KMT2A Q03164 3/20 0.68
MEN1 O00255 2/20 0.62
CYP3A4 P08684 2/20 0.62
ALOX15 P16050 2/20 0.62
SQLE Q14534 7/20 0.61
MAPT P10636 2/20 0.60
ALDH1A1 P00352 2/20 0.60
UGT1A1 P22309 1/20 0.60
KDM4E B2RXH2 2/20 0.54
POLB P06746 1/20 0.54
ATM Q13315 1/20 0.50

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
SCHEMBL2347077 1.00 KMT2A (0.68) KMT2AMEN1CYP3A4ALOX15SQLE
SCHEMBL352058 1.00 KMT2A (0.68) KMT2AMEN1CYP3A4ALOX15SQLE
SCHEMBL30531903 0.98 KMT2A (0.73) KMT2AMEN1CYP3A4ALOX15SQLE
SCHEMBL2495183 0.98 KMT2A (0.73) KMT2AMEN1CYP3A4ALOX15SQLE
Hydrochloric Acid SCHEMBL27745841 0.98 KMT2A (0.65) KMT2AMEN1CYP3A4ALOX15SQLE
SCHEMBL30531904 0.98 KMT2A (0.73) KMT2AMEN1CYP3A4ALOX15SQLE
SCHEMBL2495184 0.98 KMT2A (0.73) KMT2AMEN1CYP3A4ALOX15SQLE
SCHEMBL21260659 0.98 KMT2A (0.73) KMT2AMEN1CYP3A4ALOX15SQLE
SCHEMBL20624673 0.98 KMT2A (0.73) KMT2AMEN1CYP3A4ALOX15SQLE
SCHEMBL11892318 0.98 KMT2A (0.73) KMT2AMEN1CYP3A4ALOX15SQLE

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-117105755-A Novel method for synthesizing alpha-damascone 爱普香料集团股份有限公司 2023-11-24 CN claimed
CN-113387786-B Safener for protecting cereal from herbicide 河南省农业科学院植物保护研究所 2023-08-01 CN claimed
CN-113387786-A A safener for protecting grains from herbicide 河南省农业科学院植物保护研究所 2021-09-14 CN claimed
EP-3383200-B1 COMPOSITIONS SYMRISE AG (DE) 2019-11-06 EP claimed
US-20130267571-A1 TERPENOID ANALOGUES AND USES THEREOF FOR TREATING NEUROLOGICAL CONDITIONS NEUROQUEST INC. (CA) 2013-10-10 US claimed
EP-2616056-A1 TERPENOID ANALOGUES AND USES THEREOF FOR TREATING NEUROLOGICAL CONDITIONS Neuroquest Inc. (CA) 2013-07-24 EP claimed
CN-102030685-B Anti-beta-farnesene analog containing guanidine or nitro-ethylene as well as preparation method and applications thereof UNIV CHINA AGRICULTURAL 2013-05-29 CN claimed
WO-2012034232-A1 TERPENOID ANALOGUES AND USES THEREOF FOR TREATING NEUROLOGICAL CONDITIONS NEUROQUEST INC. (CA) 2012-03-22 WO claimed
CN-102030685-A Anti-beta-farnesene analog containing guanidine or nitro-ethylene as well as preparation method and applications thereof UNIV CHINA AGRICULTURAL 2011-04-27 CN claimed
EP-1142859-B2 Process for producing optically active 3,7-dimethyl-6-octenol and process for producing intermediate therefore TAKASAGO PERFUMERY CO LTD (JP) 2010-04-28 EP claimed
WO-2003099812-A1 PHENYL-FURAN OR PHENYL-THIOPHENE DERIVATIVES, THEIR PREPARATION AND THEIR USE AS MEDICINE PIERRE FABRE MEDICAMENT (FR) 2003-12-04 WO claimed
US-6489522-B2 ORGANOLEPTIC; FROM ALKYLAMINE AND ISOPRENE; CATALYTIC ISOMERIZATION, HEATING TAKASAGO INTERNATIONAL CORPORATION (JP) 2002-12-03 US claimed
US-6486353-B2 SUBJECTING MIXTURE OF ALKYLAMINE AND ISOPRENE TO TELOMERIZATION AT 80-100 DEGREES C.IN THE PRESENCE OF AN ALKYLLITHIUM AND/OR PHENYLLITHIUM CATALYST TAKASAGO INTERNATIONAL CORPORATION (JP) 2002-11-26 US claimed
US-20020128525-A1 Process for producing optically active 3,7-dimethyl-6-octenol and process for producing intermediate therefor TAKASAGO INTERNATIONAL CORPORATION 2002-09-12 US claimed
US-20020004620-A1 Process for producing optically active 3, 7-dimethyl-6-octenol and process for producing intermediate therefor TAKASAGO INTERNATIONAL CORPORATION (JP) 2002-01-10 US claimed
EP-1142859-A2 Process for producing optically active 3,7-dimethyl-6-octenol and process for producing intermediate therefor Takasago International Corporation (JP) 2001-10-10 EP claimed
US-4266087-A Process for preparing a myrcenol, cis-ocimenol mixture substantially free of trans-ocimenol GIVAUDAN CORPORATION (US) 1981-05-05 US claimed
US-4247480-A OXIDATION OF A SATURATED OR UNSATURATED TERT-AMINE USING HYDROGEN PEROXIDE IN THE PRESENCE OF CARBON DIOXIDE NISSAN CHEMICAL INDUSTRIES LIMITED (JP) 1981-01-27 US claimed
US-4186148-A Process for producing 3,7-dimethyl-2,6-octadienylamine derivatives NISSAN CHEMICAL INDUSTRIES LIMITED (JP) 1980-01-29 US claimed
US-4107219-A OXIDIZING UNSATURATED AMINE, THERMAL REARRANGEMENT TO FORM UNSATURATED HYDROXYLAMINE, HYDROGENATION NISSAN CHEMICAL INDUSTRIES LTD. (JP) 1978-08-15 US claimed

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-20020128525-A1 Process for producing optically active 3,7-dimethyl-6-octenol and process for producing intermediate therefor NOTUM, CYP51A1, SOAT2 KMT2A 2881/4885MEN1 1751/4885CYP3A4 49/4885
US-20020004620-A1 Process for producing optically active 3, 7-dimethyl-6-octenol and process for producing intermediate therefor NOTUM, CYP51A1, SOAT1 KMT2A 2833/4885MEN1 1625/4885CYP3A4 49/4885
US-20130267571-A1 TERPENOID ANALOGUES AND USES THEREOF FOR TREATING NEUROLOGICAL CONDITIONS PMP22, PTGES, GGPS1 KMT2A 3842/4885MEN1 2728/4885CYP3A4 488/4885

“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.