Cocarboxylase

Cocarboxylase

SCHEMBL991346

Cc1ncc(C[n+]2csc(CCOP(=O)(O)OP(=O)(O)O)c2C)c(N)n1.Cl

nearest known ligand 0.98

Full drug profile on Sugi Atlas →

Known targets — ChEMBL curated mechanism

ABL1ACEACHEACVR1ADRA1AADRA1BADRA1DADRA2AADRA2BADRA2CADRB1ADRB2ADRB3AGTR1ALKAVPR1AAVPR2BCHEBCRCA2CACNA1ACACNA1BCACNA1CCACNA1DCACNA1ECACNA1FCACNA1GCACNA1HCACNA1ICACNA1SCACNA2D1CACNA2D2CACNA2D3CACNA2D4CACNB1CACNB2CACNB3CACNB4CACNG1CACNG2CACNG3CACNG4CACNG5CACNG6CACNG7CACNG8CALCRLCASRCCR5CDK4CDK6CFBCHRM1CHRM2CHRM3CHRM4CHRM5CHRNA1CHRNA3CHRNA7CHRNB1CHRNB4CHRNDCHRNECHRNGCOXFA4COXFA4L2CRBNCSF1RCUL4ACYP19A1DDB1DPP4DRD1DRD2DRD3DRD4EDNRAEGFREML4ERBB2ERBB4ESR1ESR2FGFR1FGFR3FLT1FLT3FLT4GAAGABRA1GABRA2GABRA3GABRA4GABRA5GABRA6GABRB1GABRB2GABRB3GABRDGABREGABRG1GABRG2GABRG3GABRPGABRQGHSRGLAGNRHRGPD2GRIN1GRIN2AGRIN2BGRIN2CGRIN2DGRIN3AGRIN3BGSTP1HCN4HCRTR1HCRTR2HDAC1HDAC10HDAC11HDAC2HDAC3HDAC4HDAC5HDAC6HDAC7HDAC8HDAC9HRH1HRH2HRH3HSD11B1HSP90AA1HSP90AB1HTR1AHTR1BHTR1DHTR1EHTR1FHTR2AHTR2BHTR2CHTR3AHTR3BHTR3CHTR3DHTR3EHTR4HTR5AHTR6HTR7IMPDH1IMPDH2ITGA2BITGB3ITKJAK1JAK2KCNA1KCNA10KCNA2KCNA3KCNA4KCNA5KCNA6KCNA7KCNB1KCNB2KCNC1KCNC2KCNC3KCNC4KCND1KCND2KCND3KCNF1KCNG1KCNG2KCNG3KCNG4KCNH1KCNH2KCNH3KCNH4KCNH5KCNH6KCNH7KCNH8KCNJ2KCNJ3KCNJ5KCNK3KCNK9KCNQ1KCNQ2KCNQ3KCNQ4KCNQ5KCNS1KCNS2KCNS3KCNV1KCNV2KDRKITKLKB1LCKMMAOAMAOBMAPK14METMMP1MMP13MMP7MMP8MT-ND1MT-ND2MT-ND3MT-ND4MT-ND4LMT-ND5MT-ND6NDUFA1NDUFA10NDUFA11NDUFA12NDUFA13NDUFA2NDUFA3NDUFA5NDUFA6NDUFA7NDUFA8NDUFA9NDUFAB1NDUFAF1NDUFAF2NDUFAF3NDUFAF4NDUFB1NDUFB10NDUFB11NDUFB2NDUFB3NDUFB4NDUFB5NDUFB6NDUFB7NDUFB8NDUFB9NDUFC1NDUFC2NDUFS1NDUFS2NDUFS3NDUFS4NDUFS5NDUFS6NDUFS7NDUFS8NDUFV1NDUFV2NDUFV3NR3C1NS5ANTRK1NTRK2NTRK3ODC1OPRD1OPRK1OPRM1P2RY12PAHPARP1PDE3APDE3BPDE4APDE4BPDE4CPDE4DPDE5APDE7APDE7BPDE8APDE8BPDGFRAPDGFRBPIK3CAPIK3CDPNPPOLA1POLA2POLD1POLD2POLD3POLD4POLEPOLE2POLE3PPARGPRIM1PRIM2PRKCAPRKCBPRKCDPRKCEPRKCGPRKCHPRKCIPRKCQPRKCZPRKD1PRKD3PTGS1PTGS2RBX1RENRETROCK1ROCK2RPE65RRM1RRM2RRM2BS1PR1S1PR2S1PR3S1PR4S1PR5SCN10ASCN11ASCN1ASCN2ASCN3ASCN4ASCN5ASCN7ASCN8ASCN9ASCNN1ASCNN1BSCNN1GSIGMAR1SLC18A2SLC6A1SLC6A2SLC6A3SLC6A4SLC9A3SRCTACR1TOP1TOP2ATOP2BTTRTYMPdacAdacBdacCembAfolAftsIgyrAgyrBmrcAmrcBmrdAparCparEpolrplArplBrplCrplDrplErplFrplIrplJrplKrplLrplMrplNrplOrplPrplQrplRrplSrplTrplUrplVrplWrplXrplYrpmArpmBrpmCrpmDrpmErpmE2rpmFrpmGrpmG1rpmG2rpmG3rpmHrpmIrpmJrpsArpsBrpsCrpsDrpsErpsFrpsGrpsHrpsIrpsJrpsKrpsLrpsMrpsNrpsOrpsPrpsQrpsRrpsSrpsTrpsUykgMykgO

The experimentally established mechanism targets of Cocarboxylase. The predicted profile below is derived independently by chemical similarity — agreement is a validation signal, a miss is honest.

Predicted protein targets (top 7)

geneUniProtsupporting neighboursconfidence
HSP90AA1 known ✓ P07900 1/20 0.63
LMNA P02545 1/20 0.98
TKT P29401 7/20 0.84
TDP1 Q9NUW8 1/20 0.84
ALDH1A1 P00352 2/20 0.57
KDM4E B2RXH2 1/20 0.53
PPP5C P53041 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
Cocarboxylase SCHEMBL23151792 1.00 LMNA (0.98) LMNATKTTDP1HSP90AA1ALDH1A1
Cocarboxylase SCHEMBL4315554 0.99 LMNA (0.96) LMNATKTTDP1HSP90AA1ALDH1A1
Cocarboxylase SCHEMBL662896 0.99 LMNA (0.96) LMNATKTTDP1HSP90AA1ALDH1A1
Cocarboxylase SCHEMBL23151791 0.99 LMNA (0.96) LMNATKTTDP1HSP90AA1ALDH1A1
Cocarboxylase SCHEMBL80028 0.99 LMNA (1.00) LMNATKTTDP1HSP90AA1ALDH1A1
Cocarboxylase SCHEMBL30192281 0.99 LMNA (1.00) LMNATKTTDP1HSP90AA1ALDH1A1
Hydrochloric Acid SCHEMBL23151779 0.98 LMNA (0.94) LMNATKTTDP1HSP90AA1ALDH1A1
Cocarboxylase SCHEMBL23151785 0.98 LMNA (0.98) LMNATKTTDP1HSP90AA1ALDH1A1
Cocarboxylase SCHEMBL8923435 0.98 LMNA (0.98) LMNATKTTDP1HSP90AA1ALDH1A1
Cocarboxylase SCHEMBL28756433 0.98 LMNA (0.98) LMNATKTTDP1HSP90AA1ALDH1A1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-108191912-A The preparation method of 12 kinds of vitamin raw materials Cocarboxylase Tetrahydrates of injection 山西普德药业有限公司 2018-06-22 CN claimed
WO-2025052869-A1 EXTERNAL-USE COMPOSITION AND METHOD FOR ENHANCING FRAGRANCE OF SAME ロート製薬株式会社 2025-03-13 WO disclosed
CN-117545459-A Cleaning composition and method for producing same 日本乐敦制药株式会社 2024-02-09 CN disclosed
CN-116870157-A Composition for improving skin disorders 日本乐敦制药株式会社 2023-10-13 CN disclosed
EP-3995151-B1 LIPID COMPOSITION FOR ENCAPSULATING AN ACTIVE SUBSTANCE AND ALLOWING CONTROL OF THE SPEED OF RELEASE OF SAID ACTIVE SUBSTANCE SOC DEXPLOITATION DE PRODUITS POUR LES INDUSTRIES CHIMIQUES SEPPIC (FR) 2023-09-13 EP disclosed
CN-116685305-A Cleaning composition 日本乐敦制药株式会社 2023-09-01 CN disclosed
CN-111107831-B Composition for supplementing the taste of young women 日本乐敦制药株式会社 2022-11-25 CN disclosed
US-11246853-B2 Method for evaluating the ability of a composition to prevent muscle damage and fatigue; food supplement and drug SOCIETE D'EXPLOITATION DE PRODUITS POUR LES INDUSTRIES CHIMIQUES SEPPIC (FR) 2022-02-15 US disclosed
US-11248156-B2 Borehole fluid with a thiamine-based shale inhibitor HALLIBURTON ENERGY SERVICES, INC. (US) 2022-02-15 US disclosed
US-20210338633-A1 METHOD FOR EVALUATING THE ABILITY OF A COMPOSITION TO PREVENT MUSCLE DAMAGE AND FATIGUE; FOOD SUPPLEMENT AND DRUG SOCIETE D'EXPLOITATION DE PRODUITS POUR LES INDUSTRIES CHIMIQUES SEPPIC (FR) 2021-11-04 US disclosed
CN-106456484-A External preparation 乐敦制药株式会社 2017-02-22 CN disclosed
US-20130210921-A1 Method for Giving Warmth to Skin ROHTO PHARMACEUTICAL CO., LTD. (JP) 2013-08-15 US disclosed
CN-102232952-A Photoaging inhibitor and skin thinning inhibitor ROHTO PHARMA 2011-11-09 CN disclosed
US-20110027326-A1 External Composition for Skin ROHTO PHARMACEUTICAL CO., LTD. (JP) 2011-02-03 US disclosed
EP-2269652-A1 COMPOSITION FOR EXTERNAL APPLICATION TO SKIN Rohto Pharmaceutical Co., Ltd. (JP) 2011-01-05 EP disclosed
US-20100209364-A1 Emulsified Composition ROHTO PHARMACEUTICAL CO., LTD. (JP) 2010-08-19 US disclosed
US-20100021405-A1 EXTERNAL PREPARATION FOR SKIN ROHTO PHARMACEUTICAL CO., LTD. (JP) 2010-01-28 US disclosed
US-20090186358-A1 Pathway Analysis of Cell Culture Phenotypes and Uses Thereof WYETH (US) 2009-07-23 US disclosed
US-20080207560-A1 Composition For External Use ROHTO PHARMACEUTICAL CO., LTD. (JP) 2008-08-28 US disclosed
EP-1849481-A1 COMPOSITION FOR EXTERNAL USE ROHTO PHARMACEUTICAL CO., LTD. (JP) 2007-10-31 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-11246853-B2 Method for evaluating the ability of a composition to prevent muscle damage and fatigue; food supplement and drug GYS1, PYGM, MYOF HSP90AA1 2398/4885LMNA 1680/4885TKT 3096/4885
US-20210338633-A1 METHOD FOR EVALUATING THE ABILITY OF A COMPOSITION TO PREVENT MUSCLE DAMAGE AND FATIGUE; FOOD SUPPLEMENT AND DRUG PYGM, TNNC1, GYS1 HSP90AA1 600/4885LMNA 369/4885TKT 3160/4885

“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.