SCHEMBL932338

SCHEMBL932338

C=C(C)CCC(=O)OCC

nearest known ligand 0.50

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
GAA P10253 2/20 0.50
MGAM O43451 1/20 0.50
SI P14410 1/20 0.50
MGAM2 Q2M2H8 1/20 0.50
CYP1A2 P05177 1/20 0.50
ALDH1A1 P00352 5/20 0.46
TRPA1 O75762 1/20 0.46
LMNA P02545 2/20 0.46
HSD17B10 Q99714 1/20 0.46
TSHR P16473 2/20 0.43
POLB P06746 2/20 0.43
CYP4F2 P78329 2/20 0.41
CYP4A11 Q02928 2/20 0.41
SMN1; SMN2 Q16637 1/20 0.41
NR1I2 O75469 1/20 0.40
PGR P06401 1/20 0.40
ADORA3 P0DMS8 1/20 0.40
PTGS2 P35354 1/20 0.40
PDE4D Q08499 1/20 0.40
L3MBTL1 Q9Y468 1/20 0.40

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
Fluoromethane SCHEMBL28248919 0.96 CYP1A2 (0.47) GAAMGAMSIMGAM2CYP1A2
SCHEMBL9083407 0.86 CYP1A2 (0.57) GAAMGAMSIMGAM2CYP1A2
SCHEMBL9816382 0.86 CYP1A2 (0.57) GAAMGAMSIMGAM2CYP1A2
Succinic Acid Diethyl Ester SCHEMBL29266181 0.85 GAA (0.60) GAAMGAMSIMGAM2CYP1A2
Succinic Acid Diethyl Ester SCHEMBL27768067 0.84 GAA (0.67) GAAMGAMSIMGAM2CYP1A2
Succinic Acid Diethyl Ester SCHEMBL22780 0.84 GAA (0.67) GAAMGAMSIMGAM2CYP1A2
SCHEMBL6178625 0.83 GAA (0.52) GAAMGAMSIMGAM2CYP1A2
SCHEMBL8879326 0.83 GAA (0.54) GAAMGAMSIMGAM2CYP1A2
Succinic Acid Diethyl Ester SCHEMBL28197993 0.82 GAA (0.57) GAAMGAMSIMGAM2CYP1A2
Succinic Acid Diethyl Ester SCHEMBL4324913 0.82 GAA (0.63) GAAMGAMSIMGAM2CYP1A2

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-11440920-B2 Chemical method of producing SMTP groups or SMTP-7 and intermediates used in the method SHOWA UNIVERSITY (JP) 2022-09-13 US claimed
CN-113773438-B Carbon dioxide thickener for medium-high permeability oil reservoir and preparation method and technology thereof 德仕能源科技集团股份有限公司 2022-03-08 CN claimed
CN-113773438-A Carbon dioxide thickener for medium-high permeability oil reservoir and preparation method and technology thereof 德仕能源科技集团股份有限公司 2021-12-10 CN claimed
US-20200140450-A1 CHEMICAL METHOD OF PRODUCING SMTP GROUPS OR SMTP-7 AND INTERMEDIATES USED IN THE METHOD SHOWA UNIVERSITY (JP) 2020-05-07 US claimed
US-7615650-B2 Process for producing chroman compound MITSUBISHI GAS CHEMICAL COMPANY, INC. (JP) 2009-11-10 US claimed
US-20070179304-A1 Process for producing chroman compound MITSUBISHI GAS CHEMICAL COMPANY, INC. (JP) 2007-08-02 US claimed
EP-3882252-B1 BETA-LACTAMASE INHIBITORS VENATORX PHARMACEUTICALS INC (US) 2025-11-19 EP disclosed
WO-2025224262-A1 COMBINATION THERAPIES COMPRISING A CDK2 DEGRADER AND A CDK4/6 INHIBITOR MONTE ROSA THERAPEUTICS AG (CH) 2025-10-30 WO disclosed
WO-2025224249-A1 COMPOUNDS THAT MEDIATE PROTEIN DEGRADATION AND METHODS OF USE THEREOF MONTE ROSA THERAPEUTICS AG (CH) 2025-10-30 WO disclosed
EP-4608816-A1 COMPOUNDS THAT MEDIATE PROTEIN DEGRADATION AND METHODS OF USE THEREOF Monte Rosa Therapeutics AG (CH) 2025-09-03 EP disclosed
US-20250263395-A1 COMPOUNDS THAT MEDIATE PROTEIN DEGRADATION AND METHODS OF USE THEREOF MONTE ROSA THERAPEUTICS AG (CH) 2025-08-21 US disclosed
CN-119039195-A Preparation method of beta-thiocyanate alcohol derivative 山东省分析测试中心 2024-11-29 CN disclosed
WO-2024092039-A1 COMPOUNDS THAT MEDIATE PROTEIN DEGRADATION AND METHODS OF USE THEREOF MONTE ROSA THERAPEUTICS, INC. (US) 2024-05-02 WO disclosed
EP-0294229-B1 NOVEL HETEROCYCLIC PESTICIDAL COMPOUNDS THE WELLCOME FOUNDATION LIMITED (GB) 1992-12-02 EP disclosed
EP-0294229-A2 Novel heterocyclic pesticidal compounds THE WELLCOME FOUNDATION LIMITED (GB) 1988-12-07 EP disclosed
US-4786750-A Pentene derivatives ICI AMERICAS INC. (US) 1988-11-22 US disclosed
US-4709063-A Preparation of 2-halo-5-methylpyridines from 4-methyl-4-pentene derivatives ICI AMERICAS INC. (US) 1987-11-24 US disclosed
US-4628096-A Preparation of 2-halo-5-methylpyridines from 4-methyl-4-pentene derivatives ICI AMERICAS INC. (US) 1986-12-09 US disclosed
US-4504664-A 2-Piperidones ICI AMERICAS INC. (US) 1985-03-12 US disclosed
US-4234741-A BENZENESELENYL HALIDE REACTANT, SELENIUM-CONTAINING INTERMEDIATES FIRMENICH, S.A. (CH) 1980-11-18 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 (4 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-20200140450-A1 CHEMICAL METHOD OF PRODUCING SMTP GROUPS OR SMTP-7 AND INTERMEDIATES USED IN THE METHOD TST, SMS, TMSB4X GAA 3536/4885MGAM 4507/4885SI 618/4885
US-20070179304-A1 Process for producing chroman compound TAF9, TAF1, CHD1 GAA 488/4885MGAM 847/4885SI 737/4885
US-11440920-B2 Chemical method of producing SMTP groups or SMTP-7 and intermediates used in the method SMS, TST, TES GAA 2241/4885MGAM 3700/4885SI 244/4885
US-20250263395-A1 COMPOUNDS THAT MEDIATE PROTEIN DEGRADATION AND METHODS OF USE THEREOF CDK2, SKP2, CDK1 GAA 2291/4885MGAM 3000/4885SI 3055/4885

“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.