Carbon Monoxide

Carbon Monoxide

SCHEMBL204677

CC1=C(C)C(C)(C)C([Rh])=C1C.[C]=O.[C]=O

nearest known ligand 0.36

Full drug profile on Sugi Atlas →

Predicted protein targets (top 1)

geneUniProtsupporting neighboursconfidence
CTSD P07339 1/20 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
SCHEMBL2851519 0.92 CTSD (0.35) CTSD
Formaldehyde SCHEMBL16161196 0.90 CTSD (0.41) CTSD
Formaldehyde SCHEMBL15319409 0.90 CTSD (0.41) CTSD
SCHEMBL14954190 0.89 CTSD (0.33) CTSD
Iodide SCHEMBL810380 0.89 CTSD (0.33) CTSD
Hydrochloric Acid SCHEMBL23388159 0.89 CTSD (0.33) CTSD
Fluoride SCHEMBL14954087 0.89 CTSD (0.33) CTSD
Bromide SCHEMBL809754 0.89 CTSD (0.33) CTSD
Hydrochloric Acid SCHEMBL810310 0.89 CTSD (0.33) CTSD
Bicarbonate SCHEMBL29009439 0.85 CTSD (0.33) CTSD

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-4591122-A1 BAKE-SENSITIVE UNDERLAYERS TO REDUCE DOSE TO SIZE OF EUV PHOTORESIST Lam Research Corporation (US) 2025-07-30 EP disclosed
WO-2024064071-A1 BAKE-SENSITIVE UNDERLAYERS TO REDUCE DOSE TO SIZE OF EUV PHOTORESIST LAM RESEARCH CORPORATION (US) 2024-03-28 WO disclosed
US-9758499-B2 Stereo controlled synthesis of (E,Z)-dienals via tandem Rh(I) catalyzed propargyl claisen rearrangement The Florida State University Research Foundation, Inc. (US) 2017-09-12 US disclosed
US-20170129865-A1 STEREO CONTROLLED SYNTHESIS OF (E,Z)-DIENALS VIA TANDEM RH(I) CATALYZED PROPARGYL CLAISEN REARRANGEMENT The Florida State University Research Foundation, Inc. 2017-05-11 US disclosed
US-9573871-B2 Stereo controlled synthesis of (E,Z)-dienals via tandem Rh(I) catalyzed propargyl claisen rearrangement The Florida State University Research Foundation, Inc. (US) 2017-02-21 US disclosed
EP-2537839-B1 B-DIHYDROFURAN DERIVING COMPOUND, METHOD FOR PRODUCING B-DIHYDROFURAN DERIVING COMPOUND OR B-TETRAHYDROFURAN DERIVING COMPOUND, B -GLYCOSIDE COMPOUND, METHOD FOR PRODUCING B-GLYCOSIDE COMPOUND, AND METHOD FOR PRODUCING 4'-ETHYNYL D4T AND ANALOGUE COMPOUNDS THEREOF NISSAN CHEMICAL IND LTD (JP) 2016-12-14 EP disclosed
US-20150361019-A1 STERO CONTROLLED SYNTHESIS OF (E,Z)-DIENALS VIA TANDEM RH(I) CATALYZED PROPARGYL CLAISEN REARRANGEMENT The Florida State University Research Foundation, Inc. 2015-12-17 US disclosed
US-9212174-B2 Certain β-dihydrofuran derivatives NISSAN CHEMICAL INDUSTRIES, LTD. (JP) 2015-12-15 US disclosed
EP-2537851-B1 PROCESS FOR PREPARATION OF B-GLYCOSIDE COMPOUNDS NISSAN CHEMICAL IND LTD (JP) 2015-06-10 EP disclosed
US-8975394-B2 Process for preparation of β-glycoside compounds NISSAN CHEMICAL INDUSTRIES, LTD. (JP) 2015-03-10 US disclosed
US-20100197938-A1 Process for producing indole compoud NISSAN CHEMICAL INDUSTRIES, LTD. (JP) 2010-08-05 US disclosed
US-7732626-B2 Fused cyclic compounds TAKEDA PHARMACEUTICAL COMPANY LIMITED (JP) 2010-06-08 US disclosed
US-20100004312-A1 FUSED CYCLIC COMPOUNDS TAKEDA PHARMACEUTICAL COMPANY LIMITED (JP) 2010-01-07 US disclosed
US-20070083053-A1 Process for producing indole compound NISSAN CHEMICAL INDUSTRIES, LTD. (JP) 2007-04-12 US disclosed
US-20050267229-A1 Method for producing poly(methyl methacrylate)-metal cluster composite NATIONAL INSTITUTE OF ADVANCED INDUSTRIAL SCIENCE AND TECHNOLOGY (JP) 2005-12-01 US disclosed
EP-0711760-B1 METHOD OF ALKYLATING TRIAZINE DERIVATIVE NISSAN CHEMICAL IND LTD (JP) 2002-05-15 EP disclosed
US-6130332-A USING A GROUP 8 METAL CATALYST AND ALDEHYDES OR KETONE NISSAN CHEMICAL INDUSTRIES, LTD. (JP) 2000-10-10 US disclosed
US-5792867-A Method of alkylating of triazine derivatives NISSAN CHEMICAL INDUSTRIES, LTD. (JP) 1998-08-11 US disclosed
EP-0760369-A1 PROCESS FOR ALKYLATING TRIAZINE DERIVATIVE NISSAN CHEMICAL INDUSTRIES, LIMITED (JP) 1997-03-05 EP disclosed
EP-0711760-A1 METHOD OF ALKYLATING TRIAZINE DERIVATIVE NISSAN CHEMICAL INDUSTRIES, LIMITED (JP) 1996-05-15 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 (5 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-20170129865-A1 STEREO CONTROLLED SYNTHESIS OF (E,Z)-DIENALS VIA TANDEM RH(I) CATALYZED PROPARGYL CLAISEN REARRANGEMENT EPRS1, DHPS, RPL14 CTSD 1679/4885
US-20150361019-A1 STERO CONTROLLED SYNTHESIS OF (E,Z)-DIENALS VIA TANDEM RH(I) CATALYZED PROPARGYL CLAISEN REARRANGEMENT EPRS1, DHPS, LSS CTSD 2658/4885
US-20100004312-A1 FUSED CYCLIC COMPOUNDS GPR119, GLP1R, GPR65 CTSD 3140/4885
US-20100197938-A1 Process for producing indole compoud IDO1, IDO2, NOS2 CTSD 526/4885
US-20070083053-A1 Process for producing indole compound IDO2, IDO1, TDO2 CTSD 2830/4885

“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.