Fluciclatide

This drug entry is a stub and has not been fully annotated. It is scheduled to be annotated soon.

Identification

Generic Name
Fluciclatide
DrugBank Accession Number
DB14842
Background

Fluciclatide, an investigational radiotracer intended for PET imaging, was under investigation in clinical trials NCT00565721 and NCT01961583 to evaluate its ability to detect tumors and angiogenesis. The conditions targeted by [18F]Fluciclatide in these studies include high-grade glioma, lung cancer, and kidney neoplasms

Type
Small Molecule
Groups
Investigational
Structure
Weight
Average: 1816.02
Monoisotopic: 1814.7325222
Chemical Formula
C75H115FN18O27S3
Synonyms
Not Available
External IDs
  • AH-111585

Pharmacology

Indication

Not Available

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Contraindications & Blackbox Warnings
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Pharmacodynamics

Not Available

Mechanism of action
Not Available
Absorption

Not Available

Volume of distribution

Not Available

Protein binding

Not Available

Metabolism
Not Available
Route of elimination

Not Available

Half-life

Not Available

Clearance

Not Available

Adverse Effects
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Toxicity

Not Available

Pathways
Not Available
Pharmacogenomic Effects/ADRs
Not Available

Interactions

Drug Interactions
This information should not be interpreted without the help of a healthcare provider. If you believe you are experiencing an interaction, contact a healthcare provider immediately. The absence of an interaction does not necessarily mean no interactions exist.
Not Available
Food Interactions
Not Available

Categories

Drug Categories
Classification
Not classified
Affected organisms
Not Available

Chemical Identifiers

UNII
UQ6CV583Q3
CAS number
879894-00-5
InChI Key
VXFFXZSNVKXXIB-XVUFQIMXSA-N
InChI
InChI=1S/C75H115FN18O27S3/c76-52-13-11-51(12-14-52)39-87-121-45-65(100)83-19-23-113-27-31-117-34-36-118-35-33-116-30-26-112-22-18-82-64(99)44-120-43-62(97)80-15-5-4-9-54-70(106)93-58-47-123-124-48-59(94-72(108)56(38-67(102)103)89-61(96)40-86-68(104)53(90-73(58)109)10-6-16-85-75(78)79)74(110)91-55(37-50-7-2-1-3-8-50)71(107)92-57(46-122-49-66(101)88-54)69(105)84-20-24-114-28-32-115-29-25-111-21-17-81-63(98)42-119-41-60(77)95/h1-3,7-8,11-14,39,53-59H,4-6,9-10,15-38,40-49H2,(H2,77,95)(H,80,97)(H,81,98)(H,82,99)(H,83,100)(H,84,105)(H,86,104)(H,88,101)(H,89,96)(H,90,109)(H,91,110)(H,92,107)(H,93,106)(H,94,108)(H,102,103)(H4,78,79,85)/b87-39+/t53-,54-,55-,56?,57-,58-,59-/m0/s1
IUPAC Name
2-[(1R,4S,10R,13S,16R,19S,25S)-13-benzyl-25-(3-carbamimidamidopropyl)-10-({2-[2-(2-{2-[2-(carbamoylmethoxy)acetamido]ethoxy}ethoxy)ethoxy]ethyl}carbamoyl)-4-{4-[2-({[17-(2-{[(E)-[(4-fluorophenyl)methylidene]amino]oxy}acetamido)-3,6,9,12,15-pentaoxaheptadecan-1-yl]carbamoyl}methoxy)acetamido]butyl}-3,6,12,15,18,21,24,27-octaoxo-8,29,30-trithia-2,5,11,14,17,20,23,26-octaazabicyclo[14.11.4]hentriacontan-19-yl]acetic acid
SMILES
NC(=O)COCC(=O)NCCOCCOCCOCCNC(=O)[C@@H]1CSCC(=O)N[C@@H](CCCCNC(=O)COCC(=O)NCCOCCOCCOCCOCCOCCNC(=O)CO\N=C\C2=CC=C(F)C=C2)C(=O)N[C@H]2CSSC[C@H](NC(=O)[C@H](CC(O)=O)NC(=O)CNC(=O)[C@H](CCCNC(N)=N)NC2=O)C(=O)N[C@@H](CC2=CC=CC=C2)C(=O)N1

References

General References
Not Available
Not Available

Clinical Trials

Clinical Trials
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PhaseStatusPurposeConditionsCountStart DateWhy Stopped100+ additional columns
2CompletedDiagnosticBreast Cancer / Head And Neck Cancer / High Grade Glioma (HGG) / Lung Cancer / Renal Cell Carcinoma (RCC) / Sarcomas / Solid Tumors1somestatusstop reasonjust information to hide
2CompletedDiagnosticHead And Neck Cancer / High Grade Glioma (HGG) / Lung Cancer / Melanoma / Sarcomas1somestatusstop reasonjust information to hide
2TerminatedDiagnosticRenal Cell Carcinoma (RCC)1somestatusstop reasonjust information to hide
2TerminatedDiagnosticRenal Neoplasms1somestatusstop reasonjust information to hide
2WithdrawnDiagnosticMonoclonal Gammopathy of Undetermined Significance (MGUS) / Multiple Myeloma (MM) / Smoldering Multiple Myeloma (SMM)1somestatusstop reasonjust information to hide

Pharmacoeconomics

Manufacturers
Not Available
Packagers
Not Available
Dosage Forms
Not Available
Prices
Not Available
Patents
Not Available

Properties

State
Not Available
Experimental Properties
Not Available
Predicted Properties
PropertyValueSource
Water Solubility0.0858 mg/mLALOGPS
logP-0.25ALOGPS
logP-11Chemaxon
logS-4.3ALOGPS
pKa (Strongest Acidic)3.51Chemaxon
pKa (Strongest Basic)11.87Chemaxon
Physiological Charge0Chemaxon
Hydrogen Acceptor Count31Chemaxon
Hydrogen Donor Count18Chemaxon
Polar Surface Area634.48 Å2Chemaxon
Rotatable Bond Count56Chemaxon
Refractivity455.28 m3·mol-1Chemaxon
Polarizability188.7 Å3Chemaxon
Number of Rings4Chemaxon
Bioavailability0Chemaxon
Rule of FiveNoChemaxon
Ghose FilterNoChemaxon
Veber's RuleNoChemaxon
MDDR-like RuleYesChemaxon
Predicted ADMET Features
Not Available

Spectra

Mass Spec (NIST)
Not Available
Spectra
Not Available
Chromatographic Properties
Collision Cross Sections (CCS)
Not Available

Drug created at May 20, 2019 14:30 / Updated at September 18, 2024 01:28