SCHEMBL301026

SCHEMBL301026

COc1ccc(P(c2ccc(OC)cc2)c2ccc3ccccc3c2-c2c(P(c3ccc(OC)cc3)c3ccc(OC)cc3)ccc3ccccc23)cc1

nearest known ligand 0.51

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
MAPT P10636 2/20 0.51
CYP1A2 P05177 3/20 0.43
RAB9A P51151 2/20 0.43
CYP2A6 P11509 1/20 0.43
MAPK9 P45984 1/20 0.40
MAPK14 Q16539 1/20 0.40
TDP1 Q9NUW8 3/20 0.40
KMT2A Q03164 3/20 0.40
ALDH1A1 P00352 2/20 0.40
LMNA P02545 2/20 0.40
MEN1 O00255 2/20 0.40
CDK4 P11802 1/20 0.40
CCND1 P24385 1/20 0.40
GAA P10253 1/20 0.40
ALOX12 P18054 1/20 0.40
HIF1A Q16665 1/20 0.40
PHLPP2 Q6ZVD8 1/20 0.40
HSD17B10 Q99714 1/20 0.40
TUBB4A P04350 1/20 0.39
TUBB P07437 1/20 0.39

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
SCHEMBL7795643 0.90 MAPT (0.45) MAPTCYP1A2RAB9ACYP2A6MAPK9
SCHEMBL1606348 0.84 MAPT (0.67) MAPTCYP1A2RAB9AKMT2AALDH1A1
SCHEMBL29496547 0.84 MAPT (0.67) MAPTCYP1A2RAB9AKMT2AALDH1A1
SCHEMBL29834220 0.84 MAPT (0.67) MAPTCYP1A2RAB9AKMT2AALDH1A1
SCHEMBL6401400 0.83 RAB9A (0.49) MAPTCYP1A2RAB9ACYP2A6TDP1
SCHEMBL7948363 0.83 L3MBTL1 (0.43) MAPTCYP1A2RAB9ATDP1KMT2A
SCHEMBL7804747 0.83 MAPT (0.59) MAPTCYP1A2RAB9AKMT2AALDH1A1
SCHEMBL1305818 0.83 CYP1A2 (0.46) MAPTCYP1A2RAB9ACYP2A6KMT2A
SCHEMBL29176 0.81 MAPT (0.39) MAPTCYP1A2RAB9ACYP2A6TDP1
SCHEMBL29361524 0.81 MAPT (0.39) MAPTCYP1A2RAB9ACYP2A6TDP1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
JP-1068386-A None JP disclosed
US-20220169600-A1 METHOD FOR PRODUCING PKROSTAGLANDIN KYOWA PHARMA CHEMICAL CO., LTD. (JP) 2022-06-02 US disclosed
EP-3950672-A1 METHOD FOR PRODUCING PKROSTAGLANDIN Kyowa Pharma Chemical Co., Ltd. (JP) 2022-02-09 EP disclosed
US-20210347769-A1 METHOD FOR PRODUCING OPTICALLY ACTIVE COMPOUND DAY ONE BIOPHARMACEUTICALS, INC. 2021-11-11 US disclosed
US-10988469-B2 Method for producing optically active compound DOT THERAPEUTICS-1, INC. (US) 2021-04-27 US disclosed
US-20200317659-A1 METHOD FOR PRODUCING OPTICALLY ACTIVE COMPOUND DAY ONE BIOPHARMACEUTICALS, INC. 2020-10-08 US disclosed
US-10710989-B2 Method for producing heterocyclic compound TAKEDA PHARMACEUTICAL COMPANY LIMITED (JP) 2020-07-14 US disclosed
EP-3632441-A2 METHOD FOR PRODUCING OPTICALLY ACTIVE COMPOUND Millennium Pharmaceuticals, Inc. (US) 2020-04-08 EP disclosed
US-20180079741-A1 PROCESS FOR PRODUCING HETEROCYCLIC COMPOUND TAKEDA PHARMACEUTICALS COMPANY LIMITED (JP) 2018-03-22 US disclosed
US-9896402-B2 Method for preventing decrease in optical purity TAKASAGO INTERNATIONAL CORPORATION (JP) 2018-02-20 US disclosed
EP-0478147-B1 Process for producing optically active gamma-butyrolactone derivatives TAKASAGO PERFUMERY CO LTD (JP) 1996-11-06 EP disclosed
US-5420306-A Process for producing optically active γ-butyrolactone derivatives TAKASAGO INTERNATIONAL CORPORATION (JP) 1995-05-30 US disclosed
US-5412109-A Process for preparing optically active 4-methyl-2-oxetanone TAKASAGO INTERNATIONAL CORPORATION (JP) 1995-05-02 US disclosed
US-5349107-A Ruthenium optically active phosphine complex TAKASAGO INTERNATIONAL CORPORATION (JP) 1994-09-20 US disclosed
EP-0592881-A2 Process for producing optically active gamma-hydroxyketones Takasago International Corporation (JP) 1994-04-20 EP disclosed
EP-0580336-A1 Process for preparing optically active 4-methyl-2-oxetanone TAKASAGO INTERNATIONAL CORPORATION (JP) 1994-01-26 EP disclosed
US-5198562-A Assymetric reactions TAKASAGO INTERNATIONAL CORPORATION (JP) 1993-03-30 US disclosed
EP-0478147-A1 Process for producing optically active gamma-butyrolactone derivatives Takasago International Corporation (JP) 1992-04-01 EP disclosed
EP-0470756-A2 Ruthenium-phosphine complex useful as catalyst and intermediate for synthesis thereof Takasago International Corporation (JP) 1992-02-12 EP disclosed
JP-S6468386-A 2,2'-BIS(DI-(P-METHOXYPHENYL)PHOSPHINO)-1,1'-BINAPHTHYL TAKASAGO PERFUMERY CO LTD 1989-03-14 JP 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 (6 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-20220169600-A1 METHOD FOR PRODUCING PKROSTAGLANDIN PTGS1, PTGER1, RACK1 MAPT 4859/4885CYP1A2 472/4885RAB9A 3323/4885
US-10988469-B2 Method for producing optically active compound DHPS, QDPR, SPR MAPT 3660/4885CYP1A2 1113/4885RAB9A 1416/4885
US-20180079741-A1 PROCESS FOR PRODUCING HETEROCYCLIC COMPOUND DHPS, QDPR, DPYD MAPT 3357/4885CYP1A2 28/4885RAB9A 3014/4885
US-20200317659-A1 METHOD FOR PRODUCING OPTICALLY ACTIVE COMPOUND DHPS, QDPR, SPR MAPT 3660/4885CYP1A2 1113/4885RAB9A 1416/4885
US-10710989-B2 Method for producing heterocyclic compound APP, THOP1, TALDO1 MAPT 16/4885CYP1A2 1870/4885RAB9A 4326/4885
US-20210347769-A1 METHOD FOR PRODUCING OPTICALLY ACTIVE COMPOUND DHPS, QDPR, SPR MAPT 3660/4885CYP1A2 1113/4885RAB9A 1416/4885

“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.